Bosch E P, Gowans J D, Munsat T
Muscle Nerve. 1979 Jan-Feb;2(1):73-7. doi: 10.1002/mus.880020111.
A 75-year-old French-Canadian woman with familial oculopharyngeal dystrophy demonstrated histopathologic alterations similar to those of idiopathic polymyositis. A second biopsy obtained 15 months later was more consistent with previously reported cases. It is suggested that certain patients with oculopharyngeal dystrophy may pass through an initial phase of secondary muscle inflammation similar to that seen in some other heritable myopathies.
一名患有家族性眼咽型肌营养不良的75岁法裔加拿大女性表现出与特发性多发性肌炎相似的组织病理学改变。15个月后进行的第二次活检结果与先前报道的病例更为相符。这表明某些眼咽型肌营养不良患者可能会经历一个继发性肌肉炎症的初始阶段，类似于其他一些遗传性肌病中所见的情况。
