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肝黏液表皮样癌:一例罕见病例报告及文献复习。

Mucoepidermoid carcinoma of the liver: report of a rare case and review of the literature.

机构信息

Department of Surgery, Institute of Health Biosciences, University of Tokushima, Tokushima, Japan.

出版信息

Hepatol Res. 2008 Jul;38(7):736-42. doi: 10.1111/j.1872-034X.2008.00335.x. Epub 2008 Mar 10.

Abstract

Although a mucoepidermoid carcinoma is sometimes seen as a neoplasm originating from the salivary glands, its origination from the liver is rare. A review of the medical literature in the English language disclosed only 16 cases originating from the hepatic system. The case explored here is that of an 81-year-old female, without any significant medical history, who was referred to our hospital for elevated liver function tests. Computed tomography (CT) showed a huge tumor, 10 cm in diameter, in the right lobe of the liver. The central part of the tumor was consistently un-enhanced, suggesting a large necrotic area. The liver tumor was diagnosed as mucoepidermoid carcinoma by a percutaneous biopsy. Despite chemotherapy with radiation therapy, the tumor showed very aggressive malignancy, resulting in early mortality. We herein report on a rare case of primary mucoepidermoid carcinoma of the liver with pulmonary and lymph node metastasis, confirmed by autopsy, and review the literature.

摘要

虽然黏液表皮样癌有时被认为是起源于唾液腺的肿瘤,但它起源于肝脏的情况很少见。对英文医学文献的回顾仅发现了 16 例源自肝系统的病例。本文探讨的病例是一位 81 岁女性,无任何重大病史,因肝功能检查升高而被转至我院。计算机断层扫描(CT)显示肝脏右叶有一个直径 10 厘米的巨大肿瘤。肿瘤的中央部分始终未增强,提示存在大的坏死区域。经皮肝肿瘤活检诊断为黏液表皮样癌。尽管进行了化疗和放疗,但肿瘤表现出非常侵袭性的恶性,导致早期死亡。我们在此报告一例经尸检证实的罕见原发性肝黏液表皮样癌伴肺和淋巴结转移病例,并复习文献。

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