This document describes the embryology and anatomy of the kidney. It discusses how the kidney develops from the intermediate mesoderm through the pronephros, mesonephros and metanephros stages. The metanephros forms the permanent kidney, with nephrons developing from the interaction of the ureteric bud and metanephric mesenchyme. The document also describes the positioning of the kidneys in the retroperitoneum and their blood supply, as well as the anatomy of the kidney including dimensions, surfaces, borders, poles and surrounding structures.
The document provides information on the surgical anatomy of the kidney and ureter. It discusses the embryology, gross anatomy including orientation and position of the kidneys. It describes the microscopic anatomy including the nephron. It details the coverings of the kidney including the fibrous capsule, perinephric fat, Gerota's fascia and paranephric fat. It outlines the relations of the kidney to surrounding structures like ribs, diaphragm and pleura. It also discusses the blood supply, lymphatic drainage and nerve supply of the kidneys.
This document provides an overview of the embryology, anatomy, and physiology of the ureter. It discusses the embryonic development of the ureter from the ureteric bud. Anatomically, it describes the course, relations, blood supply, innervation, and sites of narrowing of the ureter. Physiologically, it explains the electrical and contractile properties of ureteral smooth muscle cells, the generation and propagation of action potentials, the role of neurotransmitters and second messengers in contraction, and the mechanical properties and pressure-length relationships of the ureter. The nervous system is noted to have a modulatory rather than essential role in ureteral peristalsis.
This document discusses the normal anatomy of the male and female urethra and various pathologies that can affect the urethra, as seen on medical imaging. For the male urethra, it describes the anatomy in detail and covers acquired inflammatory diseases like gonorrhea and nonspecific urethritis. It also discusses strictures, calculi, condyloma, and other conditions. For the female urethra, it briefly outlines the anatomy and mentions acquired urethral diverticula. Various imaging techniques for evaluating the urethra are also reviewed, including retrograde urethrography, ultrasonography, and others.
This document discusses various congenital anomalies of the genitourinary system, including anomalies related to position (pelvic and ectopic kidneys), form (horseshoe kidney, pancake kidney, crossed renal ectopia), number (unilateral/bilateral renal agenesis, supernumerary kidney, duplex collecting system), and development of specific structures (ureterocele, congenital megacalices, megaureter). It provides detailed descriptions and examples of imaging findings for each anomaly. The goal is to help readers learn as much as possible about congenital anomalies to facilitate successful management.
This document discusses various congenital anomalies of the kidney. It begins by describing bilateral renal agenesis, which is incompatible with life due to the lack of kidneys necessary for waste excretion and amniotic fluid production. Unilateral renal agenesis is also covered, which allows for survival due to having one functioning kidney. Other topics include supernumerary kidneys, anomalies of renal ascent, form and fusion, rotation, and collecting system. Causes, diagnoses, associated anomalies, and clinical implications are described for each congenital kidney anomaly.
Embryonic development of the urogenital systemAsheer Khan
The urogenital system develops from the intermediate mesenchyme. The urinary system develops from the nephrogenic cord, while the genital system develops from the gonadal ridge. Three sets of kidneys develop in embryos - the pronephroi, mesonephroi, and metanephroi. The metanephroi form the permanent kidneys. The kidneys and ureters develop from the ureteric bud and metanephrogenic blastema. Congenital anomalies that can occur include renal agenesis, malrotated kidneys, ectopic kidneys, horseshoe kidneys, and duplications of the urinary tract. The urinary bladder develops mainly from the vesical
The document summarizes the embryology and molecular mechanisms of kidney development. It discusses that the kidney develops from the intermediate mesoderm and progresses through pronephros, mesonephros, and metanephros stages. The ureteric bud invades the metanephric mesenchyme and branches to form the collecting system. GDNF signaling from the metanephric mesenchyme induces branching of the ureteric bud. Defects in genes involved in these signaling pathways, such as PAX2, EYA1, and WT1, can lead to kidney abnormalities. The molecular mechanisms demonstrate the importance of epithelial-mesenchymal interactions in nephrogenesis.
This document provides an overview of the anatomy of the male urethra. It discusses the embryology, parts including the prostatic, membranous, bulbar, and penile urethra. It describes the gross structure, relations, blood supply, innervation and clinical correlations like injuries and strictures. Additionally, it briefly covers the anatomy of the female urethra. The document is intended as an educational guide for medical students and residents in the department of urology.
The document provides information on the surgical anatomy of the kidney and ureter. It discusses the embryology, gross anatomy including orientation and position of the kidneys. It describes the microscopic anatomy including the nephron. It details the coverings of the kidney including the fibrous capsule, perinephric fat, Gerota's fascia and paranephric fat. It outlines the relations of the kidney to surrounding structures like ribs, diaphragm and pleura. It also discusses the blood supply, lymphatic drainage and nerve supply of the kidneys.
This document provides an overview of the embryology, anatomy, and physiology of the ureter. It discusses the embryonic development of the ureter from the ureteric bud. Anatomically, it describes the course, relations, blood supply, innervation, and sites of narrowing of the ureter. Physiologically, it explains the electrical and contractile properties of ureteral smooth muscle cells, the generation and propagation of action potentials, the role of neurotransmitters and second messengers in contraction, and the mechanical properties and pressure-length relationships of the ureter. The nervous system is noted to have a modulatory rather than essential role in ureteral peristalsis.
This document discusses the normal anatomy of the male and female urethra and various pathologies that can affect the urethra, as seen on medical imaging. For the male urethra, it describes the anatomy in detail and covers acquired inflammatory diseases like gonorrhea and nonspecific urethritis. It also discusses strictures, calculi, condyloma, and other conditions. For the female urethra, it briefly outlines the anatomy and mentions acquired urethral diverticula. Various imaging techniques for evaluating the urethra are also reviewed, including retrograde urethrography, ultrasonography, and others.
This document discusses various congenital anomalies of the genitourinary system, including anomalies related to position (pelvic and ectopic kidneys), form (horseshoe kidney, pancake kidney, crossed renal ectopia), number (unilateral/bilateral renal agenesis, supernumerary kidney, duplex collecting system), and development of specific structures (ureterocele, congenital megacalices, megaureter). It provides detailed descriptions and examples of imaging findings for each anomaly. The goal is to help readers learn as much as possible about congenital anomalies to facilitate successful management.
This document discusses various congenital anomalies of the kidney. It begins by describing bilateral renal agenesis, which is incompatible with life due to the lack of kidneys necessary for waste excretion and amniotic fluid production. Unilateral renal agenesis is also covered, which allows for survival due to having one functioning kidney. Other topics include supernumerary kidneys, anomalies of renal ascent, form and fusion, rotation, and collecting system. Causes, diagnoses, associated anomalies, and clinical implications are described for each congenital kidney anomaly.
Embryonic development of the urogenital systemAsheer Khan
The urogenital system develops from the intermediate mesenchyme. The urinary system develops from the nephrogenic cord, while the genital system develops from the gonadal ridge. Three sets of kidneys develop in embryos - the pronephroi, mesonephroi, and metanephroi. The metanephroi form the permanent kidneys. The kidneys and ureters develop from the ureteric bud and metanephrogenic blastema. Congenital anomalies that can occur include renal agenesis, malrotated kidneys, ectopic kidneys, horseshoe kidneys, and duplications of the urinary tract. The urinary bladder develops mainly from the vesical
The document summarizes the embryology and molecular mechanisms of kidney development. It discusses that the kidney develops from the intermediate mesoderm and progresses through pronephros, mesonephros, and metanephros stages. The ureteric bud invades the metanephric mesenchyme and branches to form the collecting system. GDNF signaling from the metanephric mesenchyme induces branching of the ureteric bud. Defects in genes involved in these signaling pathways, such as PAX2, EYA1, and WT1, can lead to kidney abnormalities. The molecular mechanisms demonstrate the importance of epithelial-mesenchymal interactions in nephrogenesis.
This document provides an overview of the anatomy of the male urethra. It discusses the embryology, parts including the prostatic, membranous, bulbar, and penile urethra. It describes the gross structure, relations, blood supply, innervation and clinical correlations like injuries and strictures. Additionally, it briefly covers the anatomy of the female urethra. The document is intended as an educational guide for medical students and residents in the department of urology.
The three kidney systems - pronephros, mesonephros, and metanephros - develop sequentially in humans. The pronephros is rudimentary and nonfunctional, while the mesonephros may function briefly in early fetal development. The metanephros forms the permanent kidneys. It develops from the ureteric bud and metanephric mesoderm, with the bud forming the collecting system and mesoderm forming nephrons. Nephrons continue developing until birth, and urine production begins early in gestation. The kidneys ascend from the pelvis to the abdomen during development. The urinary bladder and urethra also develop from the urogenital sinus and
The document discusses kidney development from the formation of the three germ layers during gastrulation to the development of the pronephros, mesonephros, and metanephros. It describes how the intermediate mesoderm forms the nephrogenic cord which develops into the metanephros. The ureteric bud branches to form the collecting system and induces nephron formation from the surrounding metanephric mesenchyme. Congenital anomalies of kidney development including anomalies of number, ascent, form and fusion, rotation, and the collecting system and vasculature are also summarized.
