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一例描述髓过氧化物酶抗中性粒细胞胞浆抗体相关血管炎与类风湿关节炎同时发生的罕见病例报告。

A Case Report Describing a Rare Presentation of Simultaneous Occurrence of MPO-ANCA-Associated Vasculitis and Rheumatoid Arthritis.

作者信息

Foray Nathalie, Hudali Tamer, Papireddy Muralidhar, Gao John

机构信息

Department of Internal Medicine, Southern Illinois University, 751 North Rutledge, Springfield, IL 62702, USA.

Department of Pathology, Memorial Medical Center, 701 North 1st Street, Springfield, IL 62781, USA.

出版信息

Case Rep Nephrol. 2016;2016:9340524. doi: 10.1155/2016/9340524. Epub 2016 Nov 6.

Abstract

. Renal-limited myeloperoxidase vasculitis with simultaneous rheumatoid arthritis is reported as a rare occurrence. Review of literature suggests that most patients had a diagnosis of rheumatoid arthritis for several years prior to presenting with renal failure from myeloperoxidase vasculitis. . A 58-year-old Caucasian male presented to the hospital experiencing malaise, fevers, decreased oral intake, nausea, and vomiting for one week duration. His past medical history consisted of newly diagnosed but untreated rheumatoid arthritis, hypertension, and non-insulin-dependent diabetes mellitus. He was found to have acute renal failure, proteinuria, and hypoglycemia. Standard therapy, including intravenous fluids, did not improve his acute renal failure. A vasculitis workup resulted in a positive myeloperoxidase anti-neutrophil cytoplasmic antibody (MPO-ANCA). Renal biopsy revealed crescentic glomerulonephritis (GN) pauci-immune type, suggestive of MPO-ANCA-associated vasculitis (MPO-AAV). Treatment consisted of prednisone, cyclophosphamide, and seven cycles of plasmapheresis, in addition to hemodialysis for uremia. Upon discharge, he received hemodialysis for another week and continued treatment with cyclophosphamide and prednisone. . Patients with longstanding rheumatoid arthritis may develop renal failure due to nonsteroidal anti-inflammatory medication use and AA type amyloidosis; however, necrotizing glomerulonephritis with crescent formation has been rarely reported. This stresses the importance of early recognition and swift initiation of treatment.

摘要

据报道,肾局限性髓过氧化物酶血管炎合并类风湿关节炎的情况较为罕见。文献回顾表明,大多数患者在因髓过氧化物酶血管炎出现肾衰竭之前,已确诊类风湿关节炎数年。一名58岁的白人男性因全身不适、发热、食欲减退、恶心和呕吐一周入院。他既往有新诊断但未治疗的类风湿关节炎、高血压和非胰岛素依赖型糖尿病病史。检查发现他患有急性肾衰竭、蛋白尿和低血糖。包括静脉补液在内的标准治疗未能改善其急性肾衰竭。血管炎检查发现髓过氧化物酶抗中性粒细胞胞浆抗体(MPO-ANCA)呈阳性。肾脏活检显示为寡免疫型新月体性肾小球肾炎(GN),提示MPO-ANCA相关性血管炎(MPO-AAV)。治疗包括泼尼松、环磷酰胺和七个疗程的血浆置换,此外还针对尿毒症进行了血液透析。出院时,他又接受了一周的血液透析,并继续使用环磷酰胺和泼尼松治疗。长期患类风湿关节炎的患者可能因使用非甾体抗炎药和AA型淀粉样变性而出现肾衰竭;然而,伴有新月体形成的坏死性肾小球肾炎鲜有报道。这凸显了早期识别和迅速开始治疗的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4683/5116358/f27109911b6f/CRIN2016-9340524.001.jpg

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