This document presents a case report of a 6 day old female infant referred to the hospital with vomiting since the 5th day of life. On examination, the infant was found to have bilious vomiting but no other symptoms of obstruction. Initial investigations and a barium meal were unremarkable. However, over the course of her hospital stay her symptoms persisted and she was eventually found to have a duodenal web, which was surgically corrected. This case highlights some of the challenges in diagnosing intestinal obstruction in newborns, including the need for high clinical suspicion and the potential limitations of initial radiological investigations.
Common problems in paediatric surgery.pptxQaviSekander
This document discusses common pediatric surgical problems including neonatal intestinal obstruction, anorectal malformations, infantile hypertrophic pyloric stenosis, inguinoscrotal swellings, abnormalities of the urinary opening, and hypospadias. Key points include the clinical presentations, diagnostic evaluations, and management approaches for these common congenital anomalies and acquired pediatric surgical conditions. Accurate diagnosis and timely intervention are emphasized to optimize outcomes for affected children.
This document discusses several common causes of childhood intestinal obstruction including:
1. Rotation defects that can cause midgut volvulus like malrotation or incomplete rotation.
2. Duodenal atresia which presents with jaundice and bilious vomiting in newborns.
3. Meconium ileus which is thick meconium causing ileal obstruction in cystic fibrosis patients.
4. Congenital hypertrophic pyloric stenosis causing projectile vomiting in infants.
5. Intussusception where one segment of bowel slides into another causing obstruction.
6. Hirschsprung disease where absence of ganglion cells in a segment of colon causes constipation.
Mesenteric ischemia presentation by Dr.NOSHI Capital Hospital Islamabad Paki...drfarhanali2008
The document describes a case of mesenteric ischemia in a 36-year-old male patient who presented with lower abdominal pain and vomiting. Key details include:
- The patient reported 4 days of lower abdominal pain that became severe and was accompanied by vomiting for 1 day.
- Examination found abdominal tenderness and guarding. Imaging showed fatty liver and mild ascites.
- Exploratory laparotomy revealed infarcted small intestine requiring a double barrel stoma.
- The patient was optimized after surgery and underwent stoma reversal surgery.
- Mesenteric ischemia occurs when blood supply to the intestine is inadequate and can be acute or chronic, having various etiologies including embol
NEC is a devastating condition affecting premature infants. It involves necrosis of the intestinal tissue. Key factors that increase risk are prematurity, enteral feeding, and circulatory instability in the intestines. Clinically, infants may experience apnea, feeding intolerance, and abdominal distension. Diagnosis involves blood tests showing infection and inflammation as well as imaging showing abnormalities in the intestines. Treatment involves bowel rest, antibiotics, and sometimes surgery. Outcomes depend on severity but mortality can be over 40% in very premature infants and survivors face long-term complications.
The spleen is normally located in the left upper quadrant of the abdomen. This case presents a 20-year-old female with abdominal pain who was found to have a torsed wandering spleen at the center of her abdomen. Wandering spleen is a condition where the spleen lacks normal ligamentous support, causing it to be mobile within the abdomen. At surgery, her enlarged spleen was found to have torsed along its vascular pedicle, cutting off its blood supply. A splenectomy was performed to remove the non-viable spleen. Histopathology confirmed splenic infarction due to the torsion.
pre and post operative management of paediatric Splenectomy patientsVernon Pashi
1. Splenectomy is the surgical removal of the spleen and has a long history dating back to ancient China and Europe in the 15th-16th centuries.
2. The spleen develops from embryonic mesoderm and has important peritoneal attachments and ligaments that connect it to surrounding structures.
3. Anatomically, the spleen is located in the left upper abdominal quadrant and has characteristic shapes, sizes, vascular supply, and segmental variations.
4. Diseases of the spleen include hypersplenism, splenomegaly, and trauma-related injuries. Splenectomy techniques aim to ligate vessels and detach ligaments to safely remove the spleen.
