gastroenterology Flashcards

1
Q

Vit A deficiency

A

night blindness, xerophthalmia

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2
Q

vit d def

A

rickets/osteomalacia, dental caries, hypocalcemia, hypophosphatemia

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3
Q

vit e def

A

anemia/hemolysis, neuro deficicts, altered prostaglandin synthesis

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4
Q

vit k def

A

coagulopathy/prolonged prothrombin tiome, abnormal bone matrix synthesis

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5
Q

vit b1 (thiamine) def

A

beriberi (cardiac failure, peripheral neuropathy, hoarsenss or aphonia, wernicke’s)

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6
Q

vit B6 (pyridoxine) def

A

dermatitis, cheilosis, glossitis, microcytic anemia, peripheral neuritis

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7
Q

vit B12 (cobalamin) def

A

megaloblastic anemia, demyelination, methylmalonic acidemia

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8
Q

vit c def

A

scurvy (heme abnl, edema, spongy swelling of gums, poor wound healing, impaired collagen synthesis)

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9
Q

folic acid def

A

megaloblastic anemia, neutropenia, impaired growth, diarrhea

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10
Q

niacin def

A

pellagra (diarrhea, dermatitis, dementia), glossitis, stomatitis

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11
Q

zinc def

A

skin lesions, poor wound healing, immune dysfunction, diarrhea, growth failure

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12
Q

celiac disease

A

intolerance to gluten, autoimmune
- age 6 months and 2 years
Sx: diarrhea, vomiting, bloating, anorexia, failure to thrive
- foul smelling stools, abd pain
Dx: small bowel biopsy (GOLD STANDARD) –> short flat villi, deep crypts, vacuolated epithelium with lymph
- serum IgA endomysial and serum tissue transglutaminase antibody testing

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13
Q

sandifer syndrome

A

torticollis with arching of back caused by painful esophagitis –> related to GERD

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14
Q

Diagnosis of GERD

A

pH probe measurement gold standard –> correlate with clinical findings

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15
Q

pyloric stenosis

A

first born boys
Sx: non bilious milky fluid vomiting, projectile
- irritable patients but hungry
- olive sign on physical examination
- hypochloremic hypokalemic metablic alkalosis
Dx: ultrasound, string sign on UGI
Tx: surgical correction with partial pyloromyotomy

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16
Q

malrotation/volvulus

A

males
Sx: bilious vomiting, sudden onset abd pain in otherwise healthy infant
Tx: surgical emergency to untwist gut, fluid resuscitation, nasogastric suctioning, abx

17
Q

Duodenal atresia and stenosis

A

congenital obstruction of duodenum by failure of lumen to recanalize at 8-10 weeks gestation
- most common cause of obstruction in neonate, males, associated with downs
Sx: polyhydramnios, scaphoid abd with epi distension, emesis, weight loss FTT
Dx: double bubble sign, intestinal contrast studies
Tx: decompression, hydration, duodenoduodenostomy

18
Q

intussusception

A

males, 3-9 months
- ileocolic most common
Sx: colicky/crampy abdominal pain with vomiting and lethargy
- currant jelly stools, sausage mass possible
Tx: fluids, air or contrast enema gold standard

19
Q

gray turner sign

A

bluish discoloration of flanks in acute pancreatitis

20
Q

cullen sign

A

bluish discoloration of periumbilical area in acute pancreatitis

21
Q

most common cause of organic constipation in children

A

hirschprung disease

22
Q

Serologic testing for UC and Crohn’s

A

antineutrophil cytoplasmic antibody and anti saccharomyces cerevisisae antibody

23
Q

extraintestinal manifestations UC

A

uveitis, arthropathy, pyoderma gangrenosum, sclerosing cholangitis

24
Q

extraintestinal manifestations crohns

A

FTT, delayed sex development, oral aphthous ulcers, erythema nodosum, arthritis, renal stones

25
Q

cause of false negative result of GUAIAC

A

large doses of vit C

26
Q

cause of false positive GUAIAC

A

iron, red meats, beets

27
Q

necrotizing enterocolitis

A

considered in any newborn with rectal bleeding, feeding intolerance, or abd distension

28
Q

juvenile polyps

A

most common cause of significant GI bleeding beyond infancy

29
Q

meckel’s diverticulum

A

outpouching of bowel in terminal ileum in 2% of infants
- cause of lower GI bleeding in infants and children
- ectopic gastric mucosa that produces acid
Sx: painless acute rectal bleeding

30
Q

infant jaundice

A

conjugated (direct) hyperbilirubinemia is marker for cholestasis
Cause: neonatal hepatitis or biliary atresia

31
Q

gilbert’s syndrome

A

50% UDP glucuronyl transferase deficiency, mild unconjugated bilirubinemia

32
Q

crigler najjar type 1

A

auto rec 100% deficiency in UDP glucuronyl transferase

unconjugated bilirubinemia

33
Q

crigler najjar type 2

A

auto dom 90% deficiency in UDP glucuronyl transferase

unconjugated bilirubinemia

34
Q

biliary atresia

A

progressive fibrosclerotic disease affecting extrahepatic biliary tree
- 4-6 weeks have jaundice, dark urine, pale stools
- elevated bilirubin levels
Path: bile duct obliteration and cirrhosis by 4 months of age
Sx: HSM, ascites, poor growth, steatorrhea, periph edema, coagulopathy
Tx: kasai portoenterostomy, liver transplant, supportive

35
Q

alagille syndrome

A
auto dom, paucity of intrahepatic bile ducts
Sx: cholestatic liver dx, pruritus
- broad forehead, deep set and wide spaced eyes, saddle nose, pointed chin, large ears
- cardiac disease
- renal disease
- eye abnl
- butterfly vertebrae and broad thumbs
- growth failure and short stature
- pancreatic insufficiency
- hyper cholesterolemia
36
Q

serology of autoimmune hepatitis

A

ANA or anti smooth muscle antibody - Type 1