Chapter 14: Liver tumors Flashcards

1
Q

A liver mass is incidentally seen on imaging in a middle-aged woman with a history of contraceptive use.

The mass is tan and lobulated beneath the liver capsule - this one has ruptured, hemorrhage. Can cause intraperitoneal bleeding.

Microscopically, hepatocytes appear benign but are not arranged in lobular architecture.

A

Hepatic adenoma.

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2
Q

A liver mass is removed and examined histologically. It has multiple fibrous septa and regenerative nodules.

A

Focal nodular hyperplasia - nodular lesion that resembles cirrhosis. Not neoplastic, not associated with contraceptives.

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3
Q

A patient presents with portal hypertension and a liver mass. Small hyperplastic nodules are found without fibrosis in an otherwisenormal liver.

A

Nodular Regenerative Hyperplasia

A cause of portal hypertension. Oral contraceptives? Anabolic steroids? Extrahepatic infections?

Not pre-neoplastic.

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4
Q

A patient at autopsy is found to have a small liver mass unrelated to the cause of death. Biopsy is shown below.

A

Cavernous hemangioma.

Most common tumor of the liver.

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5
Q

A patient presents with small cystic bild ducts embedded ina fibrous stroma.

A

Bile duct microhamartomas (Von Meyenburg Complexes).

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6
Q

What are the most common causes of hepatocellular carcinoma?

A

Hepatitis B virus: Integration, not necessarily cirrhosis.

Hepatitis C virus: Interaction HCV with core protein?

Alcoholic cirrhosis

Hemochromatosis and alpha1-antitrypsin deficiency.

Aflatoxin B1.

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7
Q

A middle-aged male with a history of chronic hepatitis C presents with a painful and enlarging mass in the RUQ. Biopsy is taken.

A

Hepatocellular Cracinoma:

Poorly circumscribed, nodular area of yellow partially hemorrhagic hepatocellular carcinoma.

B. Acinar pattern, surround concretions of inspissated bile.

Paraneoplastic manifedstations: Polycythemia, hypoglycemia, hypercalcemia. AFP levels elevated.

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8
Q

An adolescent patient presents with an enlarging, painful RUQ mass. A biopsy is taken.

A

Fibrolamellar hepatocellular carcinoma: Uncommon. Adolescents and young adults. Eosinophilic, neoplastic hepatocytes arranged in clusters and surrounded by delicate collagen fibers.

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9
Q

A patient with a past medical history of primary sclerosing cholangitis and infection with liver fluke (C. sinensis) presents with an enlarging RUQ mass. A biopsy is taken and shows well-differentiated neoplastic glands in a dense fibrous stroma.

A

Cholangiocarcinoma (bile duct carcinoma). Arises from biliary epithelium at any part of the biliary tree.

Metastasize throughout the body. Liver transplant rarely successful.

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10
Q

A neonate presents with abdominal enlargement, vomiting, and failure to thrive. Serum AFP is elevated.

A liver mass is found that is circumscribed and partially necrotic and hemorrhagic, with epithelial and mesenchymal cells. The cells are small and fusiform and are arranged in ribbons or rosettes.

A

Hepatoblastoma.

Other associations: Cardiac and renal malformations, hemihypetrtrophy, macroglossia.

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11
Q

A patient with known exposure to thorium dioxide presents with a liver mass. A biopsy is taken and shows multicentric tumor with multiple hemorrhagic nodules. Spindle-shaped neoplastic endothelial cells line sinusoids and compress liver cell plates.

Presents with hepatomegaly, jaundice, and ascites. Pancytopenia, hemolytic anemia.

A

Hemangiosarcoma

Thorium dioxide, vinyl chloride, or inorganic arsenic.

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12
Q

A patient presents with massive hepatomegaly. The liver is imaged and contains many nodules. It is removed.

A

Metastatic carcinoma in the liver.

This one is metastatic colon cancer. GI, breast, and lung common.

Pancreatic, melanoma, and hematologic malignancies often involve the liver.

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13
Q

A patient presents soon after a liver transplant with jaundice. A biopsy is taken.

A

Acute rejection of a liver transplant.

Portal triad expanded by polymorphous inflammatory infiltrate - small and large lymphocytes, plasma cells, macrophages, neutrophils. Bile ducts damaged.

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14
Q

A patient presents after 2 months of allograft rejection. Biopsy shows damaged interlobular bile ducts, leading to persistent cholestasis.

A

Chronic ductopenic rejection or Vanishing bile duct syndrome.

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