Probst A, Ulrich J, Kaeser H E, Heitz P
Eur Neurol. 1977;16(1-6):181-96. doi: 10.1159/000114899.
Morphological findings of 3 cases of Kaeser's scapulo-peroneal muscular atrophy are described. 1 of them is the first complete autopsy report on this disease. While the number of motor neurons in the spinal cord was grossly normal, the neuropil of the anterior horn exhibited axonal swellings, accumulations of possibly pathological lipofuscin and intra-axonal corpora amylacea. In the muscles, changes were partly those of neurogenic atrophy, partly of a primary myopathy. There was also an accumulation of neutral fat in the muscle fibres, mainly of those of type I.
本文描述了3例凯泽氏肩胛-腓骨肌萎缩症的形态学发现。其中1例是关于该疾病的首例完整尸检报告。虽然脊髓中的运动神经元数量总体正常,但前角的神经纤维网出现轴突肿胀、可能为病理性脂褐素的积聚以及轴突内淀粉样小体。在肌肉中,变化部分为神经源性萎缩,部分为原发性肌病。肌纤维中也有中性脂肪的积聚,主要在I型肌纤维中。