Sakakihara Y
Department of Pediatrics, Faculty of Medicine, University of Tokyo.
Nihon Rinsho. 1992 Apr;50(4):811-7.
Among many metabolic disorders, porphyrias and Fabry disease are known to affect autonomic nervous system. In patients with acute intermittent porphyria, hereditary coproporphyria, and variegate porphyria, autonomic symptoms such as abdominal pain, vomiting, hypertension and tachycardia are among the most prominent clinical manifestations. Fabry disease is clinically characterized by severe limb pain, hypohidrosis, angiokeratomas and various autonomic symptoms. In both porphyrias and Fabry disease, pathological changes in the central and peripheral autonomic nervous system have been documented. In porphyrias, a loss of myelinated fibers, axonal degeneration, and segmental demyelination in peripheral autonomic nerves as well as chromatolysis of several brain stem nuclei have been found. In Fabry disease, abnormal amount of the substrates of alpha-galactosidase, i.e. ceramide di- and trihexoside, are found to be accumulated in the central and peripheral autonomic nerves.
在众多代谢紊乱疾病中,已知卟啉病和法布里病会影响自主神经系统。在急性间歇性卟啉病、遗传性粪卟啉病和杂合性卟啉病患者中,腹痛、呕吐、高血压和心动过速等自主神经症状是最突出的临床表现。法布里病的临床特征为严重的肢体疼痛、少汗、血管角质瘤和各种自主神经症状。在卟啉病和法布里病中,中枢和外周自主神经系统均有病理改变记录。在卟啉病中,已发现外周自主神经中有髓纤维丢失、轴突变性和节段性脱髓鞘,以及几个脑干核的染色质溶解。在法布里病中,发现α-半乳糖苷酶的底物,即神经酰胺二己糖苷和神经酰胺三己糖苷,在中枢和外周自主神经中异常蓄积。