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富含T细胞的B细胞淋巴瘤(TCRBCL):细针穿刺细胞诊断的局限性

T-cell-rich B-cell lymphoma (TCRBCL): limitations in fine-needle aspiration cytodiagnosis.

作者信息

Das Dilip K, Pathan Shahed K, Mothaffer Fatma J, John Bency, Mallik Mrinmay K, Sheikh Zafar A, Haji Bahiyah E, Amir Thasneem, Francis Issam M

机构信息

Department of Pathology, Faculty of Medicine, Kuwait University, Kuwait.

出版信息

Diagn Cytopathol. 2012 Nov;40(11):956-63. doi: 10.1002/dc.21683. Epub 2011 Apr 6.

Abstract

Exclusive reports on fine needle aspiration (FNA) cytodiagnosis of T-cell-rich B-cell lymphoma (TCRBCL) are scarce in literature. This report reflects the diagnostic difficulties associated with cytodiagnosis of this rare variant of diffuse large B-cell lymphoma. The study is based on 11 cases with age ranging from 16 to 63 years and a median of 50 years. Male to female ratio was 6:5. Ten cases presented with lymphadenopathy and one had lymphadenopathy as well as extranodal solid tumor. The initial cytodiagnosis was suggestive of TCRBCL in one case, TCRBCL/Hodgkin's lymphoma (HL) in three cases, TCRBCL/HL/anaplastic large cell lymphoma (ALCL) in two cases, TCRBCL/ALCL in one case, and TCRBCL/non-Hodgkin lymphoma (NHL) T-cell/ALCL in one case. There was also a cytologically diagnosed HL case, which on review turned out to be HL/TCRBCL. Histopathological diagnosis was HL in all these nine cases. There were two histologically diagnosed TCRBCL cases during this period, with cytodiagnoses of NHL other than TCRBCL in one and HL in the other. While highlighting the difficulties associated with the cytodiagnosis of TCRBCL, this study conveys a word of caution that adequate immunocytochemical studies should be performed before diagnosing this rare neoplasm with a varied cytomorphology.

摘要

关于富含T细胞的B细胞淋巴瘤(TCRBCL)细针穿刺抽吸(FNA)细胞诊断的独家报道在文献中很少见。本报告反映了这种罕见的弥漫性大B细胞淋巴瘤变体的细胞诊断所面临的困难。该研究基于11例患者,年龄从16岁到63岁不等,中位数为50岁。男女比例为6:5。10例表现为淋巴结病,1例既有淋巴结病又有结外实体瘤。最初的细胞诊断中,1例提示为TCRBCL,3例提示为TCRBCL/霍奇金淋巴瘤(HL),2例提示为TCRBCL/HL/间变性大细胞淋巴瘤(ALCL),1例提示为TCRBCL/ALCL,1例提示为TCRBCL/非霍奇金淋巴瘤(NHL)T细胞/ALCL。还有1例经细胞学诊断为HL的病例,复查后发现是HL/TCRBCL。这9例经组织病理学诊断均为HL。在此期间有2例经组织学诊断为TCRBCL的病例,其中1例细胞诊断为非TCRBCL的NHL,另1例为HL。在强调TCRBCL细胞诊断困难的同时,本研究提醒注意,在诊断这种具有多种细胞形态的罕见肿瘤之前,应进行充分的免疫细胞化学研究。

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