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113 Cards in this Set

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  • Back
Plain xray findings with appendicitis
"sentinel loop" and absence of air in RLQ
presentation of acute mesenteric lymphadenitis
acute abdomen, but less toxic appearing than appendicitis
mechanism of NSAID induced dyspepsia/peptic ulcer disease
inhibits cyclooxygenase (enzyme that is essential for prostaglandin synthesis)
Definition of Recurrent/Chronic Abdominal Pain
3 or more episodes of abdominal pain over greater than 3 months, severe enough to interrupt normal activity
Classic parasite that causes abdominal pain
Giardia lamblia
Symptoms of Giardia infection
Several weeks of intermittent watery diarrhea, abdominal distention, anorexia. Afebrile.
Historical clues that suggest Giardia infection
Drinking bad water on a camping trip, or a child attending daycare
Consequences of untreated Giardia infection
Persistent diarrhea with malabsorption
Diagnostic test for Giardia
String test (ELISA).

(O&P: poor sensitivity (only ~50%); ideally would need to test 3 samples.)
Treatment for Giardia
Flagyl x 7 days, OR nitazoxanide x 3 days
Where does watery diarrhea come from?
Small intesting; typically high volume but not bloody.
Testing for a patient with watery diarrhea
No specific tests needed; exceptions: suspicion of C. difficile or cholera
Optimal mixture of oral rehydration solution
2% glucose and 90mEq NaCl
Stool test most indicitave of bacterial diarrhea
Neutrophils
What do you use to find WBCs in stool?
methylene blue
4 most common causes of viral diarrhea
NARC: Norwalk virus, Adenovirus, Rotavirus, Coronavirus
Enteropathogenic E. coli causes what?
acute and chronic diarrhea (nonbloody), commonly with fever and vomiting, in neonates and young children (especially in areas with poor sanitation)
Enterotoxigenic E. coli causes what?
self limited severe diarrhea and cramping - TRAVELER'S DIARRHEA; infantile diarrhea in 3rd world countries (comes from contaminated food and water)

Think entero-TACO-genic
Prophylaxis for traveler's diarrhea
Not typically indicated, but if asked: bismuth subsalicylate or an antibiotic such as Bactrim
Enterohemorrhagic E. coli causes what?
diarrhea, HUS (Shiga toxin); food, water, and person-to-person spread
Enteroinvasive diarrhea causes what?
Similar picture to shigella: fever, stools with blood and mucous, tenesmus; contaminated food
Classic description of bacterial diarrhea
High fever, small frequent stools, mucous or blood
Classic presentation of salmonella diarrhea
Green, malodorous stools (NOT bloody) 2 days after a picnic (transmitted by contaminated food)
Which can present in a newborn: Salmonella or Shigella?
Salmonella
Symptoms of typhoid fever
Fever, headache, abdominal pain, muscle aches, rose spots
Treatment of typhoid fever
Ceftriaxone/cefotaxime (only if <1 year or increased risk of systemic illness, such as colitis or immunocompromised) -- typically not recommended because they do not shorten clinical course and can extend the carrier state
Classic presentation of shigella diarrhea
several days after ingestion: watery diarrhea, fever; bloody diarrhea appears after fever subsides; increased bands on CBC regardless of actual WBC count
Treatment of shigella diarrhea
Bactrim
Transmission method of Shigella
person to person (VERY contagious; if no sick contacts, it's not Shigella!)
Which can be found in asymptomatic carriers: Salmonella or Shigella?
Salmonella
What infectious diarrhea can present with similar picture to Shigella?
Campylobacter
Treatment for Campylobacter diarrhea
erythromycin or azithromycin
Risk factors for C. diff colitis
Recent antibiotic use; repeated enemas; prolonged NG tube placement
Treatment for asymptomatic 5 month old with positive C. diff in stool?
Treatment not indicated in children younger than 6 months, unless symptomatic.
Infection with Yersinia can present with clinical picture similar to:
Appendicitis
Treatment for Yersinia
When limited to GI tract: benign and self-limited; no treatment required.
Screening tests for malabsorption of sugars
1. Clinitest (tests for reducing substances = all dietary sugars except sucrose); presence of reducing substances correlates with sugar malabsorption

2. Hydrogen Breath Test (normal gut "ferments" sugar --> hydrogen produced --> excreted in lungs); positive test correlates with sugar malabsorption
Screening tests for malabsorption of fat
1. Fecal fat measurement (requires 3 day stool collection)

