• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/294

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

294 Cards in this Set

  • Front
  • Back

viral gastro bugs

Noro, Cox A1, echo, adeno, Rota in children
bacterial gastro bugs that cause bloody diarrhea
C.jejuni, EC O157:H7 (entrohemorrhagic), Salmonella, Shigella, Yersinia, sometimes CDiff
bacterial gastro bugs that have risk of HUS
EC O157:H7, Shigella
HUS characteristics
thrombocytopenia, hemolytic anemia, renal failure
hepatitis h/p
RUQ pain, jaundice, scleral icterus, hepatomegaly, splenomegaly, LAD, fatigue, malaise
hepatitis treatments
A and E: supportive
B: HBVax immediately after exp; interferon or antivirals
C:IFN and maybe ribavarin
D: IFN
which Hepatitis has vaccines
A, B, D
complications of Hepatitis?
B: 5% dev chronic hepatitis, cirrhosis, 3-5% dev hepatocellular carcinoma
C: 80% dev chronic hepatitis, 50% dev cirrhosis, slightly increased risk of hepatocellular carcinoma
E: high infant mort when preg women get it
what can cause salivary duct obstruction
sialolithiasis in any salivary gland, sarcoid, infection, neoplasms
salivary gland disorder h/p
enlarged, painful glands, pain worsens with eating, painless swelling
what can cause dysphagia
achalasia, motility disorders, scleroderma, peptic strictures, esophageal webs or rings, cancer, radiation fibrosis
dysphagia labs
esophageal manometry
dysphagia rads
barium swallow, esophagogastroduodenoscopy (EGD)
what can cause achalasia
Chagas, scleroderma, neoplasms
achalasia h/p
progressive dysphagia, regurg, cough, aspiration, heartburn, weight loss
achalasia rads
barium swallow: bird's beak, need EGD to rule out cancer
achalasia tx
pneumatic dilation, botox injections, myotomy can cause GERD
diffuse esophageal spasm h/p
chest pain, dysphagia
diffuse esophageal spasm rads
barium swallow shows corkscrew pattern
diffuse esophageal spasm tx
ca channel blockers, nitrates relieve pain but worsen GERD, TCAs
what is Zenker diverticulum
divert of upper posterior esophagus from smooth muscle weakness
Zenker's divert h/p
bad breath, difficulty swallowing, regurg of food several days after eating, dysphagia, feeling of aspiration
Zenker's divert rads
barium swallow
Zenker's divert tx
cricopharyngeal myotomy/ diverticulectomy
risk factors for GERD
obesity, hiatal hernia, preg, scleroderma
what can worsen GERD
alcohol, smoking, fatty foods
GERD h/p
burning chest pain, sour taste in mouth, regurg, dysphagia, odynophagia, nausea, cough, pain worse with lying down relieved by standing
GERD labs
esophageal pH monitoring
GERD rads
not necessary, but EGD/cxr/barium swallow can r/o neoplasm Barrett's esophagus, hiatal hernia
GERD tx
elevate head of bed, WL, diet mod, Antacids with H2 blockers/PPIs
tx of refractory GERD
Nissen fundoplication, hiatal hernia repair
complications of GERD
Barrett's esophagus, ulceration, strictures, adenocarcinoma
2 types of esophageal cancer
squamous (more common) and adeno (less common)
what usually precedes adenocarcinoma of esophagus
Barrett's esophagus
risk factors for adeno esophageal cancer
alcohol, tobacco, GERD, obesity
2 types of hiatal hernia
1. sliding
2. Paraesophageal
Tx of hiatal hernias
sliding: reflux control
paraesophageal: surgical Nissen or gastropexy
hiatal hernia complications
incarceration
esophageal spasm rads
corkscrew on barium swallow
side effects of H2 antagonists
HA, diarrhea, thrombocytopenia rare, cimetidine can cause gynecomnastia and impotence
side effects of PPIs
may increase effects of Warfarin, benzos, phenytoin, dig, carbamazepine
Type A vs type B chronic gastritis
A: Fundus, autoAb against parietal cells leads to pernicious anemia, decreased gastric acid level and decreased gastrin, achlorhydria, thyroiditis
B: Antrum, Hpylori infection, increased gastric acid level, PUD, gastric cancer
acute vs chronic gastritis
acute is erosive, chronic is not
how does a urea breath test work
detects increase in pH from ammonia producing H pylori
tx of all acute and chronic gastritis
acute: stop offending agents like alcohol, acidic foods, give H2 antagonists or PPIs
Chronic: type A give B12
type B triple therapy vs HPylori:
PPI+Clarithro+ Amox/Metro for 7-14 days
causes of gastric ulcers mnemonic
ANGST HAM: aspirin, NSAIDS, Gastrinoma, Steroids, Tobacco, HPylori, Alcohol, MEN1
gastric ulcers from stress for severe burns and intracranial injuries are called what
Curling's and Cushing's ulcers
how to diff b/w gastric and deodenal ulcer?
