Gastroenterology Flashcards

(50 cards)

1
Q

What are the major gastrointestinal hormones involved in food digestion?

A

Gastrin, Cholecystokinin (CCK), Secretin, Vasoactive Intestinal Peptide (VIP), and Somatostatin.

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2
Q

What is the source and stimulus for Gastrin secretion?

A

G cells in the antrum of the stomach. Stimulus: Distension of the stomach, swallowing, vagus nerve stimulation, luminal peptides/amino acids, acetylcholine, and histamine. Inhibited by low antral pH and somatostatin.

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3
Q

What are the actions of Gastrin?

A

Increases HCl, pepsinogen, and intrinsic factor secretion; increases gastric motility; stimulates parietal cell maturation.

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4
Q

What is the source and stimulus for Cholecystokinin (CCK) secretion?

A

I cells in the upper small intestine. Stimulus: Partially digested proteins and triglycerides.

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5
Q

What are the actions of Cholecystokinin (CCK)?

A

Stimulates gallbladder contraction, increases secretion of enzyme-rich fluid from the pancreas, relaxes the sphincter of Oddi, decreases gastric emptying, and induces satiety.

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6
Q

What is the source and stimulus for Secretin secretion?

A

Source: S cells in the upper small intestine. Stimulus: Acidic chyme and fatty acids.

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7
Q

What are the actions of Secretin?

A

Increases secretion of bicarbonate-rich fluid from the pancreas and liver; decreases gastric acid secretion.

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8
Q

What is the source and stimulus for Vasoactive Intestinal Peptide (VIP) secretion?

A

Source: Small intestine and pancreas. Stimulus: Neural stimulation.

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9
Q

What are the actions of Vasoactive Intestinal Peptide (VIP)?

A

Acts as a vasodilator, regulates smooth muscle activity, epithelial cell secretion, and gastrointestinal blood flow; stimulates secretion by the pancreas and intestines; inhibits acid secretion.

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10
Q

What is the source and stimulus for Somatostatin secretion?

A

Source: D cells in the pancreas and stomach. Stimulus: Fat, bile salts, and glucose in the intestinal lumen.

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11
Q

What are the actions of Somatostatin?

A

Inhibits all gastrointestinal endocrine secretions, decreases acid and pepsin secretion, decreases gastrin secretion, decreases pancreatic enzyme secretion, decreases insulin and glucagon secretion, and stimulates gastric mucous production.

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12
Q

What is VIPoma?

A

A vasoactive intestinal polypeptide (VIP)-secreting tumor, mainly occurring in the pancreas, causing symptoms like watery diarrhea, dehydration, hypokalemia, and achlorhydria.

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13
Q

What is the treatment for VIPoma?

A

Somatostatin analogs, codeine for diarrhea, and surgical resection for non-metastatic tumors.

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14
Q

What are the indications for upper GI endoscopy in GERD?

A

Age > 55 years, symptoms > 4 weeks, dysphagia, relapsing symptoms, and weight loss.

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15
Q

What is the gold standard test for diagnosing GERD?

A

24-hour esophageal pH monitoring.

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16
Q

What is Barrett’s esophagus?

A

Metaplasia of the lower esophageal mucosa, where squamous epithelium is replaced by columnar epithelium, associated with GERD and increased risk of esophageal adenocarcinoma.

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17
Q

What is the management of Barrett’s esophagus?

A

High-dose PPIs for 8-12 weeks, endoscopic surveillance, cryotherapy, and esophagectomy in severe cases.

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18
Q

What are the risk factors for esophageal cancer?

A

Smoking, alcohol, GERD, Barrett’s esophagus, achalasia, Plummer-Vinson syndrome, and rare associations like celiac disease and scleroderma.

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19
Q

What is Achalasia?

A

Failure of esophageal peristalsis and relaxation of the lower esophageal sphincter due to degenerative loss of ganglia from Auerbach’s plexus.

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20
Q

What is the gold standard test for diagnosing Achalasia?

A

Esophageal manometry.

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21
Q

What is the treatment for Achalasia?

A

Heller cardiomyotomy, balloon dilation, botulinum toxin injection, and drug therapy with nifedipine or nitrates.

22
Q

What is Boerhaave’s syndrome?

A

Spontaneous esophageal rupture, often due to vomiting, presenting with severe epigastric pain, pleural effusion, and respiratory distress.

23
Q

What is the diagnostic test for esophageal rupture?

A

Gastrografin swallow.

24
Q

What is the acute treatment for variceal hemorrhage?

