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Zorluk: ZorPathology and Biopsy Interpretation

Match each focal hepatic lesion to its characteristic histopathologic and immunohistochemical findings typically seen on a needle core biopsy or surgical resection.

  • Focal nodular hyperplasiaNodular architecture with a central fibrous scar containing thick-walled dystrophic vessels and bile ductular proliferation; demonstrates a geographic, 'map-like' pattern of glutamine synthetase expression.
  • Beta-catenin-activated hepatocellular adenomaBenign proliferation of hepatocytes frequently showing cytologic atypia and pseudoglandular formation; immunohistochemistry demonstrates strong, diffuse nuclear staining for beta-catenin.
  • Well-differentiated hepatocellular carcinomaProliferation of hepatocytes arranged in broadened trabeculae (greater than 3 cells thick) with a decreased reticulin framework; demonstrates diffuse CD34 staining outlining capillarized sinusoids.
  • Fibrolamellar hepatocellular carcinomaLarge polygonal cells with abundant intensely eosinophilic granular cytoplasm and prominent nucleoli, interspersed with dense, parallel bands of collagen; often occurs in young patients without cirrhosis.

Cevap

Focal nodular hyperplasia pairs with the 'map-like' glutamine synthetase staining and central scar; Beta-catenin-activated hepatocellular adenoma pairs with diffuse nuclear beta-catenin staining; Well-differentiated hepatocellular carcinoma pairs with broadened trabeculae and CD34-positive capillarized sinusoids; Fibrolamellar hepatocellular carcinoma pairs with large eosinophilic cells and dense lamellar collagen bands.
Accurate interpretation of liver biopsy findings is crucial for establishing the diagnosis of focal hepatic lesions, as management ranges from observation to major resection or transplant. Focal nodular hyperplasia is identified by a central scar and geographic glutamine synthetase staining. Beta-catenin-activated adenomas show diffuse nuclear beta-catenin and require resection due to malignancy risk. Hepatocellular carcinoma is characterized by thickened trabeculae, loss of reticulin, and sinusoidal capillarization (CD34+). Fibrolamellar hepatocellular carcinoma has distinctive large oncocytic cells with dense lamellar fibrosis.

Adım Adım Çözüm

1
Evaluate the histologic and immunohistochemical description featuring the 'map-like' glutamine synthetase pattern.
This pattern, along with a central fibrous scar and bile ductular proliferation, is diagnostic of focal nodular hyperplasia.
Recognizing this specific IHC pattern differentiates focal nodular hyperplasia from true neoplastic hepatic adenomas.
2
Evaluate the description featuring diffuse nuclear beta-catenin and cytologic atypia.
This identifies a beta-catenin-activated hepatocellular adenoma.
This specific subtype of hepatic adenoma is critical to identify due to its significantly higher risk of malignant transformation compared to other adenoma subtypes.
3
Analyze the description of broadened trabeculae and CD34 staining outlining sinusoids.
These features define a well-differentiated hepatocellular carcinoma.
CD34 highlights capillarization of sinusoids, a hallmark of malignant vascularization in hepatocellular carcinoma that distinguishes it from benign nodules.
4
Analyze the description of large eosinophilic cells with lamellar collagen bands.
This is the classic appearance of fibrolamellar hepatocellular carcinoma.
This distinct clinical and pathologic variant occurs in non-cirrhotic livers of young patients and has unique morphological features requiring differentiation from standard hepatocellular carcinoma.

Anahtar Kavram

Histopathologic and immunohistochemical differentiation of focal hepatic lesions
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