This document provides an overview of the anatomy of the retroperitoneum and kidney development. It describes the boundaries and contents of the retroperitoneum, including fascial layers like Gerota fascia. It discusses the early development of the pronephros and mesonephros kidneys before focusing on the metanephros, the definitive kidney. The document is intended as a reference for medical students and residents in learning retroperitoneal anatomy and kidney embryology.
This document discusses the embryological development of the urinary and genital systems from the mesoderm. It describes the formation and regression of the three kidney systems - pronephros, mesonephros, and metanephros. The metanephros (permanent kidney) develops from the ureteric bud and metanephric mesoderm. Molecular signals between the bud and mesoderm regulate nephron formation. Genes involved and some clinical correlates of kidney defects are also mentioned.
The document summarizes the stages of kidney development from the intermediate mesoderm to the metanephros stage. It describes the development of the nephron, collecting system, and vasculature. Key signaling pathways involved include WT1, GDNF-RET, BMP, FGF, PAX-2, and WNT-4. Stages include pronephros regression by 5 weeks, mesonephros functioning until metanephros at 5 weeks, and ascent of kidneys to lumbar region between 6-9 weeks. Applied aspects discussed include anomalies in kidney number, position, ascent, and polycystic kidney disease.
This document provides an overview of kidney and ureter embryology and surgical anatomy. It discusses the development of the pronephros, mesonephros and metanephros. The mesonephric duct gives rise to the ureteric bud which develops into the collecting system. Congenital anomalies including renal agenesis, horseshoe kidney and duplex collecting system are described. The surgical anatomy of the kidneys and their blood supply from the renal arteries is summarized. The relationships of the kidneys to surrounding structures and fascial layers including Gerota's fascia are also outlined.
The document describes the retroperitoneal space and structures contained within it. The retroperitoneal space lies between the peritoneum and posterior abdominal wall from the diaphragm to the pelvic floor. It contains various organs like the kidneys, ureters, parts of the colon, pancreas and more. The space is further divided into the anterior pararenal space, perirenal space, and posterior pararenal space by fascial planes. The document outlines the boundaries and structures of the retroperitoneal space.
This document provides an overview of the anatomy and physiology of the urinary bladder. It describes the bladder's location, shape, relations to surrounding structures, blood supply, innervation, and histological layers. Key points include that the bladder is a hollow, retroperitoneal organ located in the pelvis that stores and empties urine. It has multiple ligaments attaching it to surrounding structures. The document also summarizes the normal filling and voiding functions of the lower urinary tract and the roles of the detrusor muscle, urethral sphincter, and neural control.
This document discusses ectopic ureters and ureteroceles. Some key points:
1. Ectopic ureters and ureteroceles are congenital abnormalities that occur due to abnormal development of the ureter and urinary tract.
2. Clinical presentations can include urinary tract infections, incontinence, pain, and obstruction. Evaluation involves ultrasound, voiding cystourethrogram, nuclear scans, and possibly MRI.
3. Management depends on factors like obstruction, reflux, and renal function. Options include observation, acute decompression, definitive surgery like reimplantation, and in some cases total reconstruction or upper pole nephrectomy. Complications
The document discusses renal vascular anatomy and its implications for surgery. It notes that the renal arteries typically enter the kidney through the hilum and branch into segmental arteries that do not anastomose. It also describes variations such as accessory renal arteries. The segmental arteries further branch within the kidney and an avascular plane exists between anterior and posterior branches. Venous drainage parallels the arterial supply. Imaging like CTA can accurately map the vasculature preoperatively to aid surgery. Understanding variations and collateral circulation is important for procedures like donor nephrectomy.
This document discusses ureteroceles, which are cystic dilations of the terminal ureter. It describes classifications of ureteroceles and their embryology. Diagnosis can be made through prenatal ultrasound or MRI showing hydronephrosis and the intravesical cyst. Evaluation involves ultrasound, intravenous pyelography, voiding cystourethrography, and nuclear scans. Management is individualized and may include prenatal decompression or postnatal surgical procedures to preserve renal function, eliminate infection/obstruction/reflux, and maintain continence. Treatment aims to minimize morbidity while meeting these goals.
Development and congenital anomalies of urogenital systemJayeta Choudhury
The document discusses development and congenital anomalies of the urogenital system. It begins by explaining how the urinary and genital systems develop from a common ridge in the embryo and open into a common channel, the cloaca. It then describes the development of the three kidney systems - pronephros, mesonephros, and metanephros. Next, it discusses anomalies that can occur, including anomalies of form (agenesis, hypoplasia, supernumerary kidneys), position (malrotation, ectopic kidneys), and fusion (horseshoe kidney, crossed fused renal ectopia, cake kidney). It concludes by covering congenital cystic renal diseases and the approach to differentiating them using ultrasound findings
The document discusses the anatomy and embryology of the prostate gland. It describes the prostate's shape, size, surfaces, lobes, capsule, fascia, venous and arterial supply, pelvic plexus, lymphatic drainage and embryological development. The prostate develops from the urogenital sinus in males through androgen-dependent budding and condensation of epithelial cells. Its anatomy includes zones, glandular and fibromuscular composition, and relationship to surrounding structures like the bladder neck.
Megaureter ppt. Types, pathophysiology, evaluation and management.Hussain Shah
- Megaureter (MGU) is defined as a ureteral diameter greater than 7 mm. MGU can be classified based on its cause as refluxing, obstructed, both refluxing and obstructed, or nonrefluxing and nonobstructed.
- MGU is a common finding in neonates referred for urologic evaluation and accounts for up to 23% of cases of urinary tract dilatation seen on prenatal ultrasound.
- Evaluation of MGU involves ultrasound to assess anatomy and severity, VCUG to check for reflux, renal scan to evaluate function, and potentially MRI urography.
- Management depends on etiology but
This document provides a summary of kidney anatomy and ultrasound appearance in 3 paragraphs:
The kidneys have a complex internal architecture visible on ultrasound, including echogenic renal sinuses containing vessels and collecting systems. Each kidney contains lobes with a medullary pyramid, cortex, and vessels. In adults there are typically 11 pyramids and 9 calices. The kidneys have a slightly ovoid shape viewed longitudinally from the front or back. Normal kidney size varies by individual but is around 10.5-11cm on average.
Ultrasound is used to image the kidneys using curvilinear probes from various approaches. The native kidneys are best seen from the back using adjacent organs as an acoustic window.
This document provides information about retrocaval ureter, including its etiology, diagnosis, and management. Retrocaval ureter is a rare congenital anomaly where the ureter passes behind the inferior vena cava. It occurs due to persistence of the subcardinal veins during embryonic development. Clinical presentations include flank pain, hematuria, urinary tract infections, and urolithiasis. Diagnosis involves imaging tests like intravenous urogram, CT urography, and renography. Surgical management includes open or laparoscopic pyeloplasty to reposition the ureter anterior to the inferior vena cava. Preserving the retrocaval ureter segment may be
1. Urodynamics describes physiological tests used to investigate lower urinary tract function, with cystometry being the most important test. Cystometry measures pressure-volume relationships during bladder filling and voiding.
2. Urodynamics tests the storage and evacuation of urine to reproduce a patient's symptoms and determine their underlying cause. Tests include cystometry, uroflowmetry, and pressure-flow studies.
3. Urodynamics is indicated for incontinence, suspected outflow obstruction, neurogenic bladder dysfunction, and children with voiding issues. It helps characterize detrusor and bladder outlet function and diagnose neuropathies.
This document provides information about ultrasound use in urology. It discusses the history of ultrasound in urology from 1963 onwards. It then covers basic ultrasound principles including modes, probes, imaging planes and documentation. Applications to the kidney, bladder, prostate and testes are described. Common abnormalities like hydronephrosis, cysts, masses and infections are outlined. In summary, the document is an overview of ultrasound techniques and their use in evaluating the urinary tract and common urologic conditions.
The document summarizes the development of the pancreas. It notes that the pancreas develops from two buds that arise from the posterior foregut and later fuse. After fusion, the three main cell types of the pancreas - acinar, ductal, and islet cells - differentiate. The development of the ductal system is also described. Key transcription factors involved in pancreatic development like Pdx1 and Hlxb9 are discussed. Some congenital anomalies of the pancreas including annular pancreas and pancreatic divisum are then outlined, describing their presentations, diagnoses, and management approaches.
1. The document describes the development of the urinary and genital systems from the intermediate mesoderm.
2. Three kidney systems form sequentially - the pronephros, mesonephros, and metanephros. The metanephros persists to form the permanent kidneys.
3. The kidneys ascend from the pelvic region to the abdomen during development. The urinary bladder and urethra develop from the urogenital sinus which divides the cloaca.
The kidney develops from intermediate mesoderm along the posterior abdominal wall. It progresses through three stages - the pronephros, mesonephros and metanephros. The metanephros forms the permanent kidney. The ureteric bud induces metanephric mesenchyme to form nephrons. Nephrogenesis is complete by birth. The kidney ascends from the pelvis to the abdomen during development. Genetic factors like WT1 regulate kidney development. Anomalies can occur in kidney number, position, rotation and ascent during embryogenesis.
