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肝上皮样血管内皮瘤:细针穿刺细胞学诊断中的一个陷阱。

Hepatic epithelioid hemangioendothelioma: A diagnostic pitfall in aspiration cytology.

作者信息

Gupta Ruchika, Mathur Sandeep R, Gupta S Datta, Durgapal Prashant, Iyer Venkateswaran K, Das Chandan Jyoti, Acharya Subrat K

机构信息

Department of Pathology, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Cytojournal. 2010 Jan 15;6:25. doi: 10.4103/1742-6413.58951.

Abstract

Hepatic epithelioid hemangioendothelioma (EH) is a rare vascular neoplasm. An accurate radiologic diagnosis is usually difficult due to the presence of multiple nodules, simulating metastatic carcinoma. Though histologic features of this tumor are well described, cytologic reports of hepatic EH are very few in the available literature. We describe a case of a young healthy adult male who was found to have multiple hepatic masses on radiologic investigations. A guided fine needle aspiration demonstrated a poorly differentiated neoplasm. The diagnosis was made on core biopsy assisted by immunohistochemistry, which showed characteristic features of EH. He is doing well 14 months after diagnosis, without surgical excision or chemotherapy. An accurate diagnosis of hepatic EH on aspiration cytology requires an adequate specimen and awareness of its cytologic features, including discohesive atypical cells with intracytoplasmic lumina and intranuclear inclusions. Since this tumor is usually unresectable but has a favorable prognosis as compared to hepatocellular carcinoma, a correct diagnosis is essential for appropriate management and prognostication.

摘要

肝上皮样血管内皮瘤(EH)是一种罕见的血管肿瘤。由于存在多个结节,类似转移性癌,准确的放射学诊断通常很困难。尽管该肿瘤的组织学特征已有详细描述,但在现有文献中,肝EH的细胞学报告非常少。我们描述了一例年轻健康成年男性,其在放射学检查中发现有多个肝脏肿块。一次引导下细针穿刺显示为低分化肿瘤。通过免疫组织化学辅助的核心活检做出了诊断,显示出EH的特征性表现。诊断后14个月他情况良好,未进行手术切除或化疗。在细针穿刺细胞学上准确诊断肝EH需要足够的标本以及对其细胞学特征的认识,包括具有胞质内管腔和核内包涵体的分散性非典型细胞。由于该肿瘤通常无法切除,但与肝细胞癌相比预后良好,正确诊断对于恰当的管理和预后判断至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3693/2822180/4926de7eed12/CJ-06-25-g001.jpg

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