This document presents a case report of a 6 day old female infant referred to the hospital with vomiting since the 5th day of life. On examination, the infant was found to have bilious vomiting but no other symptoms of obstruction. Initial investigations and a barium meal were unremarkable. However, over the course of her hospital stay her symptoms persisted and she was eventually found to have a duodenal web, which was surgically corrected. This case highlights some of the challenges in diagnosing intestinal obstruction in newborns, including the need for high clinical suspicion and the potential limitations of initial radiological investigations.
Common problems in paediatric surgery.pptxQaviSekander
This document discusses common pediatric surgical problems including neonatal intestinal obstruction, anorectal malformations, infantile hypertrophic pyloric stenosis, inguinoscrotal swellings, abnormalities of the urinary opening, and hypospadias. Key points include the clinical presentations, diagnostic evaluations, and management approaches for these common congenital anomalies and acquired pediatric surgical conditions. Accurate diagnosis and timely intervention are emphasized to optimize outcomes for affected children.
This document discusses several common causes of childhood intestinal obstruction including:
1. Rotation defects that can cause midgut volvulus like malrotation or incomplete rotation.
2. Duodenal atresia which presents with jaundice and bilious vomiting in newborns.
3. Meconium ileus which is thick meconium causing ileal obstruction in cystic fibrosis patients.
4. Congenital hypertrophic pyloric stenosis causing projectile vomiting in infants.
5. Intussusception where one segment of bowel slides into another causing obstruction.
6. Hirschsprung disease where absence of ganglion cells in a segment of colon causes constipation.
Mesenteric ischemia presentation by Dr.NOSHI Capital Hospital Islamabad Paki...drfarhanali2008
The document describes a case of mesenteric ischemia in a 36-year-old male patient who presented with lower abdominal pain and vomiting. Key details include:
- The patient reported 4 days of lower abdominal pain that became severe and was accompanied by vomiting for 1 day.
- Examination found abdominal tenderness and guarding. Imaging showed fatty liver and mild ascites.
- Exploratory laparotomy revealed infarcted small intestine requiring a double barrel stoma.
- The patient was optimized after surgery and underwent stoma reversal surgery.
- Mesenteric ischemia occurs when blood supply to the intestine is inadequate and can be acute or chronic, having various etiologies including embol
NEC is a devastating condition affecting premature infants. It involves necrosis of the intestinal tissue. Key factors that increase risk are prematurity, enteral feeding, and circulatory instability in the intestines. Clinically, infants may experience apnea, feeding intolerance, and abdominal distension. Diagnosis involves blood tests showing infection and inflammation as well as imaging showing abnormalities in the intestines. Treatment involves bowel rest, antibiotics, and sometimes surgery. Outcomes depend on severity but mortality can be over 40% in very premature infants and survivors face long-term complications.
The spleen is normally located in the left upper quadrant of the abdomen. This case presents a 20-year-old female with abdominal pain who was found to have a torsed wandering spleen at the center of her abdomen. Wandering spleen is a condition where the spleen lacks normal ligamentous support, causing it to be mobile within the abdomen. At surgery, her enlarged spleen was found to have torsed along its vascular pedicle, cutting off its blood supply. A splenectomy was performed to remove the non-viable spleen. Histopathology confirmed splenic infarction due to the torsion.
pre and post operative management of paediatric Splenectomy patientsVernon Pashi
1. Splenectomy is the surgical removal of the spleen and has a long history dating back to ancient China and Europe in the 15th-16th centuries.
2. The spleen develops from embryonic mesoderm and has important peritoneal attachments and ligaments that connect it to surrounding structures.
3. Anatomically, the spleen is located in the left upper abdominal quadrant and has characteristic shapes, sizes, vascular supply, and segmental variations.
4. Diseases of the spleen include hypersplenism, splenomegaly, and trauma-related injuries. Splenectomy techniques aim to ligate vessels and detach ligaments to safely remove the spleen.
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.
Dr. Maimuna Sayeed presented the case of an 11-month-old boy with breathing difficulties for 2 days, vomiting since 3 months of age, and dribbling of urine since birth. Examination found the boy to be dyspneic, pale, and hypertensive with ballotable kidneys and palpable bladder. Investigations supported chronic kidney disease stage 5 due to posterior urethral valve, with hydronephrosis, hydroureters, and vesicoureteral reflux seen on imaging. The boy was managed conservatively with antibiotics and peritoneal dialysis, showing improvement over follow-ups. Surgery consultation was planned to address the underlying valve abnormality.
