Meckel's diverticulum is the most common congenital abnormality of the gastrointestinal tract, affecting approximately 2% of the population. It is a true diverticulum that forms from incomplete closure of the vitelline duct during fetal development. Meckel's diverticulum can contain heterotopic gastric or pancreatic tissue which can lead to ulceration and bleeding. Clinical presentations include hemorrhage, intestinal obstruction, diverticulitis, and intussusception. Diagnosis is often made through scans like a Meckel's scan or CT scan, and treatment involves surgical resection of the diverticulum.
Meckel's diverticulum is a vestigial remnant of the omphalomesenteric duct that connects the fetal intestine to the umbilical cord. It is the most common congenital anomaly of the gastrointestinal tract, affecting approximately 2% of the population. Meckel's diverticulum can occur anywhere along the small intestine but is usually located about 2 feet from the ileocecal valve. It often contains heterotopic or abnormal tissue such as gastric or pancreatic cells. Symptoms generally occur in children under 2 years of age and include bleeding, intestinal obstruction, or diverticulitis. Diagnosis can be made through scintigraphy or surgery is usually recommended for symptomatic cases.
Hirschsprung disease is a disorder where part or all of the large intestine lacks nerves and cannot function properly. This causes severe constipation or abdominal distension in infants. It occurs when neural crest cells fail to migrate during development. Diagnosis involves abdominal x-rays, barium enema, rectal biopsies and manometry. Treatment is surgical removal of the affected portion of intestine. The most common procedures are Swenson, Duhamel and Soave operations, which have mortality rates of 1-6% and risks of complications like leakage or enterocolitis.
Abdominal surgery and stomas are discussed, including:
- Common abdominal procedures for colorectal cancer like right/left hemicolectomy and anterior resection are described.
- Complications of surgery like anastomotic leaks and paralytic ileus are also covered.
- Stomas, specifically ileostomies and colostomies, are defined as ways to divert feces after removal of part of the colon and rectum. Differences between ileostomies and colostomies and potential complications are outlined.
This document provides an overview of Mirizzi's syndrome, including:
- The history and classification of Mirizzi's syndrome based on involvement of the bile duct.
- The predisposing factors, typical presentations, and diagnostic challenges of Mirizzi's syndrome, which can include obstructive jaundice.
- Treatment typically involves surgical approaches like cholecystectomy and bile duct repair, with risks of complications higher than typical cholecystectomy. Preoperative diagnosis is important for surgical planning.
MECKEL’S DIVERTICULUM- Pediatric Surgery
Dear Viewers,
Greetings from “Surgical Educator”
Today I have uploaded a video on Meckel’s diverticulum. This is a great imitator because of its varied ways of presentation. It can present as bleeding per rectum, intestinal obstruction, pain abdomen and fecal umbilical discharge. I have discussed the epidemiology, etiology, embryology, clinical features, investigations, differential diagnosis and treatment of Meckel’s diverticulum in this video. Hope you will enjoy the video. You can watch the video in the following links:
surgicaleducator.blogspot.com
youtube.com/c/surgicaleducator
Thank you for watching the video.
This document discusses obstructed defecation syndrome (ODS). It defines ODS as difficulty evacuating the rectum that may be associated with constipation. Common causes include diet, medications, and pelvic floor disorders. ODS is caused by abnormal function of muscles involved in defecation or anatomical abnormalities of pelvic organs. Diagnosis involves questionnaires, tests like defecography, and the ODS score. Treatment depends on the underlying cause and may include conservative options, biofeedback, or surgical procedures like STARR to repair defects.
The document summarizes information about the spleen, including its anatomy, development, location in the body, blood supply, histology, and functions. It then discusses splenic trauma and injuries, describing grading scales for injuries and treatment approaches. For minor injuries, nonoperative management is often adequate but more severe injuries may require splenectomy or partial resection to control bleeding.
Meckel's diverticulum is the most common congenital abnormality of the gastrointestinal tract, affecting approximately 2% of the population. It is a true diverticulum that forms from incomplete closure of the vitelline duct during fetal development. Meckel's diverticulum can contain heterotopic gastric or pancreatic tissue which can lead to ulceration and bleeding. Clinical presentations include hemorrhage, intestinal obstruction, diverticulitis, and intussusception. Diagnosis is often made through scans like a Meckel's scan or CT scan, and treatment involves surgical resection of the diverticulum.
Meckel's diverticulum is a vestigial remnant of the omphalomesenteric duct that connects the fetal intestine to the umbilical cord. It is the most common congenital anomaly of the gastrointestinal tract, affecting approximately 2% of the population. Meckel's diverticulum can occur anywhere along the small intestine but is usually located about 2 feet from the ileocecal valve. It often contains heterotopic or abnormal tissue such as gastric or pancreatic cells. Symptoms generally occur in children under 2 years of age and include bleeding, intestinal obstruction, or diverticulitis. Diagnosis can be made through scintigraphy or surgery is usually recommended for symptomatic cases.
Hirschsprung disease is a disorder where part or all of the large intestine lacks nerves and cannot function properly. This causes severe constipation or abdominal distension in infants. It occurs when neural crest cells fail to migrate during development. Diagnosis involves abdominal x-rays, barium enema, rectal biopsies and manometry. Treatment is surgical removal of the affected portion of intestine. The most common procedures are Swenson, Duhamel and Soave operations, which have mortality rates of 1-6% and risks of complications like leakage or enterocolitis.
Abdominal surgery and stomas are discussed, including:
- Common abdominal procedures for colorectal cancer like right/left hemicolectomy and anterior resection are described.
- Complications of surgery like anastomotic leaks and paralytic ileus are also covered.
