Thomas Khoo, Sarah Saxon, Barbara Koszyca, Bernice Gutschmidt, Vidya Limaye
{"title":"肌肉血管炎:一种不同亚群疾病的新描述。","authors":"Thomas Khoo, Sarah Saxon, Barbara Koszyca, Bernice Gutschmidt, Vidya Limaye","doi":"10.1002/acr2.70062","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>The objective of this study was to assess the clinical and histopathologic features of muscle vasculitis.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":93845,"journal":{"name":"ACR open rheumatology","volume":"7 6","pages":"e70062"},"PeriodicalIF":2.8000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12169899/pdf/","citationCount":"0","resultStr":"{\"title\":\"Muscle Vasculitis: A Novel Delineation of Distinct Subsets of Disease.\",\"authors\":\"Thomas Khoo, Sarah Saxon, Barbara Koszyca, Bernice Gutschmidt, Vidya Limaye\",\"doi\":\"10.1002/acr2.70062\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>The objective of this study was to assess the clinical and histopathologic features of muscle vasculitis.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>\",\"PeriodicalId\":93845,\"journal\":{\"name\":\"ACR open rheumatology\",\"volume\":\"7 6\",\"pages\":\"e70062\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12169899/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACR open rheumatology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/acr2.70062\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"RHEUMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACR open rheumatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/acr2.70062","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"RHEUMATOLOGY","Score":null,"Total":0}
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.