HIRSCHSPRUNG DISEASE of neonate wrr.pptxShambelNegese
disease is a condition that affects the large intestine (colon) and causes problems with passing stool. The condition is present at birth (congenital) as a result of missing nerve cells in the muscles of the baby's colon.
Pancreatic agenesis with congenital diabetes mellitus (case study).Azad Haleem
A 5-year-old boy was diagnosed with diabetes at 1 week of age and treated with insulin but without control. He also experienced abdominal distention and bulky stool. Investigations did not identify a diagnosis. He was diagnosed with agenesis of the pancreas based on imaging. Insulin therapy and pancreatic enzyme replacement controlled his diabetes and malabsorption symptoms. Routine imaging is recommended for young diabetes patients with atypical features to identify conditions like agenesis of the pancreas.
Infantile hypertrophic pyloric stenosis is a condition characterized by thickening of the pyloric muscle which causes projectile vomiting in infants usually starting around 3 weeks of age. It occurs more commonly in males and the risk is increased if the father also had IHPS. Diagnosis is suggested by symptoms and confirmed by ultrasound showing thickening of the pyloric wall over 4mm. Treatment involves rehydration followed by pyloromyotomy surgery to cut the thickened pyloric muscle and relieve the obstruction.
Case presntation of Mucopolysaccharidosesmaliha shah
This document presents the case of a 15-year-old female patient admitted with short stature, body aches, loss of appetite, and joint pain. Her examination revealed short stature, coarse facies, widened bones, and limited joint mobility. Skeletal survey showed narrow pelvis, short stubby bones, and irregular bone growth. Differential diagnoses included Mucopolysaccharidoses (MPS), Ehlers-Danlos syndrome, and Mucolipidoses. MPS Type IV was considered most likely given skeletal findings and enzyme deficiency causing lysosomal storage.
A 37-year-old male presented with abdominal pain and fever and was found to have a large splenic hematoma due to Plasmodium vivax malaria infection. He underwent an emergency splenectomy. Histopathology confirmed the presence of malaria parasites. Malaria, especially P. vivax, is a known cause of spontaneous splenic rupture in endemic areas like India due to splenic congestion and hematoma formation from infected red blood cells accumulating in the spleen.
Approach to Inborn errors of metabolism with Case of Maple Syrup Urine diseas...Aheed Khan
A case of MSUD and its course in the NICU. with brief description to approach to inborn errors of metabolism and how to identify and lab work of suspected neonatal encephalopathy
A case study of prolapse in female .pptxRaviChahar11
This document presents a case of a 50-year-old woman with a chief complaint of vaginal prolapse, increased urinary frequency, and lower back pain. She has a history of 6 vaginal births without proper prenatal or postnatal care. On examination, she has a 3rd degree uterovaginal prolapse with cystocele protruding 8cm from the hymenal ring. Laboratory tests and ultrasound are normal. The diagnosis is 3rd degree uterovaginal prolapse with cystocele. The planned management is a vaginal hysterectomy with pelvic floor repair.
This patient presented with symptoms of difficulty breathing, lower limb swelling, decreased urine output, and pallor. Her labs showed kidney dysfunction with elevated creatinine and liver enzymes. Her history of abruptio placenta and recent pregnancy termination suggested HELLP syndrome. A kidney biopsy was considered but the patient refused. Her kidney function and labs gradually improved with aggressive fluid management and medications.
A 45-year-old male presented with fever, abdominal pain, and jaundice. Examination found tender hepatomegaly. Tests found elevated inflammatory markers and mildly abnormal liver enzymes. Imaging showed a large abscess in the right lobe of the liver. Needle aspiration yielded anchovy paste-like pus. Given the patient's history, physical exam findings, and imaging results, he was diagnosed with amoebic liver abscess. He was treated medically and surgically with drainage but later developed complications of sepsis and a right pleural effusion, which also resolved with treatment. Amoebic liver abscess most commonly presents as this case outlines.
