Chapter 18 part 6: Gallbladder Flashcards

1
Q

Congenital anomalies of the gallbladder

A
  • can be congenitally absent or exist in aberrant locations (embedded in hepatic substance)
  • other variants include folded fundus (phrygian cap) or duplicated or bilobed gallbladder
  • agenesisi of common or hepatic bile ducts or hypoplastic narrowing of biliary channels
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2
Q

Cholelithiasis (gallstones)

A
  • 95% of biliary tract disease attributed to this
  • 90% are cholesterol stones with remainder being pigmented (bilirubin calcium salts); vast majority remain asymptomatic for decades
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3
Q

Risk factors for cholesterol gallstones

A
  • related to increased hepatic cholesterol uptake or synthesis or increased biliary cholesterol secretion
  • Native Americans (75% in Hopi, Navajo and Pima groups)
  • Industrialized countries
  • increasing age, female more than males
  • Estrogenic influences, including oral contraception and pregnancy
  • Obesity, metabolic syndromes, hypercholestrolemia, and rapid weight loss
  • Gallbladder stasis, like in spinal cord injury
  • Heritable conditions related to hepatic biliary transport (common variants of adenosine triphosphate [ATP]-binding cassette sterol transported encoded by ABCG8 gene
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4
Q

Pathogenesis of Cholesterol stones

A

-When cholesterol concentration exceed solubilizing capacity of bile salts (supersaturation), cholesterol nucleates into solid cholesterol monohydrate crystals

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5
Q

Four conditions that contribute to cholesterol stone formation

A

1) Bile must be supersaturated with cholesterol
2) Gallbladder hypomotility promotes crystal nucleation
3) Cholesterol nucleation in bile is accelerated by microprecipitates of calcium salts (inorganic or bilirubin salts)
4) Mucus hypersecretion in gallbladder traps the cyrstals permitting aggregation into stones

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6
Q

Pathogenesis of pigment stones

A
  • form in setting of unconjugated bilirubin (most commonly due to chronic hemolytic conditions) and precipitation of calcium bilirubin salts
  • In underdeveloped countries, pigmented stones are often formed bc biliary infections (with E. Coli, Ascaris lumbricoides, or O. sinensis) promote bilirubin glucuronide deconjugation
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7
Q

Morphology of cholesterol stones

A
  • arise exclusively in gallbladder and are classically hard and pale yellow
  • bilirubin salts can impart a black color
  • when composed mostly of cholesterol, they are radiolucent; calcium carbonate deposition in 10-20% of stones is sufficient to render them radiopaque
  • single stones are ovoid; multiple stones are faceted
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8
Q

Morphology of pigmented stones

A
  • can be black (sterile gallbladder bile) or brown (with infection)
  • Both are soft and usually multiple and most are radiopaque
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9
Q

Clinical features of gallstones

A
  • 70-80% asymptomatic in life
  • become symptomatic at a rate of 1-4% per year with risk diminishing with time
  • S/S: spasmodic, colicky pain, due to passing stones in bile ducts (smaller stones more commonly cause symptoms than large stones)
  • Associated gallbladder inflammation (cholecystitis) generates right upper-abdominal pain
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10
Q

Severe complications of gallstones

A
  • Empyema, perforation, fistulas, biliary tree inflammation (cholangitis), obstructive cholestasis or pancreatitis and erosion of gallstone into adjacent bowel (gallstone ileus)
  • Clear mucinous secretions in obstructed gallbladder distend the gallbladder (mucocele)
  • also increased risk for gallbladder carcinoma
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11
Q

Cholecystitis

A
  • Can be acute or chronic

- Acute divided into acute calculous colecystitis (WITH gallstones) and acute acalculus cholecystitis

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12
Q

Acute cholecystitis

A
  • acute inflammation of gallbladder precipitated most frequently by gallstone obstruction
  • 10% of cases without gallstone obstruction usually occur in severely ill patients
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13
Q