Gastric: younger <50, NSAID users, pain SOON and worse after eating, normal/low gastric acid level, HIGH gastrin level
Duodenal: Younger, pain 2-4 h after eating which can initially improve sxs, high gastric acid level with normal Gastrin level
PUD rads
axr to detect perfs, barium swallow can collect in ulcerations (abnormal mucosal folds/mass/filling defects in region of ulcer suggests malig), EGD for biopsy and active bleeds
surgical tx of non neoplastic refractory PUD
antrectomy/ parietal cell vagotomy
complications of PUD
hemorrhage: posterior ulcers erode into GDA, anterior ulcers more likely to perf
where gastrinomas usually found
duodenum (70%) or pancreas
ZE h/p
refractory PUD
ZE labs
increased fasting gastrin, positive secretin stim test (give secretin and higher than expected levels of gastrin result)
ZE rads
somatostatin receptor imaging with SPECT
ZE Tx
surgery for nonmetastatic, PPI and H2Inhibitors can ease sxs, octreotide can also help in metastatic cases
MEN1
Parathyroid hyperplasia/adenoma with hypercal
Pancreatic islet cell neoplasia (Gastrin, VIP, insulin, glucagon)
Pituitary adenomas
MEN2A
Parathyroid hyperplasic (15-20% hypercal)
Pheo
MTC
MEN2B
MTC
Pheo
Mucosal and GI neuromas
2 types of gastric cancer
Adeno (common) and squam (less common usually from esophagus)
4 subtypes of gastric cancer
Ulcerating, Polypoid, Superficial spreading (only mucosal and submucosal good prog), Linitis plastica (all layers, decreased stomach elasticity, bad prog)
gastric cancer risk factors
HPylori, fam hx, Japanese person in Japan, tobacco, alcohol, vitamin C def, high consumption of preserved foods, males>females
gastric cancer h/p
WL, anorexia, pain, early satiety, enlarged left supraclavicular LN (Virchow's node), periumbilical node (Sister Mary Joseph's node)
gastric ca labs
inc CEA, inc glucuronidase in gastric secretions
gastric ca rads
barium swallow: thickened leather bottle stomach= linitis plastica, do an EGD for biopsy and visuals
gastric ca tx
subtotal gastrectomy: for lesions in distal third of stomach
Total gastrectomy: for lesions in middle or upper third of stomach or invasive lesions, needs adj chemo and rad
gastric cancer prog
early detection: 70% cure rate but poor prog in later detection <15% 5 year survival
autoantibodies that cause celiac sprue
antiendomysial
antigliadin
where in GI tract does celiac sprue affect
duodenal/jejunal mucosa
celiac sprue labs
antiendomysial
antigliadin abs
biopsy shows loss of duodenal and jejunal villi
diff b/w tropical and celiac sprue
no autoabs, tropical is for people who have spent time in tropics, removal of gluten from diet has no effect on tropical sprue
h/p of malabsorption disorders
WL, diarrhea, steatorrhea, bloating, glossitis, dermatitis, edema
Tx of sprues
removal of gluten and steroids for celiac
FA replacement and tetracycline for tropical
where in GI tract is lactose normally absorbed
jejunum
what is lactose tolerance/breath test
give lactose, minimal increase in glucose in serum/breath hydrogen test after lactose meal
what bug causes Whipple's dz
Tropheryma whippelii
Whipple's dz risk factors
white male european
Whipple's dz h/p
same as for other malabsorption disorders: WL, joint pain, abd pain, diarrhea, dementia, cough, bloating, steatorrhea, fever, vision abn, LAD, new heart murmur, severe wasting late
Whipple's dz labs
PAS stain on jejunal biopsy shows foamy macros and villous atrophy
Whipple's dz tx
Bactrim or Ceftriaxone for 1 year
what test detects steatorrhea
Sudan stain
when do you work up acute diarrhea? how
with high fever/bloody/>5d
1. if yes, stool culture, stool acid-fast, fecal leuks for enteroinvasive bacteria, O+Px3, hydration and abx
2. If no, hydration, antimotility agents unless there's no resolution then goto 1
3 types of chronic diarrhea
