Hughes J T, Brownell B
J Neurol Neurosurg Psychiatry. 1972 Oct;35(5):648-57. doi: 10.1136/jnnp.35.5.648.
Four cases of peroneal muscular atrophy (Charcot-Marie-Tooth disease) are described in which observations were made from the necropsy examination of the central nervous system, the peripheral nervous system, and the skeletal muscles. The pattern of nerve degeneration in these various locations is described and the conclusion is drawn that the basis of the disease is a very chronic progressive neuropathy. To the pathological descriptions of previous observers is added the finding of fibrosis affecting the muscle spindles which was present in all four of the cases. The literature of the case reports with necropsy examination is reviewed.
本文描述了4例腓骨肌萎缩症(夏科-马里-图思病),对其进行了中枢神经系统、周围神经系统及骨骼肌的尸检观察。描述了这些不同部位的神经变性模式,并得出结论:该病的基础是一种非常慢性的进行性神经病变。在以往观察者的病理描述基础上,补充了所有4例均存在的肌梭纤维化这一发现。对有尸检检查的病例报告文献进行了综述。