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附睾原发性滤泡性淋巴瘤,t(14;18)(q32;q21)/IGH-BCL2 阳性且 BCL2 蛋白表达阴性:一例报告

Primary follicular lymphoma of the epididymis positive for t(14;18)(q32;q21)/IGH-BCL2 and negative for BCL2 protein expression: a case report.

作者信息

Tralongo Vincenzo, Becchina Gaspare, Nagar Claudia, Ottoveggio Gabriella, Mason Silvia, Seno Barbara, Sessa Francesca, Frattini Milo, Genovese Francesco

机构信息

Department of Diagnostic Laboratory, U,O,C, of Pathologic Anatomy, "G,F, Ingrassia" Hospital, ASP Palermo, Italy.

出版信息

J Med Case Rep. 2012 Jan 18;6:24. doi: 10.1186/1752-1947-6-24.

Abstract

INTRODUCTION

Non-Hodgkin lymphoma (NHL) can involve the paratesticular organs as the primary disease, as primary testicular lymphoma that secondarily involves the paratesticular structures, as the initial site of presentation of occult nodal disease or as the result of disease dissemination. Primary follicular lymphoma of the epididymis in an adult is extremely rare. Little is known about primary adult paratesticular/epididimal lymphomas.

CASE PRESENTATION

We report a rare case of primary follicular non-Hodgkin lymphoma of the epididymis in a 90-year-old Caucasian man who presented with a left scrotal mass. Bone marrow biopsy was negative and computed tomography of the total body revealed no evidence of extratesticular involvement. Macroscopically, the epididymis was replaced completely by a uniform mass. Histologic studies revealed a dense lymphoid infiltrate predominantly composed of centrocytes with admixed centroblasts. Immunohistochemical analyses demonstrated that neoplastic cells strongly expressed CD45RB, CD20, CD79a, bcl-6 and CD10; bcl-2 immunostaining was negative. Molecular studies showed the presence of the monoclonal IgH gene rearrangement and the IgH/BCL2 rearrangement. The lymphoma was classified as follicular lymphoma, low grade, grade 1-2. The patient subsequently underwent radical orchiectomy, did not receive chemotherapy and post-operative follow-up showed absence of disease recurrence.

CONCLUSIONS

The case of primary follicular lymphoma of epididymis, reported here, is considered a very rare event. It is characterized by clinically indolent localized disease, a good clinical outcome, lack of expression of BCL2 protein and the presence of the t(14;18)(q32;q21)/IGH-BCL2. Even if it is a single case, the primary follicular lymphoma epididymis with t(14;18) could represent either a variant of the previously reported t(14;18)-negative primary paratesticular follicular lymphoma or a distinct biological entity. To report additional cases in the future would be helpful in resolving this question.

摘要

引言

非霍奇金淋巴瘤(NHL)可作为原发性疾病累及睾丸旁器官,可作为原发性睾丸淋巴瘤继而累及睾丸旁结构,可作为隐匿性淋巴结疾病的初始表现部位,也可作为疾病播散的结果。成人原发性附睾滤泡性淋巴瘤极为罕见。关于成人原发性睾丸旁/附睾淋巴瘤知之甚少。

病例报告

我们报告一例罕见的90岁白人男性原发性附睾滤泡性非霍奇金淋巴瘤,患者表现为左侧阴囊肿块。骨髓活检阴性,全身计算机断层扫描未发现睾丸外受累证据。肉眼可见,附睾完全被一个均匀的肿块取代。组织学研究显示密集的淋巴细胞浸润,主要由中心细胞组成,并伴有中心母细胞。免疫组化分析表明,肿瘤细胞强烈表达CD45RB、CD20、CD79a、bcl-6和CD10;bcl-2免疫染色阴性。分子研究显示存在单克隆IgH基因重排和IgH/BCL2重排。该淋巴瘤被分类为滤泡性淋巴瘤,低级别,1-2级。患者随后接受了根治性睾丸切除术,未接受化疗,术后随访显示无疾病复发。

结论

本文报道的原发性附睾滤泡性淋巴瘤病例被认为是非常罕见的事件。其特点是临床惰性局限性疾病、良好的临床结局、BCL2蛋白表达缺失以及存在t(14;18)(q32;q21)/IGH-BCL2。即使这是一个单病例,伴有t(14;18)的原发性附睾滤泡性淋巴瘤可能代表先前报道的t(14;18)阴性原发性睾丸旁滤泡性淋巴瘤的一种变体,或者是一个独特的生物学实体。未来报告更多病例将有助于解决这个问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f34/3314557/25d9d79cda5b/1752-1947-6-24-1.jpg

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