[口服皮质类固醇治疗原发性积液性淋巴瘤1例]。

Takashi Shimizu, Masaaki Okajima, Natsue Shimizu, Kazuaki Morohashi, Tatsuki Ohara, Jozi Toyama
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摘要

原发性积液性淋巴瘤是一种罕见的淋巴瘤类型,它局限于与人类疱疹病毒8感染有关的体腔。我们报告一例93岁男性胸膜原发积液性淋巴瘤,但疱疹病毒8感染阴性。胸部计算机断层扫描显示双侧胸腔积液,但未显示任何肿瘤肿块或淋巴结肿大的证据。胸膜积液细胞学分析显示非典型淋巴样细胞,免疫表型CD10、CD19和CD20阳性。免疫球蛋白重链基因克隆重排经Southern blot检测,诊断为原发性积液性淋巴瘤。虽然出现呼吸困难和严重缺氧,并伴有胸腔积液增加,但由于患者的年龄,不需要化疗。因此,我们尝试口服皮质类固醇治疗以减轻病情,结果导致他的胸腔积液显著减少。我们报告一例罕见的原发性积液性淋巴瘤,经皮质类固醇治疗有效控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[A case of primary effusion lymphoma effectively treated by oral corticosteroid therapy].

Primary effusion lymphoma is a rare type of lymphoma which is confined to those body cavities associated with human herpes virus 8 infection in its development. We describe a 93-year-old man with primary effusion lymphoma in the pleura, but who was negative for herpes virus 8 infection. Chest computed tomography revealed bilateral pleural effusion, but did not show any evidence of a tumor mass or lymph node enlargement. Cytological analysis of his pleural effusion revealed atypical lymphoid cells with immunophenotypes which were positive for CD10, CD19 and CD20. Clonal rearrangement of the immunoglobulin-heavy chain gene was detected by Southern blot analysis, and a diagnosis of primary effusion lymphoma was made. Although dyspnea and severe hypoxia developed, accompanied with increased pleural effusion, chemotherapy was not indicated because of his age. We thus tried oral corticosteroid therapy for palliation which resulted in a dramatic, long-term decrease of his pleural effusion. We present a rare case of primary effusion lymphoma effectively controlled by corticosteroid therapy.

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