原发性肝上皮样血管内皮瘤1例。

Changgeng yi xue za zhi Pub Date : 1999-09-01
C H Shen, M H Tsai, T C Chen, N J Liu, I S Sheen
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引用次数: 0

摘要

肝上皮样血管内皮瘤(HEH)是一种非常罕见的肝脏血管肿瘤。它通常影响成年女性,表现为多发肝结节,主要分布于周围。由于其临床表现和影像学表现非特异性,极易被病理误诊,给临床医生诊治带来特殊困难。其临床病程和预后不一,但应介于血管瘤和血管肉瘤之间。主要的治疗选择是根治性切除或肝移植。我们报告一位62岁男性右上腹腹痛持续数天,最初被误诊为肝脓肿。最后通过肿瘤细胞viii因子相关抗原免疫组化染色阳性诊断为HEH。这个病例可以突出诊断这种罕见肿瘤的缺陷。提高怀疑指数,熟悉肿瘤的放射学和组织学特征,有助于准确诊断,从而避免不必要的干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary hepatic epithelioid hemangioendothelioma: case report.

Hepatic epithelioid hemangioendothelioma (HEH) is a very rare vascular tumor of the liver. It usually affects adult women and presents as multiple hepatic nodules with mainly peripheral distribution. It poses special difficulties for clinicians in its diagnosis and treatment because of its non-specific clinical manifestations and findings on imaging, and it is easy to be misdiagnosed pathologically. Its clinical course and prognosis are variable but supposed to be intermediate between hemangioma and angiosarcoma. The primary treatments of choice are radical resection or liver transplantation. We report a 62-year-old man with right upper quadrant abdominal pain of several days' duration, who was initially misdiagnosed as having a liver abscess. Finally, HEH was diagnosed on the basis of positive immunohistochemical staining for factor VIII-related antigen in tumor cells. This case could serve to highlight the pitfalls in diagnosing this rare tumor. Increasing the index of suspicion and familiarity with the radiological and histological characteristics of this tumor would facilitate the accurate diagnosis and thus avoid unnecessary interventions.

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