The three kidney systems - pronephros, mesonephros, and metanephros - develop sequentially in humans. The pronephros is rudimentary and nonfunctional, while the mesonephros may function briefly in early fetal development. The metanephros forms the permanent kidneys. It develops from the ureteric bud and metanephric mesoderm, with the bud forming the collecting system and mesoderm forming nephrons. Nephrons continue developing until birth, and urine production begins early in gestation. The kidneys ascend from the pelvis to the abdomen during development. The urinary bladder and urethra also develop from the urogenital sinus and
The document discusses kidney development from the formation of the three germ layers during gastrulation to the development of the pronephros, mesonephros, and metanephros. It describes how the intermediate mesoderm forms the nephrogenic cord which develops into the metanephros. The ureteric bud branches to form the collecting system and induces nephron formation from the surrounding metanephric mesenchyme. Congenital anomalies of kidney development including anomalies of number, ascent, form and fusion, rotation, and the collecting system and vasculature are also summarized.
This document provides an overview of the anatomy of the retroperitoneum and kidney development. It describes the boundaries and contents of the retroperitoneum, including fascial layers like Gerota fascia. It discusses the early development of the pronephros and mesonephros kidneys before focusing on the metanephros, the definitive kidney. The document is intended as a reference for medical students and residents in learning retroperitoneal anatomy and kidney embryology.
This document discusses the embryological development of the urinary and genital systems from the mesoderm. It describes the formation and regression of the three kidney systems - pronephros, mesonephros, and metanephros. The metanephros (permanent kidney) develops from the ureteric bud and metanephric mesoderm. Molecular signals between the bud and mesoderm regulate nephron formation. Genes involved and some clinical correlates of kidney defects are also mentioned.
The document summarizes the stages of kidney development from the intermediate mesoderm to the metanephros stage. It describes the development of the nephron, collecting system, and vasculature. Key signaling pathways involved include WT1, GDNF-RET, BMP, FGF, PAX-2, and WNT-4. Stages include pronephros regression by 5 weeks, mesonephros functioning until metanephros at 5 weeks, and ascent of kidneys to lumbar region between 6-9 weeks. Applied aspects discussed include anomalies in kidney number, position, ascent, and polycystic kidney disease.
This document provides an overview of kidney and ureter embryology and surgical anatomy. It discusses the development of the pronephros, mesonephros and metanephros. The mesonephric duct gives rise to the ureteric bud which develops into the collecting system. Congenital anomalies including renal agenesis, horseshoe kidney and duplex collecting system are described. The surgical anatomy of the kidneys and their blood supply from the renal arteries is summarized. The relationships of the kidneys to surrounding structures and fascial layers including Gerota's fascia are also outlined.
The document describes the retroperitoneal space and structures contained within it. The retroperitoneal space lies between the peritoneum and posterior abdominal wall from the diaphragm to the pelvic floor. It contains various organs like the kidneys, ureters, parts of the colon, pancreas and more. The space is further divided into the anterior pararenal space, perirenal space, and posterior pararenal space by fascial planes. The document outlines the boundaries and structures of the retroperitoneal space.
This document provides an overview of the anatomy and physiology of the urinary bladder. It describes the bladder's location, shape, relations to surrounding structures, blood supply, innervation, and histological layers. Key points include that the bladder is a hollow, retroperitoneal organ located in the pelvis that stores and empties urine. It has multiple ligaments attaching it to surrounding structures. The document also summarizes the normal filling and voiding functions of the lower urinary tract and the roles of the detrusor muscle, urethral sphincter, and neural control.
This document discusses ectopic ureters and ureteroceles. Some key points:
1. Ectopic ureters and ureteroceles are congenital abnormalities that occur due to abnormal development of the ureter and urinary tract.
2. Clinical presentations can include urinary tract infections, incontinence, pain, and obstruction. Evaluation involves ultrasound, voiding cystourethrogram, nuclear scans, and possibly MRI.
3. Management depends on factors like obstruction, reflux, and renal function. Options include observation, acute decompression, definitive surgery like reimplantation, and in some cases total reconstruction or upper pole nephrectomy. Complications
The document discusses renal vascular anatomy and its implications for surgery. It notes that the renal arteries typically enter the kidney through the hilum and branch into segmental arteries that do not anastomose. It also describes variations such as accessory renal arteries. The segmental arteries further branch within the kidney and an avascular plane exists between anterior and posterior branches. Venous drainage parallels the arterial supply. Imaging like CTA can accurately map the vasculature preoperatively to aid surgery. Understanding variations and collateral circulation is important for procedures like donor nephrectomy.
This document discusses ureteroceles, which are cystic dilations of the terminal ureter. It describes classifications of ureteroceles and their embryology. Diagnosis can be made through prenatal ultrasound or MRI showing hydronephrosis and the intravesical cyst. Evaluation involves ultrasound, intravenous pyelography, voiding cystourethrography, and nuclear scans. Management is individualized and may include prenatal decompression or postnatal surgical procedures to preserve renal function, eliminate infection/obstruction/reflux, and maintain continence. Treatment aims to minimize morbidity while meeting these goals.
Development and congenital anomalies of urogenital systemJayeta Choudhury
The document discusses development and congenital anomalies of the urogenital system. It begins by explaining how the urinary and genital systems develop from a common ridge in the embryo and open into a common channel, the cloaca. It then describes the development of the three kidney systems - pronephros, mesonephros, and metanephros. Next, it discusses anomalies that can occur, including anomalies of form (agenesis, hypoplasia, supernumerary kidneys), position (malrotation, ectopic kidneys), and fusion (horseshoe kidney, crossed fused renal ectopia, cake kidney). It concludes by covering congenital cystic renal diseases and the approach to differentiating them using ultrasound findings
The document discusses the anatomy and embryology of the prostate gland. It describes the prostate's shape, size, surfaces, lobes, capsule, fascia, venous and arterial supply, pelvic plexus, lymphatic drainage and embryological development. The prostate develops from the urogenital sinus in males through androgen-dependent budding and condensation of epithelial cells. Its anatomy includes zones, glandular and fibromuscular composition, and relationship to surrounding structures like the bladder neck.
Megaureter ppt. Types, pathophysiology, evaluation and management.Hussain Shah
- Megaureter (MGU) is defined as a ureteral diameter greater than 7 mm. MGU can be classified based on its cause as refluxing, obstructed, both refluxing and obstructed, or nonrefluxing and nonobstructed.
- MGU is a common finding in neonates referred for urologic evaluation and accounts for up to 23% of cases of urinary tract dilatation seen on prenatal ultrasound.
- Evaluation of MGU involves ultrasound to assess anatomy and severity, VCUG to check for reflux, renal scan to evaluate function, and potentially MRI urography.
- Management depends on etiology but
This document provides a summary of kidney anatomy and ultrasound appearance in 3 paragraphs:
The kidneys have a complex internal architecture visible on ultrasound, including echogenic renal sinuses containing vessels and collecting systems. Each kidney contains lobes with a medullary pyramid, cortex, and vessels. In adults there are typically 11 pyramids and 9 calices. The kidneys have a slightly ovoid shape viewed longitudinally from the front or back. Normal kidney size varies by individual but is around 10.5-11cm on average.
Ultrasound is used to image the kidneys using curvilinear probes from various approaches. The native kidneys are best seen from the back using adjacent organs as an acoustic window.
This document provides information about retrocaval ureter, including its etiology, diagnosis, and management. Retrocaval ureter is a rare congenital anomaly where the ureter passes behind the inferior vena cava. It occurs due to persistence of the subcardinal veins during embryonic development. Clinical presentations include flank pain, hematuria, urinary tract infections, and urolithiasis. Diagnosis involves imaging tests like intravenous urogram, CT urography, and renography. Surgical management includes open or laparoscopic pyeloplasty to reposition the ureter anterior to the inferior vena cava. Preserving the retrocaval ureter segment may be
1. Urodynamics describes physiological tests used to investigate lower urinary tract function, with cystometry being the most important test. Cystometry measures pressure-volume relationships during bladder filling and voiding.
2. Urodynamics tests the storage and evacuation of urine to reproduce a patient's symptoms and determine their underlying cause. Tests include cystometry, uroflowmetry, and pressure-flow studies.
3. Urodynamics is indicated for incontinence, suspected outflow obstruction, neurogenic bladder dysfunction, and children with voiding issues. It helps characterize detrusor and bladder outlet function and diagnose neuropathies.
This document provides information about ultrasound use in urology. It discusses the history of ultrasound in urology from 1963 onwards. It then covers basic ultrasound principles including modes, probes, imaging planes and documentation. Applications to the kidney, bladder, prostate and testes are described. Common abnormalities like hydronephrosis, cysts, masses and infections are outlined. In summary, the document is an overview of ultrasound techniques and their use in evaluating the urinary tract and common urologic conditions.
