Fernandez C, Attarian S, Figarella-Branger D, Disdier P, Grob J-J, Pouget J, Pellissier J-F
Service d'Anatomie Pathologique et de Neuropathologie, Hôpital d'Adultes de la Timone, Marseille.
Rev Neurol (Paris). 2003 Apr;159(4):425-33.
Granulomatous inflammation is infrequently observed in muscle biopsy. We report a series of 7 patents presenting with granulomas in muscle. Two of them had a history of sarcoidosis In 4 other cases, muscle Involvement revealed systemic sarcoidosis. Among the 6 cases of sarcoidosis, we observed 2 with acute myositis and 4 chronic forms. The last patient presented with polymyositis in association with melanoma. In sarcoidosis, muscle biopsy showed a granulomatous inflammation of varying intensity, which was generally associated with mononuclear inflammatory cells. Most of granulomas were located in the perimysium and the endomysium and necrosis was absent. Inflammatory cells were predominantly macrophages and CD4 positive lymphocytes. On the contrary, in the case of paraneoplastic polymyositis,granulomas were rare, most of inflammatory cells were CD8 positive lymphocytes and numerous areas of necrosis were observed. Class I MHC molecules were expressed on the membrane of muscle fibers. As a general rule, requisite examinations must be performed to search for sarcoidosis in patients exhibiting granulomas on muscle biopsy.
肉芽肿性炎症在肌肉活检中很少见。我们报告了一系列7例肌肉出现肉芽肿的患者。其中2例有结节病病史。在其他4例中,肌肉受累提示全身性结节病。在这6例结节病中,我们观察到2例急性肌炎和4例慢性形式。最后1例患者表现为与黑色素瘤相关的多发性肌炎。在结节病中,肌肉活检显示不同程度的肉芽肿性炎症,通常伴有单核炎性细胞。大多数肉芽肿位于肌束膜和肌内膜,无坏死。炎性细胞主要是巨噬细胞和CD4阳性淋巴细胞。相反,在副肿瘤性多发性肌炎病例中,肉芽肿罕见,大多数炎性细胞是CD8阳性淋巴细胞,且观察到许多坏死区域。I类MHC分子在肌纤维膜上表达。一般来说,对于肌肉活检显示肉芽肿的患者,必须进行必要的检查以寻找结节病。