坏疽性脓皮病合并骨髓增生异常综合征并发快速进展的脓胸相关淋巴瘤1例报告。

Akiko Goto, Satoshi Yamamoto, Atsushi Notoya, Akio Takada, Masaya Mukai
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引用次数: 0

摘要

本报告描述了一例坏疽性脓皮病(PG)并发骨髓增生异常综合征(MDS),随后迅速进展的脓胸相关淋巴瘤(PAL)。一名74岁男性因与MDS相关的皮肤坏疽入院。我们诊断他患有PG,并开始大剂量口服强的松龙。入院两个月后,他迅速发展为淋巴瘤。尽管接受了放射治疗,病人还是死了。尸检病理诊断为弥漫性大细胞淋巴瘤。在淋巴瘤细胞中检测eb病毒(EBV)编码RNA和eb病毒编码核抗原(EBNA)。该病例提示免疫抑制治疗可能有利于ebv感染细胞的克隆增殖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pyoderma gangrenosum complicated with myelodysplastic syndrome followed by rapidly progressing pyothorax-associated lymphoma: a case report.

This report describes a patient with pyoderma gangrenosum (PG) complicated with myelodysplastic syndrome (MDS) followed by rapidly progressing pyothorax-associated lymphoma (PAL). A 74-year-old man was admitted with cutaneous gangrene associated with MDS. We diagnosed him as having PG, and high-dose oral prednisolone was started. Two months after admission he developed lymphoma rapidly. The patient died in spite of radiation therapy. On autopsy, the pathological diagnosis was diffuse large cell lymphoma. Epstein-Barr virus (EBV)-encoded RNA, and EBV-encoded nuclear antigen (EBNA) were detected in lymphoma cells. This case suggested that immunosuppressive therapy might favour the clonal proliferation of EBV-infected cells.

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