Journal List > Korean J Gastroenterol > v.68(2) > 1007545

Yun, Kim, Lee, Kim, Kim, Jung, Lee, and Song: A Case of Composite Hepatocellular Carcinoma and Neuroendocrine Carcinoma in a Patient with Liver Cirrhosis Caused by Chronic Hepatitis B

Abstract

Primary hepatic neuroendocrine carcinoma (PHNEC) is rare and its origin is not clearly understood. The coexistence of PHNEC and hepaotcellular carcinoma has been reported in only a few cases. We report a rare case of combined PHNEC and hepaotcellular carcinoma in a patient with liver cirrhosis caused by chronic hepatitis B that resulted in aggressive behavior and poor prognosis.

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Fig. 1.
Abdominal CT scan showing tumor of S3 with a high density area in the peripheral part of the mass. (A) Arterial phase showed about 2.4 cm hypervascular nodule in S3 of liver. (B) Portal phase showed heterogeneous enhancing mass. (C) Delayed phase showed pseudo washout sign underlying liver cirrhosis.
kjg-68-109f1.tif
Fig. 2.
(A) MRI showed peripheral hypervascular mass with pseudo washout appearance and heterogeneous T2 signal. (B) MRI showed restricted diffusion.
kjg-68-109f2.tif
Fig. 3.
Cut section of the specimen showed 2.5 cm light gray mass with clear distinction underlying liver cirrhosis.
kjg-68-109f3.tif
Fig. 4.
(A) The neoplastic cells of the neuroendocrine carcinoma (NEC) are separated from hepatocellular carcinoma (HCC) (H&E, ×40). (B) The transition between HCC (left) and NEC (right) (H&E, ×100). (C) Immunostain for CD56 are strongly positive in small round cells (×200). (D) Immunostain for hepatocyte specific antigen showed positive for HCC (×200).
kjg-68-109f4.tif
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