복강 내 거대 종양형태로 발생한 간세포암종 분화성 위선암

Hepatoid adenocarcinoma is a rare variant of adenocarcinoma of the stomach. The tumor has been found to be an alpha-fetoprotein (AFP) producing carcinoma arising in extrahepatic organs, and it mimics hepatocellular carcinoma in terms of morphology and function. Vascular invasion, usually prominent,...

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Published inAnnals of surgical treatment and research Vol. 66; no. 2; pp. 153 - 158
Main Authors 남소현(So Hyun Nam), 장혁재(Hyuk Jai Jang), 김용호(Yong Ho Kim), 조용필(Yong Pil Cho), 나병규(Pyung Kyu Na), 안재홍(Jae Hong Ahn), 강길현(Kil Hyun Kang), 한명식(Myeng Sik Han)
Format Journal Article
LanguageKorean
Published 대한외과학회 01.02.2004
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ISSN2288-6575
2288-6796

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Summary:Hepatoid adenocarcinoma is a rare variant of adenocarcinoma of the stomach. The tumor has been found to be an alpha-fetoprotein (AFP) producing carcinoma arising in extrahepatic organs, and it mimics hepatocellular carcinoma in terms of morphology and function. Vascular invasion, usually prominent, is often complicated by extensive liver metastases, and vascular permeation, especially in the veins, has been described as a characteristic finding of this tumor. A patient with hepatoid adenocarcinoma of the stomach with a huge mass is described. Gastrofiberscopy revealed an elevated lesion with a central depression on the greater curvature of the antrum and with extrinsic compression on the lesser curvature and the duodenum. Computed tomography revealed a large lobulated mass in the lesser curvature of the stomach, attached from the liver, gall bladder and porta hepatitis to the pancreas. The AFP serum level was markedly elevated. After a diagnosis was made of AFP-producing stomach carcinoma with huge lymph node metastasis, subtotal gastectomy with wedge resection of the liver, and cholecystectomy including the huge mass ware performed. Microscopically, the tumor and intraabdominal huge mass showed mainly hepatoid differentiation. The tumor showed immunohistochemical positivity for AFP and huge lesser omental metastasis with adhesion to the liver and extensive venous invasion. Lymph node metastasis was not found. According to these histopathological findings, the tumor was diagnosed as hepatoid adenocarcinoma of the stomach with venous invasion. We report this rare variant of adenocarcinoma of the stomach, which mimics hepatocellular carcinoma in its propensity for venous permeation. KCI Citation Count: 1
Bibliography:G704-000991.2004.66.02.009
http://kmbase.medric.or.kr/Main.aspx?d=KMBASE&m=VIEW&i=0371320040660020153
ISSN:2288-6575
2288-6796