De Reuck J, Van den Bossche H, De Coster W, Hooft C
Eur Neurol. 1978;17(3):142-8. doi: 10.1159/000114937.
A right gastrocnemius muscle biopsy of a 13-month-old floppy male infant, which appeared at a more advanced age to suffer from an infantile spinal muscular atrophy, showed unusual histochemical changes: the chequer-board distribution was replaced by three groups of muscle fibers with a same mean narrow diameter of 12.5 micrometer. The smallest groups could easily be recognized as type I and type IIB fibers, while the largest group, involving more than 75% of the whole biopsy, revealed an intermediate hybrid fiber population, which would be classified as type I, if based on their phosphorylase and myofibrillar ATPase activities alone. The pathogenesis of this unusual finding is discussed.
一名13个月大的男性软瘫婴儿,其右腓肠肌活检显示出异常的组织化学变化。该婴儿在稍大年龄时被诊断为患有婴儿型脊髓性肌萎缩症。活检结果显示,正常的棋盘状分布被三组平均直径狭窄(12.5微米)的肌纤维取代。最小的两组很容易被识别为I型和IIB型纤维,而最大的一组,占整个活检样本的75%以上,显示出中间型混合纤维群。仅根据其磷酸化酶和肌原纤维ATP酶活性,该组纤维应被归类为I型。本文讨论了这一异常发现的发病机制。