secretory, osmotic, inflammatory
how do you work up chronic diarrhea (>2wks)
1. r/o infection, recent surg, meds
2. sudan stain for fecal fat: malabsorption
3. FOB, WBC, Lactoferrin, Calpotectin for inflammatory causes: do stool Cx and colonoscopy
4. measure stool pH and lactose tol test for lactase def
5. If normal, do stool lytes and osmolality: stool mOsm/kg= 290 - 2(Na+K)
>50 is high osmotic gap=osmotic cause: lactase def
<50 is normal osmotic gap = secretory: do CT, colonoscopy, hormone levels
6. If high osmotic gap, could be lax abuse or lac def
7. If normal osmotic gap, do stool weight for IBS (normal)
Rome III criteria for IBS
recurrent abd pain for 3 or more days over the last 3 mo plus 2 of the following:
improvement with def
pain then change in freq of stool
pain then change in form of stool
Manning Criteria for IBS
1. pain improves with def
2. pain then change in freq of stool
3. pain then change in form of stool
4. visible abd distension
5. passage of mucus with stool
6. feeling of incomplete defecation
what ages does IBS usually start
teens or young adulthood
workup for IBS
axr, abd ct, barium to rule out other GI causes, colonoscopy in older to r/o cancer
IBS tx
assurance, high fiber diet, psychosocial tx, antidepressants
Crohn's vs UC sites
Crohn's: skip lesions and entire bowel wall involved
UC: continuous starting at rectum, only mucosa and submucosa affected
Crohn's vs UC sxs
Crohn's: abd pain, WL, watery dia
UC: abd pain, urgency, tenesmus, bloody diarrhea
Crohn's vs UC physical
Crohn's: fever, RLQ mass, perianal fissures/fistulas, oral ulcers
UC: fever, orthostatic, tachy, gross blood on rectal exam
Crohn's vs UC extraintestinal manifestation
Both have arthritis, uveitis, ankylosing spondylitis, PSC, erythema nodosum, fatty liver
nephrolithiasis more common with Crohns
pyoderma gangrenosum more common with UC
Crohn's vs UC labs
Crohn's: ASCA+, pANCA rare
UC: ASCA rare, pANCA+
Crohn's vs UC rads
Crohn's: cobblestoning, fissures, skip lesions, string sign
UC: continuous, lead pipe
Crohn's vs UC tx
Both: Mesalamine, steroids, immunosuppressives
Crohn's: surgical resection of severely affected areas/strictures/fistulas
UC: total colectomy is curative
Crohn's vs UC comps
Both: Toxic Megacolon
Crohn's: abscess/fistulas/fissures
UC: increased risk of Colon Cancer
most common causes of obstruction
adhesions, hernias, neoplasms (large bowel)
which part of GI tract is usually spared from ischemia
rectum cause there's collateral circ
which is the most painful type of GI ischemia
small bowel ischemia: pain out of proportion to exam
which part of GI tract is usually involved in ischemic colitis
left colon
what causes ischemic colitis
embolus, obstruction, inadequate perfusion, medication, surgery-induced vascular compromise
ischemic colitis risk factors
DM, athero, CHF, peripheral vasc, lupus
ischemic colitis h/p
abd pain, bloody diarrhea, vomiting, mild tenderness
ischemic colitis labs
inc WBC and lactate
ischemic colitis rads
thumb printing
ischemic colitis tx
fluids bowel rest, abx, resection of necrotic bowel
RLQ pain differential mnemonic
APPENDICITIS: Appendicitis, PID/Period, Pancreatitis, Ectopic/Endometriosis, Neoplasm, Diverticulitis(rare), Intussusception, Crohns/Cyst ovarian, IBD, Torsion, IBS, Stones (kidney, gallbladder)
causes of appendicitis by age
children: lymphoid hyperplasia
adults: fibroid bands, fecaliths
appendicitis h/p
periumbilical tenderness moves to RLQ at McBurney's point (1/3 from R ASIS to umbilicus), rebound, Psoas sign, Rovsing's sign (RLQ pain with LLQ palp),
appendicitis labs
WBC with left shift (more leukocytes vs neutrophils)
appendicitis rads
free air under diaphragm if perfed, CT is most sens
appendicitis tx
appendectomy, abx for ruptured
appendicitis complications
abscess form, perf
how long does postop ileus last?
