Clarren S K, Hall J G
J Neurol Sci. 1983 Jan;58(1):89-102. doi: 10.1016/0022-510x(83)90112-0.
The lumbosacral cord segments of 10 infants with varying clinical forms of neurogenic arthrogryposis were compared with similar spinal cord segments from an infant with congenital contractures secondary to uterine constraint, 8 infants with Werdnig-Hoffman syndrome, and 11 age-matched controls. Neuronal numbers, sizes, and distribution were measured within the anterior horns. In addition to the classical reduction in the numbers of alpha motor neurons in both pathologic states, this study found the smaller neurons of the anterior horn were absent or diminished in Werdnig-Hoffman syndrome, while those cells were present in increased numbers with abnormal histology in all the patients with arthrogryposis. In 5 of the patients with arthrogryposis, the pathologic pattern was consistent throughout each cord segment; in 5 others, normal alpha neurons were retained and unequally distributed in the anterior horn segments. This unequal distribution predicted the muscle group involvement and suggested the mechanism for intrauterine joint fixation in these patients. The pathologic changes in the patients with arthrogryposis appear to be unique in spite of the heterogeneity of etiology and the clinical presentation.
将10例患有不同临床类型神经源性关节挛缩症婴儿的腰骶段脊髓,与1例因子宫压迫继发先天性挛缩的婴儿、8例患有韦尼克 - 霍夫曼综合征的婴儿以及11例年龄匹配的对照者的相似脊髓段进行了比较。在前角内测量神经元的数量、大小和分布。除了在两种病理状态下经典的α运动神经元数量减少外,本研究发现,韦尼克 - 霍夫曼综合征中前角较小的神经元缺失或减少,而在所有关节挛缩症患者中,这些细胞数量增加且组织学异常。在5例关节挛缩症患者中,每个脊髓节段的病理模式一致;在另外5例中,正常的α神经元保留在前角节段且分布不均。这种不均一分布预示了肌肉群受累情况,并提示了这些患者子宫内关节固定的机制。尽管病因和临床表现存在异质性,但关节挛缩症患者的病理变化似乎是独特的。