DeReuck J, Van Landegem W
J Neurol. 1987 Apr;234(3):187-90. doi: 10.1007/BF00314142.
The histological, histochemical and biometric findings in the posterior crico-arytenoid muscle in two patients with Shy-Drager syndrome were compared with those found in cases of carcinoma of the larynx. In biopsy specimens from the patients with laryngeal carcinoma, neurogenic atrophy and various structural changes in the muscle fibres were the prominent features. In the two patients with Shy-Drager syndrome these changes were not present and the only significant finding was the more pronounced type I fibre atrophy, with type II fibre predominance in the more severely affected case. These findings do not permit the vocal cord paralysis seen in the Shy-Drager syndrome to be explained by motorneuron loss and denervation. It is postulated that a possible cause may be a biochemical defect in the brain.
将两名Shy-Drager综合征患者的环杓后肌的组织学、组织化学和生物测量结果与喉癌患者的结果进行了比较。在喉癌患者的活检标本中,神经源性萎缩和肌纤维的各种结构变化是突出特征。在两名Shy-Drager综合征患者中,这些变化并不存在,唯一显著的发现是I型纤维萎缩更为明显,在受影响更严重的病例中II型纤维占优势。这些发现无法用运动神经元丧失和去神经支配来解释Shy-Drager综合征中所见的声带麻痹。据推测,一个可能的原因可能是大脑中的生化缺陷。