The document summarizes the development of the pancreas. It notes that the pancreas develops from two buds that arise from the posterior foregut and later fuse. After fusion, the three main cell types of the pancreas - acinar, ductal, and islet cells - differentiate. The development of the ductal system is also described. Key transcription factors involved in pancreatic development like Pdx1 and Hlxb9 are discussed. Some congenital anomalies of the pancreas including annular pancreas and pancreatic divisum are then outlined, describing their presentations, diagnoses, and management approaches.
1. The document describes the development of the urinary and genital systems from the intermediate mesoderm.
2. Three kidney systems form sequentially - the pronephros, mesonephros, and metanephros. The metanephros persists to form the permanent kidneys.
3. The kidneys ascend from the pelvic region to the abdomen during development. The urinary bladder and urethra develop from the urogenital sinus which divides the cloaca.
The kidney develops from intermediate mesoderm along the posterior abdominal wall. It progresses through three stages - the pronephros, mesonephros and metanephros. The metanephros forms the permanent kidney. The ureteric bud induces metanephric mesenchyme to form nephrons. Nephrogenesis is complete by birth. The kidney ascends from the pelvis to the abdomen during development. Genetic factors like WT1 regulate kidney development. Anomalies can occur in kidney number, position, rotation and ascent during embryogenesis.
1. The urinary and genital systems develop from a common intermediate mesoderm and initially share a common cavity called the cloaca.
2. The kidneys develop through three successive stages - the pronephros, mesonephros, and metanephros - with the metanephros forming the permanent kidneys.
3. The ureters develop from the mesonephric ducts and later join the bladder, which develops from the urogenital sinus. The bladder remains connected to the umbilicus by the urachus in early development.
The urinary system develops from the intermediate mesoderm and includes three successive kidney structures - the pronephros, mesonephros, and metanephros. The metanephros forms the permanent kidneys. It develops from the ureteric bud penetrating the metanephric mesoderm and inducing nephron formation. The kidneys ascend into the abdominal cavity during development and become fully functional by 12 weeks of gestation. The urinary bladder and urethra also develop from the intermediate mesoderm through partitioning of the cloaca.
This document discusses renal embryology and kidney development. It begins by outlining the three main stages of kidney development - the pronephros, mesonephros, and metanephros. It then provides details on the development of each of these stages, including how they form from the intermediate mesoderm and their roles. The document also discusses genetic factors involved in kidney differentiation, abnormal kidney development including anomalies in number and position, and applied aspects such as hereditary polycystic kidneys.
• Describe the development of gonads (indifferent stage) and sex determination.
• Describe the development of testis and ovaries and the related structures.
• Describe the development of the genital ducts.
• Describe the development of male and female glands.
• Describe the development of the male and female external genitalia. • Discuss the related developmental anomalies.
• Both the urinary &reproductive systems are closely related (structurally & developmentally)
• Urogenital system develop from the intermediate mesoderm
• Urogenital ridge is a longitudinal elevation of the mesoderm lateral to the dorsal aorta
• Nephrogenic cord (ridge) develop in the urogenital ridge
• Gives rise to part of the urinary system
• Genital (gonadal) ridge develop close to the nephrogenic cord
• Gives rise to part of the genital system
The kidneys develop from intermediate mesoderm and progress through three stages - pronephros, mesonephros and metanephros. The metanephros forms the permanent kidneys. It develops from interaction between the ureteric bud and metanephric mesenchyme. Nephrons develop from mesenchyme and the collecting system from the ureteric bud. The kidneys ascend during development due to body growth. Common anomalies include horseshoe kidney and abnormal rotation or position of the kidneys.
This document summarizes the development of the urinary system and suprarenal gland. It discusses how they both originate from the intermediate mesoderm. It describes the development of the pronephros, mesonephros, and metanephros, which give rise to the permanent kidneys. It also discusses the development of the ureters, bladder, and collecting system from the ureteric bud. Finally, it summarizes how the suprarenal glands develop from mesenchyme and neural crest cells to form the cortex and medulla, respectively.
Development & histology of GIT & clinical considerations by Shapi. MD.pdfShapi. MD
A well summarized presentation on the Basics in the science of the Human Anatomy that'll effectively deliver information in an incredibly remarkable way to the reader.
This document provides an overview of the anatomy of the urinary bladder, including its embryology, gross anatomy, histology, vascular and nerve supply, and surgical considerations. It describes the bladder's location in the pelvis, layers, relationships to surrounding organs, and changes during filling and voiding. Key structures like the trigone and bladder neck are emphasized. Modulators of bladder function from the brain and spinal cord through peripheral nerves are reviewed.
The document describes the embryological development of the urinary tract and various congenital anomalies that can occur. It discusses the formation of the urogenital sinus, cloaca, trigone, and bladder. It then categorizes and describes anomalies in number (agenesis, duplication), size (hypoplasia, megacystis), and form (exstrophy epispadias complex, diverticula, fistulas). Specific anomalies like complete duplication, sagittal septum, and classic bladder exstrophy are explained in detail.
UROGENITAL SYSTEM LECTURE SLIDES for medical studentsymusa1334
The document summarizes the development of the urogenital system from the intermediate mesenchyme. It describes how the urinary system begins with the formation of the pronephros, mesonephros, and metanephros kidneys. The metanephros becomes the permanent kidneys through the interaction of the ureteric bud and metanephric mesenchyme. The kidneys ascend into the abdomen as the embryo grows. The ureters, bladder, and urethra also develop to complete the urinary system. Common abnormalities like renal agenesis and horseshoe kidney are also discussed.
This document discusses phimosis and circumcision. It provides background information on phimosis including definitions, types, epidemiology, embryology, anatomy, etiology, pathophysiology, prognosis, history and physical examination. It also discusses the medical and surgical treatment of phimosis, including conservative surgical alternatives and conventional male circumcision. The document is authored by multiple professors and assistant professors from the Department of Urology at Govt Royapettah Hospital and Kilpauk Medical College in Chennai, India.
This document discusses abnormalities of the female urogenital tract, including their embryological development and classification. It notes that the urinary and genital systems develop from a common intermediate mesoderm and cloaca. Abnormalities can include defects in the development of the uterus, vagina, or urogenital sinus. Evaluation involves history, physical exam, imaging like ultrasound and MRI, and hormonal/genetic testing. Classification systems relate to the level of confluence between the urethra and vagina. Treatment is multidisciplinary and involves gender assignment and surgical reconstruction if needed.
This document discusses the diagnosis and management of posterior urethral valves. It begins by defining PUV as a congenital obstructing membrane in the urethra that causes lower urinary tract obstruction. PUV is the most common cause of urinary outflow obstruction in pediatric patients and can lead to renal failure if not treated. The document then covers the pathophysiology, prenatal diagnosis, postnatal evaluation and various treatment approaches for PUV including endoscopic valve ablation, vesicostomy, and nephroureterectomy in severe cases.
Bladder anatomy & embryology of bladder and urethra-convertedGovtRoyapettahHospit
This document discusses the developmental anatomy of the bladder and urethra. It begins with an introduction to the development of the urinary and reproductive systems during the first and second trimesters of pregnancy. It then describes the formation of the bladder, ureters, urethra and trigone from the urogenital sinus. It discusses normal development and abnormalities that can occur, along with clinical correlations for conditions like vesicoureteral reflux and bladder exstrophy. The document is intended to provide an overview of normal bladder and urethra development as well as abnormalities that can occur.
Development of kidney, its function and kftAshikMajumder1
This document discusses the development and functional anatomy of the kidney. It begins by describing the embryonic development of the kidney through the pronephros, mesonephros, and metanephros stages. It then discusses the structure and function of the nephron, including filtration in the glomerulus and reabsorption/secretion in the tubules. Finally, it covers kidney function tests such as creatinine clearance and serum creatinine levels, which are used to evaluate kidney function.
This document describes the renogram procedure. It provides details on:
- The radiopharmaceuticals used, including 99mTc-DTPA, 99mTc-MAG3, and 99mTc-DMSA
- How the procedure is performed, including patient preparation, image acquisition, and time-activity curve analysis
- The roles of the radiopharmaceuticals in evaluating renal blood flow, glomerular filtration rate, and renal handling and excretion
- Factors that can affect the procedure such as hydration, medications, and kidney positioning
This document provides information about an X-ray KUB (kidneys, ureters, bladder) exam performed by the Department of Urology at Govt Royapettah Hospital and Kilpauk Medical College in Chennai, India. It lists the moderators and their qualifications. It then discusses the history of X-rays, how they are produced, standard views, and how to systematically read an X-ray KUB. It describes how to assess technical quality and what to look for, including renal calcifications which are most commonly due to kidney stones. It also discusses mimics of urinary calcifications like gallstones.
This document provides information about a KUB (kidney, ureter, bladder) x-ray performed at the Department of Urology, Government Royapettah Hospital and Kilpauk Medical College in Chennai. It lists the professors and assistant professors in the department and provides details on the history, physics, techniques, anatomical landmarks, disorders, and interpretations of renal calculi, ureter, bladder, and other findings that can be seen on a KUB x-ray.
