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Castleman病的细针穿刺抽吸结果。

Fine-needle aspiration findings in Castleman's disease.

作者信息

Meyer L, Gibbons D, Ashfaq R, Vuitch F, Saboorian M H

机构信息

Department of Pathology, University of Texas Southwestern Medical Center, Dallas 75235-9072, USA.

出版信息

Diagn Cytopathol. 1999 Jul;21(1):57-60. doi: 10.1002/(sici)1097-0339(199907)21:1<57::aid-dc16>3.0.co;2-a.

Abstract

Castleman's disease of the hyaline vascular subtype is an uncommon lesion; experience with fine-needle aspiration (FNA) of this tumor is limited to rare case reports. We describe the cytologic, flow cytometric, and immunohistochemical findings in two cases initially sampled by FNA. Two females, aged 40 and 26 yr, were found incidentally to have an oropharyngeal and a mediastinal mass, respectively. Neither complained of systemic symptoms, and both had a normal routine laboratory workup. FNA followed by surgical excision in both cases was consistent with Castleman's disease of the hyaline vascular type. In the appropriate clinical context, a mature small lymphoid population associated with larger atypical cells, which are consistent with follicular dendritic cells, can be suggestive of Castleman's disease. Confirmation of a polytypic B-cell population by flow cytometry, supported by immunohistochemistry, is very helpful. However, definitive distinction from Hodgkin's lymphoma on FNA is probably not possible.

摘要

透明血管型Castleman病是一种罕见病变;关于该肿瘤细针穿刺抽吸活检(FNA)的经验仅限于少数病例报告。我们描述了两例最初通过FNA取样的病例的细胞学、流式细胞术和免疫组化结果。两名女性,年龄分别为40岁和26岁,分别偶然发现口咽和纵隔肿块。两人均无全身症状,且常规实验室检查均正常。两例均经FNA后手术切除,结果均符合透明血管型Castleman病。在适当的临床背景下,与较大的非典型细胞相关的成熟小淋巴细胞群,与滤泡树突状细胞一致,可能提示Castleman病。通过流式细胞术确认多型B细胞群,并得到免疫组化支持,非常有帮助。然而,FNA时可能无法与霍奇金淋巴瘤进行明确区分。

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