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Classical hodgkin lymphoma and spontaneous regression

机译:经典霍奇金淋巴瘤和自发消退

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摘要

Mohsen and colleagues describe an interesting case of an 86-year-old woman with biopsyproven classical Hodgkin lymphoma (HL), mixed cellularity type, who initially presented with diffuse myalgia, pancytopenia, lymphadenopathy, splenomegaly, bilateral pleural effusions, and pulmonary nodules. She experienced near-complete regression of lymphoma shortly after diagnosis, before any tumor-specific therapy could be initiated. The authors hypothesize that the constitutional symptoms reported by the patient may reflect an underlying immunologic milieu contributing to this remission. Thorough testing was performed as part of the rheumatologic workup in order to rule out a concurrent underlying autoimmune disease due to the association between immunologic dysfunction and lymphomagenesis, as explained below.
机译:Mohsen及其同事描述了一个有趣的案例,该患者有活检证明的经典霍奇金淋巴瘤(HL),混合细胞型,年龄86岁,最初表现为弥漫性肌痛,全血细胞减少,淋巴结肿大,脾肿大,双侧胸腔积液和肺结节。诊断后不久,在开始任何肿瘤特异性治疗之前,她经历了淋巴瘤几乎完全消退。作者假设患者报告的体质症状可能反映了导致这种缓解的潜在免疫环境。作为风湿病检查的一部分,进行了彻底的测试,以排除由于免疫功能障碍和淋巴瘤发生之间的关联而导致的潜在基础自身免疫疾病,如下所述。

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