2. Serum carotene and PT (indirect tests; correlate with vitamin A and vitamin K absorption)
Screening tests for malabsorption of protein
Albumin level, total protein
Which 2 malabsorptions (sugars, fat, protein) typically occur together?
fat and protein
Definition of chronic diarrhea
Diarrhea beyond 2 weeks that cannot be attributed to an acute gastroenteritis; nutrition and growth are affected
What tumor can cause diarrhea and why?
neuroblastoma -- produces vasoactive intestinal peptides
Normal time course for transient lactase deficiency to resolve
3-6 months
Protozoan parasite that can cause chronic diarrhea in immunocompetent child
Cryptosporidium (especially child in day care); severe cases can result in malabsorption
Most common cause of chronic diarrhea in children up to age 3
Toddler's diarrhea
Classic description of toddler's diarrhea (chronic nonspecific diarrhea)
Formed stool in the morning which become progressively looser as the day progresses; growth and development are normal, no fever or melena
Treatment of toddler's diarrhea
Limit carbs, increase fat and fiber intake, remove cold foods and liquids that stimulate colonic activity
Chronic diarrhea following acute gastroenteritis
Malnutrition from treatment with high osmolar solutions -- frequent passing of loose green stools ("starvation stools")
What is abetalipoproteinemia?
rare autosomal recessive disorder that interferes with the normal absorption of fat and fat-soluble vitamins from food. It is caused by a deficiency of apolipoprotein B-48 and B-100, which are used in the synthesis and exportation of chylomicrons and VLDL respectively

(from Wikipedia)
Symptoms of abetalipoproteinemia
steatorrhea, acanthocytosis (RBCs with spiney projections -- like a porcupine), retinal damage, neurological sequelae
Predisposing factors to protracted diarrhea
Malnutrition
Chronic infection
Systemic disease
Immunodeficiency
What is intestinal lymphangiectasia?
a protein losing enteropathy that results in hypoproteinemia, hypogammaglobulinemia, steatorrhea, lymphedema, lymphopenia
Causes of neonatal vomiting associated with polyhydramnios
antral web, annular pancreas
Imaging studies with a radiolucent filling defect in the prepyloric region
antral web
Elevated indirect bili can occur in what cause of neonatal vomiting?
pyloric stenosis (in up to 2.5%)
Diagnostic criteria for pyloric stenosis on ultrasound
pyloric length greater than 14mm, or pyloric muscle thickness greater than 4mm
Air in distal small bowel excludes what 2 causes of neonatal vomiting?
duodenal atresia and annulal pancreas
Term neonate with bilious vomiting, abdominal tenderness, abdominal distention, possibly passing blood per rectum
Malrotation

(NEC is similar, but less common in term infant)
Neonate with bilious vomiting and right sided abdominal distention
Volvulus