- Stomas, specifically ileostomies and colostomies, are defined as ways to divert feces after removal of part of the colon and rectum. Differences between ileostomies and colostomies and potential complications are outlined.
This document provides an overview of Mirizzi's syndrome, including:
- The history and classification of Mirizzi's syndrome based on involvement of the bile duct.
- The predisposing factors, typical presentations, and diagnostic challenges of Mirizzi's syndrome, which can include obstructive jaundice.
- Treatment typically involves surgical approaches like cholecystectomy and bile duct repair, with risks of complications higher than typical cholecystectomy. Preoperative diagnosis is important for surgical planning.
MECKEL’S DIVERTICULUM- Pediatric Surgery
Dear Viewers,
Greetings from “Surgical Educator”
Today I have uploaded a video on Meckel’s diverticulum. This is a great imitator because of its varied ways of presentation. It can present as bleeding per rectum, intestinal obstruction, pain abdomen and fecal umbilical discharge. I have discussed the epidemiology, etiology, embryology, clinical features, investigations, differential diagnosis and treatment of Meckel’s diverticulum in this video. Hope you will enjoy the video. You can watch the video in the following links:
surgicaleducator.blogspot.com
youtube.com/c/surgicaleducator
Thank you for watching the video.
This document discusses obstructed defecation syndrome (ODS). It defines ODS as difficulty evacuating the rectum that may be associated with constipation. Common causes include diet, medications, and pelvic floor disorders. ODS is caused by abnormal function of muscles involved in defecation or anatomical abnormalities of pelvic organs. Diagnosis involves questionnaires, tests like defecography, and the ODS score. Treatment depends on the underlying cause and may include conservative options, biofeedback, or surgical procedures like STARR to repair defects.
The document summarizes information about the spleen, including its anatomy, development, location in the body, blood supply, histology, and functions. It then discusses splenic trauma and injuries, describing grading scales for injuries and treatment approaches. For minor injuries, nonoperative management is often adequate but more severe injuries may require splenectomy or partial resection to control bleeding.
Meckel's diverticulum is the most common congenital anomaly of the small bowel. It is a remnant of the vitelline duct that normally disappears during fetal development. Meckel's diverticulum occurs in approximately 2% of the population and is located in the ileum about 2 feet from the ileocecal junction. It can contain ectopic gastric, pancreatic, or colonic mucosa. While often asymptomatic, complications can include bleeding, diverticulitis, intestinal obstruction, and intussusception. Treatment of symptomatic Meckel's diverticulum involves surgical resection of the diverticulum through open or laparoscopic surgery.
This document provides an overview of hernias, including relevant anatomy, common sites, causes, types, clinical features, investigations, and treatment. It focuses on inguinal hernias, describing the anatomy of the inguinal canal, types of inguinal hernias (indirect, direct), clinical exam findings, and surgical repair techniques including open and laparoscopic approaches. Post-operative complications are also outlined.
This document discusses Mirizzi syndrome, which refers to common hepatic duct obstruction caused by an impacted gallstone. It can occur in 0.1-2.5% of gallstone cases. Large stones can impact in the cystic duct or gallbladder neck, causing mechanical obstruction or inflammation of the common hepatic duct. Patients often present with jaundice, abdominal pain, or cholangitis. Diagnosis is difficult but can be aided by imaging like MRCP or ERCP. Surgical treatment depends on the classification and may involve cholecystectomy with possible bile duct repair or bypass. Complications can include bile duct injury, bleeding, or stricture.
This document discusses various congenital anomalies requiring surgery in neonates. It begins by providing statistics on birth rates and the percentage of babies born with conditions needing surgical treatment. Specific conditions discussed include esophageal atresia, gastroschisis, omphalocele, intestinal malrotations, intestinal obstructions, Hirschsprung's disease, congenital hypertrophic pyloric stenosis, anorectal malformations, and tracheoesophageal fistula. For each condition, the document provides details on incidence, embryology, clinical presentation, diagnosis, and treatment approaches. It emphasizes the importance of timely surgical intervention to improve outcomes for babies born with these rare but serious birth defects.
The document summarizes the evolution of bowel anastomosis techniques from the early 19th century to modern practices. It describes early techniques such as Glover's suture and Lembert's suture. Lembert introduced the concept of sero-serous sutures rather than muco-mucosal sutures. It also discusses modified techniques by Dupuytren, Jobert, Czerny, and Kocher. Modern techniques now use a double layer approach with synthetic absorbable sutures. Key considerations for a successful anastomosis include minimizing tension, ensuring blood supply is maintained, and allowing for physiological healing over 10-14 days.
This document discusses the history, types, diagnosis and management of intussusception. It notes that intussusception occurs most often in children under 2 years old and presents with abdominal pain and vomiting. Ultrasound is the primary diagnostic tool, showing a target or doughnut-shaped mass. Management involves attempting non-operative reduction with hydrostatic or pneumatic enemas under radiologic guidance. Surgery is reserved for failed non-operative reduction or if signs of bowel ischemia are present. Recurrence rates after initial reduction are approximately 5-20%.
Gastroschisis and omphalocele are the two most common abdominal wall defects. Gastroschisis involves intestines protruding through an abdominal wall defect without a membrane covering, while omphalocele involves intestines covered by a membrane through an umbilical defect. Outcomes depend on associated anomalies, which are more common with omphalocele. Prenatal diagnosis allows for delivery planning, and management focuses on stabilization, careful examination for other issues, and surgical closure of the abdominal wall defect. Long-term outcomes depend on the presence of other anomalies.
Acute Diverticulitis is an inflammation of diverticula in the large intestine that commonly occurs in the sigmoid colon. It presents with lower abdominal pain, fever, and changes in bowel habits. Diagnosis is made through CT scan findings and blood tests. Treatment depends on severity and complications, ranging from oral antibiotics for uncomplicated cases to emergency surgery for perforated diverticulitis with peritonitis. Long term risks include recurrence requiring further treatment or surgery.