A

ABC resuscitation, correction of clotting, vasoactive agents (terlipressin), prophylactic antibiotics, endoscopic variceal band ligation, and Sengstaken-Blakemore tube if uncontrolled.

25
What is the prophylaxis for variceal hemorrhage?
Propranolol and endoscopic variceal band ligation (EVL).
26
What is the Rockall scoring system used for?
Stratifying patients with gastrointestinal bleeding into high and low-risk groups based on age, comorbidities, shock, endoscopic abnormalities, and evidence of bleeding.
27
What is Meckel's diverticulum?
A vestigial remnant of the omphalomesenteric duct, located in the terminal ileum, which can contain ectopic gastric mucosa and cause complications like bleeding, diverticulitis, and obstruction.
28
What is the diagnostic test for Meckel's diverticulum?
Tc-99m pertechnetate scan.
29
What are the associations of Helicobacter pylori?
Peptic ulcer disease, gastric cancer, B-cell lymphoma of MALT tissue, and atrophic gastritis.
30
What is the treatment for H. pylori eradication?
Triple therapy with a PPI, amoxicillin, and clarithromycin or metronidazole for 7 days.
31
What is Zollinger-Ellison syndrome?
A condition characterized by excessive gastrin secretion, usually from a gastrin-secreting tumor in the duodenum or pancreas, causing multiple gastroduodenal ulcers and diarrhea.
32
What is the diagnostic test for Zollinger-Ellison syndrome?
Fasting gastrin levels on 3 different days and secretin stimulation test.
33
What are the risk factors for gastric cancer?
Chronic H. pylori infection, blood group A, gastric adenomatous polyps, pernicious anemia, smoking, alcohol, and dietary factors like salty, spicy, and smoked foods.
34
What is non-alcoholic fatty liver disease (NAFLD)?
A spectrum of liver disease ranging from steatosis to steatohepatitis (NASH), fibrosis, and cirrhosis, often associated with obesity and insulin resistance.
35
What is the management of NAFLD?
Lifestyle changes (weight loss, low-fat diet), supervised exercise, and monitoring. Medications like pioglitazone and orlistat may be used in some cases.
36
What is autoimmune hepatitis?
A chronic liver disease of unknown etiology, most common in young females, associated with other autoimmune disorders and hypergammaglobulinemia.
37
What is the treatment for autoimmune hepatitis?
Steroids and immunosuppressants like azathioprine.
38
What is the most common cause of hepatocellular carcinoma (HCC) worldwide?
Chronic hepatitis B.
39
What is the treatment for hepatocellular carcinoma (HCC)?
Surgical resection or liver transplantation for localized disease. Non-surgical options include percutaneous ethanol injection, TACE, and radiofrequency ablation.
40
What is primary biliary cirrhosis (PBC)?
A chronic liver disease characterized by immune-mediated destruction of intrahepatic bile ducts, leading to cholestasis, fibrosis, and cirrhosis, often associated with antimitochondrial antibodies (AMA).
41
What is the treatment for primary biliary cirrhosis (PBC)?
Ursodeoxycholic acid, cholestyramine for pruritus, fat-soluble vitamin supplementation, and liver transplantation in advanced cases.
42
What is primary sclerosing cholangitis (PSC)?
A chronic cholestatic liver disease characterized by inflammation and fibrosis of intra- and extrahepatic bile ducts, often associated with ulcerative colitis.
43
What is the gold standard diagnostic test for PSC?
ERCP, though MRCP is often used initially due to its non-invasive nature.
44
What is Gilbert's syndrome?
An autosomal recessive condition causing mild unconjugated hyperbilirubinemia due to a deficiency of UDP glucuronyl transferase.
45
What is the management of Gilbert's syndrome?
No treatment is required. Phenobarbitone can be used in severe cases.
46
What is Budd-Chiari syndrome?
Obstruction of hepatic venous outflow, often due to thrombosis, leading to hepatomegaly, ascites, and abdominal pain.
47
What is the treatment for Budd-Chiari syndrome?
Anticoagulation, portocaval shunts, TIPSS, and liver transplantation.
48
What is hereditary hemochromatosis?
An autosomal recessive disorder of iron metabolism leading to iron accumulation in organs like the liver, heart, and pancreas, caused by mutations in the HFE gene.
49
What is the treatment for hereditary hemochromatosis?
Repeated venesection to remove excess iron, iron chelation with desferrioxamine in rare cases, and liver transplantation in advanced disease.
50
What is the diagnostic test for hereditary hemochromatosis?
Elevated transferrin saturation (>45%), genetic testing for HFE mutations, and liver biopsy with Perl's stain for iron quantification.