Familial adenomatous polyposis

Last updated: November 01, 2022

Familial adenomatous polyposis

gıt

gıt

Pancreatitis: Pathology review
Appendicitis: Pathology review
Diverticular disease: Pathology review
Cirrhosis: Pathology review
Malabsorption syndromes: Pathology review
Gastrointestinal bleeding: Pathology review
Colorectal polyps and cancer: Pathology review
Esophageal disorders: Pathology review
Congenital gastrointestinal disorders: Pathology review
GERD, peptic ulcers, gastritis, and stomach cancer: Pathology review
Jaundice: Pathology review
Viral hepatitis: Pathology review
Inflammatory bowel disease: Pathology review
Gallbladder disorders: Clinical
Gastrointestinal bleeding: Clinical
Cirrhosis: Clinical
Appendicitis: Clinical
Pancreatitis: Clinical
Inflammatory bowel disease: Clinical
Peptic ulcers and stomach cancer: Clinical
Laxatives and cathartics
Acid reducing medications
Antidiarrheals
Pediatric gastrointestinal bleeding: Clinical
Malabsorption: Clinical
Colorectal cancer: Clinical
Gastroesophageal reflux disease (GERD): Clinical
Diverticular disease: Clinical
Esophageal disorders: Clinical
Viral hepatitis: Clinical
Gastroparesis: Clinical
Esophagitis: Clinical
Diarrhea: Clinical
Jaundice: Clinical
Hepatitis A and Hepatitis E virus
Hepatitis B and Hepatitis D virus
Hepatocellular carcinoma
Alcohol-associated liver disease
Pyloric stenosis
Congenital diaphragmatic hernia
Esophageal web
Tracheoesophageal fistula
Aphthous ulcers
Sialadenitis
Oral candidiasis
Achalasia
Barrett esophagus
Boerhaave syndrome
Diffuse esophageal spasm
Gastroesophageal reflux disease (GERD)
Mallory-Weiss syndrome
Plummer-Vinson syndrome
Zenker diverticulum
Esophageal cancer
Peptic ulcer
Cyclic vomiting syndrome
Gastric dumping syndrome
Gastritis
Gastroparesis
Gastric cancer
Gastroenteritis
Hirschsprung disease
Intestinal atresia
Gastroschisis
Omphalocele
Imperforate anus
Intestinal malrotation
Meckel diverticulum
Intussusception
Necrotizing enterocolitis
Celiac disease
Lactose intolerance
Tropical sprue
Protein losing enteropathy
Small bowel bacterial overgrowth syndrome
Whipple's disease
Ulcerative colitis
Gallstone ileus
Volvulus
Intestinal adhesions
Bowel obstruction
Femoral hernia
Inguinal hernia
Abdominal hernias
Small bowel ischemia and infarction
Ischemic colitis
Colorectal polyps
Familial adenomatous polyposis
Colorectal cancer
Peutz-Jeghers syndrome
Juvenile polyposis syndrome
Gardner syndrome
Appendicitis
Diverticulosis and diverticulitis
Irritable bowel syndrome
Anal fissure
Anal fistula
Hemorrhoid
Rectal prolapse
Biliary atresia
Crigler-Najjar syndrome
Dubin-Johnson syndrome
Gilbert's syndrome
Rotor syndrome
Autoimmune hepatitis
Viral hepatitis
Wilson disease
Primary biliary cholangitis
Primary sclerosing cholangitis
Hemochromatosis
Jaundice
Non-alcoholic fatty liver disease
Cholestatic liver disease
Neonatal hepatitis
Cirrhosis
Benign liver tumors
Hepatic encephalopathy
Budd-Chiari syndrome
Portal hypertension
Hepatocellular adenoma
Acute cholecystitis
Chronic cholecystitis
Ascending cholangitis
Gallbladder carcinoma
Gallstones
Biliary colic
Cholangiocarcinoma
Chronic pancreatitis
Pancreatic cancer
Acute pancreatitis
Pancreatic pseudocyst
Zollinger-Ellison syndrome
Pancreatic neuroendocrine neoplasms

Transcript

Watch video only

With familial adenomatous polyposis, or simply FAP, familial refers to the fact that the disease runs in the family, and adenomatous polyposis refers to the fact that people affected develop multiple polyps that arise from the glands in the large intestine, which includes the colon and the rectum.

Now, the walls of the gastrointestinal tract are composed of four layers.

The outermost layer is called serosa.

Then there’s the muscular layer, which contracts in a synchronized way to move food through the bowel.

Then there is the submucosa, which consists of a dense layer of tissue through which blood vessels, lymphatics, and nerves run and branch into the mucosa and the muscular layer.

Finally, the inner lining of the intestine is called the mucosa; it surrounds the lumen of the gastrointestinal tract, and comes into direct contact with digested food.

The mucosa is organized as invaginations called the intestinal glands or colonic crypts, lined with large cells that are specialized in absorption.

Familial adenomatous polyposis is caused by an autosomal dominant mutation in the adenomatous polyposis coli gene or APC gene on chromosome 5q, which is a tumor suppressor gene.

Tumor suppressor genes stop cells from dividing uncontrollably.

But if the gene is mutated and the cell is without a functioning APC, the intestinal gland cells are more likely to accumulate mutations and start dividing faster than usual - ultimately giving rise to polyps, which are benign outgrowths of intestinal gland tissue.

Even though for any single polyp the chance that it evolves into cancer is generally quite low, polyps might accumulate additional mutations in other genes like the p53 gene (another tumor suppressor) or K-ras gene (a proto-oncogene), and with enough mutations, a cell might become completely unregulated and might start invading nearby tissue and become malignant.

Polyps can be classified by their gross appearance.

Some are flat, which means that they don’t protrude into the lumen and are flat up against the mucosa.

Some are pedunculated which means that they do protrude into the lumen and remain attached to the wall by a stalk, just like a mushroom.

And some are sessile which means that they also protrude into the lumen, but have their base firmly attached to the mucosa.

People with familial adenomatous polyposis develop a specific kind of polyp called adenomatous polyps or simply adenomas, and they’re usually pedunculated or sessile.

Under the microscope, the cells look like normal colonic mucosa cells.

There are three types of adenomas based on histology: tubular, with little hollow tubes within it, villous, with tiny tree-like branches, and tubulovillous, which look like a mix of the two with hollow tubes and tree-like branches.

Tubular adenomas are the most common type and have less malignant potential than villous adenomas, while tubulovillous adenomas have intermediate malignant potential.

Key Takeaways

Familial adenomatous polyposis (FAP) is a rare, autosomal dominant condition characterized by the development of many polyps in the colon and rectum. These polyps can become cancerous over time, leading to a high risk of developing colorectal cancer. Surgery is often recommended to remove the polyps and prevent cancer from developing.

FAP is caused by mutations in the adenomatous polyposis coli (APC) gene. This gene normally helps to suppress tumor growth in the colon. When it is mutated, this function is lost, resulting in an increased risk of developing tumors. FAP can be diagnosed through genetic testing.