Choledochal cysts are congenital dilations of the bile duct that can be extrahepatic or intrahepatic. There are several proposed causes including abnormalities in the common bile duct that allow pancreatic juices to damage the duct wall. Histologically they show chronic inflammation and metaplasia. Todani classification divides choledochal cysts into 5 types based on location and extent of dilation. Clinical features include jaundice, abdominal pain, and palpable mass. Diagnosis involves imaging like ultrasound, CT, MRCP and biopsy. Treatment involves surgical excision and reconstruction, with more extensive procedures like liver transplantation needed for severe cases.
Biliary stricture is an abnormal narrowing of the bile duct. The most common cause is injury during cholecystectomy, accounting for 80% of non-malignant strictures. Bile duct injury can cause inflammation, fibrosis, scarring, and cirrhosis. Surgical treatment depends on when the injury is recognized, with immediate repair during surgery or delayed repair weeks later being options. Roux-en-Y hepaticojejunostomy is a common repair method that involves a mucosa-to-mucosa anastomosis of the bile duct to the jejunum. Factors like multiple prior repairs, proximal strictures, and surgeon inexperience can lead to poor outcomes.
This document discusses intestinal atresias and meconium ileus. It begins by describing duodenal atresia and stenosis, including historical aspects, incidence, embryology, theories of development, classification, and associated anomalies. It then covers clinical features, diagnosis including imaging studies, and management including surgical techniques like duodenoduodenostomy. Post-operative care and long-term complications are also summarized. The document concludes with a brief section on jejunoileal atresia.
1) Inguinal hernias are common, with approximately 700,000 repairs performed annually in the US, mostly occurring in males.
2) There are two main types of inguinal hernias - indirect and direct. Indirect hernias are congenital while direct hernias are acquired lesions that occur through the posterior inguinal wall.
3) Common surgical repair options include the Lichtenstein tension-free repair using mesh, the Shouldice repair with overlapping tissue layers, and laparoscopic repairs like TAPP and TEP which utilize a mesh placed laparoscopically.
The document discusses various tumors and conditions of the small intestine. The common benign and malignant tumors of the small intestine are listed. Details are provided about carcinoid tumors, including their classification and characteristics. Megaolon is described as a dilatation of the colon that can be congenital or acquired. Hirschsprung's disease is mentioned as a congenital form. Other topics covered include the carcinoid syndrome, Meckel's diverticulum, volvulus, and intussusception - the telescoping of one segment of intestine into another.
This document discusses different types of ventral hernias, including umbilical, epigastric, incisional, and paraumbilical hernias. It describes the causes, clinical features, diagnosis, and treatment options for each type. For treatment, it compares open surgical repair techniques like primary closure or mesh placement versus laparoscopic approaches. Complications of surgery like seroma, infection, and injury are also reviewed.
1. Choledochal cysts are abnormal dilations of the bile ducts that are more common in Asia and women.
2. They are classified into 5 types based on location and extent of dilation.
3. Presentation varies from jaundice and abdominal mass in children to pain and cholangitis in older patients.
4. Investigation involves ultrasound, CT, MRCP and cholangiography to determine type and rule out complications.
5. Treatment is complete excision of the cysts and biliary tree with Roux-en-Y hepaticojejunostomy, except for type III which can be managed endoscopically.
Choledochal cyst is a rare congenital dilatation of the bile duct that occurs in 1 in 100,000 people. It is more common in Asian populations and women. The pathogenesis is typically due to an anomalous pancreaticobiliary junction, where the pancreatic and biliary ducts fuse before entering the duodenum. This allows pancreatic secretions to reflux into the bile duct and cause inflammation and cystic degeneration. Choledochal cysts are classified into 5 types based on their location and extent. Patients typically present with jaundice, right upper quadrant pain, or a palpable mass. Investigations include ultrasound, CT, MRCP and ERCP to establish the diagnosis and classification. Complications include
Ventral hernias occur when abdominal contents protrude through weaknesses in the abdominal wall. There are several types of ventral hernias including umbilical, epigastric, incisional, and parastomal hernias. Incisional hernias occur through surgical scars and are more common with obesity, advanced age, and emergency surgeries. Treatment depends on hernia size but may involve primary repair for small defects or prosthetic mesh placement for larger defects. Laparoscopic repair is preferred when feasible due to benefits like fewer infections and shorter recovery.
This document discusses various causes and types of intestinal obstruction, including their presentation, diagnosis and management. It covers mechanical obstructions caused by adhesions, hernias, volvulus and intussusception. It also discusses paralytic ileus and pseudo-obstruction which are adynamic obstructions without a mechanical cause. The management involves supportive care, surgical correction of the underlying cause, and resection of non-viable intestine. Early diagnosis and treatment are important to prevent complications like strangulation.
This document discusses abdominal abscesses, including:
- Definitions and types of abdominal abscesses
- Pathophysiology, factors that favor abscess formation, and clinical features
- Diagnostic tests including X-ray, CT scan, USG, and MRI
- Management including adequate resuscitation, antimicrobial therapy, and source control through percutaneous or surgical drainage
- Specific discussions of pyogenic liver abscesses, amoebic liver abscesses, prerequisites and complications of percutaneous drainage, and criteria for drain removal
Hydatid cyst of the liver, also known as echinococcosis, is caused by the larval stage of the Echinococcus tapeworm. Humans can become infected by ingesting tapeworm eggs from infected animal feces. The parasite then develops into a hydatid cyst in the liver or lungs. A hydatid cyst grows slowly and can reach a large size, sometimes replacing an entire liver lobe. It consists of an outer layer (ectocyst) and inner layer (endocyst) that produces cyst fluid and daughter cysts. Rupture of the cyst can lead to spread of the parasite within the abdomen or chest. Imaging such as ultrasound and CT are important for diagnosis and show cyst
This document describes a case of a 12-year-old female who presented with abdominal pain and signs of peritonitis. She underwent an exploratory laparotomy which revealed a Meckel's diverticulum with gastric mucosa and a jejunal perforation. She had a complicated postoperative course requiring a second surgery. Meckel's diverticulum is a common congenital abnormality caused by incomplete vitelline duct obliteration. It can contain heterotopic gastric or pancreatic mucosa and commonly presents in children with GI bleeding. Surgical resection is often required for complications like perforation or obstruction.
