Biliary tumors Flashcards
demographics of gallbladder cancer
- 3X more common in women
- more common in people over 65, whites
- most common GI malignancy in native americans
etiology of gallbladder cancer
- gallbladder disease (especially if >40)
- calcification of GB
- usually associated with cholesterol stones
- Salmonella typhi carriage increases risk
gastric surgery and cancers
- gastric surgery INCREASES risk of gallbladder cancer after 20 years
- gastric surgery DOES NOT INCREAsE the risk of bile duct cancer
most common benign tumor of gallbladder
- adenoma
most common malignant tumor of gallbladder
- adenocarcinoma
- lymphatic, neural, vascular spread due to lack of well-defined muscularis
- direct extension to liver, bile duct, colon, duodenum
location of gallbladder cancer
- 60% in fundus
- 30% in body
- 10% in neck
Krukenberg tumor
- adenocarcinoma that starts in the stomach or gallbladder and spreads to the pelvis (intraperitoneal spread)
symptoms of gallbladder cancer
- PAIN is the most common complaint
- hepatomegaly
- palpable mass
- ascites
- jaundice
diagnosis of gallbladder cancer
- increased ALP and bilirubin
- CEA and CA 19-9 may be elevated
- US, CT, MRI
treatment of gallbladder cancer
- 80% are unresectable
- chemo and radiation do not work
etiology of bile duct cancer
- no association with cirrhosis
- most intrahepatic cancers in China and Southeast Asia are from liver flukes
- associated with PSC, CUC (10X)
- occurs in younger age with CUC and without stones
- occurs after 15 years of CUC
Klatskin tumor
- cholangiocarcinoma at junction of left and right hepatic ducts
- presents with PAINLESS jaundice
- death from hepatic failure or cholangitis
clinical manifestations of bile duct cancer
- N/V, anorexia, weight loss, rarely painful unless with stone, PAINLESS jaundice
- increased ALP and bilirubin
- often bilirubin > 12 - cancer until proven otherwise
- best diagnosed with EUS
treatment of bile duct cancer
- intrahepatic, Klatskin, or mild bile duct tumor - resection
- distal bile duct - whipple procedure
pancreatic exocrine tumors
- 95% are pancreatic ductal adenocarcinoma
pancreaticoblastoma
- found in CHILDREN
risk factors for pancreatic adenocarcinoma
- 80% occur between 60-80
- male and urban setting
- if < 40, usually female
- diabetes and chronic pancreatitis
- 5X risk for hereditary pancreatitis
most common pancreatic exocrine tumor
- ductal cell mucin-producing adenocarcinoma
symptoms of ductal adenocarcinoma
- if its in the head - jaundice
- if its behind the ampulla - pancreatic insufficiency and chronic obstructive pancreatitis
- if its in the body/tail - severe back pain and weight loss
clinical manifestations of pancreatic adenocarcinoma
- ab pain
- > 10% weight loss
- worse when supine
insulinoma
- secretes excessive insulin thus causing hypoglycemia
- 60% are women
- headache, confusion, light-headedness, VISUAL SYMPTOMS, irrational behavior, DROWSINESS, coma
insulinoma diagnosis
- Hypoglycemia plus elevated insulin levels in patient with pancreatic mass
- determined during 72 hour fast with close observation
- insulin/glucose > 0.3 = insulinoma
- tumor of BETA islet cell
VIPoma
- secretes vasoactive intestinal peptide
- AKA pancreatic cholera - fasting large volume diarrhea, hypokalemia, hypochlorohydria
VIPoma diagnosis
- diarrhea with increased serum VIP
glucagonoma symptoms
- secrete glucagon
- dermatitis (necrolytic migratory erythema) - snake like rash on skin that is improved with amino acids
- angular chelitis, glucose intolerance, anemia
- nail dystrophy, thinning hair, weight loss
- thromboemboli are common
- tumor of the ALPHA islet cell
somatostatinoma
- can be in pancreas or intestine
- somatostatin stops things from being secreted - gastric acid, insulin, CCK, etc.
- 2X more common in females
- intestinal tumors usually in men
- somatostatin normally produced by D islet cells
symptoms of somatostatinoma
- mild DM, GB disease, weight loss, megaloblastic anemia, diarrhea, steatorrhea, hypochlorhydria
GRFoma
- causes acromegaly
- tumor usually > 6 cm
- associated with Zollinger-Ellison syndrome and MEN1
GRFoma diagnosis
- acromegaly
- increased GH
- pancreatic mass
ampullary carcinoma
- tumor of ampulla of Vater
- presents with jaundice, iron deficiency, weight loss
- treated with whipple procedure
jaundice due to malignancy
- tumor in the liver
- malignant nodes in porta heptatis
- Klatskin tumor
- ampullary/pancreatic carcinoma
- GB tumor