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多脏器移植6年后免疫抑制患者发生血管肉瘤的细胞学诊断:病例报告及文献复习

Cytological diagnosis of angiosarcoma arising in an immunosuppressed patient 6 years after multi-visceral transplantation: a case report and literature review.

作者信息

Chen Xiaowei, Lagana Stephen M, Poneros John, Kato Tomoaki, Remotti Fabrizio, He Huangjun, Kaminsky Dmitry, Hamele-Bena Diane

机构信息

Department of Pathology and Cell Biology, Columbia University Medical Center, New York, New York.

出版信息

Diagn Cytopathol. 2014 Oct;42(10):884-9. doi: 10.1002/dc.23068. Epub 2013 Nov 7.

Abstract

Angiosarcoma is a rare and aggressive malignant tumor of soft tissue. It can arise in almost any part of the body, most commonly in the skin and the superficial soft tissue in the head and neck region. Although the etiology of angiosarcoma is unknown, there are several well-known risk factors, such as chronic lymphedema, exposure to radiation, toxins, and foreign bodies. It rarely occurs in transplant patients. Cytological criteria for the diagnosis of angiosarcoma have not been fully established, having been described only in a few cases, mostly fine-needle aspiration biopsies (FNAB). Herein, we present a case of angiosarcoma arising in an immunosuppressed patient status post multi-visceral transplantation and diagnosed by cytology. To the best of our knowledge, this is the first report of such a case in the English literature. The cytological findings from endoscopic ultrasound-guided FNAB and ascites fluid are discussed.

摘要

血管肉瘤是一种罕见的侵袭性软组织恶性肿瘤。它几乎可发生于身体的任何部位,最常见于皮肤以及头颈部的浅表软组织。尽管血管肉瘤的病因尚不清楚,但有几个众所周知的危险因素,如慢性淋巴水肿、接触辐射、毒素和异物。它很少发生在移植患者中。血管肉瘤的细胞学诊断标准尚未完全确立,仅在少数病例中有所描述,大多是细针穿刺活检(FNAB)。在此,我们报告一例多脏器移植术后免疫抑制状态下发生的血管肉瘤,并通过细胞学诊断。据我们所知,这是英文文献中首例此类病例报告。本文讨论了内镜超声引导下细针穿刺活检及腹水的细胞学检查结果。

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