Meckel's diverticulum is a congenital diverticulum that arises from the terminal ileum due to incomplete closure of the vitellointestinal duct during fetal development. It is the most common congenital anomaly of the small intestine. Symptomatic cases typically present with severe hemorrhage in children under 2 years old. A technetium scan is a useful diagnostic tool to detect Meckel's diverticulum, including cases with minimal bleeding. Treatment involves resection of the affected segment of ileum containing the diverticulum.
Meckel's diverticulum is the most common congenital anomaly of the small bowel. It is a remnant of the vitelline duct that normally disappears during fetal development. Meckel's diverticulum occurs in approximately 2% of the population and is located in the ileum about 2 feet from the ileocecal junction. It can contain ectopic gastric, pancreatic, or colonic mucosa. While often asymptomatic, complications can include bleeding, diverticulitis, intestinal obstruction, and intussusception. Treatment of symptomatic Meckel's diverticulum involves surgical resection of the diverticulum through open or laparoscopic surgery.
This document provides an overview of hernias, including relevant anatomy, common sites, causes, types, clinical features, investigations, and treatment. It focuses on inguinal hernias, describing the anatomy of the inguinal canal, types of inguinal hernias (indirect, direct), clinical exam findings, and surgical repair techniques including open and laparoscopic approaches. Post-operative complications are also outlined.
This document discusses Mirizzi syndrome, which refers to common hepatic duct obstruction caused by an impacted gallstone. It can occur in 0.1-2.5% of gallstone cases. Large stones can impact in the cystic duct or gallbladder neck, causing mechanical obstruction or inflammation of the common hepatic duct. Patients often present with jaundice, abdominal pain, or cholangitis. Diagnosis is difficult but can be aided by imaging like MRCP or ERCP. Surgical treatment depends on the classification and may involve cholecystectomy with possible bile duct repair or bypass. Complications can include bile duct injury, bleeding, or stricture.
This document discusses various congenital anomalies requiring surgery in neonates. It begins by providing statistics on birth rates and the percentage of babies born with conditions needing surgical treatment. Specific conditions discussed include esophageal atresia, gastroschisis, omphalocele, intestinal malrotations, intestinal obstructions, Hirschsprung's disease, congenital hypertrophic pyloric stenosis, anorectal malformations, and tracheoesophageal fistula. For each condition, the document provides details on incidence, embryology, clinical presentation, diagnosis, and treatment approaches. It emphasizes the importance of timely surgical intervention to improve outcomes for babies born with these rare but serious birth defects.
The document summarizes the evolution of bowel anastomosis techniques from the early 19th century to modern practices. It describes early techniques such as Glover's suture and Lembert's suture. Lembert introduced the concept of sero-serous sutures rather than muco-mucosal sutures. It also discusses modified techniques by Dupuytren, Jobert, Czerny, and Kocher. Modern techniques now use a double layer approach with synthetic absorbable sutures. Key considerations for a successful anastomosis include minimizing tension, ensuring blood supply is maintained, and allowing for physiological healing over 10-14 days.
This document discusses the history, types, diagnosis and management of intussusception. It notes that intussusception occurs most often in children under 2 years old and presents with abdominal pain and vomiting. Ultrasound is the primary diagnostic tool, showing a target or doughnut-shaped mass. Management involves attempting non-operative reduction with hydrostatic or pneumatic enemas under radiologic guidance. Surgery is reserved for failed non-operative reduction or if signs of bowel ischemia are present. Recurrence rates after initial reduction are approximately 5-20%.
Gastroschisis and omphalocele are the two most common abdominal wall defects. Gastroschisis involves intestines protruding through an abdominal wall defect without a membrane covering, while omphalocele involves intestines covered by a membrane through an umbilical defect. Outcomes depend on associated anomalies, which are more common with omphalocele. Prenatal diagnosis allows for delivery planning, and management focuses on stabilization, careful examination for other issues, and surgical closure of the abdominal wall defect. Long-term outcomes depend on the presence of other anomalies.
Acute Diverticulitis is an inflammation of diverticula in the large intestine that commonly occurs in the sigmoid colon. It presents with lower abdominal pain, fever, and changes in bowel habits. Diagnosis is made through CT scan findings and blood tests. Treatment depends on severity and complications, ranging from oral antibiotics for uncomplicated cases to emergency surgery for perforated diverticulitis with peritonitis. Long term risks include recurrence requiring further treatment or surgery.
Choledochal cysts are congenital dilations of the bile duct that can be extrahepatic or intrahepatic. There are several proposed causes including abnormalities in the common bile duct that allow pancreatic juices to damage the duct wall. Histologically they show chronic inflammation and metaplasia. Todani classification divides choledochal cysts into 5 types based on location and extent of dilation. Clinical features include jaundice, abdominal pain, and palpable mass. Diagnosis involves imaging like ultrasound, CT, MRCP and biopsy. Treatment involves surgical excision and reconstruction, with more extensive procedures like liver transplantation needed for severe cases.