Acute calculus cholecystitis

A
  • with gallstones
  • initiated by chemical irritation of gallbladder by retained bile acids; subsequent release of inlammatory mediators (lysolecithin, prostaglandins) and gallbladder develops dysmotility
  • In severe cases, distention and increased luminal pressures compromise mucosal blood flow causing ischemia; bacterial contamination can be late complication
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14
Q

Acute acalculous cholecystitis

A
  • results from ischemia due to diminished flow in end-arterial cystic artery circulation
  • occurs in setting of sepsis with hypotension and multiorgan failure, immunosuppression, major trauma or burns, DM, or infections
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15
Q

Morphology of acute cholecystitis

A
  • enlarged, tense, bright red to blotchy green-black gallbladder with serosal fibrinous exudate
  • Luminal contents range from turbid to purulent
  • In severe cases, gallbladder is transformed into green-black necrotic organ (gangrenous cholecystitis) with multiple perforations
  • In milder cases only gallbladder wall edema and hyperemia
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16
Q

Clinical features of acute cholecystitis

A

-may be mild and intermittent or may be a surgical emergency
S/S: RUQ or epigastric pain, fever, anorexia, tachycardia, diaphoresis, and nausea and vomiting
-jaundice suggests common bile duct obstruction

17
Q

Cholecystitis prognosis

A
  • Slef limited attacks subside over several days
  • 25% develop more severe symptoms and require surgical intervention
  • In severely ill paients with acalculus cholecystitis, symptoms may not be evident due to comorbid conditions and mortality rate is higher
18
Q

Chronic cholecystitis

A
  • consequence of repeated bouts of acute cholecystitis but often develops without antecedent attacks
  • although gallstones are usually present (90%), they may not play a role in initiating inflammation
  • Rather chronic bile supersaturation with cholesterol permits cholesterol suffusion of gallbladder wall and initiation of inflammation and gallbladder dysmotility
  • Pt. populations and symptoms are same as for acute cholecystitis
19
Q

Morphology of chronic cholecystitis

A
  • contracted gallbladders (from fibrosis), normal size or enlarged (from obstruction)
  • wall is variably thickened and gray-white
  • mucosa is generally preserved but may be atrophied
  • cholesterol-laden macrophages in lamina propria (cholesterolosis) and gallstones frequent
  • Variable inflammation with occasional mucosal outpouchings (Rokitansky-Aschoff sinuses)
  • Rarely see mural dystrophic calcifications (porcelain gallbladder) or a fibrosed, nodular gallbladder with marked histiocytic inflammation (xanthogranulomatous cholecystitis)
20
Q

Clinical features of chronic cholecystitis

A
  • Recurrent attacks of steady or colicky epigastric or RUQ pain
  • Complications: same as for acute including bacterial superinfection, gallbladder perforation and abscess formation or peritonitis and formation of biliary-enteric fistulas
21
Q

Carcinoma of the gallbladder

A
  • slightly more common in women, age over 70
  • gallstones coexist in 95% of US patients
  • chronic gallbladder inflammation (with or without stones) is critical risk factor)
  • Gallstones less common precursor in Asian populations where pyogeniic and parasitic diseases dominate as causes
  • Gallbladder cancers harbor recurrent molecular alterations; ERBB2 (Her-2/neu) is overexpressed in 30-60% of cases and mutations of chromatin remodeling genes (PBRM1 and MLL3) occur in 25%
22
Q

Morphology of gallbladder carcinoma

A
  • tumors may be INFILTRATING with diffuse gallbladder thickening and induration, or EXOPHYTIC–growing into lumen as irregular, cauliflower-like mass
  • Most gallbladder carcinomas are adenocarcinomas
  • Histo varies from papillary to infiltrating and can range from moderately differentiated to undifferentiated
  • Rarely there are squamous, adenosquamous, carcinoid or mesenchymal variants
  • spread by local invasion of liver, extension to cystic duct and portohepatic lymph nodes and metastatic seeding of peritoneum, viscera and lungs
23
Q

Clinical features of gallbladder carcinoma

A
  • S/S: insiduous and indistinguishable from those caused by cholelithasis
  • Tumors usually unresectable when discovered