GI/GU tracts Flashcards
eosinophilic esophagitis mechanism
allergic
Symptoms similar to GERD
Treatment
RX: avoidance of food allergens/ steroids
Echogenic bowel on prenatal ultrasound
enema shows microcolon from disuse
CF with meconium ileus
The most serious complication of ulcerative
colitis is___________-
toxic megacolon, ↑ risk of intestinal perforation
intussusception work up
air, barium, or saline enema
therapeutic as well as diagnostic
hydrostatic effects reduce the intussusception
Most common cause of bacterial sinusitis
strep pneumo
CF men are infertile because?
congenital absence of vas deferens
What does rubella have that measles does not?
arthritis= rubella
measles will have a high fever
When do teeth erupt
5 to 7 months- mandibular then maxillary
weaning from the bottle should be discussed with the parents toward the _________ (time)
end of the first year of life
What does charcol not work on?
Compounds not adsorbed by charcoal: alcohols acids/ strong bases ( drain cleaners/ oven cleaners) ferrous sulfate cyanide lithium potassium
Labial adhesion rx
estrogen cream x 1 week
Cause of diabetes insipidus
primary unresponsiveness of the distal tubule
and collecting duct to vasopressin.
Fanconi syndrome
collection of abnormalities arising from the defective transport of water, sodium, potassium, glucose, phosphate, bicarbonate, and amino acids from the kidneys
Fanconi syndrome acid base
metabolic acidosis (proximal renal tubular acidosis).
Renal tubular acidosis (RTA) type 1 is a distal RTA, and has a___________, as does RTA type 4.
positive urine anion gap
diagnosed in a child with absent abdominal muscular tone, undescended testes, and urinary tract anomalies including hydronephrosis and dilated ureters and bladder
Prune belly syndrome
intermediate stage between acute pyelonephritis and renal abscess, and is a focal region of interstitial nephritis. It appears as a wedge of poorly perfused renal parenchyma, without a cortical rim sign.
Lobar nephronia
rx: prolonged IV and then PO antibiotics
Generalized reabsorptive defect in PCT.
Associated with ↑ excretion of nearly all amino acids, glucose
Fanconi syndrome
results from IgA deposits within the mesangium of the glomerulus in the absence of systemic disease; it can
be associated with microscopic or gross hematuria
Berger nephropathy (IgA nephropathy)
pulmonary hemorrhages in addition to the signs and symptoms of glomerulonephritis
Goodpasture syndrome
Lobar nephronia
intermediate stage between acute pyelonephritis and renal abscess, and is a focal region of interstitial nephritis. It appears as a wedge of poorly perfused renal parenchyma, without a cortical rim sign.
Prune belly syndrome
diagnosed in a child with absent abdominal muscular tone, undescended testes, and urinary tract anomalies including hydronephrosis and dilated ureters and bladder
Fanconi syndrome causes
Wilson disease, tyrosinemia, glycogen storage disease, cystinosis
ischemia
multiple myeloma
nephrotoxins/drugs (eg, ifosfamide, cisplatin, tenofovir,
expired tetracyclines)
lead poisoning.