Sladek G D, Vasey F B, Sieger B, Behnke D A, Germain B F, Espinoza L R
J Rheumatol. 1983 Jun;10(3):467-70.
We report 3 male patients with a unique eosinophilic myositis of unknown etiology who appear to have a benign course. The most striking feature in 2 patients was relapsing myalgias with lower extremity predilection and tendency for spontaneous recovery. Laboratory studies showed peripheral eosinophilia, elevated CPK, and EMG consistent with a myositic pattern. Muscle biopsies showed myositis characterized by focal necrosis and degeneration with an inflammatory infiltrate predominantly composed of histiocytes and eosinophils. Skin and fascia were normal.
我们报告了3例病因不明的独特嗜酸性粒细胞性肌炎男性患者,其病程似乎呈良性。2例患者最显著的特征是复发性肌痛,以下肢为主,且有自发恢复的倾向。实验室检查显示外周血嗜酸性粒细胞增多、肌酸磷酸激酶(CPK)升高,肌电图符合肌炎模式。肌肉活检显示肌炎的特征为局灶性坏死和变性,炎症浸润主要由组织细胞和嗜酸性粒细胞组成。皮肤和筋膜正常。