Parambil Joseph G, Keogh Karina A, Fervenza Fernando C, Ryu Jay H
Division of Pulmonary and Critical Care Medicine, Desk East 18, Mayo Clinic, 200 1st St SW, Rochester, MN 55905, USA.
Am J Kidney Dis. 2006 Nov;48(5):827-31. doi: 10.1053/j.ajkd.2006.07.020.
A variety of autoimmune diseases has been associated with thymoma, and thymectomy does not always induce remission of these disorders. This case report describes a 50-year-old man who presented with migratory polyarthritis and an anterior mediastinal mass that proved to be a thymoma. Five months after thymectomy, the patient presented with worsening polyarthritis, hematuria, and azotemia. Based on elevated titers of antineutrophil cytoplasmic antibodies directed against myeloperoxidase and renal biopsy showing crescentic necrotizing glomerulonephritis, microscopic polyangiitis was diagnosed. After remission-induction therapy with prednisone and cyclophosphamide, articular symptoms and renal manifestations resolved. Microscopic polyangiitis was not associated previously with thymoma, and this case broadens the spectrum of autoimmune disorders seen with this tumor. Progressive disease seen after thymectomy in this patient has potential implications regarding the pathophysiological characteristics of microscopic polyangiitis and management of patients with this clinical association.
多种自身免疫性疾病与胸腺瘤相关,而胸腺切除术并不总能使这些疾病缓解。本病例报告描述了一名50岁男性,他出现游走性多关节炎和前纵隔肿块,经证实为胸腺瘤。胸腺切除术后五个月,患者出现多关节炎加重、血尿和氮质血症。基于抗髓过氧化物酶抗中性粒细胞胞浆抗体滴度升高以及肾活检显示新月体坏死性肾小球肾炎,诊断为显微镜下多血管炎。在使用泼尼松和环磷酰胺进行诱导缓解治疗后,关节症状和肾脏表现消失。显微镜下多血管炎此前与胸腺瘤无关,该病例拓宽了与此肿瘤相关的自身免疫性疾病谱。该患者胸腺切除术后出现的疾病进展对显微镜下多血管炎的病理生理特征及有此临床关联患者的管理具有潜在意义。