| Literature DB >> 20107963 |
Tomohiko Akahoshi1, Hidefumi Higashi, Satoru Tsuruta, Kouichiro Tahara, Toshifumi Matsumoto, Hideya Takeuchi, Shoichi Era, Fuminori Fujita, Yoichi Muto.
Abstract
Primary hepatic neuroendocrine carcinoma is an extremely rare liver tumor. We herein report a case of primary hepatic neuroendocrine carcinoma coexisting with a hemangioma in a 66-year-old man. Ultrasonography, computed tomography, and magnetic resonance imaging showed a tumor (1.5 cm in diameter) coexisting with a hemangioma in the lateral segment of the liver. Liver biopsy showed malignant cells, and several examinations revealed no alternative primary source. We performed a lateral segmentectomy. Microscopically, the tumor cells had round to oval nuclei and eosinophilic cytoplasm, proliferated in thick trabeculae or solid nests, and formed a focal rosette pattern. Mitotic cells were frequently observed. Immunohistochemically, the tumor cells were positive for the endocrine markers chromogranin A, neuron-specific enolase, and neural cell adhesion molecule, but negative for alpha-fetoprotein and hepatocyte-specific antigen. The patient is still alive after 3 months, without recurrence.Entities:
Mesh:
Year: 2010 PMID: 20107963 DOI: 10.1007/s00595-009-4018-5
Source DB: PubMed Journal: Surg Today ISSN: 0941-1291 Impact factor: 2.549