GASTROENTEROLOGY Flashcards
Which conditions show dysphagia to solids AND liquids
MOTILITY/NEUROLOGICAL conditions
-DES
-Achalasia
-Systemic sclerosis
Which conditions show dysphagia to solids THEN liquids
ANATOMIC conditions
-stricture (progressive)
-cancer (progessive)
- schatzki ring (intermittent)
DX: EGD
What is dyspepsia. What is managment for individual <60yrs with no RFs
Dyspepsia: chronic/intermittent pain in upper abd ESPECIALLY after meals
2 options in pts w/dyspepsia and no RFs and <60yrs:
(1) Test and tx for H pylori, then
(2) Trial with PPI for 4-8 wks
What is tx for H pylori
(1) No previous macrolide use/ macrolide-resistance low: triple therapy–>omeprazole+ ampicillin +clarithromycin for 14 days
All others receive:
(1) levofloxacin triple therapy for 14 days
(2) bismuth quardruple tx for 14 days
What is bismuth quadruple tx for H pylori
bismuth + metronidazole + tetracyline + PPI for 14 days
What is levofloxacin triple tx for H pylori
levo + amoxicillin + PPI for 14 days
List characteristics of achalasia. What about pseudo achalasia?
ACHALASIA:
-dysphagia solids AND liqs
-regurge WORSE AT NIGHT
-long standing (usu years)
-Dx: barium swallow (bird’s beak), EGD (r/o obstruction), manometry (confirms)
-Tx: opening/relaxing LES –>surgery or dilation. IF poor surgical candidate, botulism toxin
Think PSEUDOACHALASIA
-Same sx as achalasia BUT
-wt loss
->60yrs
-progressive
-Dx: EGD!!
List characteristics of Diffuse Esophageal Spasm
DES
-spasms, precipitated BY COLD
-Dx: barium swallow (corkscrew pattern IF done at time of spasms)
-Tx: reassurance. IF want more
(1st line): CCB
(2nd line): isosorbide, sildenafil
(3rd line): bot injection
What is acute cholangitis? What 3 things do you expect to see?
ACUTE CHOLANGITIS
-inflammation of the bile ducts 2/2 stones
-Sx: (1) biliay colic (2)jaundice (3) fever w/chills
-Tx: β-lactam/β-lactamase inhibitor or a third-generation cephalosporin plus metronidazole + ERCP
Describe PBC–sx, dx, tx, associated dx
PRIMARY BILIARY CHOLANGITIS
-progressive, autoimmune liver dx
-women aged 40-60yrs
(1) Symptoms: fatigue, wt loss, hyperpigmentations
(2) Diagnosis: +antimicrobial antibody, alk phos >=1.5 ULN
(3) Tx: Ursodeoxycholic acid
(4) Associated dx: thyroid dx (TSH q1yr); DEXA; men/or pts w/cirrhosis–screen for hepatocellular cancer
Describe PSC–sx, dx, tx, associated dx
PRIMARY SCLEROSIS CHOLANGITIS
-progressive liver dx charac by bile duct destruction/billiary dx
(1) Symptoms: pruiritis, elevated Alk phos, elevated total bil,
(2) Dx: MRCP –“string of beads”
(3) Tx: liver transplantation
(4) Associated dx: IBD (85% UC) –>colon cancer (colonoscopy q2yrs); gallbladder cancer; cholangiocarcinoma
Periumbilical pain that becomes RLQ pain + fever should make you think of what condition
Appendicitis
-starts periumbilical and then migrates to RLQ
-note: iverticulitis–>LLQ pain
Describe carcinoid syndrome
CARCINOID SYDROME
-Conditions causing increased cortisol (including carcinoid dx)
-Sx: flushing, hypotension, tachycardia, explosive diarrhea + NIACIN deficiency (rash, thickened tongue, angular chelitis)
Describe Chron’s dx vs Ulcerative Colitis. What 4 sx do you see w/Chron’s
CHRON’S
-more indolent, less responsive to tx
-more likely to have strictures, inflammatory masses, associated obstruction
-4 Sx: (1) rectal SPARING (2) skip lesions (3) perianal dx (4) ileocecal involement
-DX: endoscopic findings of pathchy, focal, transmural ulcers. +granulomas +/- string sign.