Biliary stricture is an abnormal narrowing of the bile duct. The most common cause is injury during cholecystectomy, accounting for 80% of non-malignant strictures. Bile duct injury can cause inflammation, fibrosis, scarring, and cirrhosis. Surgical treatment depends on when the injury is recognized, with immediate repair during surgery or delayed repair weeks later being options. Roux-en-Y hepaticojejunostomy is a common repair method that involves a mucosa-to-mucosa anastomosis of the bile duct to the jejunum. Factors like multiple prior repairs, proximal strictures, and surgeon inexperience can lead to poor outcomes.
This document discusses intestinal atresias and meconium ileus. It begins by describing duodenal atresia and stenosis, including historical aspects, incidence, embryology, theories of development, classification, and associated anomalies. It then covers clinical features, diagnosis including imaging studies, and management including surgical techniques like duodenoduodenostomy. Post-operative care and long-term complications are also summarized. The document concludes with a brief section on jejunoileal atresia.
1) Inguinal hernias are common, with approximately 700,000 repairs performed annually in the US, mostly occurring in males.
2) There are two main types of inguinal hernias - indirect and direct. Indirect hernias are congenital while direct hernias are acquired lesions that occur through the posterior inguinal wall.
3) Common surgical repair options include the Lichtenstein tension-free repair using mesh, the Shouldice repair with overlapping tissue layers, and laparoscopic repairs like TAPP and TEP which utilize a mesh placed laparoscopically.
The document discusses various tumors and conditions of the small intestine. The common benign and malignant tumors of the small intestine are listed. Details are provided about carcinoid tumors, including their classification and characteristics. Megaolon is described as a dilatation of the colon that can be congenital or acquired. Hirschsprung's disease is mentioned as a congenital form. Other topics covered include the carcinoid syndrome, Meckel's diverticulum, volvulus, and intussusception - the telescoping of one segment of intestine into another.
This document discusses different types of ventral hernias, including umbilical, epigastric, incisional, and paraumbilical hernias. It describes the causes, clinical features, diagnosis, and treatment options for each type. For treatment, it compares open surgical repair techniques like primary closure or mesh placement versus laparoscopic approaches. Complications of surgery like seroma, infection, and injury are also reviewed.
1. Choledochal cysts are abnormal dilations of the bile ducts that are more common in Asia and women.
2. They are classified into 5 types based on location and extent of dilation.
3. Presentation varies from jaundice and abdominal mass in children to pain and cholangitis in older patients.
4. Investigation involves ultrasound, CT, MRCP and cholangiography to determine type and rule out complications.
5. Treatment is complete excision of the cysts and biliary tree with Roux-en-Y hepaticojejunostomy, except for type III which can be managed endoscopically.
Choledochal cyst is a rare congenital dilatation of the bile duct that occurs in 1 in 100,000 people. It is more common in Asian populations and women. The pathogenesis is typically due to an anomalous pancreaticobiliary junction, where the pancreatic and biliary ducts fuse before entering the duodenum. This allows pancreatic secretions to reflux into the bile duct and cause inflammation and cystic degeneration. Choledochal cysts are classified into 5 types based on their location and extent. Patients typically present with jaundice, right upper quadrant pain, or a palpable mass. Investigations include ultrasound, CT, MRCP and ERCP to establish the diagnosis and classification. Complications include
Ventral hernias occur when abdominal contents protrude through weaknesses in the abdominal wall. There are several types of ventral hernias including umbilical, epigastric, incisional, and parastomal hernias. Incisional hernias occur through surgical scars and are more common with obesity, advanced age, and emergency surgeries. Treatment depends on hernia size but may involve primary repair for small defects or prosthetic mesh placement for larger defects. Laparoscopic repair is preferred when feasible due to benefits like fewer infections and shorter recovery.
This document discusses various causes and types of intestinal obstruction, including their presentation, diagnosis and management. It covers mechanical obstructions caused by adhesions, hernias, volvulus and intussusception. It also discusses paralytic ileus and pseudo-obstruction which are adynamic obstructions without a mechanical cause. The management involves supportive care, surgical correction of the underlying cause, and resection of non-viable intestine. Early diagnosis and treatment are important to prevent complications like strangulation.
This document discusses abdominal abscesses, including:
- Definitions and types of abdominal abscesses
- Pathophysiology, factors that favor abscess formation, and clinical features
- Diagnostic tests including X-ray, CT scan, USG, and MRI
- Management including adequate resuscitation, antimicrobial therapy, and source control through percutaneous or surgical drainage
- Specific discussions of pyogenic liver abscesses, amoebic liver abscesses, prerequisites and complications of percutaneous drainage, and criteria for drain removal
Hydatid cyst of the liver, also known as echinococcosis, is caused by the larval stage of the Echinococcus tapeworm. Humans can become infected by ingesting tapeworm eggs from infected animal feces. The parasite then develops into a hydatid cyst in the liver or lungs. A hydatid cyst grows slowly and can reach a large size, sometimes replacing an entire liver lobe. It consists of an outer layer (ectocyst) and inner layer (endocyst) that produces cyst fluid and daughter cysts. Rupture of the cyst can lead to spread of the parasite within the abdomen or chest. Imaging such as ultrasound and CT are important for diagnosis and show cyst
This document describes a case of a 12-year-old female who presented with abdominal pain and signs of peritonitis. She underwent an exploratory laparotomy which revealed a Meckel's diverticulum with gastric mucosa and a jejunal perforation. She had a complicated postoperative course requiring a second surgery. Meckel's diverticulum is a common congenital abnormality caused by incomplete vitelline duct obliteration. It can contain heterotopic gastric or pancreatic mucosa and commonly presents in children with GI bleeding. Surgical resection is often required for complications like perforation or obstruction.
