Khoo Thomas, Saxon Sarah, Koszyca Barbara, Gutschmidt Bernice, Limaye Vidya
Faculty of Health and Medical Sciences, University of Adelaide, Rheumatology Unit, Royal Adelaide Hospital, and Rheumatology Unit, Southern Adelaide Local Health Network, Adelaide, South Australia, Australia.
Anatomical Pathology, SA Pathology, Adelaide, South Australia, Australia.
ACR Open Rheumatol. 2025 Jun;7(6):e70062. doi: 10.1002/acr2.70062.
The objective of this study was to assess the clinical and histopathologic features of muscle vasculitis.
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.
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.
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.
本研究旨在评估肌肉血管炎的临床和组织病理学特征。
检索SA病理学电子数据库(2000 - 2023年),该数据库评估了南澳大利亚所有的肌肉活检样本,以识别血管炎病例。病例分为系统性血管炎(SV)或孤立性肌肉血管炎(IMV)。IMV又分为局限性肌肉疾病(IMV-LMD)或合并已知结缔组织病(IMV-CTD)。对肌肉血管炎与经活检证实的特发性炎性肌病(IIM)进行临床和组织学比较。
在3090份肌肉活检样本中,59份显示血管炎(女性占47.5%,中位年龄64.1岁[四分位间距(IQR)51.5 - 75.3岁])。59例中32例为SV,59例中15例为IMV-LMD,59例中10例为IMV-CTD。SV和IMV-LMD患者的肌酸激酶(CK)水平常正常(SV:中位值58.5[IQR 25 - 152]IU/L;IMV-LMD:中位值34.5[IQR 21.5 - 88.5]IU/L)。抗中性粒细胞胞浆抗体(ANCA)仅限于SV患者(髓过氧化物酶-ANCA[32例中的13例]对比蛋白酶3-ANCA[32例中的2例])。与IIM患者相比,肌肉血管炎患者的肌无力症状较少见(59例中的29例对比369例中的305例;P < 0.01),但远端肌肉症状较多见(59例中的21例对比360例中的74例;P = 0.02),且C反应蛋白水平升高(59例中的35例对比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)在肌肉血管炎中出现的频率低于IIM(P < 0.01),提示尽管血管存在病变,但肌纤维保持完整。
肌肉血管炎可与SV同时发生或局限于肌肉,很少与CTD相关。与IIM不同,肌肉血管炎常缺乏肌纤维坏死和/或浸润;因此,肌肉力量保存和CK水平正常不应妨碍进行肌肉活检。