-LAB: ASCA
-Extraintestinal: Osteoperosis (2/2 chronic steroid use)
UCLERATIVE COLITIS
-inflammation ALWAYS starts in rectum–extends proximally; CONFINED to colon
-continuous mucosal inflammation w/shallow ulcers
-Sx: abdominal pain + bloody diarrhea +/- tenesum (painful anal spasms) +/- constipation
-LAB: p-ANCA
-Extraintestinal: “Joints-skin-eyes-mouth” –> skin lesions (erythema nodosum/pyoderma gangrensum), joints (anklosising spondylitis, RF-negative polyarthritis), eyes (iritis), mouth) apthous ulcers) ALSO PSC (think jaundice, itching, cholestatic LFTs)
Describe Whipple disease–sx, dx, tx
WHIPPLE
-caused by bacteria: gram + T whipple. Bacteria obstruct lympatics in intestine which cause malabsorption.
-Sx: 4 things (1) abdominal pain (2) diarrhea (3) wt loss (4) joint pain +NEURO sx
-Dx: foamy macrophages, + PAS
-Does NOT improve w/gluten free diet. No villi blunting on bx
-Tx: IV ceftriaxone, yr of bactrim
Describe olmesartan-induced enteropathy
This ARB causes sx IDENTICAL (clinical and histopathologically) to celiac. Has FDA black box warning!
Describe TROPICAL SPRUE
TROPICAL SPRUE
-Caused by an unknown organism
-Megaloblastic anemia (B12 deficiency); travel to equatorial areas
-does NOT improve w/gluten free diet. Villi blunting on bx
-Tx: tetracycline or doxycycline x 6mos
What skin condition and anemia is strongly associated with CELIAC SPRUE
CELIAC SPRUE (aka Celiac Disease, nontropical sprue)
-DERMATITIS herpetiformis–tx w/dapsone
-Iron deficiency (microcytic anemia–2/2 iron being absorbed in the duodenum)
-DOES improve with gluten free diet. Villi blunting on bx
**Note, tropical sprue associated w/megaloblastic anemia (B12 deficiency)
Describe celiac dx (nontropical sprue)
CELIAC
-inflammatory response to dietary gluten that damagess intestinal mucosa
-dx: antibodies (IgA anti-tissue transglutaminase); anti DGP in case of IgA deficiency
-Tx: gluten free diet
EXTRAINTESTINAL MANIFESTATIONS
-DM1, adrenal insufficiency
-dermatitis herptiformis (responds to dapsone)
-osteoperosis
-neuropathies
-non-hodgkin lymphoma
-thyroid/esophageal cancer
What do you generally treat invasive diarrhea with? What 2 bugs are the exception
GENERALLY tx invasive diarrhea with quinolones (esp ciprofloxacin) BUT macrolides for campy and metronidazole for amebiasis
EXCEPTIONS–NO abx:
1) EHEC –> symptomatic tx only. Abx incr risk for TTP/HUS!
2) Salmonella–>symptomatic tx only. Abx may prolong infection
What do you generally treat invasive diarrhea with? What 2 bugs are the exception
GENERALLY tx invasive diarrhea with quinolones (esp ciprofloxacin) BUT macrolides for campy and metronidazole for amebiasis
EXCEPTIONS–NO abx:
1) EHEC –> symptomatic tx only. Abx incr risk for TTP/HUS!
2) Salmonella–>symptomatic tx only. Abx may prolong infection
What kind of bilirubin is elevated in Gilbert syndrome
Unconjugated = indirect= without bilirubinemia.
Describe hemochromatosis.
Hemochromatosis:
-autosomal recessive; increased intestinal absorption of IRON
-Labs: transferrin saturation, serum ferritin
-Tx: phlebotomy
-f/u: screen for HCC q6mos if cirrhosis
Describe Wilson’s dx
Wilson’s dx:
-autosomal recessive; decr excretion of COPPER
-Sx: hx of psychiatric disorders, and/or cathetoid movements
-Labs: (1) elevated urine copper (2) low serum ceruplasmin (3) slit lamp eye exam –>Kayser Fleischer rings +hemolytic anemia +elevated alkphos
-Tx: D-pencillamine
*elevated copper in PBC, PSC**
How do you tx autoimmune hepatitis (AIH)?
prednisone/budenosine +/- azathioprine
What demographics are generally invovled with PSC, PBC, and autoimmune hepatitis
PSC: middle-aged men
PBC: middle-aged woman
Autoimmune hepatitis: young woman
What hepatitis is associated with leukocytoclastic vasculitis
HCV
Describe Irritable bowel SYNDROME
IBS
-Note, it’s NOT inflammatory bowel dx (IBD –Chron’s, UC)
-Sx: alternating constipation/diarrhea w/normal colonoscopy +/- abd pain
-dx: sx for >3mos with @ least 2 of the following: pain-related defecation, change in stool consistency, change in stool frequency