Meckel's diverticulum is a congenital diverticulum that arises from the terminal ileum due to incomplete closure of the vitellointestinal duct during fetal development. It is the most common congenital anomaly of the small intestine. Symptomatic cases typically present with severe hemorrhage in children under 2 years old. A technetium scan is a useful diagnostic tool to detect Meckel's diverticulum, including cases with minimal bleeding. Treatment involves resection of the affected segment of ileum containing the diverticulum.
Meckel`s Diveticulum.pptx Meckel's diverticulum is the most common congenital...DrSabinShrestha1
Meckel's diverticulum is the most common congenital anomaly of the gastrointestinal tract. It results from incomplete obliteration of the vitelline duct leading to the formation of a true diverticulum of the small intestine.
The embryology, clinical features, diagnosis, and treatment of Meckel's diverticulum are reviewed here. The clinical evaluation of various gastrointestinal symptoms (abdominal pain, gastrointestinal bleeding, bowel obstruction) in children and adults is found in separate topic reviews. General considerations for the management of other congenital anomalies of the gastrointestinal tract are reviewed elsewhere.
Meckel's diverticulum is a true diverticulum, containing all layers of the small bowel wall. It arises from the antimesenteric surface of the middle-to-distal ileum. The diverticulum represents a persistent remnant of the omphalomesenteric duct, which connects the midgut to the yolk sac in the fetus.
The omphalomesenteric duct normally involutes between the fifth and sixth weeks of human gestation as the bowel settles into its permanent position within the abdominal cavity.
Meckel's diverticulum is the most common congenital malformation of the gastrointestinal tract [1]. There is probably no familial predisposition for Meckel's diverticulum, although a few cases of occurrence within the same family have been reported . The prevalence of Meckel's diverticulum is increased in children born with major malfo
Meckel diverticulum is a congenital abnormality caused by persistence of the omphalomesenteric duct, which normally disappears by gestational week 9. It occurs in about 2% of the population and is most common in children under age 2. Complications include bleeding from ulceration caused by ectopic gastric tissue, intestinal obstruction, and diverticulitis. Symptoms include painless rectal bleeding in infants and intestinal obstruction presenting as vomiting and abdominal distension in newborns. Diagnosis involves scans concentrating isotopes in ectopic gastric mucosa or x-rays showing dilated bowel loops. Surgical removal of the diverticulum is treatment for complications like bleeding or obstruction.
This document discusses neonatal abdominal emergencies, including their causes, embryology, and anomalies. It begins by introducing abdominal emergencies in neonates, infants, and children. It then covers the embryology of the gastrointestinal tract, including the development of the foregut, midgut, and hindgut. Specific anomalies are discussed such as Meckel's diverticulum and intestinal malrotation. Diagnosis and treatment of some conditions are also mentioned.
The document summarizes Meckel's diverticulum, which is the most common congenital abnormality of the gastrointestinal tract. It arises from incomplete obliteration of the vitelline duct during fetal development. Key points include:
- Meckel's diverticulum contains all three layers of the bowel and can contain ectopic gastric or pancreatic tissue.
- It is usually found within 2 feet of the ileocecal valve and is symptomatic in only about 2% of adults but more commonly in children under 2 years old.
- Common presentations include bleeding, intestinal obstruction, diverticulitis, and intussusception. Bleeding can be caused by ulceration from acidic secretions of
Meckel's diverticulum is the most common congenital abnormality of the gastrointestinal tract, occurring in approximately 2% of the population. It results from incomplete obliteration of the vitelline duct during fetal development. While most cases are asymptomatic, Meckel's diverticulum can cause complications like bleeding, diverticulitis, intestinal obstruction, and intussusception due to heterotopic gastric or pancreatic tissue. Diagnosis is often made through scans like a technetium-99m pertechnetate scan or CT scan. Treatment involves surgical resection of the diverticulum and adjacent bowel segment for symptomatic cases.
Meckel's diverticulum is the most common congenital anomaly of the gastrointestinal tract, affecting approximately 2% of the population. It results from incomplete obliteration of the omphalomesenteric (vitelline) duct during fetal development. While most cases are asymptomatic, complications can include bleeding, intestinal obstruction, and diverticulitis. Diagnosis is often incidental but can be aided by imaging like CT scans. Treatment involves surgical removal of the diverticulum (diverticulectomy).
This document provides an overview of Meckel's diverticulum, including its embryology, epidemiology, clinical presentation, diagnosis, treatment, and references for further information. Meckel's diverticulum results from incomplete obliteration of the vitelline duct during fetal development, leading to a true diverticulum of the small intestine. It most commonly presents with gastrointestinal bleeding, intestinal obstruction, or inflammation/intussusception in children under 2 years old. Diagnosis involves imaging scans or surgical exploration. Treatment is diverticulectomy, which can be performed open or laparoscopically.
1. The midgut forms a U-shaped loop that herniates through the umbilical ring and undergoes two rotations to return to the abdominal cavity, positioning the appendix on the right.
2. Failure of the midgut to return or complete rotation can result in defects like omphalocele, malrotation, intestinal atresia or stenosis.
3. Common midgut defects include Meckel's diverticulum from persistence of the vitelline duct and intestinal malrotation from incomplete rotation.
1. The midgut forms a U-shaped loop that herniates through the umbilical ring and undergoes two rotations to return to the abdominal cavity, positioning the appendix on the right.
2. Failure of the midgut to return or complete rotation can result in defects like omphalocele, malrotation, intestinal atresia or stenosis.
3. Common midgut defects include Meckel's diverticulum from persistence of the vitelline duct and intestinal malrotation from incomplete rotation.