This document contains a patient case report for Januka Katuwal, a 32-year-old female presenting with cessation of menstruation for over a month, abdominal pain for 8 hours, and vomiting for 8 hours. Her examination and investigations revealed a ruptured ectopic pregnancy in her right fallopian tube, which was then managed via an emergency laparotomy and right salpingectomy with left tubal ligation. The document also provides definitions, classifications, risk factors, clinical approaches, diagnostic methods, and management options for ectopic pregnancies.
Cervical incompetence is the inability for the cervix to retain an intra-uterine pregnancy till term as a result of structural and functional defects of the cervix
Primary intestinal lymphangiectasia (PIL) case presentationAzad Haleem
- An 11-year-old girl presented with abdominal pain, swelling, periorbital swelling, diarrhea, vomiting, stiffness, and weight loss. Investigations found hypoproteinemia, hypocalcemia, and elevated stool alpha-1 antitrypsin. Endoscopy showed dilated intestinal lacteals.
- She was diagnosed with primary intestinal lymphangiectasia (PIL), a rare disease characterized by dilated intestinal lacteals causing lymph leakage into the bowel.
- Treatment included a high-protein, low-fat diet with medium chain triglycerides, albumin infusion, calcium, magnesium, vitamin D supplementation, octreotide, and tranexamic acid. Her condition improved with management
Zakiya, a 5-year-old girl, presented with a single opening in front of her anus through which she urinates. She strains during urination but has normal bowel movements. On examination, she has an enlarged clitoris and incomplete fusion of her labia. Imaging found a urogenital sinus, bladder cystitis, and vesicoureteral reflux. She was diagnosed with urogenital sinus anomaly and a heart condition. The treatment plan is for endoscopic evaluation and further treatment.
A case presentation and discussion of ALL presented in a Tertiary Care Hospital ER. Includes presenting complaints, work-up, diagnosis and relevant case discussion.
Strategies for Effective Upskilling is a presentation by Chinwendu Peace in a Your Skill Boost Masterclass organisation by the Excellence Foundation for South Sudan on 08th and 09th June 2024 from 1 PM to 3 PM on each day.
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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.
Dr. Maimuna Sayeed presented the case of an 11-month-old boy with breathing difficulties for 2 days, vomiting since 3 months of age, and dribbling of urine since birth. Examination found the boy to be dyspneic, pale, and hypertensive with ballotable kidneys and palpable bladder. Investigations supported chronic kidney disease stage 5 due to posterior urethral valve, with hydronephrosis, hydroureters, and vesicoureteral reflux seen on imaging. The boy was managed conservatively with antibiotics and peritoneal dialysis, showing improvement over follow-ups. Surgery consultation was planned to address the underlying valve abnormality.
HIRSCHSPRUNG DISEASE of neonate wrr.pptxShambelNegese
disease is a condition that affects the large intestine (colon) and causes problems with passing stool. The condition is present at birth (congenital) as a result of missing nerve cells in the muscles of the baby's colon.
Pancreatic agenesis with congenital diabetes mellitus (case study).Azad Haleem
A 5-year-old boy was diagnosed with diabetes at 1 week of age and treated with insulin but without control. He also experienced abdominal distention and bulky stool. Investigations did not identify a diagnosis. He was diagnosed with agenesis of the pancreas based on imaging. Insulin therapy and pancreatic enzyme replacement controlled his diabetes and malabsorption symptoms. Routine imaging is recommended for young diabetes patients with atypical features to identify conditions like agenesis of the pancreas.
Infantile hypertrophic pyloric stenosis is a condition characterized by thickening of the pyloric muscle which causes projectile vomiting in infants usually starting around 3 weeks of age. It occurs more commonly in males and the risk is increased if the father also had IHPS. Diagnosis is suggested by symptoms and confirmed by ultrasound showing thickening of the pyloric wall over 4mm. Treatment involves rehydration followed by pyloromyotomy surgery to cut the thickened pyloric muscle and relieve the obstruction.
