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一名原发性干燥综合征日本女孩同时患有急性链球菌感染后肾小球肾炎和急性风湿热。

Coexistence of acute poststreptococcal glomerulonephritis and acute rheumatic fever in a Japanese girl with primary Sjögren's syndrome.

机构信息

Center for Pediatric Allergy and Rheumatology, KKR Sapporo Medical Center, Sapporo, Japan.

Faculty of Medicine and Graduate School of Medicine, Department of Pediatrics, Hokkaido University, Sapporo, Japan.

出版信息

Mod Rheumatol Case Rep. 2020 Jul;4(2):262-266. doi: 10.1080/24725625.2020.1728060. Epub 2020 Feb 18.

Abstract

Although acute poststreptococcal glomerulonephritis (APSGN) and acute rheumatic fever (ARF) are well-known complications of group A streptococcus infection, concomitant occurrence of both diseases is rare. We report an 11-year-old Japanese girl with primary Sjögren's syndrome complicated by acute renal failure about 2 weeks after the onset of pharyngitis. Although histopathological findings of the kidney were not confirmative, APSGN was suggested by the spontaneous recovery of her renal function, typical latent period with high levels of antistreptolysin O and low serum levels of C3 but not of C4. In addition, cardiac hypomotility and regurgitation of the 4 valves progressed in the convalescent phase of APSGN, which was accompanied by elevation of serum C-reactive protein and plasma brain natriuretic peptide (BNP) levels. Myocarditis was suggested by delayed gadolinium-enhancement of cardiac walls on cardiac magnetic resonance imaging. She was diagnosed with APSGN and ARF and was treated with a combination of short course prednisolone and prophylactic penicillin G. There is no relapse of renal or cardiac symptoms during 6 years follow-up. Unexpected elevation of plasma BNP in a convalescent stage of APSGN suggests the development of ARF. Underlying Sjögren's syndrome (SS) may modify the histopathological findings and make it difficult to differentiate APSGN from CTD-associated nephritis such as lupus nephritis (LN) even by renal biopsy.

摘要

虽然急性链球菌后肾小球肾炎 (APSGN) 和急性风湿热 (ARF) 是 A 组链球菌感染的已知并发症,但这两种疾病同时发生的情况很少见。我们报告了一例 11 岁日本女孩,在咽炎发作约 2 周后并发原发性干燥综合征和急性肾衰竭。尽管肾脏的组织病理学发现不具确诊性,但根据肾功能的自发恢复、抗链球菌溶血素 O 水平升高和 C3 但 C4 血清水平降低的典型潜伏期,提示为 APSGN。此外,在 APSGN 的恢复期,心脏运动功能减退和四个瓣膜反流进展,同时伴有血清 C 反应蛋白和血浆脑钠肽 (BNP) 水平升高。心脏磁共振成像上心脏壁的延迟钆增强提示心肌炎。她被诊断为 APSGN 和 ARF,并接受了短程泼尼松龙和预防性青霉素 G 联合治疗。在 6 年的随访中,肾脏或心脏症状没有复发。APSGN 恢复期血浆 BNP 的意外升高提示 ARF 的发生。潜在的干燥综合征 (SS) 可能会改变组织病理学发现,即使通过肾活检也难以将 APSGN 与 CTD 相关的肾炎(如狼疮性肾炎 [LN])区分开来。

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