肌肉血管炎:一种不同亚群疾病的新描述。

IF 2.8 Q2 RHEUMATOLOGY
Thomas Khoo, Sarah Saxon, Barbara Koszyca, Bernice Gutschmidt, Vidya Limaye
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引用次数: 0

摘要

目的:本研究的目的是评估肌肉血管炎的临床和组织病理学特征。方法:检索南澳所有肌肉活检样本的SA病理学电子数据库(2000-2023年),确定血管炎病例。病例分为系统性血管炎(SV)和孤立性肌肉血管炎(IMV)。IMV可发生为局部肌肉疾病(IMV- lmd)或已知结缔组织疾病(IMV- ctd)。临床和组织学比较肌肉血管炎和活检证实的特发性炎性肌病(IIM)。结果:在3090份肌肉活检样本中,59份显示血管炎(47.5%为女性,中位年龄64.1岁[四分位间距(IQR) 51.5-75.3]岁)。59例中有32例存在SV, 59例中有15例存在IMV-LMD, 59例中有10例存在IMV-CTD。SV和IMV-LMD患者通常有正常的肌酸激酶(CK)水平(SV:中位数58.5 [IQR 25-152] IU/L;IMV-LMD:中位数34.5 [IQR 21.5-88.5] IU/L。抗中性粒细胞胞浆抗体(ANCAs)仅限于SV患者(髓过氧化物酶- anca [13 / 32] vs蛋白酶3-ANCA[2 / 32])。与IIM患者相比,肌肉血管炎患者的虚弱发生率较低(59例中的29例对369例中的305例;P < 0.01),但远端肌肉症状较多(59例中的21例对360例中的74例;P = 0.02)和c反应蛋白水平升高(59例中的35例vs 82例中的20例;P < 0.01)。IIM的显著组织学特征(肌纤维淋巴细胞浸润、肌纤维坏死、主要组织相容性复合体I类上调)在肌血管炎中出现的频率低于IIM (P < 0.01),提示尽管在脉管系统中病理存在肌纤维完整性。结论:肌肉血管炎可伴SV发生或孤立于肌肉,很少与CTD相关。与IIM不同,肌血管炎通常缺乏肌纤维坏死和/或浸润;因此,肌肉力量和正常CK水平的保存不应阻止肌肉活检。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Muscle Vasculitis: A Novel Delineation of Distinct Subsets of Disease.

Objective: The objective of this study was to assess the clinical and histopathologic features of muscle vasculitis.

Methods: The electronic database of SA Pathology, wherein all muscle biopsy samples in South Australia are assessed, was searched (2000-2023), identifying cases of vasculitis. Cases were classified as systemic vasculitis (SV) or isolated muscle vasculitis (IMV). IMV occurred as either localized muscle disease (IMV-LMD) or with known connective tissue disease (IMV-CTD). Clinical and histologic comparisons between muscle vasculitis and biopsy-proven idiopathic inflammatory myopathy (IIM) were made.

Results: From 3,090 muscle biopsy samples, 59 showed vasculitis (47.5% female, median age 64.1 [interquartile range (IQR) 51.5-75.3] years). SV was present in 32 of 59, IMV-LMD was present in 15 of 59, and IMV-CTD was present in 10 of 59. Patients with SV and IMV-LMD frequently had normal creatine kinase (CK) levels (SV: median 58.5 [IQR 25-152] IU/L; IMV-LMD: median 34.5 [IQR 21.5-88.5] IU/L). Antineutrophil cytoplasmic antibodies (ANCAs) were restricted to those with SV (myeloperoxidase-ANCA [13 of 32] vs proteinase 3-ANCA [2 of 32]). Compared to patients with IIM, patients with muscle vasculitis had less frequent weakness (29 of 59 vs 305 of 369; P < 0.01) but more distal muscle symptoms (21 of 59 vs 74 of 360; P = 0.02) and elevated C-reactive protein levels (35 of 59 vs 20 of 82; P < 0.01). Salient histologic features of IIM (lymphocytic infiltration of myofibers, myofiber necrosis, major histocompatibility complex class I up-regulation) occurred less frequently in muscle vasculitis than IIM (P < 0.01), suggesting myofiber integrity despite pathology in the vasculature.

Conclusion: Muscle vasculitis can occur with SV or be isolated to the muscles and is rarely associated with CTD. Distinct from IIM, muscle vasculitis frequently lacks myofiber necrosis and/or infiltration; consequent preservation of muscle power and normal CK levels should not deter from muscle biopsy.

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CiteScore
5.80
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