This document describes a voiding cystourethrogram (VCUG) conducted by the Department of Urology at GRH and KMC in Chennai, India. It lists the professors and assistant professors moderating the VCUG. The document provides details on the indications, techniques, and pediatric applications of VCUGs, focusing on evaluating conditions like vesicoureteral reflux, posterior urethral valves, bladder diverticula, and ectopic ureters. It compares VCUG to nuclear cystography and voiding sonography as diagnostic tools.
The document provides information about urodynamics testing performed at the Department of Urology, Government Royapettah Hospital and Kilpauk Medical College in Chennai. It discusses the professors and assistant professors who moderate the tests. It then describes the purpose and components of urodynamics testing, which involves a series of tests to evaluate urine storage and evacuation. The key components reviewed include uroflowmetry, measurement of post-void residual urine, cystometrogram, pressure flow studies, and videourodynamics. The document provides details on performing each test and interpreting the results.
This document provides an overview of MRI in urology, with a focus on MRI of the prostate. It discusses the moderators and professors of the department of urology. It then covers the basic principles of MRI, including magnetic field strength, radiofrequency pulses, T1/T2 weighting, and contrast agents. Applications of MRI for prostate imaging and prostate cancer detection are described, including T2-weighted imaging, diffusion-weighted imaging, and magnetic resonance spectroscopy. The PIRADS scoring system and assessment of extracapsular extension on MRI are also summarized.
This document provides information about intravenous urography (IVU), including its definition, history, indications, contraindications, technique, phases, and what is evaluated. Some key points:
- IVU involves injecting iodine contrast intravenously and taking x-ray images as it passes through the kidneys, ureters, and bladder. It was introduced in 1929 by American urologist Moses Swick.
- Indications include evaluating for ureteral obstruction, trauma, congenital anomalies, hematuria, infection, or uncontrolled hypertension. Contraindications include contrast allergy and renal impairment.
- The technique involves injecting contrast as a rapid bolus,
This patient presented with anterior urethral stricture and multiple abnormal connections (fistulas) between the prostate gland/urethra and the skin, resulting in urine leakage to the skin. Treatment will require surgical repair of the strictures and closure of all abnormal connections to restore normal urinary flow and continence.
This document provides information about intravenous urography (IVU), including:
- IVU involves injecting contrast media intravenously and imaging the kidneys, ureters, and bladder.
- It has indications like evaluating suspected obstruction, assessing integrity after trauma, and investigating hematuria or infection.
- Contraindications include contrast allergy and renal failure. Advantages include clearly outlining the urinary system, while disadvantages include need for contrast and radiation exposure.
- The document describes the IVU technique, expected timing of images, and what should be evaluated on the images.
- It also covers normal anatomy, types of contrast media, and abnormal findings that could be
This document discusses urinary extravasation, which is when urine leaks out of the urinary tract into other body cavities. It defines two types - superficial and deep extravasation. Superficial extravasation occurs above the perineal membrane and is usually caused by injuries to the penile urethra during instrumentation. Deep extravasation occurs below the perineal membrane due to injuries of the membranous urethra or extraperitoneal bladder from pelvic trauma. Management involves pain relief, antibiotics, suprapubic catheterization, and sometimes surgical exploration and drainage of collections.
This document provides information about urodynamic evaluation of voiding dysfunction. It discusses the history of urodynamics, aims, equipment used including catheters, flowmeters and EMG equipment. It describes how to conduct urodynamic evaluations including uroflowmetry, cystometrogram, and considerations for filling rate and medium. Key points covered are the indications for urodynamics, preparation of patients, types of equipment and how to interpret uroflow curves and cystometrogram measurements.
This document provides information about various tumor markers used in urology, including prostate-specific antigen (PSA) markers for prostate cancer screening and diagnosis, tumor markers for testicular cancer such as alpha-fetoprotein (AFP) and human chorionic gonadotropin (HCG), and urine-based markers for bladder cancer screening like NMP22 and BTA. It also discusses guidelines for PSA screening and interpretation, as well as clinical applications of different tumor markers for diagnosis, prognosis, monitoring treatment response, and detecting recurrence of urological cancers.
This document discusses transitional urology, which involves the planned movement of adolescents and young adults with chronic urological conditions from pediatric to adult-centered care. It provides an overview of common urological conditions seen in transitional urology, including spina bifida, bladder exstrophy, hypospadias, posterior urethral valves, vesicoureteral reflux, and pediatric genitourinary cancers. It also discusses specific issues in transitional urology like urinary tract infections in neurogenic/reconstructed bladders, troubleshooting continent catheterizable channels, risks of malignancy with augmentation cystoplasty, and presentation of BPH and pelvic organ prolapse in patients with neurogenic
This document provides information about retroperitoneal fibrosis (RPF), including its pathogenesis, clinical presentations, investigations, and management. RPF is characterized by extensive fibrosis in the retroperitoneum that can encase the aorta, vena cava, and ureters. Patients typically present with nonspecific symptoms like back pain, but late presentations can include urinary obstruction and vascular complications. Diagnosis is often made using CT or MRI imaging showing soft tissue surrounding retroperitoneal structures. Treatment involves medications like corticosteroids to reduce inflammation or surgical procedures to decompress the urinary system if obstructed.
The document describes urodynamic evaluation (UDE) performed in the Department of Urology at Govt Royapettah Hospital and Kilpauk Medical College in Chennai. It lists the professors and assistant professors in the department and provides an introduction to UDE. It then describes the various components of UDE including uroflowmetry, cystometry, pressure flow studies and videourodynamics. It outlines the procedure for setting up and performing UDE, and analyzes storage and voiding phases and parameters measured.
This document discusses urinary obstruction, including its pathophysiology, causes, effects on renal physiology and function, histological changes, clinical impact, and renal recovery after relief of obstruction. It provides an overview of how urinary obstruction can lead to permanent kidney damage depending on the severity, chronicity, and baseline kidney condition. Both unilateral and bilateral obstruction are examined, along with the triphasic response and changes in renal blood flow, filtration, and tubular transport that occur.
This document describes uroflowmetry - a noninvasive test used to evaluate urine flow. It discusses the normal and abnormal flow patterns seen in uroflowmetry and their clinical significance. Uroflowmetry provides parameters like maximum flow rate, average flow rate and voided volume. It can detect bladder outlet obstruction, detrusor underactivity or overactivity. However, pressure-flow studies are needed to precisely define lower urinary tract function. Uroflowmetry is useful for screening and monitoring treatment response, though invasive therapy should not be based on uroflowmetry alone per AUA guidelines.
Pathophysiology of pneumoperitoneum and complications of laproscopic surgeryGovtRoyapettahHospit
This document provides information about the Department of Urology at Govt Royapettah Hospital and Kilpauk Medical College in Chennai, India. It lists the professors and assistant professors in the department and provides an introduction to laparoscopy. The rest of the document discusses the history of laparoscopy, choices of insufflation gas, physiological effects of pneumoperitoneum, and potential complications of laparoscopy procedures. It provides details on cardiovascular, respiratory, renal, and other organ system effects of increased abdominal pressure during laparoscopy. The document also outlines potential complications from veress needle placement, trocar insertion, insufflation, and electrosurgery and their management.
This document discusses the history and types of endoscopes used in urology. It describes rigid endoscopes which use a series of lenses to transmit images and how the rod lens system improved image quality. Flexible endoscopes transmit images using fiber optic bundles and have the advantage of being able to flex and access different areas. Newer digital endoscopes replace lenses with CCD chips to provide superior quality images electronically. The document outlines the benefits of different endoscope technologies and future trends including 3D imaging and wireless capabilities.
This document discusses various positioning techniques used in urological procedures. It describes the lithotomy, lateral decubitus, prone, supine, and Trendelenburg positions. For each position, it provides details on how to properly position the patient, including flexion angles, padding of pressure points, and risks of nerve injuries if not performed correctly. It aims to ensure patient safety and provide optimal surgical exposure while avoiding iatrogenic injuries during urological procedures.
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Here is the updated list of Top Best Ayurvedic medicine for Gas and Indigestion and those are Gas-O-Go Syp for Dyspepsia | Lavizyme Syrup for Acidity | Yumzyme Hepatoprotective Capsules etc
Osteoporosis - Definition , Evaluation and Management .pdfJim Jacob Roy
Osteoporosis is an increasing cause of morbidity among the elderly.
In this document , a brief outline of osteoporosis is given , including the risk factors of osteoporosis fractures , the indications for testing bone mineral density and the management of osteoporosis
Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Kat...rightmanforbloodline
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
8 Surprising Reasons To Meditate 40 Minutes A Day That Can Change Your Life.pptxHolistified Wellness
We’re talking about Vedic Meditation, a form of meditation that has been around for at least 5,000 years. Back then, the people who lived in the Indus Valley, now known as India and Pakistan, practised meditation as a fundamental part of daily life. This knowledge that has given us yoga and Ayurveda, was known as Veda, hence the name Vedic. And though there are some written records, the practice has been passed down verbally from generation to generation.
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Rasamanikya is a excellent preparation in the field of Rasashastra, it is used in various Kushtha Roga, Shwasa, Vicharchika, Bhagandara, Vatarakta, and Phiranga Roga. In this article Preparation& Comparative analytical profile for both Formulationon i.e Rasamanikya prepared by Kushmanda swarasa & Churnodhaka Shodita Haratala. The study aims to provide insights into the comparative efficacy and analytical aspects of these formulations for enhanced therapeutic outcomes.
