Graveleau P, Gray F, Plas J, Graveleau J, Brion S
Rev Neurol (Paris). 1985;141(11):713-8.
A 39 year-old man with mild stable mental retardation, without family history, developed progressively a gait disturbance and intellectual deterioration. CT scan showed a low density of the periventricular hemispheric white matter which increased on subsequent examinations. Eight months before death he presented with several Grand Mal seizures. He died 29 months after the onset of the clinical disorders. Neuropathological studies included light and electron microscopy of a cerebral biopsy and a post-mortem examination of the brain. It showed a sudanophilic leukodystrophy with unusual features: cavitation of the white matter, oligodendrocyte proliferation and lamellar "fingerprint" dense cytoplasmic inclusions in the oligodendrocytes. Only 3 similar cases have been previously reported.
一名39岁男性,患有轻度稳定型智力障碍,无家族病史,逐渐出现步态障碍和智力衰退。CT扫描显示脑室周围半球白质密度减低,后续检查中该情况有所加重。在死亡前八个月,他出现了几次大发作癫痫。临床症状出现29个月后他去世。神经病理学研究包括对脑活检组织进行光镜和电镜检查以及对大脑进行尸检。结果显示为一种具有不寻常特征的嗜苏丹性脑白质营养不良:白质空洞形成、少突胶质细胞增生以及少突胶质细胞内出现层状“指纹”样致密胞质内包涵体。此前仅报道过3例类似病例。