Gastroenterology Flashcards

1
Q

What ages does pyloric stenosis develop?

A

Between 3-8 weeks of life (would not suspect in a brand new neonate)

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2
Q

GI manifestations associated with Down’s Syndrome

A

Duodenal atresia, imperforate anus, Hirschsprung’s disease

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3
Q

Family history of liver cirrhosis and transplantation at a young age, hematemesis, elevated AST/ALT and anemia, neuropsychiatric symptoms (ataxia, choreathetoid movements), Kayser-Fleischer rings. Name the disorder ?

A

Wilson’s disease (autosomal recessive)–accumulation of Copper in liver and brain–> cirrhosis and esophageal varices. Defect in movement of copper from liver to bile.
Labs- low serum Cu2+ and low ceruloplasmin (but Cu overload–deposited in the tissues), high urine Copper excretion
Treatment: chelation (D-penicillamine), decreased Cu intake, intake of Zn (competes with Cu for absorption)

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4
Q

How do you definitively diagnose a biliary atresia?

A

Intraoperative cholangiogram (fluoroscopy during surgery watching contrast flow through the biliary tree); HIDA scan is not specific enough

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5
Q

Is achalasia associated with an increased or decreased LES resting tone?

A

Increased tone/pressure, aganglionic distal portion of the esophagus–does not relax and so you have a functional distal obstruction of the esophagus

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6
Q

GI disorders associated with Erythema nodosum?

A

Crohn’s, Ulcerative colitis

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7
Q

Bifid thumbs and other bony deformities, greasy foul-smelling stools, failure to thrive, normal sweat chloride testing; cyclic neutropenia

A

Schwachman-Diamond Syndrome (Autosomal recessive)
(Bone and bone marrow problems)– skeletal deformities, neutropenia +/- anemia/thrombocytopenia, so increased risk of bacterial infections
(Pancreatic exocrine insufficiency)– foul, smelling stools, FTT, poor absorption of ADEK vitamins

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8
Q

Pyoderma gangrenosum is commonly associated with which GI disorder? Also areas where lesions can be located?

A

IBD (Crohn’s and Ulcerative colitis); starts of raised violaceous, maculopapular and then becomes necrotic and pustular (autoimmune); can be located on the shins, head and anogenital regions commonly

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9
Q

Causes of Autoimmune Hepatitis? What is an associated lab finding with this disorder?

A

Medications (Isoniazid, Minocycline, Nitrofurantoin, Sulfonamides); associated with hypergammaglobulinemia (increased antibodies against smooth muscle, liver, kidney, mitochondria, etc); check total IgG level

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10
Q

What conditions can make you more susceptible to SMA?

A

SMA- Superior Mesenteric Artery Syndrome; LOSING WEIGHT; loss of mesenteric fat leads to tightening of space within the bifurcation of the aorta into the SMA and abdominal aorta; the duodenum 2-3rd portions lie within this space and gets squished

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11
Q

What kind of positioning leads to improvement of SMA syndrome related nausea and vomiting?

A

Knee to chest, left lateral side lay; relieves the functional duodenal obstruction by widening this space

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12
Q

Acrodermatitis Enteropathica usually coincides with the removal of what from the diet?

A

Breast-Milk; autosomal recessive absence of Zinc-binding ligand in the GI tract of affected infants–breast milk has zinc-binding ligand

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13
Q

Symptoms of acrodermatitis enteropathica?

A

Loose stools, FTT, irritability, mucosal bullous lesion that bursts and crusts over

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14
Q

Celiac disease– intestinal mucosa finding? What skin condition is celiac disease associated with?

A

Effacement of microvilli, scalloping (bumpiness) of intestinal mucosa; dermatitis herpetiformis (IgA deposition in the skin preceded by herpetic appearing vesicular lesions that burst and scar)

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15
Q

Blood in stools, otherwise asymptomatic exam– how do you diagnose this condition?

A

Technetium 99 scan–although low negative predictive value, so would still need surgical management if you are unable to find it on imaging; meckel’s diverticulum (ectopic gastric tissue)

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16
Q

Foul, smelling loose stools and gets sick very often, FTT; sweat chloride test negative; what is the diagnosis?

A

Shwachman-Diamond Syndrome- 1. (bony abnormalities at metaphyses and growth plate of bones + bone marrow hypoplasia– neutropenia, anemia, thrombocytopenia); 2. pancreatic exocrine insufficiency (loose stools)

17
Q

Peutz-Jeghers syndrome signs and symptoms?

A

Blue-black mucocutaneous macules (nose, mouth, elbows, hands) and intestinal hamartomas (increased risk of GI adenocarcinomas and intussusception).

18
Q

Risk factors for intestinal atresia?

A

Maternal tobacco and cocaine use, low birth weight, multiple births

19
Q

Autoimmune hepatitis presentation?

A

Sudden onset jaundice and evidence of hepatitis in someone who was previously healthy; Type I (10-20 years old, usually female); Type II (younger children, usually more serious); may need steroids and immunosuppressive meds; Type III is for adults

20
Q

Gallbladder hydrops is commonly associated with which disorder?

A

Kawasaki disease (distention of gallbladder by sterile bile)

21
Q

Triple A or Allgrove Syndrome features?

A

Achalasia (failure of esophageal relaxation at the LES–> bird’s beak), alacrima (reduced ability to produce tears), and Adrenal insufficiency (primary); associated with autonomic dysfunction

22
Q

Crohn’s disease can be associated with which eye condition?

A

Anterior uveitis

23
Q

Antibodies associated with Type I Autoimmune Hepatitis

A

Anti-smooth muscle and ANA antibodies

24
Q

Antibodies associated with Type II Autoimmune Hepatitis

A

Anti-liver and anti-liver-kidney antibodies (more severe because targets organs–this is only a mnemonic)

25
Q

PRSS1 gene mutation is related to which disorder?

A

Hereditary pancreatitis– converts trypsinogen into active trypsin while still in the pancreas, instead of waiting for it to be released into the stomach lumen

26
Q

What is Reye’s syndrome?

A

Swelling of the brain and liver 2/2 to taking salicylates while have the chicken pox or flu or either vaccines. Can have behavioral changes related to brain swelling.

27
Q

How long should you avoid salicylates after receiving Influenza or VZV vaccines?

A

6 weeks