This document discusses acquired intestinal ileus, which can be paralytic or mechanical in nature. Paralytic ileus is caused by medications, surgery, infection, or other insults and results in paralysis of intestinal movement. Mechanical obstruction can be caused by hernias, adhesions, tumors or other structural issues that physically block intestinal contents. Symptoms include abdominal pain, distension and inability to pass gas or stool. Diagnosis involves physical exam, imaging and labs. Treatment focuses on restoring bowel motility with decompression, fluids and electrolyte replacement. The document also discusses specific causes like intussusception, adhesions and their signs, symptoms, diagnosis and management.
1. Acute appendicitis is caused by obstruction of the appendix lumen leading to increased intraluminal pressure, edema, and bacterial invasion.
2. Signs and symptoms include migratory pain that localizes to the right lower quadrant, nausea, vomiting, anorexia, and rebound tenderness.
3. Treatment is surgical removal of the appendix, which can be done through open or laparoscopic approaches. Complications include bleeding, infection, and abscess formation if not treated promptly.
1. Imperforate anus is a birth defect where the rectum is not connected to the anus. It requires surgery to create an opening for stool passage.
2. Surgery for high or intermediate cases first creates a temporary colostomy. After months of growth, a more complex procedure connects the rectum to the new anus.
3. Necrotizing enterocolitis is a disease that affects premature infants, causing parts of the intestine to die. It requires stopping feeds, antibiotics, and may necessitate surgery to remove dead sections of bowel.
Meckel diverticulum is the most common congenital malformation of the gastrointestinal tract, occurring in approximately 2% of the population. It is a remnant of the fetal ombilical cord that fails to close off after birth. Common complications include bleeding, bowel obstruction, and inflammation. Symptoms may include abdominal pain, bloody stools, and anemia. Diagnosis is often made through scans or nuclear imaging studies. Treatment involves surgical removal of the diverticulum. With early diagnosis and treatment, prognosis is typically good, but untreated cases have mortality rates as high as 15%.
Acute appendicitis is inflammation of the appendix that is most common in people aged 5-35. It occurs when the appendix becomes blocked, usually by a fecalith, causing bacterial infection and tissue damage. Common symptoms include abdominal pain localized to the lower right side, nausea, vomiting, and fever. A physical exam may reveal tenderness at McBurney's point. Imaging tests and bloodwork can help diagnose appendicitis, and it is scored using the Alvarado scale. Treatment involves antibiotics, IV fluids, and an appendectomy to remove the inflamed appendix. Complications can include perforation, abscess formation, and infection spread.
The document discusses the anatomy and abnormalities of the abdominal wall and retroperitoneum. It describes the layers of the abdominal wall including the innervation of muscles. It also discusses congenital abnormalities such as omphalocele and gastroschisis. Acquired conditions like rectus diastasis and rectus sheath hematoma are also summarized. Common malignancies, diseases of the omentum and mesentery are briefly described.
- A 49-year-old man presented with abdominal pain and vomiting. Imaging showed a partial small bowel obstruction.
- During surgery, a Meckel's diverticulum was found torsed around the small bowel, causing the obstruction. The Meckel's diverticulum was resected.
- Meckel's diverticulum is the most common congenital gastrointestinal abnormality, occurring in about 2% of the population. It can cause bleeding, intestinal obstruction, or inflammation/perforation from diverticulitis.
Meckel's diverticulum is the most common congenital anomaly of the gastrointestinal tract, occurring in approximately 2% of the population. It results from the incomplete obliteration of the vitelline duct during embryonic development. While most cases are asymptomatic, complications can include bleeding, intestinal obstruction, or diverticulitis. Symptomatic cases often present with painless rectal bleeding in children or intestinal obstruction in adults. Surgical resection is the treatment for symptomatic diverticula, while the management of asymptomatic cases remains controversial.
11. Other Problems in Inflammatory Response.pptxJRRolfNeuqelet
This document discusses several inflammatory conditions that can affect different body systems. It provides details on the causes, symptoms, diagnostic tests and treatments for appendicitis, peritonitis, pancreatitis, cholecystitis, and cystitis. Appendicitis is caused by obstruction of the appendix, usually by a fecalith, and requires appendectomy to prevent rupture. Peritonitis is inflammation of the abdominal lining that can result from a perforated appendix or other infections. Pancreatitis may be due to gallstones or alcohol and causes abdominal pain. Cholecystitis is gallbladder inflammation often from gallstones blocking the cystic duct. Cystitis is a urinary tract infection.
- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
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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.
3. INTRODUCTION:
● Meckel’s diverticulum is the abnormality /
pathology in the last part of small intestine ( ie in
ileum ) and it is a congenital condition.
● It was reported initially in 1598 by Hildanus and
then described in detail by Johann Meckel in
1809.
● Diverticulum - an abnormal pouch or sac ,
opening from a hollow organ
6. VITELLOINTESTINAL DUCT :
● Aka vitelline duct , yolk stalk ,
omphalomesenteric duct ,
omphaloenteric duct
● It connects midgut with yolk
sac.
● It appears at the end of 4th
week and disappears by 8th to
9th week of Intrauterine life
after the placenta replaces the
yolk sac.
7. What if vitellointestinal duct doesn’t obliterates (or)
disappears?
The failure to disappear completely or
any part of the duct doesn’t disappear it
will produce anomalies of vitellointestinal
duct . They are :
● Meckel’s diverticulum
● Umbilical sinus
● Umbilical ( vitelline fistula )
● Vitelline cyst
9. Meckel’s diverticulum - Definition:
● A congenital anomaly in which a small
part of vitellointestinal duct persists
close to midgut ( ileum ) . It present as
an outpouching or bulge in the small
intestine (terminal / end of ileum) .