Case presntation of Mucopolysaccharidosesmaliha shah
This document presents the case of a 15-year-old female patient admitted with short stature, body aches, loss of appetite, and joint pain. Her examination revealed short stature, coarse facies, widened bones, and limited joint mobility. Skeletal survey showed narrow pelvis, short stubby bones, and irregular bone growth. Differential diagnoses included Mucopolysaccharidoses (MPS), Ehlers-Danlos syndrome, and Mucolipidoses. MPS Type IV was considered most likely given skeletal findings and enzyme deficiency causing lysosomal storage.
A 37-year-old male presented with abdominal pain and fever and was found to have a large splenic hematoma due to Plasmodium vivax malaria infection. He underwent an emergency splenectomy. Histopathology confirmed the presence of malaria parasites. Malaria, especially P. vivax, is a known cause of spontaneous splenic rupture in endemic areas like India due to splenic congestion and hematoma formation from infected red blood cells accumulating in the spleen.
Approach to Inborn errors of metabolism with Case of Maple Syrup Urine diseas...Aheed Khan
A case of MSUD and its course in the NICU. with brief description to approach to inborn errors of metabolism and how to identify and lab work of suspected neonatal encephalopathy
A case study of prolapse in female .pptxRaviChahar11
This document presents a case of a 50-year-old woman with a chief complaint of vaginal prolapse, increased urinary frequency, and lower back pain. She has a history of 6 vaginal births without proper prenatal or postnatal care. On examination, she has a 3rd degree uterovaginal prolapse with cystocele protruding 8cm from the hymenal ring. Laboratory tests and ultrasound are normal. The diagnosis is 3rd degree uterovaginal prolapse with cystocele. The planned management is a vaginal hysterectomy with pelvic floor repair.
This patient presented with symptoms of difficulty breathing, lower limb swelling, decreased urine output, and pallor. Her labs showed kidney dysfunction with elevated creatinine and liver enzymes. Her history of abruptio placenta and recent pregnancy termination suggested HELLP syndrome. A kidney biopsy was considered but the patient refused. Her kidney function and labs gradually improved with aggressive fluid management and medications.
A 45-year-old male presented with fever, abdominal pain, and jaundice. Examination found tender hepatomegaly. Tests found elevated inflammatory markers and mildly abnormal liver enzymes. Imaging showed a large abscess in the right lobe of the liver. Needle aspiration yielded anchovy paste-like pus. Given the patient's history, physical exam findings, and imaging results, he was diagnosed with amoebic liver abscess. He was treated medically and surgically with drainage but later developed complications of sepsis and a right pleural effusion, which also resolved with treatment. Amoebic liver abscess most commonly presents as this case outlines.
This document contains a patient case report for Januka Katuwal, a 32-year-old female presenting with cessation of menstruation for over a month, abdominal pain for 8 hours, and vomiting for 8 hours. Her examination and investigations revealed a ruptured ectopic pregnancy in her right fallopian tube, which was then managed via an emergency laparotomy and right salpingectomy with left tubal ligation. The document also provides definitions, classifications, risk factors, clinical approaches, diagnostic methods, and management options for ectopic pregnancies.
Cervical incompetence is the inability for the cervix to retain an intra-uterine pregnancy till term as a result of structural and functional defects of the cervix
Primary intestinal lymphangiectasia (PIL) case presentationAzad Haleem
- An 11-year-old girl presented with abdominal pain, swelling, periorbital swelling, diarrhea, vomiting, stiffness, and weight loss. Investigations found hypoproteinemia, hypocalcemia, and elevated stool alpha-1 antitrypsin. Endoscopy showed dilated intestinal lacteals.
- She was diagnosed with primary intestinal lymphangiectasia (PIL), a rare disease characterized by dilated intestinal lacteals causing lymph leakage into the bowel.
- Treatment included a high-protein, low-fat diet with medium chain triglycerides, albumin infusion, calcium, magnesium, vitamin D supplementation, octreotide, and tranexamic acid. Her condition improved with management
Zakiya, a 5-year-old girl, presented with a single opening in front of her anus through which she urinates. She strains during urination but has normal bowel movements. On examination, she has an enlarged clitoris and incomplete fusion of her labia. Imaging found a urogenital sinus, bladder cystitis, and vesicoureteral reflux. She was diagnosed with urogenital sinus anomaly and a heart condition. The treatment plan is for endoscopic evaluation and further treatment.
