GI Flashcards

(36 cards)

1
Q

Sandifer syndrome

A

spasmodic tordional dystonia; opsthotonic posturing, mainly involving the neck, back and upper extremities, associated with GERD

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2
Q

Diagnosis of reflux/aspiration

A

video barium swallow

milk scan (less specific, more sensitive)

Salivagram (if likely upper airway secretion aspiration)

BAL (lipid-laden macrophage = aspiration)

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3
Q

evaluation of elevated LFTs in obese child

A

Don’t forget hepatitis B and C
PSC
autoimmune hepatitis

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4
Q

Tx of hospitalized patients with acute severe colitis

A

IV steroids
Infliximab
Colectomy if no response 10-12 days after initiation

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5
Q

Fecal lactoferrin

A

iron-binding protein found inside neutrophils
Sensitive and specific for detecting IBD (but can be positive for any intestinal inflammation)

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6
Q

Appendicitis tx

A

surgery here in US
Abx only ok in europe

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7
Q

Ddx of infant who is not able to swallow solids

A

congenital esophageal stricture
Vascular ring

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8
Q

What is the Apt-Downey test and what is the oldest age to test it on

A

detects fetal hemoglobin
+ means it’s from the baby
- means its maternal

8 week old

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9
Q

How does secondary lactose intolerance happen in celiac disease?

A

atropy of lactase-containing vili

will resolve when celiac is treated (gluten-free diet)

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10
Q

How do you diagnose lactose intolerance

A

lactose breath testing
intestinal biopsy (less commonly done)

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11
Q

Chronic vs. acute recurrent vs. acute pancreatitis

A

Acute (2/3):
1. abd pain epigastric
2. serum amylase/lipase 3x ULN
3. Imaging finding consistent with pancreatitis

Acute recurrent:
At least 2 episodes of AP and 1 of the following
- Complete resolution of pain between AP episodes
- complete normalization of pancreatic enzyme measurements between AP episodes

Chronic (any below)
- Abd pain consistent with pancreatitis
- evidence of exocrine pancreatic insufficiency
- evidence of endocrine pancreatic insufficiency
- biopsy

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12
Q

Causes of Acute recurrent pancreatitis or chronic pancreatitis

A

CF
Pancreas divisum, annular pancreas
HLD, medications (VPA or 6-MP)
autoimmune pancreatitis
Primary sclerosing cholangitis

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13
Q

What is rectal suction biopsy used to detect?

A

Hirschsprung

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14
Q

What neonatal diseases is AFP elevated in

A

omphalocele, gastrocschisis, neural tube defects

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15
Q

High bHCG in early pregnancy ddx

A

trisomy 21
placental tumor
molar pregnancy

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16
Q

Celiac lab findings

A

normal pancreatic elastase and elevated fecal fat from fat malabsorption

17
Q

Syndrome associated with exocrine pancreatic insufficiency

A

Shwachman Diamond syndrome

18
Q

Juvenile polyp, signs symptoms, age onset, treatment

A

1-7 yo
Painless, intermittent rectal bleeding
Polyp in distal colon

Tx: resection. No further follow up for colonoscopy is indicated

UNLESS there is >5 polyps. Then Juvenile polyposis syndrome. Need colonoscopy q1-3y

19
Q

Villous atrophy and intraepithelial lymphocytosis. dx?

20
Q

Common causes of cholestasis in first few months of life. Labs to get

A

biliary atresia
idiopathic neonatal cholestasis
parenteral nutrition-associated cholestasis (TPN)
Obstruction (bile stone, choledochal cyst)
CF
Metabolic/endocrine disorder (e.g. tyrosinemia)
Panhypopituitarism
Alagille syndrome

Labs: alpha1 antitrypsin lvl, TFT, Abd US, review newborn screen

21
Q

Liber biopsy for those with biliatry atresia would show

A

evidence of fibrosis
bile duct plugging
bile ductal proliferation

22
Q

Tx of biliary atresia

A

Kasai hepatoportoenterostomy (HPE) – re-establish bile flow before age 90 days

May need liver transplant (cirrhosis, portal htn)

23
Q

Ddx of rectal prolapse, when to be concerned

A

<4yo due to normal anatomy
If >4yo, usually abnormal

Usual etiology:
constipation, severe chronic cough.
Rectal poplyp
Hirschsprung

24
Q

Causes of dysphagia in young people (teen and young adult)

25
Tx of EoE
3-6 food elimination topical steroids (fluticasone or oral viscous budesonide) PPI If doesnt respond, may need elemental formula
26
When does biliary atresia present?
After the first few weeks of life
27
Crigler-Najjar. Problem is conjugated or unconjugated hyperbilirubinemia?
unconjugated
28
Gilbert syndrome, conjugated or unconjugated problem hyperbilirubinemia?
unconjugated
29
Physiologic neonatal jaundice is caused by what immature enzyme?
bilirubin uridine diphosphate-glucoronosyltransferase BUGT Also increased enterohepatic circulation of unconjugated bilirubin, and increased bilirubin from hemolysis of RBCs
30
Physiologic neonatal jaundice is caused by what immature enzyme?
bilirubin uridine diphosphate-glucoronosyltransferase BUGT Also increased enterohepatic circulation of unconjugated bilirubin, and increased bilirubin from hemolysis of RBCs
31
Dx of functional constipation
2 or less defacations in the toilet per week At least 1 episode of fecal incontinence per week, history of stool retention, hx of painful/hard bowel movements, rectal fecal mass, large-diameter stools that may obstruct the toilet
32
CF in infants, signs/symptoms
hepatomegaly steatorrhea severe diaper dermatitis malnutrition
33
Superior Mesenteric artery syndrome sx
significant weight loss followed by bilious emesis
34
Causes of emesis you should not forget about
malrotation volvulus (corkscrew) duodenal atresia (double bubble) EoE abdominal migraine pyloric stenosis
35
How does hypophosphatemia occur in refeeding syndrome?
increased phosphate use in production of ATP
36
Other electrolyte abnormalities in refeeding sd besides hypophos
- hypomag - hypo K (increased insulin from sudden hyperglycemia) - hypo-thiamine