Meola G, Sansone V, Rotondo G, Jabbour A
Department of Neurology, University of Milan, San Donato Hospital, Italy.
Muscle Nerve. 1996 Nov;19(11):1476-80. doi: 10.1002/(SICI)1097-4598(199611)19:11<1476::AID-MUS12>3.0.CO;2-R.
We describe clinical, pathological, and muscle imaging findings in a patient with an early adult-onset progressive muscular weakness in association with atrophy beginning in the legs and involving both gastrocnemi in particular. Muscle biopsy findings showed a severe dystrophic process with no vacuoles, consistent with Miyoshi's myopathy. Computerized tomography and magnetic resonance imaging scans were used to provide an ongoing permanent record of the various stages of the disease.
我们描述了一名成年早期发病的进行性肌无力患者的临床、病理及肌肉影像学表现，该患者伴有萎缩，始于腿部，尤其累及双侧腓肠肌。肌肉活检结果显示为严重的营养不良过程，无空泡，符合三泽肌病。计算机断层扫描和磁共振成像扫描用于对疾病的各个阶段进行持续的永久记录。