<5 days. Small bowel recovers in 24h, stomach in 48-72h, and large bowel in 3-5 days
what causes ileus
postop, infection, ischemia, DM, opioid use
ileus h/p
pain, nausea, bloating, no bowel mvmts, can't eat, no rebound
ileus rads
distention of bowel, air-fluid levels
ileus tx
stop opioids, NPO, colonoscopic decompression if no resolution
where in GI tract does volvulus mostly occur
cecum, sigmoid
who gets volvulus usually
infants and elderly
volvulus rads
double bubble on axr, barium enema shows birds beak for distal volvulus
volvulus tx
maybe self limited, colonoscopic detorsion of sigmoid volvulus, resection maybe required in cecal volvulus if can't detorse
most common cause of acute lower GI bleeding over 40y
diverticulitis
diverticulitis more commonly occurs where
sigmoid colon
what is diverticulitis
outpouchings of colonic mucosa and submucosa that herniate through muscular layer
diverticulitis h/p
LLQ pain, nausea, vomiting, melena, hematochezia, tenderness, fever, distension
diverticulitis labs
WBC, guaiac pos
diverticulitis rads
free air under diaphragm if perfed, tics on barium enema/colonoscopy, CT shows soft tissue density , bowel wall thickening, possible abscess
diverticulitis tx
no perf: bowel rest, liquids only for 3 days, abx: Fluoro+Metro OR Bactrim+Metro OR Augmentin
Perf: resect segment of colon, diverting colostomy for 3 mo in cases of peritonitis + Broad spec abx
diverticulitis comp
abscess, fistula, sepsis
where to internal/external hemorrhoids get their blood supply from
internal: superior rectal veins above pectinate line
external: inferior rectal veins below pectinate line
which type of hemorrhoids are painful
external only
cell types for internal/external hemorrhoids
internal: columnar rectal epith
external: squamous rectal epith
hemmorrhoids rads
sigmoidoscopy to r/o other caues of bleeding
hemmorhoids tx
warm baths, increase in fiber, sclerotx, ligation, excision
tx for anal fissures
stool softeners, topical nitro, partial spincterotomy if recurrent
where do pilonidal cysts occur
superior gluteal cleft
where are carcinoids usually found
appendix, ileum, rectum, stomach
carcinoids h/p
abd pain, carcinoid syndrome: flushing, diarrhea, bronchoconstriction, valvular dz, caused by serotonin secretion by tumor (only seen with liver mets or extra-GI involvement)
carcinoids labs
inc 5HIAA in urine, inc serum serotonin
carcinoids rads
CT/ Indium-labeled octreotide scintigraphy
carcinoid tx
tumors <2cm low incidence of mets and can be resected
tumors >2cm higher risk of mets need greater extent of resection, tx with IFNa, octreotide, embolization
colorectal ca most common type
adeno
colorectal ca risk factors
fam hx, UC, polyps, hereditary polyposis syndromes, low fiber high fat diet, prev colon ca, alcohol, smoking, DM
colorectal ca most common mets to
lung and liver
colorectal ca h/p
change in bowel habits (more common in left sided ca), weakness, pain, constipation, hematochezia, melena, WL, abd or rectal mass
colorectal ca labs
guiac, anemia, CEA increased in 70% of pts, useful for monitoring purposes, biopsy is diagnostic
colorectal ca rads
barium enema, colonoscopy, CT/PET can det extent and mets
Fe def anemia in old men is what until proven otherwise
colorectal ca
which hereditary polyposis syndromes are caused by mutation in APC gene
FAP, Gardner's, Turcot
Duke's criteria for prognosis of colorectal ca
Class A: TMN1: tumor confined to bowel wall: cure rate 90%
