Chen B F
Department of Pathology, Fujian Medical College, Fuzhon.
Zhonghua Bing Li Xue Za Zhi. 1991 Mar;20(1):38-40.
The basic lesions in the muscle biopsies of 11 cases of severe infantile spinal muscular atrophy showed typical neurogenic fascicular muscular atrophy. It was found through histochemistry staining that both types of muscle fibres were involved which were characterised by the presence of type grouping of the damaged fibers, anyhow, the original mosaic pattern of both types were still partially reserved. With anti-laminin immunofluorescence staining, it was demonstrated that the basal membrane of atrophied small muscle fibre was still intact. It is considered that the main manifestation of damage on spinal anterior horn neuron is denervation of the skeletal muscle; meanwhile, the function of the muscle fibre in regulations carbohydrate metabolism is not apparently obstructs. The pathologic process of this disease develops from denervation to renervation and then back to denervation again. Therefore the clinical feature of muscle atrophy in this disease is progressive and developmental.
11例严重婴儿脊髓性肌萎缩症患者肌肉活检的基本病变显示典型的神经源性束状肌萎缩。通过组织化学染色发现,两种类型的肌纤维均受累,其特征为受损纤维出现群组化,无论如何,两种类型的原始镶嵌模式仍部分保留。抗层粘连蛋白免疫荧光染色显示,萎缩的小肌纤维的基底膜仍然完整。认为脊髓前角神经元损伤的主要表现是骨骼肌去神经支配;同时,肌纤维在调节碳水化合物代谢中的功能未明显受阻。该疾病的病理过程从去神经支配发展到再支配,然后再次回到去神经支配。因此,该疾病肌肉萎缩的临床特征是进行性和发展性的。