A case presentation and discussion of ALL presented in a Tertiary Care Hospital ER. Includes presenting complaints, work-up, diagnosis and relevant case discussion.
Strategies for Effective Upskilling is a presentation by Chinwendu Peace in a Your Skill Boost Masterclass organisation by the Excellence Foundation for South Sudan on 08th and 09th June 2024 from 1 PM to 3 PM on each day.
Chapter wise All Notes of First year Basic Civil Engineering.pptxDenish Jangid
Chapter wise All Notes of First year Basic Civil Engineering
Syllabus
Chapter-1
Introduction to objective, scope and outcome the subject
Chapter 2
Introduction: Scope and Specialization of Civil Engineering, Role of civil Engineer in Society, Impact of infrastructural development on economy of country.
Chapter 3
Surveying: Object Principles & Types of Surveying; Site Plans, Plans & Maps; Scales & Unit of different Measurements.
Linear Measurements: Instruments used. Linear Measurement by Tape, Ranging out Survey Lines and overcoming Obstructions; Measurements on sloping ground; Tape corrections, conventional symbols. Angular Measurements: Instruments used; Introduction to Compass Surveying, Bearings and Longitude & Latitude of a Line, Introduction to total station.
Levelling: Instrument used Object of levelling, Methods of levelling in brief, and Contour maps.
Chapter 4
Buildings: Selection of site for Buildings, Layout of Building Plan, Types of buildings, Plinth area, carpet area, floor space index, Introduction to building byelaws, concept of sun light & ventilation. Components of Buildings & their functions, Basic concept of R.C.C., Introduction to types of foundation
Chapter 5
Transportation: Introduction to Transportation Engineering; Traffic and Road Safety: Types and Characteristics of Various Modes of Transportation; Various Road Traffic Signs, Causes of Accidents and Road Safety Measures.
Chapter 6
Environmental Engineering: Environmental Pollution, Environmental Acts and Regulations, Functional Concepts of Ecology, Basics of Species, Biodiversity, Ecosystem, Hydrological Cycle; Chemical Cycles: Carbon, Nitrogen & Phosphorus; Energy Flow in Ecosystems.
Water Pollution: Water Quality standards, Introduction to Treatment & Disposal of Waste Water. Reuse and Saving of Water, Rain Water Harvesting. Solid Waste Management: Classification of Solid Waste, Collection, Transportation and Disposal of Solid. Recycling of Solid Waste: Energy Recovery, Sanitary Landfill, On-Site Sanitation. Air & Noise Pollution: Primary and Secondary air pollutants, Harmful effects of Air Pollution, Control of Air Pollution. . Noise Pollution Harmful Effects of noise pollution, control of noise pollution, Global warming & Climate Change, Ozone depletion, Greenhouse effect
Text Books:
1. Palancharmy, Basic Civil Engineering, McGraw Hill publishers.
2. Satheesh Gopi, Basic Civil Engineering, Pearson Publishers.
3. Ketki Rangwala Dalal, Essentials of Civil Engineering, Charotar Publishing House.
4. BCP, Surveying volume 1
Communicating effectively and consistently with students can help them feel at ease during their learning experience and provide the instructor with a communication trail to track the course's progress. This workshop will take you through constructing an engaging course container to facilitate effective communication.
Main Java[All of the Base Concepts}.docxadhitya5119
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How to Make a Field Mandatory in Odoo 17Celine George
In Odoo, making a field required can be done through both Python code and XML views. When you set the required attribute to True in Python code, it makes the field required across all views where it's used. Conversely, when you set the required attribute in XML views, it makes the field required only in the context of that particular view.
