Seitz R J, Wechsler W, Mosny D S, Lenard H G
Neuropediatrics. 1986 Aug;17(3):132-6. doi: 10.1055/s-2008-1052514.
A female newborn delivered at 32 weeks of gestation presented with multiple joint contractures consistent with arthrogryposis multiplex congenita (AMC). The girl died after a four days course of severe respiratory distress. Autopsy revealed slightly hypoplastic and immature lungs with acute necrotizing bronchopneumonia, and marked consecutive hypoxic brain lesions with severe periventricular haemorrhages. The peripheral nerves including the cranial and spinal nerve roots showed a hypomyelination radiculoneuropathy with well preserved axons and a normal content of Schwann cells. In the skeletal muscles of the arms and legs some fascicles of the extensors were replaced by lipomatous tissue. Since myelination of the white matter in the central nervous system was adequate to the age, this case represents an exclusive maturation disorder of the peripheral myelin sheaths that may be considered causal for AMC.
一名孕32周出生的女婴出现了与先天性多发性关节挛缩症(AMC)相符的多处关节挛缩。该女婴在经历了四天的严重呼吸窘迫后死亡。尸检显示肺部轻度发育不全且不成熟,伴有急性坏死性支气管肺炎,以及明显的连续性缺氧性脑损伤和严重的脑室周围出血。包括颅神经和脊神经根在内的周围神经表现为脱髓鞘性神经根神经病,轴突保存完好,雪旺细胞含量正常。在手臂和腿部的骨骼肌中,一些伸肌束被脂肪组织取代。由于中枢神经系统白质的髓鞘形成与年龄相符,该病例代表了一种外周髓鞘的排他性成熟障碍,可能是AMC的病因。