Cell Therapy Expansion and Challenges in Autoimmune DiseaseHealth Advances
There is increasing confidence that cell therapies will soon play a role in the treatment of autoimmune disorders, but the extent of this impact remains to be seen. Early readouts on autologous CAR-Ts in lupus are encouraging, but manufacturing and cost limitations are likely to restrict access to highly refractory patients. Allogeneic CAR-Ts have the potential to broaden access to earlier lines of treatment due to their inherent cost benefits, however they will need to demonstrate comparable or improved efficacy to established modalities.
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Despite these headwinds, industry leaders and investors remain confident that cell therapies are poised to address significant unmet need in patients suffering from autoimmune disorders. However, the extent of this impact on the treatment landscape remains to be seen, as the industry rapidly approaches an inflection point.
1. EMBRYOLOGY AND ANATOMY OF
KIDNEY
Dept of Urology
Govt Royapettah Hospital and Kilpauk Medical College
Chennai
1
2. Moderators:
Professors:
• Prof. Dr. G. Sivasankar, M.S., M.Ch.,
• Prof. Dr. A. Senthilvel, M.S., M.Ch.,
Asst Professors:
• Dr. J. Sivabalan, M.S., M.Ch.,
• Dr. R. Bhargavi, M.S., M.Ch.,
• Dr. S. Raju, M.S., M.Ch.,
• Dr. K. Muthurathinam, M.S., M.Ch.,
• Dr. D. Tamilselvan, M.S., M.Ch.,
• Dr. K. Senthilkumar, M.S., M.Ch.
Dept of Urology, GRH and KMC, Chennai. 2
4. EMBRYOLOGY OF KIDNEY
• Develop from a common mesodermal ridge
(intermediate mesoderm) along the posterior
wall of the abdominal cavity.
– pronephros, (rudimentary and nonfunctional)
– mesonephros, (function for a short time during
the early fetal period)
– metanephros, (forms the permanent kidney)
4
Dept of Urology, GRH and KMC, Chennai.
5. PRONEPHROS
• At 3rd week of gestation
• Develops as five to seven solid cell groups
• starts at the cranial end of the nephrogenic
cord and progresses caudally
• As each tubule matures it immediately begins
to degenerate along with the segment of the
nephric duct
5
Dept of Urology, GRH and KMC, Chennai.
6. MESONEPHROS
• Around 24th day, mesonephric vesicles begin to form.
– Initially, several spherical mass of cells
– vesicle elongates, form an S-shaped tubule.
– The lateral end forms a bud that connects with the
nephric duct.
– The medial end lengthens and enlarges to form a cup-
shaped sac, which eventually wraps around a knot of
glomerular capillaries to form a renal corpuscle.
• The tuft of glomerular capillaries originating from a branch of
the dorsal aorta invades the developing glomerulus
6
Dept of Urology, GRH and KMC, Chennai.
8. • Ducts fuse with the cloaca and begin to form a
lumen at the caudal end and progresses cranially
• This differentiation progresses caudally and
results in the formation of 40 to 42 pairs of
mesonephric tubules,
• At any time only 30 pair tubules present,because
degeneration start simultaneously
8
Dept of Urology, GRH and KMC, Chennai.
9. – By the 4th month, the human mesonephros - completely
disappeared, except for a few elements that persist as
part of the reproductive tract.
– In males, some cranially located mesonephric tubules
become the efferent ductules of the testes , epididymis
and vas deferens .
– In females, small, nonfunctional mesosalpingeal structures
termed the epoöphoron and paroöphoron.
9
Dept of Urology, GRH and KMC, Chennai.
12. METANEPHROS
• The definitive kidney
• Excretory units develop from metanephric mesoderm
• Ureteric bud forms from distal portion of the nephric duct as
sprouting buds
• Ureteric bud come in contact with the condensing blastema of
metanephric mesenchyme = 28th day
• The ureteric bud penetrates the metanephric mesenchyme and
begins to divide dichotomously.
• As the ureteric bud divides and branches ,it gives metanephros a
lobulated appearance
12
Dept of Urology, GRH and KMC, Chennai.
13. • Mesenchymal-epithelial interaction -- induce
formation of future nephrons
• Glomerulus, proximal tubule, loop of henle,
and distal tubule = derive from the
metanephric mesenchyme
• Collecting system, consisting of collecting
ducts, calyces, pelvis, and ureter, is formed
from the ureteric bud
13
Dept of Urology, GRH and KMC, Chennai.
14. EXCRETORY SYSTEM
• Each newly formed collecting tubule is covered at its distal end by a
metanephric tissue cap.
• Cells of the tissue cap form small vesicles, the renal vesicles.
• Renal vesicles give rise to small S-shaped tubules.
• Capillaries grow into the pocket at one end of tubule and
differentiate into glomeruli.
• These tubules, together with their glomeruli, form nephrons, or
excretory units.
• The proximal end of each nephron forms Bowman’s capsule.
14
Dept of Urology, GRH and KMC, Chennai.
15. • The distal end forms an open connection with one of the collecting
tubules, establishing a passageway from Bowman’s capsule to the
collecting unit.
• Continuous lengthening of the excretory tubule results in formation
of the proximal convoluted tubule, loop of Henle, and distal
convoluted tubule.
• At birth there are approximately 1 million of nephrons in each
kidney.
• Urine production begins early in gestation, soon after
differentiation of the glomerular capillaries, which start to form by
the 10th week.
• At birth the kidneys have a lobulated appearance, which disappears
during infancy as a result of further growth of the nephrons,
without increase in number.
15
Dept of Urology, GRH and KMC, Chennai.
18. • Overall, these events are reiterated
throughout the growing kidney so that older,
more differentiated nephrons are located in
the inner part of the kidney near the
juxtamedullary region and newer, less
differentiated nephrons are found at the
periphery
18
Dept of Urology, GRH and KMC, Chennai.
19. COLLECTING SYSTEM
• The dichotomous branching of the ureteric bud
determines the eventual pelvicalyceal patterns and
their corresponding renal lobules .
• By 20 to 22 weeks, ureteric bud branching is
completed.
• Thereafter, collecting duct development occurs by
extension of peripheral branch segments.
•
• The bud dilates, forming the primitive renal pelvis,
and splits into cranial and caudal portions (the future
major calyces).
19
Dept of Urology, GRH and KMC, Chennai.
20. • Each calyx forms two new buds while penetrating the
metanephric tissue.
• These buds continue to subdivide until 12 or more
generations of tubules have formed.
• Meanwhile, at the periphery more tubules form until
the end of the fifth month.
• The tubules of the second order enlarge and absorb
those of the third and fourth generations, forming
the minor calyces of the renal pelvis.
• Collecting tubules of the fifth and successive
generations form the renal pyramid.
20
Dept of Urology, GRH and KMC, Chennai.
23. • Between 22 and 24 weeks of fetal gestation the
peripheral (cortical) and central (medullary)
develops.
• Nephrogenesis completed before birth at 32-34
weeks of gestation.
• Postnatal maturation of kidney continue till 18-
24 month of age
23
Dept of Urology, GRH and KMC, Chennai.
24. • Renal cortex
– 70% of total kidney volume at birth,
– becomes organized as a relatively compact,
– circumferential rim of tissue surrounding the periphery of
the kidney.
• Renal medulla
– 30% of total kidney volume at birth,
– modified cone shape with a broad base contiguous
with cortical tissue.
– The apex of the cone is formed by convergence of
collecting ducts in the inner medulla and is termed
the papilla.
24
Dept of Urology, GRH and KMC, Chennai.
25. GENETICS
• WT1 is normally first expressed in the intermediate mesoderm prior
to kidney formation and is then expressed in the developing kidney,
gonad, and mesothelium
• The metanephrogenic mesenchyme secretes glial-derived
neurotrophic factor (GDNF) to induce and direct the ureteric bud
• The ureteric bud secretes FGF2 and BMP7 to prevent
mesenchymal apoptosis and maintains the synthesis of WT1
•
• Leukemia inhibitory factor (LIF) from the ureteric bud induces the
mesenchyme cells to aggregate
• Lim-1 homeodomain transcription factor causes Conversion of the
aggregated cells into a nephron
• Hoxa-13 and Hoxd-13 act on urogenital deferentiation
25
Dept of Urology, GRH and KMC, Chennai.
27. POSITION OF KIDNEY
• The kidney, initially in the pelvic region,
• Around 6-7th week, ascent of the kidney is caused by
diminution of body curvature and by growth of the
body in the lumbar and sacral regions.
• In the pelvis the metanephros receives its arterial
supply from a pelvic branch of the aorta.
• During its ascent to the abdominal level, it is
vascularized by arteries that originate from the aorta
at continuously higher levels
• During 7-8week kidney rotate 90 degree with renal
hilum changing position from ventral to anteromedially
27
Dept of Urology, GRH and KMC, Chennai.