हिंदी वर्णमाला पीपीटी, hindi alphabet PPT presentation, hindi varnamala PPT, Hindi Varnamala pdf, हिंदी स्वर, हिंदी व्यंजन, sikhiye hindi varnmala, dr. mulla adam ali, hindi language and literature, hindi alphabet with drawing, hindi alphabet pdf, hindi varnamala for childrens, hindi language, hindi varnamala practice for kids, https://www.drmullaadamali.com
Temple of Asclepius in Thrace. Excavation resultsKrassimira Luka
The temple and the sanctuary around were dedicated to Asklepios Zmidrenus. This name has been known since 1875 when an inscription dedicated to him was discovered in Rome. The inscription is dated in 227 AD and was left by soldiers originating from the city of Philippopolis (modern Plovdiv).
2. NAME : MS. DHARSHINI
AGE : 11 YEARS
SEX : FEMALE
INFORMANT : MOTHER
EDUCATION OF INFORMANT : 10TH STD
RELIABILITY : GOOD
•
3. HISTORY OF PRESENTING ILLNESS
• A 11 year old 2nd born female child of NCM parents
brought by mother of good reliability who is a K/C/O
operated lipomyelomeningocele/ neurogenic bladder/
bladder outlet obstruction(BOO), came here for further
management. No complaints at present.
4. CASE EXPLAINED
Patient was noticed with a swelling only at birth in lumbosacral region,
said as fat in outside hospital (No treatment). At her 7 years of age she
developed bladder and bowel disturbance,
CT ABDOMEN : Neural tube defect at sacral bone at S1 level measuring
44mm with lipomyelomeningocele, interiorly the cor is extending upto
S2 level.
MRI ABDOMEN: Spinal dysraphism in lumbar spine, tethered cord
with overlying subcutaneous fat thickening with neural placode.
• diagnosed as Neural tube defect - Lipomyelomeningocele, and was
operated at her age of 8 years.
5. • Post surgery she had history of
» decresed food intake(solid foods)
» increased frequency of urination and defection
» vomiting on and off intermittently
» nausea/ abdominal pain for 3 days
Patient was taken to outside hospital,
• USG ABDOMEN done initially revealing chronic cystitis with
bilateral Grade II HUN.
• CT ABDOMEN WITH KUB, done and revealed, Distended urinary
bladder with mucosal irregularities, wall thickening of 5mm,
Bilateral moderate HUN due to reflux. She was started on antibiotics
and was acutely managed.
6. • Paediatric and urology opinion obtained and diagnosed as
Autonomous bladder. Neuro medicine opinion taken and
adviced for Clean intermittent catheterization( Bladder
training). Patient was catheterized for 6 months ( changes
monthly once)
• And reffered to higher centre for definitive management of
Autonomous bladder.
• Presently came to VMCH for the management.
7. • PAST HISTORY : K/C/O Lipomyelomeningocele operated at
her 8 years of age.
H/O Recurrent urinary tract infection
N/K/C/O CHD, Thyroid disorders, seizure disorder.
• ANTENATAL HISTORY : Booked and immunized, folic acid
tablets taken. No H/O GDM, GHTN
• NATAL HISTORY: Term, NVD at private hospital, cried
immediately after birth, Birth weight - 3.25kg, healthy
female child , now 11 years old. Swelling at back noticed at
birth, told as fat and was not operated.
• POSTNATAL HISTORY : No H/o NICU admission.
8. • MENSTRUAL HISTORY : Attained menarche at 9 years of age/
Regular/ 5/30 days cycle, no menstrual irregularities.
• IMMUNIZATION HISTORY: Immunized as per schedule
Last immunization was at 10 years of age.