(Ladd bands constrict large and small bowel)
Xray findings with volvulus
gastric and duodenal dilatation, decreased intestinal air, corkscrew appearance of the duodenum
GI med to avoid during fundoplication surgery
omeprazole (especially in patients with neurological impairment)
Mechanism of action of ondansetron
serotonin receptor antagonist
Pharmacologic treatment for cyclic vomiting
cyproheptadine, propranolol, TCA's (similar to migraine treatment)
Forceful vomiting, weight loss, dysphagia, FTT
achalasia
Some sx of achalasia plus abdominal pain and distension
gastric outlet obstruction
Cyst on the floor of the mouth: "mucocele" vs. "midline mass"
Mucocele = ranula (tx with excision); midline mass could be ectopic thyroid (so don't remove it!)
parotid swelling, dry mouth, poor tear production
Mikulicz's disease
Bacterial cause of parotitis
staph aureus (more marked tenderness, higher fever than with mumps)
Underdeveloped or absent teeth, absent sweat glands
Ectodermal hypoplasia; x-linked; diagnosed by skin biopsy
Earliest sign of portal hypertension is _______ followed by _________
earliest sign: splenomegaly; follwed by ascites, prominent abdominal veins, esophageal or gastric varices
Copious oral secretions, polyhydramnios, coughing and cyanosis with initial feeding
TE fistula
Treatment for NSAID induced ulcers
H2 blocker
Causes of solid food dysphagia
Reflux esophagitis (possibly with esophageal stricture) or eosinophilic esophagitis
EGD findings of eosinophilic esophagitis vs. GERD
eosinophilic esophagitis: inflammation of entire esophagus with increased eosinophils on biopsy; GERD: ulceration/injury limited to distal 5cm of esophagus
Best diagnostic test for H. pylori
EGD for biopsy
Treatment for H. pylori
"triple" therapy: PPI plus 2 antibiotics (amox + Flagyl OR amox + clarithromycin) x 14 days
Serologic testing positive for H. Pylori. Next step?
Serology has high sensitivity but lots of false positives, so must confirm with another study (fecal antigen or Urea breath test)
Zollinger-Ellison Syndrome
gastrin-secreting tumor; sx similar to peptic ulcer disease; diagnose by obtaining fasting gastrin levels
Bulky, pale, frothy and foul smelling stools; proximal muscle wasting; abdominal distention
Celiac disease
Dietary management of celiac disease
Avoid gluten (wheat, rye); some patients can tolerate oatmeal. Vitamin supplements.
Diagnose celiac disease by...
upper endoscopy, duodenal biopsy
Causes of rectal prolapse
CF; things that cause increased intraabdominal pressure (pertussis, tenesmus, chronic constipation); rare causes: meningomyelocele, parasites
Causes of malabsorption
CF, celiac disease, cow milk and soy allergies
"Ground glass" on abdominal film
meconium plug syndrome (rule out CF)
Extra teeth, premalignant polyps in large and small intestines, osteomas
Gardner's syndrome
mucosal pigmentation of lips and gums
Peutz-Jeghers Syndrome
Extraintestinal manifestations of Crohn's disease
Pyoderma gangrenosum of the food; erythema nodosum; ankylosing spondylitis/sacroiliitis; arthritis; uveitis (eyes); liver disease; renal stones
Chronic cramp and abdominal pain, fever; pain not quite as severe as intussusception
Campylobacter jejuni diarrhea or Yersinia (crampy severe periumbilical pain)
Child around age 2, afebrile, symptoms mimicking sepsis, no GI symptoms
Intussusception (afebrile child who looks toxic)
If a child older than 6 gets intussusception, must rule out:
Lymphosarcoma (could be "lead point" causing the intussusception)
GI abnormalities associated with Trisomy 21
duodenal atresia, Hirschsprung's disease
Infant with bilious vomiting, poor PO intake and abdominal distention
Hirschsprung's disease
Infant who strains to pass small liquid stools; remits by age 1
Anal stenosis
"First thing" to distinguis upper from lower GI bleeding
nasogastric lavage
Test to determine if GI blood is infant's or mother's
Apt test
Top 3 differential diagnoses for lower GI bleed in newborns
Hirschsprung's disease (with associated colitis), malrotation with associated volvulus (melena), NEC
Most common cause of lower GI bleed in 1-2 years old
Anal fissure; usually secondary to constipation
Top 4 differential diagnoses for preschool (2-5 years old) with lower GI bleed
Juvenile polyp; entamoeba histolytica (bloody diarrhea in child from Indian reservation or rural area of south, central, SW US); meckel diverticulum; juvenile polyposis (usually in a child that is older)
Labs to differentiate cholestatic jaundice from hepatocellular caused jaundice
Cholestatic disease: very high alk phos; hepatocellular disease: very high AST/ALT
Enzyme deficiency in Gilbert syndrome
Glucuronyl transferase deficiency
Lab abnormalities in Reye's syndrome
Elevated LFTs and ammonia
Most specific test to diagnose pancreatitis
Abdominal ultrasound (NOT amylase) -- lipase more specific than amylase
Most common genetic causes of recurrent pancreatitis
CF, hereditary pancreatitis
Conditions that predispose to cholecystitis
Hemolytic disease, prolonged TPN, small intestinal disease, obesity, pregnancy
Differences in presentation of cholecystitis vs. cholelithiasis
Both: dx by ultrasound; abdominanl pain, N/V; cholecystitis: shoulder pain, lethargy; cholelithiasis: hepatosplenomegaly, icterus
Best diagnostic test for Hepatitis A
IgM-specific antibody
Presence of HBsAg (Hepatitis B surface antigen)
Acute or chronic (>= 6 months) infection
Presence of Anti-HBsAg
Previous infection or positive response to immunization
Presence of HBeAg
High rate of replication --> high rate of infectivity
Presence of HBcAg
Indicates past infection (IgM to HBcAg --> recent infection (past 6 months))
HBV-DNA
Sensitive marker indicating viral replication
"Window" period with HepB infection
Disappearance of surface antigen but before appearance of antibody to surface antigen; but, should have presence of antibody to core antigen (anti-HBcAg)
Required for Hepatitis D
presence of HBsAg (provides outer coat of HepD)