Class B: TMN2: penetration of tumor into colonic serosa/perirectal fat: cure rate 80%
Class C: TMN3: LN involvement: cure rate <60%
Class D: TMN4: distant mets: cure rate <5%
colorectal ca prev
screening >50y
annual fobt
flex sig q5y
colonoscopy q10y
what about FAP
tons of polyps, almost always dev into ca, prophylactic subtotal colectomy
HNPCC
multiple mutations, usually in proximal colon
Gardner's syndrome
similar to FAP with common bone and soft tissue tumors
Peutz-Jeghers synd
polyps are hamartomas with low risk of malig; mucocutaneous pigmentation of mouth, hands, genitals
Turcot synd
many colonic adenomas with high malig potential, comorbid malignant CNS tumors
Juvenile polyposis
colon, small bowel, stomach polyps are source of GI bleeds, slightly increased risk of ca later in life
what's the first thing you have to do with upper and lower GI bleeds
NG tube and lavage
Crit goal with GI bleeds
>30%
UGIB diff
PUD, mallory weiss tears, esophagitis, esophageal varices, gastritis
LGIB diff
diverticulosis, neoplasm, UC, mesenteric ischemia, AVMs, hemorrhoids, Meckel's
GI Bleeds rads
EGD/colonoscopy, barium swallow/enema, angiography, technetium scan for Meckel's
GI bleeds tx
fluid resus, PPI for UGIB until gastric cause is ruled out, prophylactic BBlockers for known varices to decrease chance of rebleeding, sclerotx, vasopressin may stop bleeding from AVMs and diverticula
what causes pancreatitis
GET SMASHED
Gallstones
Ethanol
Trauma
Steroids
Mumps
Autoimmune
Scorpion Sting
Hypercal/Hyperlip
ERCP, Drugs like Sulfa drugs
Ranson's Criteria on admission
GA LAW:
Glucose >200
AST>250
LDH>350
Age>55
WBC >16000
Ranson's Criteria during initial 48 hours post presentation
Cal<8
Hct dec >10%
PaO2<60mmHg
BUN inc >5
Base deficit >4
Sequestration of fluid >6L
pancreatitis h/p
epigastric pain rad to back, fever, n/v, Grey Turner's sign, Cullen' sign, steatorrhea if chronic, tachy
pancreatitis labs
increased amylase and lipase, glycosuria if chronic
pancreatitis rads
dilated loops of bowel near pancrease (sentinal loop), R colon distended until near pancreas (colon cutoff sign), enlarged pancreas, pseudocyst, pancreatic calc,
pancreatitis tx
hydration, opioids, NG suction, NPO, prophylactic abx for GI bacteria, debridement, enzyme supp if chronic
pancreatitis comp
abscess, pseudocyst, necrosis, obstruction, flstula formation, shock, DIC, sepsis, cancer if chronic
Exocrine pancreatic cancer location and type
head of pancreas, adeno
Exocrine pancreatic cancer risk factors
chronic pancreatitis, DM, fam hx, tobacco, high fat diet, male
Exocrine pancreatic cancer h/p
abdominal pain rad to back, nause, vom, WL, statorrhea, jaundice if bile duct obstructed, palpable nontender gallbladder (Courvoisier's Sign for gallbladder of pancreatic malignancy)
Exocrine pancreatic cancer labs
inc CEA and CA 19-9, hypergly, increased bilis, inc alk phos with bile duct obstruction
Exocrine pancreatic cancer rads
CT mass, dilated pancreas, local spread, ERCP can locate tumors
Exocrine pancreatic cancer tx
nonmets and limited to head can be treated with Whipple procedure, enzyme replacement, stenting of ducts for pallation
Exocrine pancreatic cancer comps
usually not detected until progressed, 5yr survival <2%, 20-30% 5 year survival after successful Whipple procedure, migratory thrombophlebitis (Trousseau's syndrome)
triad to start insulinoma workup
1. sxs of hypogly when fasting
2. hypogly
3. improvement with carb load
multiple insulinomas assoc w?
