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肾移植术后患者中类似霍奇金淋巴瘤的淋巴瘤,模拟间变性大细胞淋巴瘤——罕见病例报告及文献综述

Hodgkin-like lymphoma, simulating anaplastic large cell lymphoma in the patient after renal transplantation--unusual case report and literature review.

作者信息

Ziarkiewicz-Wróblewska B, Górnicka B, Gierej B, Suleiman W, Nowacka-Cieciura E, Durlik M, Bogdańska M, Wasiutyński A, Pileri S A

机构信息

Department of Pathology, Medical University of Warsaw, Warszawa.

出版信息

Pol J Pathol. 2008;59(1):63-9.

Abstract

UNLABELLED

We report the atypical case of posttransplant lymphoproliferative disorder (PTLD) diagnosed in 55-year men 9 years after renal transplantation. It was evaluated only by bone marrow biopsy, which showed its total involvement with malignant lymphoma. It was composed of two populations of lymphoid cells: large RS-like cells and small to medium ones, with slightly angular nuclei without visible nucleoli. Both cellpopulations did not show positive reaction for typical B cell markers (CD20, CD79a). Large RS-like cells were positive with CD30 and EBV-LMP. However, negative reaction with CD15 and positive reactions with UCHL1 and EMA were not consistent with classical type of Hodgkin lymphoma. Morphological picture and immunophenotype had suggested anaplastic T cell lymphoma. Because of negative reaction with ALK1, initial diagnosis was ALCL ALK-negative. Then, additional stains with BOB1 and Oct2 were performed, which were positive. Taking it into account the diagnosis was changed; finally Hodgkin-like B lymphoma was diagnosed. The patient was treated with CHOP regimen with good response. 5 years after primary diagnose of PTLD he is steel free of disease.

CONCLUSIONS

  1. Apart from typical forms of PTLD, one may expect cases with nonspecific morphological picture and phenotype. 2. Negative reactions with typical immunohistochemical markers for lymphocytes of B cell line do not exclude the possibility of B-cell proliferation.
摘要

未标注

我们报告了一例非典型的移植后淋巴细胞增生性疾病(PTLD),该病例发生在一名55岁男性肾移植9年后。仅通过骨髓活检进行评估,结果显示其完全被恶性淋巴瘤累及。它由两类淋巴细胞组成:大的里-施(RS)样细胞和小到中等大小的细胞,细胞核略呈角形,无可见核仁。这两类细胞对典型的B细胞标志物(CD20、CD79a)均未显示阳性反应。大的RS样细胞CD30和EBV-LMP呈阳性。然而,CD15阴性反应以及UCHL1和EMA阳性反应与经典型霍奇金淋巴瘤不符。形态学表现和免疫表型提示为间变性T细胞淋巴瘤。由于ALK1阴性反应,初步诊断为ALK阴性的间变性大细胞淋巴瘤(ALCL)。随后进行了BOB1和Oct2的额外染色,结果呈阳性。综合考虑后诊断发生了改变;最终诊断为霍奇金样B淋巴瘤。该患者接受了CHOP方案治疗,反应良好。PTLD初次诊断5年后,他仍无疾病。

结论

  1. 除了典型的PTLD形式外,可能会出现形态学表现和表型不典型的病例。2. B细胞系淋巴细胞典型免疫组化标志物的阴性反应并不排除B细胞增殖的可能性。

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