28. Anomalies of shape
• Horse shoe kidney
• Pancake kidney
• Lobulated kidney
28
Dept of Urology, GRH and KMC, Chennai.
29. Abnormal rotation
• Nonrotation: The hilum is directed forward.
• Incomplete rotation
• Reverse rotation: The hilum is directed
anterolaterally.
29
Dept of Urology, GRH and KMC, Chennai.
30. Anomalies of position
• The kidneys may fail to ascend. They then lie
in the sacral region.
• Incomplete ascent = lie opposite the lower
lumbar vertebrae.
• The kidneys may ascend too far, and may even
be present within the thoracic cavity.
30
Dept of Urology, GRH and KMC, Chennai.
32. ANATOMY OF KIDNEY
• Paired ovoid, reddish-brown retroperitoneal organs
situated in the posterior part of the abdomen on each side
of the vertebral coloumn
• Lie on the psoas muscles; thus the longitudinal axes of the
kidneys are oblique .
• The upper poles more medial and posterior than the
inferior poles.
• The medial aspect of each kidney is rotated anteriorly at an
angle of approximately 30 degrees.
32
Dept of Urology, GRH and KMC, Chennai.
34. • The exact position of the kidney within the
retroperitoneum varies:
➢The kidneys move inferiorly approximately 3
cm (one vertebral body) during inspiration and
during changing body position from supine to
the erect.
34
Dept of Urology, GRH and KMC, Chennai.
35. DIMENSIONS
• Length- 10 to 12 cm
• Width- 5.0 to 7.5 cm
• Thickness- 2.5 to 3.0 cm.
➢Weight of kidney = approx. 125-170 gm. ( 10-
15 gm lighter in females)
➢Relatively larger in children and have
prominent fetal lobulations.
35
Dept of Urology, GRH and KMC, Chennai.
36. Right kidney vs left kidney
Right kidney
• Reside between the top
of the 1st lumbar
vertebra to the bottom of
the 3rd lumbar vertebra.
• The right kidney is
slightly shorter and wider
because of downward
compression by the liver.
• The right kidney is
related to the 12th rib,
Left kidney
• Between the 12th
thoracic vertebra and the
3rd lumbar vertebra.
• Dromedary hump more
common on left side.
• Left kidney is related to
the 11th and 12th ribs
36
Dept of Urology, GRH and KMC, Chennai.
37. RELATIONS
• Surfaces of kidney are - anterior and
posterior.
• Borders are - medial and lateral.
• Poles of kidney are – superior and inferior.
• Anteriorly kidney is related - abdominal
viscera
Posteriorly - osteomuscular area
37
Dept of Urology, GRH and KMC, Chennai.
38. ANTERIOR RELATIONS
RIGHT KIDNEY
• right adrenal gland
• liver,
• second part of duodenum,
• ascending colon,
• hepatic flexure of colon.
LEFT KIDNEY
• Left adrenal,
• Pancreas,
• splenic vessels,
• Stomach,
• Spleen,
• Dj flexure,
• Ligament of trietz,
• Descending colon,
• Splenic flexure of colon,
• Loops of jejunum.
38
Dept of Urology, GRH and KMC, Chennai.
41. POSTERIOR RELATIONS OF KIDNEY
LEFT KIDNEY
• Projection of 11th rib
• Area for diaphragm
• Projection of 12th rib
• Area for aponeurosis of
transversus abdominis
muscle
• Area for quadratus
lumborum muscle
• Area for psoas major muscle
RIGHT KIDNEY
• Area for diaphragm
• Projection of 12th rib
• Area for aponeurosis of
transversus abdominis
muscle
• Area for quadratus
lumborum muscle
• Area for psoas major muscle
41
Dept of Urology, GRH and KMC, Chennai.
44. APPLIED ANATOMY
• Posterior reflection of the pleura extends
inferiorly to the 12th rib
• Lung edge lies above the 11th rib (at the 10th
intercostal space)
• Risk of injury to the lung from a 10th
intercostal percutaneous approach to the
kidney
44
Dept of Urology, GRH and KMC, Chennai.
46. MEDIALBORDER
» In medial border of each kidney there is a vertical fissure
called renal hilum/porta
• Renal vessels, nerves, lymphatics, enter and exit through
through hilum
• Concavity of hilum is continous with deep declivity in
medial border of kidney called renal sinus
• Within renal sinus is renal pelvis, a funnel shaped sac
formed by widely expanded portion of proximal ureter and
by junction of major calices
46
Dept of Urology, GRH and KMC, Chennai.
47. • Intra renal pelvis denotes the pelvis that is
almost covered by renal parenchyma.
• Renal pelvis almost bifurcates or trifurcates
within the sinus producing 2/3 major calyx.
• Each major calyx again divide into 5-14 minor
calyxes receiving collecting ducts ( 500).
• Renal pelvis commonly lies posterior to renal
vessels.
• Has a capacity of 3 to 10 ml of urine.
47
Dept of Urology, GRH and KMC, Chennai.
48. • LATERAL BORDER :
Related to perirenal fascia, gerota’s fascia,
para renal fascia.
48
Dept of Urology, GRH and KMC, Chennai.
49. GEROTA’S FASCIA
• Encloses the kidney & perirenal fat and
adrenals.
• Anatomic barrier to spread of malignancy
• Superiorly and laterally it is closed
• Medially it crosses the midline to fuse with
the fellow of opp. Side
• Inferiorly it remains open- perinephric fluid
can track into pelvis
49
Dept of Urology, GRH and KMC, Chennai.
51. • Two distinct regions :-
Cortex - pale outer region,
Medulla - darker inner region
• Renal medulla - 8 to 18 striated, distinct, conically shaped areas
called renal pyramids.
• The apex of the pyramids forms the renal papilla, and each papilla is
cupped by an individual minor calyx.
• The base of the pyramids is positioned at the corticomedullary
boundary.
• Renal cortex is approximately 1 cm in thickness and covers the base
of each renal pyramid peripherally and extends downward between
the individual pyramids to form the columns of Bertin . 51
Dept of Urology, GRH and KMC, Chennai.
52. • Interlobar arteries traverse these columns of
Bertin
• Therefore percutaneous access to the collecting
system is usually performed through a renal
pyramid into a calyx to avoid these columns of
Bertin containing larger blood vessels
• The functional unit of the kidney is the nephron.
Approximately 0.4 to 1.2 million nephrons are
found in each adult kidney.
52
Dept of Urology, GRH and KMC, Chennai.
53. • The cortex made up of the glomeruli with PCT &
DCT.
• The renal pyramids are made up of loops of
Henle and collecting ducts.
• Ducts join to form the papillary ducts (about 20),
which open at the papillary surface (area cribosa)
and drain urine into the collecting system(into
the fornix of a minor calyx).
53
Dept of Urology, GRH and KMC, Chennai.
55. MINOR CALYX
• The renal papillae drain into the minor calyces,
(the most peripheral portions of the intrarenal
collecting system).
• Range in number from 5 to 14 (mean- 8)
• Simple (drains one papilla)
• Compound (drains two or three papillae)
• Compound calyces are the rule in the upper
calyceal group, are common in the lower calyceal
group, and are rare in the middle calyceal group
55
Dept of Urology, GRH and KMC, Chennai.
56. • Three calyceal groups: upper, middle, and lower.
• Minor calyces, either directly or after coalescing into
major calyces, drain by infundibula into the renal pelvis
• Compound calyces of the poles of the kidney are
oriented facing their respective poles.
• Simple calyces usually come in pairs, with one facing
anteriorly and one facing posteriorly
56
Dept of Urology, GRH and KMC, Chennai.
58. • Drainage of the upper pole into the renal pelvis is by a
single midline infundibulum in the majority of kidneys.
• Drainage from the lower pole is via a single infundibulum
in about half of human kidneys.
• The middle calyces are typically arranged in a series of
paired anterior and posterior calyces.
• In about two thirds of kidneys, there are two major calyceal
systems—an upper one and lower one—and the middle
calyces drain into either or both systems
58
Dept of Urology, GRH and KMC, Chennai.
59. CLASSIFICATION OF THE
PELVIOCALYCEAL SYSTEM
Group A (62.2%)
• Two major calyceal groups (superior and inferior)
• Midzone calyceal drainage dependent on these two
major groups
➢ Type A-I (45%). The kidney midzone is drained by minor
calyces that are dependent on the superior and/ or
inferior calyceal groups
➢ Type A-II (17.2%). The kidney midzone is drained
simultaneously by crossed calyces, one draining into
the superior calyceal group and the other draining into
the inferior calyceal group 59
Dept of Urology, GRH and KMC, Chennai.
61. Group B (37.8%)
• Midzone (hilar) calyceal drainage independent of both
the superior and inferior calyceal groups
• Type B-I (21.4%). The kidney midzone is drained by a
major calyceal group, independent of both the superior
and the inferior groups.
• Type B-II (16.4%). The kidney midzone is drained
by minor calyces (one to four) entering directly into the
renal pelvis .
61
Dept of Urology, GRH and KMC, Chennai.
