Serratrice G, Pellissier J F, Roux H, Quilichini P
Clinique des maladies du système nerveux et de l'appareil locomoteur, Faculté de médecine, Marseilles, France.
Muscle Nerve. 1990 May;13(5):385-95. doi: 10.1002/mus.880130505.
Several groups of cases of fasciitis and myositis with eosinophilia are reported. The common features are inflammation into fascia and/or perimysium, and/or muscle fibers; eosinophilia in blood and/or in muscle biopsy. The following classification of 24 cases is suggested: at one end of the spectrum are fasciitis with eosinophilia: diffuse fasciitis (Shulman syndrome): 10 cases (3 with hematological complications); 2 cases of diffuse fasciitis with muscle atrophy; 3 cases of restricted fasciitis. Relapsing perimyositis with eosinophilia belong to the same spectrum, either diffuse (5 cases) with myalgias, or localized (2 cases). Other cases are focal myositis or multiple myositis, polymyositis with eosinophilia. The relationship among these cases is discussed. There is a continuum among the different groups. The pathophysiology remains unknown.
有几组伴有嗜酸性粒细胞增多的筋膜炎和肌炎病例被报道。其共同特征为筋膜和/或肌束膜和/或肌纤维的炎症;血液和/或肌肉活检中的嗜酸性粒细胞增多。建议对24例病例进行如下分类:在谱系的一端是嗜酸性筋膜炎:弥漫性筋膜炎(舒尔曼综合征):10例(3例伴有血液学并发症);2例伴有肌肉萎缩的弥漫性筋膜炎;3例局限性筋膜炎。复发性嗜酸性肌束膜炎属于同一谱系,可为弥漫性(5例)伴肌痛,或局限性(2例)。其他病例为局灶性肌炎或多发性肌炎、嗜酸性多肌炎。讨论了这些病例之间的关系。不同组之间存在连续性。病理生理学仍然未知。