● It’s apex is usually free but sometimes
may be connected to anterior
abdominal wall by a fibrous cord ( the
obliterated remaining part of
vitellointestinal duct ) .
10. Salient features of Meckel’s diverticulum:
● Meckel's diverticulum is the most common congenital
defect of the Small intestine.
● Arises from antimesenteric border of the ileum.
● Contains all layers of bowel ( so it is called , TRUE
DIVERTICULUM )
● Meckel’s diverticulum has independent blood supply.
● A Meckel's diverticulum may ( in 20% cases ) contain
cells from both the stomach and pancreas (
HETEROTOPIC EPITHELIUM ) Cells from the
stomach can secrete acid, which can cause ulcers and
bleeding
11.
12. Rule of 2 :
● 2% of population is affected
● 2 inches long
● 2 feet proximal from the ileocecal junction
● 2% of Meckel’s diverticulum patient will be symptomatic
● 2 types of epithelium ( heterotrophic ) in 20% of
population ( that is presence of gastric and pancreatic
type of epithelial cells )
● 2:1 ratio ( m:f )
13. Clinical presentation:
● Though 2% to 3% of the population gets
Meckel's diverticulum, it causes symptoms
in only a small number of those people .
● Majority of People can live their whole lives
without ever knowing they have Meckel's
diverticulum (Asymptomatic)
● Symptoms of Meckel's diverticulum usually
occur during the first year of a child's life (
<2 years of age ), but can occur into
adulthood.
14. The patient may present with :
● Gastrointestinal bleeding ( M/C Presentation )
● Meckel’s diverticulitis
● Perforated diverticulum
● Bowel obstruction due to mesodiverticular band
● Volvulus , intussusception of small bowel
● Littre's hernia
● Tumor
15. Gastrointestinal bleeding:
● Most common presentation .
● Lower GI hemorrhage and pain due to
gastric mucosa present in diverticulum
secretes acid which causes bleeding
and ulceration resulting in rectal bleed
or Malena.
● Management - self limiting usually but if
persists embolisation / diverticulectomy
( embolisation - procedure that blocks
or closes a specific blood vessel using
embolic agents like balloons or metallic
coils )
16. Meckel’s diverticulitis:
● Infection and inflammation of Meckel’s diverticulum
due to bacterial infection which can go on to
Gangrene .
● Mimics acute appendicitis.
● Seen in 20% cases and the patient presents with
abdominal pain in right lower quadrant and rectal
bleeding .
● Diagnosis- USG , CT
● Management- diverticulectomy
17. Perforated diverticulum:
● If perforated , peritonitis occurs.
● Management- Resection and
Anastomosis ( ileocolic anastomosis )
18. Bowel obstruction:
● Due to trapping of a bowel loop by
mesodiverticular band or due to
volvulus or due to intussusception.
● Mesodiverticular band - embryological
remnant of vitelline circulation which
carries the arterial supply to the Meckel's
diverticulum
19. VOLVULUS :
● Portion of small intestine may twist around
the Meckel’s diverticulum causing
compromised blood supply ( necrosis) and
bowel obstruction.
INTUSSUSCEPTION :
● When one part of the bowel ( here
Meckel’s diverticulum) slides into the next ,
much like a pieces of telescope.
● It may be ileoileal or ileocolic
intussusception.
20. Littre’s Hernia :
● Any hernia ( femoral or inguinal )
which contains Meckel’s diverticulum
as content in the hernial sac. It can
also cause bowel obstruction.
● Management- Resection of
diverticulum and herniorrhaphy (
surgical repair of hernia and the
weakness in the abdominal wall )
21. Tumor :
● Tumor can also occur in Meckel’s
diverticulum with Neuroendocrine Tumor (
NET ) or carcinoid Tumor is the most
common malignant tumor ( in 77% of cases )
● NET - Tumor arising from neuroendocrine
cells
● Neuroendocrine cells are cells that receive
neural input and, as a consequence of this
input, release messenger molecules
(hormones) into the blood. Eg : cells in
stomach , pancreas , pituitary etc ..
23. ● Meckel's diverticulum can be difficult to diagnose
because many of the symptoms, such as vomiting,
abdominal pain, and tenderness, can occur in
several different conditions.
● 99mTc-pertechnetate scan - Radioactive
technetium is injected into the body. This
substance is absorbed by stomach cells in the
diverticulum and can be detect diverticulum
● Colonoscopy : A small, flexible tube with a camera
on the end is inserted into the rectum and colon to
look for blockages and the cause of bleeding.
● Small bowel enema / enteroclysis - x-ray
procedure that examines the small bowel using
Contrast material.
25. ● Many adults who have Meckel's
diverticulum never have symptoms.
They learn they have the condition
only after it is noticed during surgery
or during tests for another condition (
incidental finding ). In this case,
Meckel's diverticulum usually does not
have to be treated.
● Surgical management - Meckel’s
diverticulectomy with or without
small bowel resection.
26. MECKEL’S DIVERTICULECTOMY :
Surgical removal of Meckel’s diverticulum and
after resection, suture the defect at its base or
join with a linear stapler cutter.
The INDICATIONS for surgery are ,
● When the base and mouth of diverticulum
is narrow
● Lengthy diverticulum
● Presence of adhesions or any fibrous band
like mesodiverticular band
● Symptomatic Patients ( or ) patients with
complications
● If it is found in children below 2 years.
27. Complications of Meckel’s diverticulectomy:
● Damage to nearby organs in the body.
● Wound infections or the wound breaks open after
surgery.
● The edges of your intestines that are sewn or
stapled together (anastomosis) may come open.
● The area where the intestines are sewn together
can scar and create blockage of the intestine.
● Blockage of the intestine may occur later from
adhesions caused by the surgery