MEN1
What about insulinomas
HA, visual changes, confusion, weakness, mood instability, palps, diaphoresis
Inc fasting insulin, positive C peptide
Use CT/US/Indium Octreotide scan to localize
Tx: resection; diazoxide or octreotide can alleviate sxs
What about Glucagonomas
alpha cell tumor causing hypergly
refractory DM
abd pain, diarrhea, WL, MSchange, Migratory necrolytic erythema, DM sxs
hypergly, increased glucagon
CT/endoscopic US to localize
need surg, octreotide, IFNalpha, chemo, embolization
What about VIPomas
VIP from nonbeta islet cells
Water Diarrhea, weakness, N/V
high stool osmolality points to secretory cause of watery diarrhea
Rads: CT
Tx: Steroids, chemo, resection, octreotide, embolization for mets
5 Fs for patients susceptible to gallstones
Fat, Forty, Female, Fertile, Fam Hx
Cholithiasis risk factors
5 Fs, OCP use, TPN, rapid WL, DM
what are gallstones usually made of
cholesterol, unless it's calcium bilirubinate (Pigmented stones) secondary to chronic hemolysis
Cholithiasis h/p
postprandial RUQ pain, n/v, palpable gallbladder
Cholithiasis rads
US
Cholithiasis tx
bile salts dissolve stones, shock wave lithotripsy, cholecystectomy
Cholithiasis comps
recurrent stones, acute cholecystitis, pancreatitis
who can get acalculous Acute cholecystitis
TPN or critically ill
Acute cholecystitis h/p
RUQ pain rad to back, n/v, fever, tenderness
Acute cholecystitis labs
WBC, inc bilis, inc alk phos with impacted stone or cholangitis
Acute cholecystitis rads
US, HIDA scan will show that gallbladder fails to fill normally
Acute cholecystitis tx
fluids, abx, endoscopic drainage followed by cholecystectomy after it calms down, if mild can to lithitripsy and bile salts, ERCP to deliver stone solvents
Acute cholecystitis comps
perf, ileus, abscess
Charcot's triad for cholangitis
Fever, RUQ pain, Jaundice
Reynold's pentad for cholangitis
Fever, RUQ pain, Jaundice, change in MS, Hypotension
rask factors for Cholangitis
cholithiasis, anatomic defect, biliary cancer
Cholangitis labs
WBC, positive cultures, bilis, alk phos, AST/ALT increase, increased amylase
Cholangitis rads
HIDA scan more sensitive than US
Cholangitis tx
hyd, abx, endoscopic drainage with cholecystectomy, emergency bile duct decompression and relief of obstruction if emergent and sxs severe
gallbladder cancer rads
calcified gallbladder from axr or US, ERCP to bipsy
Viral hepatitis vs alcohol hepatitis enzyme patterns
Viral hep: AST and ALT equally elevated
Alcoholic AST>ALT
alcohol related liver dz h/p
ascites, HSmegaly, fever, jaundice, testicular atrophy, gynecomnastia, digital clubbing
alcohol related liver dz labs
increased AST and ALT, inc GGT, inc alk phos, inc bilis, longer PT, WBC
alcohol related liver dz tx
thiamine, folate, high caloric intake, liver txplant
alcohol related liver dz comp
hepatic encephalopathy, cirrhosis, coag disorders
causes of cirrhosis
HEPATIC
Hemochromatosis
Enzyme def (alpha antitrypsin)
PBC/PSC
Alcoholism
Tumor (hepatoma)
Infection (Hepatitis)
Chronic cholecystitis/Copper (Wilson's)
Cirrhosis h/p
GI bleeding, HSmegaly, Jaundice, ascites, Caput Medusae, Spider Telangectasias, Palmar erythema, Dupuytren's contractures in hands, testicular atrophy, gynecomnastia, MS change, asterixis
Cirrhosis labs
AST ALT GGT Alk Phos, dec alb, anemia, dec platelets, longer PT
Cirrhosis tx
treat varices with beta blockers or sclerotx, lactulose + neomycin + low protein diet can improve encephalopathy, liver txplant
Cirrhosis comp
portal htn, varices, hepatic encephalopathy, renal failure, bacterial peritonitis
Portal HTN prehepatic/hepatic/posthepatic causes
prehepatic: portal vein thrombosis
hepatic: cirrhosis, schisto, granulomatous dz
posthepatic: right sided heart failure, hepatic vein thrombosis, Budd-Chiari syndrome
5 locations of varices as a result of portal HTN
1. esophageal
2. Hemorrhoids
3. Caput medusae (paraumbilical vein to external iliacs)
4. Renal (Gastro/Splenorenal veins)
5. Paravertebral
Portal HTN h/p
ascites, pain, change in MS, GI bleeds, HSmegaly, testicular atrophy, gynecomnastia
