Heidenreich R, Natowicz M, Hainline B E, Berman P, Kelley R I, Hillman R E, Berry G T
Department of Pediatrics, University of Pennsylvania School of Medicine, Philadelphia.
J Pediatr. 1988 Dec;113(6):1022-7. doi: 10.1016/s0022-3476(88)80574-2.
We report four patients with methylmalonic acidemia who developed acute extrapyramidal disease after metabolic decompensation. The neurologic findings resulted from bilateral destruction of the globus pallidus with variable involvement of the internal capsules. This complication was unrelated to a specific gene defect responsible for methylmalonic acidemia or to cyanocobalamin administration. These lesions constitute a "metabolic stroke," probably because of the accumulation of toxic organic acid metabolites, because they cannot be accounted for by hypoxemia or vascular insufficiency.
我们报告了4例甲基丙二酸血症患者,他们在代谢失代偿后出现了急性锥体外系疾病。神经系统表现是由于双侧苍白球破坏,内囊也有不同程度受累。这种并发症与导致甲基丙二酸血症的特定基因缺陷或钴胺素的使用无关。这些病变构成了一种“代谢性中风”,可能是由于有毒有机酸代谢产物的积累,因为低氧血症或血管功能不全无法解释这些病变。