Blumbergs P C, Chin D K, Hallpike J F
Clin Exp Neurol. 1983;19:94-101.
The case is described of a man, aged 46 at his time of death, who suffered from focal motor, adversive and generalised seizures for 22 years. He developed a progressive dementia over the last 2 years of his life. Investigation, including angiography and air encephalography early in the course of the illness and repeated CT head scans later, failed to demonstrate any neoplasm. Death occurred abruptly, due to cerebellar tonsillar herniation. At postmortem an extensive diffuse low grade fibrillary astrocytoma infiltrated both cerebral hemispheres, the corpus callosum, central grey matter, midbrain and pons. Thus, there was gliomatosis cerebri. Attention is drawn to the exceptional length of the history in this case, the difficulties which may arise in displaying diffusely infiltrating low grade astrocytomas radiologically and to the rare occurrence of gliomatosis cerebri.
报道了一例患者,死亡时46岁,患有局灶性运动性、扭转性和全身性癫痫发作22年。在其生命的最后两年出现进行性痴呆。在疾病早期进行的包括血管造影和气脑造影在内的检查,以及后来多次头颅CT扫描,均未发现任何肿瘤。患者因小脑扁桃体疝突然死亡。尸检发现广泛弥漫性低度纤维型星形细胞瘤浸润双侧大脑半球、胼胝体、中央灰质、中脑和脑桥。因此,存在大脑胶质瘤病。该病例病程异常漫长,放射学上显示弥漫性浸润性低度星形细胞瘤可能存在困难,以及大脑胶质瘤病罕见,这些均引起了关注。