Frerebeau P, Marty-Double C, Castan-Tarbouriech E, Privat J M, Benezech J
Neurochirurgia (Stuttg). 1978 Nov;21(6):212-20. doi: 10.1055/s-0028-1090346.
A boy, 25 months old, presented a cerebellar syndrome with increased intracranial pressure. Despite a ventriculo-peritoneal bypass, death occurred at the age of 4 1/2 years. Autopsy revealed a very large cerebellum, presenting a "glossy" appearance, with swelling of the brain stem. Histologically, there was a very unusual lesion with a diffuse disorganization of the cortex, a neuronoglial mixed proliferation, a large number of calcospherites, small tumour-like nodules and many leptomeningeal glial bridges. The authors consider that their case is not related to L'Hermitte-Duclo's disease, nor to gangliogliomas, and they discuss the hypothesis of hamartoma.
一名25个月大的男孩出现小脑综合征并伴有颅内压升高。尽管进行了脑室-腹腔分流术,但仍在4岁半时死亡。尸检发现小脑非常大,呈现出“光滑”外观,脑干肿胀。组织学上,有一个非常不寻常的病变,表现为皮质弥漫性紊乱、神经胶质细胞混合增生、大量钙球、小肿瘤样结节以及许多软脑膜胶质桥。作者认为他们的病例与赫米特-迪克洛病无关,也与神经节胶质瘤无关,并讨论了错构瘤的假说。