DEVELOPMENTAL HISTORY: Milestones attained as per age
FAMILY HISTORY: No significant history
15 yrs 11 yrs
9. ANTHROPOMETRY
• HEIGHT - 142cm
• WEIGHT - 49kg
• BMI - 24.3kg/㎡
• WEIGHT FOR AGE - BETWEEN 90TH AND 97TH PERCENTILE
• HEIGHT FOR AGE - BETWEEN 25TH AND 50TH PERCENTILE
• BMI FOR AGE - ABOVE OBESE PERCENTILE( >95TH PERCENTILE)
• NUTRITIONAL ASSESSMENT - OVERWEIGHT
EQUIVALENT
10. • GENERAL EXAMINATION:
O/e patient concious, oriented, afebrile
No pallor, icterus, clubbing, cyanosis, pedal edema,
lymphadenopathy
• VITALS :
• HR - 94/min
• BP - 120/80mmhg
• RR - 22/min
• SPO2 - 98%
• LOCAL EXAMINATION :
Swelling over lumbosacral region
Size of 10*8cm, soft in consistency, no warmth, vertical scar of 11cm
over swelling, fluctuant +
11. SYSTEMIC EXAMINATION:
CVS - S1, S2 heard, no murmur
RS - B/L AE+, no added sounds
P/A - Soft, no tenderness, no organomegaly
CNS:
BULK: No obvious wasting
TONE: Normal in both lower and upeer limbs
POWER: 5/5 in all 4 limbs
REFLEXES : UL LL
» Biceps - ++ ++
» Triceps- ++ ++
» Supinator ++ ++
» Knee jerk +++ +++
» Ankle jerk ++ ++
» BILATERAL PLANTAR - NO RESPONSE
» SENSORY SYSTEM: NORMAL
13. TREATMENT
• ADVICED ABOUT THE STATUS AND CHRONIC CONDITION OF THE
PATIENT TO BOTH THE PATIENT AND ATTENDERS
• Initiated CLEAN INTERMITTENT CATHERIZATION
• PELVIC FLOOR EXERCISE( KEGELS EXERCISE)
• COUNCELLED ON PROPER HANDWASHING AND THE RISK OF
INFECTION OF THIS TREATMENT
• INPUT AND OUTPUT MONITORING DONE REGULARLY.
• PRESENTLY PATIENT PRACTICING FOR SELF CATHETERIZATION.
14. NEUROGENIC BLADDER
• Children with spinal dysraphism, spinal trauma, tumors may develop NEUROGENIC
BLADDER, and they also have a high risk of renal damage besides incontinence.
• They need a very long term follow up.
• Usually bladder innervation seen in spina bifida occulta, sacral agenesis, autonomic
neuropathy, spinal tumors or trauma.
EVALUATION: Firstly, they need a detailed neurological evaluation with attention
iver lower back tone, anal tone, sensations over perineum, heel besides only abdominal or
genital examination.
• USG should be carried out to see kidney size, bladder capacity, wall thickness, post
voidal residue/ MCU for vesicoureteric reflex / DMSA for renal scars, if both these are
normal, these are repeated every 12 to 18 months till 5years of age, as bladder dynamic
change with age.
• Three categories of lower tract dynamics: Bladder sphincter dysenergia
with/without bladder hypertonicity, synergic low pressure incontinent bladder
and a completely denervated bladder.
15. • .
• USG should be carried out to see kidney size, bladder capacity, wall
thickness, post voidal residue/ MCU for vesicoureteric reflex /
DMSA for renal scars, if both these are normal, these are repeated
every 12 to 18 months till 5years of age, as bladder dynamic change
with age.
• Three categories of lower tract dynamics: Bladder sphincter
dysenergia with/without bladder hypertonicity, synergic low
pressure incontinent bladder and a completely denervated
bladder.
16. MANAGEMENT
• Usually a child with spinal dysraphism lkely to have (elimination disorder) affecting evacuation of
both urinary bladder and bowel. If associated with constipation, should be treated early as it worsens
bladder.. with laxatives, a daily enema.
• Firstly, Crede’ maneuver - suprapubic massage, that results in reflux bladder contraction. Incase of
failure, go with CIC ( CLEAN INTERMITTENT CATHETERIZATION). This improves
significantly on long term followup and prevents UTI.
• Children who cannot empty their bladder spontaneously need CIC irrespective of the grade of reflux.
• Anti cholinergic for high pressurwe small volume bladder, Sympathomimmetics for who cannot stay
dry between catheterizations.
• Surgical procedures like, Vesicostomy in infants whose upper UT drainage fails even after CIC and
medications. Sphincterectomy to reduce bladder outlet obstriction. Reimplantation pf urethra in case
of reflux besides safe bladder.
• Pelvic floor exercise : KEGELS EXERCISE. To strengthen pelvic muscles in case of Urinary
incontinance, Fecal incontinance, Pelvic organ prolapse.