what does serum-ascites albumin gap (SAAG) tell you
high gradient >1.1 is portal htn
high gradient with high protein >2.5 is Budd Chiari or heart failure, with low protein <2.5 is cirrhosis of liver

Low SAAG <1.1is ascites not due to portal htn, like nephrotic synd, TB, cancer
portal htn tx
salt restriction
IV abx for bac peritonitis
Dialysis for renal failure
lactulose neomycin low protein diet for hep enc
Vasopressin/sclerotx for varices
TIPS (Transjugular Intrahepatic Portocaval shunting)
Liver txplant
portal htn labs
do a SAAG, increased serum ammonium, WBC, normal glucose
lab signs for spontaneous bac peritonitis on paracentesis
PMN>250
Total protein >1
glucose <50
LDH >Normal serum LDH
what lab signs on paracentesis make you suspicious of cancer
if very high albumin and LDH is 60% of serum LDH
hemochromotosis leads to Fe dep which organs
liver, pancreas, heart, pituitary
Hemochromatosis h/p
abd pain, polyuria, polydipsia, pigmented bronze rash, hepatomegaly, testicular atrophy, may resemble DM or CHF
Hemochromatosis labs
inc Fe, Fesat, ferritin
slightly inc AST and ALT
Hemochromatosis tx
weekly/biweekly phlebotomy, avoid alcohol, deferoxamine for chelation
Hemochromatosis comp
cirrhosis, hepatoma, CHF, DM, hypopit
Wilson's dz deposits copper where
liver, brain, cornea
Wilson's dz h/p
psych dist, personality changes, loss of coordination, tremor, Keyser-Fleischer rings, hepatomegaly
Wilson's dz labs
dec serum ceruloplasmin, inc urine copper,
Wilson's dz tx
trientine or penicillamine for copper chelation, lifelong zinc, copper restriction, B6 supp
Wilson's dz comp
hepatic failure, cirrhosis
what does alpha 1 antitrypsin def cause
cirrhosis, panlobular emphysema
what is PBC
autoimmune intrahepatic bile duct obstruction leads to accum of bili, bile acids, cholesterol
PBC risk factors
older females, autoimmune dz such as rheumatoid arth, scleroderma
PBC h/p
jaundice, HSmegaly, pruritis, skin hyperpig, xanthomas
PBC labs
inc alk phos and GGT, inc bili, but normal liver enzymes
ANA and AMA positive
PBC tx
Ursodeoxycholic acid, fat soluble vitamins
what is PSC
destruction of larger intra and extra hepatic bile ducts leading to fibrosis and cirrhosis
PSC risk factors
younger males, UC
PSC h/p
RUQ pain, pruritis, jaundice, fever, night sweats, xanthomas
PSC labs
inc alk phos and GGT, normal liver enzymes, increased bilis and cholesterol, possibly positive pANCA
PSC rads
ERCP pearls on a string bile ducts
PSC tx
Ursodeoxycholic acid, MTX, steroids, endoscopic stenting of strictures, surgical resection of affected ducts
enzyme that conjugates bilis
glucuronosyl transferase
Gilbert's dz
mild def of glucuronosyl transferase: mild jaundice after exercise, increased indirect bilis<5
Crigler-Najjar syndrome type I
severe def in glucuronosyl transferase: peristent jaundice and CNS sxs (kernicterus in infants), increased indirect >5
Crigler-Najjar tx
phototx, plasmapheresis, cal phos w/orlistat, liver tx
Crigler-Najjar syndrome type II TX
phenobarb which increases liver enzymes
benign hepatic tumor types
hepatic adenoma, focal nodular hyperplasia, hemangiomas, hepatic cysts
who gets benign hepatic tumor
women with hx of OCP use
benign hepatic tumor rads
hypervascular liver mass on CT, MRI or angio
Hepatocellular carcinoma risk factors
HBV, HCV, cirrhosis, hemochromatosis, Aspergillus infection, schisto
Hepatocellular carcinoma h/p
jaundice, diarrhea, WL, RUQ pain, hepatomegaly, bruit over liver, ascites
enzyme that conjugates bilis
glucuronosyl transferase
Gilbert's dz
mild def of glucuronosyl transferase: mild jaundice after exercise, increased indirect bilis<5
Crigler-Najjar syndrome type I
severe def in glucuronosyl transferase: peristent jaundice and CNS sxs (kernicterus in infants), increased indirect >5
Crigler-Najjar tx
phototx, plasmapheresis, cal phos w/orlistat, liver tx
Crigler-Najjar syndrome type II TX
phenobarb which increases liver enzymes
benign hepatic tumor types
hepatic adenoma, focal nodular hyperplasia, hemangiomas, hepatic cysts
who gets benign hepatic tumor
women with hx of OCP use