63. ORIENTATION OF CALYCES
• Important consideration for percutaneous surgery-
anteroposterior orientation of the calyces,
• Because access (from the typical posterior or
posterolateral approach) into a posterior calyx allows
relatively straight entry into the rest of the kidney,
whereas
• Percutaneous puncture of an anterior calyx requires
an acute angulation to enter the renal pelvis, which
may not be possible with rigid instrumentation .
63
Dept of Urology, GRH and KMC, Chennai.
64. ORIENTATION OF CALYCES
• Paired anterior and posterior calyces usually
enter at about 90 degrees from each other.
• The relative mediolateral orientation (on
anteroposterior radiography) is determined by
the relationship of this 90-degree unit to the
frontal plane of the kidney.
64
Dept of Urology, GRH and KMC, Chennai.
65. BRODEL TYPE
• Unit is rotated anteriorly, such that the posterior
calyces are about 20 degrees behind the frontal plane
• Anterior calyces are 70 degrees in front of the frontal
plane
• The posterior calyces are lateral, and the anterior
calyces are medial in this case
• Most right kidneys have a Brodel-type orientation
(posterior calyces are lateral)
65
Dept of Urology, GRH and KMC, Chennai.
66. HODSON TYPE
• Calyceal pairs are rotated posteriorly, with the
posterior calyces 70 degrees behind the
frontal plane and appearing medial
• Anterior calyces 20 degrees in front of the
frontal plane and appearing lateral
• Left kidneys have a Hodson-type orientation
(posterior calyces are medial)
66
Dept of Urology, GRH and KMC, Chennai.
68. • Mostly calyces of the upper pole are suitable
for percutaneous access from posterior
approach, whereas care must be taken to
select a posterior minor calyx in middle and
lower groups.
• Safest place to access collecting system is
directly into calyceal fornix as it will avoid
interlobar arteries and arcuate arteries…
68
Dept of Urology, GRH and KMC, Chennai.
69. FOR PERCUTANEOUS ACCESS
▪ In prone position, prefered calyx are posterior ones.
▪ Should never be directed into infundibulum or renal
pelvis.
▪ Upper pole calyx is most versatile site through which to
enter the upper urinary tract collecting system.
▪ Subcostal approach is safest route to kidney.
69
Dept of Urology, GRH and KMC, Chennai.
70. RENAL VASCULATURE
• The renal arteries arise from the aorta at the level of the intervertebral disk
between the L1 and L2 vertebrae.
• Each artery divides into five segmental end arteries that do not anastomose
significantly with other segmental arteries.
• The renal artery usually divides to form anterior and posterior divisions.
• The anterior division supplies anterior two thirds of the kidney, and the posterior
division supplies the posterior one third of the kidney.
• Typically, the anterior division divides into four anterior segmental branches:
apical, upper, middle, and lower.
• The posterior segmental artery - first and most constant branch, which separates
from the renal artery before it enters the renal hilum
70
Dept of Urology, GRH and KMC, Chennai.
71. SEGMENTAL BRANCHES
• End arteries- so injury lead to segmental infarction.
• First and most constant branch POSTERIOR SEGMENTAL
BRANCH
• Four anterior branches
• APICAL
• UPPER
• MIDDLE
• LOWER
• Posterior segmental artery passes posterior to renal pelvis,
• SURGICAL IMPORTANCE - when it passes anterior to pelvis
lead to puj obstruction..
71
Dept of Urology, GRH and KMC, Chennai.
74. • In the renal sinus, the segmental arteries branch into lobar arteries,
which further subdivide in the parenchyma to form interlobar
arteries.
• The interlobar arteries progress peripherally within the cortical
columns of Bertin, avoiding the renal pyramids but in a close
association with the minor calyceal infundibula.
• At the base (peripheral edge) of the renal pyramids, the interlobar
arteries branch into arcuate arteries.
• Instead of moving peripherally, the arcuate arteries parallel the
edge of the corticomedullary junction and move radially, where
they eventually divide to form the afferent arteries to the
glomerulus.
74
Dept of Urology, GRH and KMC, Chennai.
77. ANOMALIES OF RENAL ARTERY
• Multiple renal arteries- kidney supplied by more than
one artery..MC on left side.
• Accessory renal artery – 2 or more branch supply the
same renal segment. MC on left side 30 to 35%
• They enter either in upper pole/ lower pole of kidney.
• Such accessory artery can cause ureteric obstruction
lead to secondary HUN..
• But ligation of accessory renal artery result in a portion
of infarction
• Arterial anomalies are more common on left and
venous anomalies are more common on right.
77
Dept of Urology, GRH and KMC, Chennai.
78. COMMON ANATOMIC VARIANTS OF
VESSEL
• Occurs in 25- 40%
• M.C is supernumery arteries- More commen
on Left side.
• Lower pole arteries can cross ant to collection
system and cause PUJ obstruction
78
Dept of Urology, GRH and KMC, Chennai.
79. RENAL VEIN
• The vein is located directly anterior to the
renal artery.
• This position can vary up to 1-2 cm cranially or
caudally relative to the artery
79
Dept of Urology, GRH and KMC, Chennai.
80. LEFT RENAL VEIN
• The left renal vein - 6 to 10 cm in length and
drains into IVC after passing posterior to the
superior mesenteric artery and anterior to the
aorta
• Left renal vein enters the IVC at a slightly more
cranial level and a more anterolateral location
• The left renal vein receives the left adrenal
vein superiorly, lumbar vein posteriorly, and
left gonadal vein inferiorly
80
Dept of Urology, GRH and KMC, Chennai.
81. RIGHT RENAL VEIN
• The right renal vein is generally 2 to 4 cm in
length and enters the right lateral to
posterolateral edge of the IVC
• Right renal vein enters the IVC at a slightly
more caudal level.
• The right renal vein typically do not receive
any branches
81
Dept of Urology, GRH and KMC, Chennai.
82. • Unlike the arterial supply, the venous drainage
communicates freely through “Venous
Collars” around the infundibula,
• Extensive collateral circulation is present in
the venous drainage of the kidney.
• Surgically, this is important, because unlike the
arterial supply, occlusion of a segmental
venous branch has little effect on venous
outflow
82
Dept of Urology, GRH and KMC, Chennai.
85. BRODEL’S LINE /AVASCULAR PLANE
• Slightly behind the convex border at the
posterior half of kidney (approximately 2/3 rd
way from lateral border ).
• Incision in this area will permit to remove
stone within renal calices with minimal
damage.
85
Dept of Urology, GRH and KMC, Chennai.
87. LYMPHATICS
• Largely follow blood vessels through the column
of bertin.
• Lymphatics empty to LN near renal hilum
• L KIDNEY:-
-Lt lateral para- aortic LN
• R KIDNEY:-
-Rt inter aortocaval and Rt lateral para
caval LN and anterior and posterior inferior
venacaval nodes.
87
Dept of Urology, GRH and KMC, Chennai.
90. NERVE SUPPLY
• SYMPATHETIC - From T8 to L1 through celiac
and aortico renal ganglion
- Vasoconstriction
• PARA SYMPATHETIC- From vagus
- vasodilatation
➢Remember that kidney can function well even
without neurological control
90
Dept of Urology, GRH and KMC, Chennai.
91. APPLIED ANATOMY
• Avoid injury to T11 and T12 nerves – to avoid
post op paraesthesias and postop muscle
bulding from partial muscle paralysis.
• While suturing ensure not to entrap the lower
costal nerves.
• Injury to 12 th nerve lead to gluteal
paraesthesias.
91
Dept of Urology, GRH and KMC, Chennai.
92. RADIOLOGICAL ANATOMY OF RENAL
PARENCHYMA
• On USG- In adults normal kidneys have smooth margins
and isoechoic to liver
• Both renal cortices and pyramids are usually hypoechoic
to the liver, spleen, and renal sinus. Compared with renal
parenchyma, the renal sinus appears hyperechoic
because of the presence of hilar adipose tissue, blood
vessels, and lymphatics.
• The renal cortices of newborn kidneys are isoechoic or
hyperechoic to the liver and splenic parenchyma
• Echogenicity correlates to the severity of pathologic changes
in renal parenchyma.
92
Dept of Urology, GRH and KMC, Chennai.
93. ON CT
• On unenhanced computed tomography (CT), the renal
parenchyma is homogeneous, with a density ranging
from 30 to 60 (HU)
• After intravenous contrast injection = 80-120HU.
• Arterial phase= after 20 to 30 seconds of contrast
• The corticomedullary= 30-70 sec ( cortex brighter)
• The nephrographic CT phase= 80 to 120 seconds,
equally enhances renal cortex and medulla and is
considered to be the optimal phase for detection of
renal neoplasms.
• The excretory ct phase= more than 3 minutes after
contrast
93
Dept of Urology, GRH and KMC, Chennai.
94. ON MRI
• MRI= T1-weighted sequences show the renal
cortex much brighter than the renal medulla,
whereas the cortex is slightly less intense than
the medulla on T2-weighted sequences
• Pelvis containing fat appears hypertense on
both T1 and T2
• Nephrogenic phase= 60-90 sec
• Excretory phase= 120 sec
94
Dept of Urology, GRH and KMC, Chennai.