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与慢性粒单核细胞白血病相关的系统性中血管炎。

Systemic medium-sized vessel vasculitis associated with chronic myelomonocytic leukemia.

作者信息

Hamidou M A, Boumalassa A, Larroche C, El Kouri D, Blétry O, Grolleau J Y

机构信息

Department of Internal Medicine, Hôtel-Dieu, University Hospital Nantes, Nantes, France.

出版信息

Semin Arthritis Rheum. 2001 Oct;31(2):119-26. doi: 10.1053/sarh.2001.27717.

Abstract

OBJECTIVE

To determine the clinical aspects of systemic vasculitis associated with chronic myelomonocytic leukemia (CMML).

METHODS

In this retrospective study, 8 patients suffering from systemic vasculitis associated with CMML are described. The French and English literature on systemic vasculitis associated with myelodysplasia was reviewed.

RESULTS

All 8 patients had a systemic medium-sized vessel vasculitis which fulfilled the American College of Rheumatology criteria for polyarteritis nodosa in the setting of active CMML. Antineutrophil cytoplasmic antibodies (ANCA) were negative in 7 patients. One patient had cytoplasmic ANCA by indirect immunofluorescence without antiproteinase 3 or antimyeloperoxydase antibodies on the enzyme-linked immunosorbent assay. At presentation, 6 patients had fever of unknown origin, 5 had polymyalgia rheumatica, 3 had sensory hearing loss, and 4 had eosinophilia. None had viral infection or drug-associated vasculitis. Diagnostic procedures included renal or hepatic angiography in 6 patients which showed microaneurysms in 4, skin and temporal artery biopsy in 2 which showed vasculitis, and 1 postmortem examination which showed gastroduodenal arteritis. All patients were treated with corticosteroids, and 7 received immunosuppressive drugs. Death was attributable to vasculitis in 2 cases, infection in 3, and other vasculitis-related causes in 2. In a review of the French-English literature, we found 11 similar cases of ANCA-negative systemic vasculitis, generally associated with refractory anemia, with or without blast excess.

CONCLUSIONS

Systemic ANCA-negative polyarteritis nodosa-type vasculitis seems closely associated to CMML. Clinical presentation is nonspecific, and systemic vasculitis should be suspected when a patient with myelodysplasia develops atypical manifestations. Renal, gastrointestinal, or hepatic angiography are useful diagnostic procedures when more invasive biopsies should be avoided because of low platelet count. The prognosis of CMML-associated systemic vasculitis is poor.

摘要

目的

确定与慢性粒单核细胞白血病(CMML)相关的系统性血管炎的临床特征。

方法

在这项回顾性研究中,描述了8例患有与CMML相关的系统性血管炎的患者。回顾了关于与骨髓增生异常相关的系统性血管炎的法语和英语文献。

结果

所有8例患者均患有系统性中等大小血管血管炎,在活动性CMML背景下符合美国风湿病学会结节性多动脉炎标准。7例患者抗中性粒细胞胞浆抗体(ANCA)阴性。1例患者间接免疫荧光显示胞浆ANCA阳性,但酶联免疫吸附试验中无抗蛋白酶3或抗髓过氧化物酶抗体。就诊时,6例患者有不明原因发热,5例有多发性肌痛性风湿症,3例有感觉性听力丧失,4例有嗜酸性粒细胞增多。均无病毒感染或药物相关性血管炎。诊断程序包括6例患者进行肾或肝血管造影,其中4例显示微动脉瘤,2例进行皮肤和颞动脉活检显示血管炎,1例尸检显示胃十二指肠动脉炎。所有患者均接受了糖皮质激素治疗,7例接受了免疫抑制药物治疗。2例患者死于血管炎,3例死于感染,2例死于其他与血管炎相关的原因。在对法语-英语文献的回顾中,我们发现11例类似的ANCA阴性系统性血管炎病例,通常与难治性贫血相关,有或无原始细胞增多。

结论

系统性ANCA阴性结节性多动脉炎型血管炎似乎与CMML密切相关。临床表现不具特异性,当骨髓增生异常患者出现非典型表现时应怀疑系统性血管炎。由于血小板计数低而应避免进行更具侵入性的活检时,肾、胃肠道或肝血管造影是有用的诊断程序。CMML相关系统性血管炎的预后较差。

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