benign hepatic tumor rads
hypervascular liver mass on CT, MRI or angio
Hepatocellular carcinoma risk factors
HBV, HCV, cirrhosis, hemochromatosis, Aspergillus infection, schisto
enzyme that conjugates bilis
glucuronosyl transferase
Hepatocellular carcinoma h/p
jaundice, diarrhea, WL, RUQ pain, hepatomegaly, bruit over liver, ascites
Gilbert's dz
mild def of glucuronosyl transferase: mild jaundice after exercise, increased indirect bilis<5
Crigler-Najjar syndrome type I
severe def in glucuronosyl transferase: peristent jaundice and CNS sxs (kernicterus in infants), increased indirect >5
Crigler-Najjar tx
phototx, plasmapheresis, cal phos w/orlistat, liver tx
Crigler-Najjar syndrome type II TX
phenobarb which increases liver enzymes
benign hepatic tumor types
hepatic adenoma, focal nodular hyperplasia, hemangiomas, hepatic cysts
who gets benign hepatic tumor
women with hx of OCP use
benign hepatic tumor rads
hypervascular liver mass on CT, MRI or angio
Hepatocellular carcinoma risk factors
HBV, HCV, cirrhosis, hemochromatosis, Aspergillus infection, schisto
Hepatocellular carcinoma h/p
jaundice, diarrhea, WL, RUQ pain, hepatomegaly, bruit over liver, ascites
paraneoplastic syndrome of hepatoma
hypogly, inc RBC production, refractory watery diarrhea, hyper cal, skin lesions
Hepatocellular carcinoma labs
increased AFP,slightly inc AST and ALT, in alk phos, inc bilis t and d, biopsy has to be carefully done cause it can hemorrhage
Hepatocellular carcinoma comps
poor prog, portal vein obstruction, Budd Chiari, liver failure
what are Dubin-Johnson and Rotor's syndromes
inability to excrete conjugated bilis from liver: benign but black liver
most common type of TEF
distal fistula with proximal esophageal atresia
TEF h/p
coughing, cyanosis during feeding, food filled blind pouch, abdominal distention, hx of aspiration pna
TEF rads
do a cxr with NG tube insertion which demonstrates tube in lung or blind pouch
what about Pyloric stenosis
olive sized epigastric mass, projective vomiting, barium swallow shows thin pyloric channel (string sign), US shows inc pyloric muscle thickness
pyloric stenosis tx
pyloric myotomy
what about Necrotizing enterocolitis
risks: preterm, LBW, bilious vomiting, hematochezia, abdominal distention and tenderness, signs of shock
labs: met acidosis, hypoNa
Rads: bowel distention, air in bowel wall, portal vein gas, or free air under diaphragm.
Tx: TPN, abx, NG suction, resection of affected bowel
what about Hirschsprung's Dz
obstipation, failure to pass stool, abd distention, bowel biopsy shows absence of ganglion cells
Rads: dilated bowel, barium enema shows proximal dilation with distal narrowing (Megacolon)
Tx: colostomy and resection
what about Intussusception
most common cause of obstruction in first 2 years, most commonly at ileocecal valve
It's considered cancer in an adult until proven otherwise
risks: Meckel's, HSP, adenovirus, CF
intermittent abdominal pain, currant jelly stool, palpable sausage like abd mass
labs: inc WBC
Rads: barium enema shows obstruction, US or CT can detect abnormal bowel
Tx: barium enema can reduce, if not surg
Comp: bowel ischemia esp appendix
what about Meckels
rule of 2s: Males 2x more likely, within 2ft of ileocecal valve, 2 types of ectopic tissue (gastric/pancreatic), 2% of population, most comps before 2yrs

remnant of vitelline duct, outpouching of ileum
painless rectal bleeding, intussusception, diverticulitis
rads: detected by nuclear scan technetium
tx: surgical resection
causes of neonatal jaundice
physiologic, G6Pd, bili overproduction without hemolysis: hemm, mat-fet transfusion, Gilbert's, Crigler-Najjar, biliary atresia
kernicterus sxs
jaundice, scleral icterus, lethargy, high pitched cry, seizures, apnea
what points to nonphysiologic jaundice in newborn
total bilis >15 or direct bili >2
neonatal jaundice tx
phototx, exchange txfusion, IVIG if blood incompatibility
FTT definition
below 3rd percentile weight for age
FTT workup
UA, CBC, cultures, lytes, CF, food records, suspect neglect or abuse, parental training for feeding and nutrition