Simon M, Kafritsas D
Department of Pathology, Medical School-University of Ulm, Germany.
Clin Neuropathol. 1992 Mar-Apr;11(2):71-3.
In a 48-year-old man, marked unilateral cerebellar hypoplasia was diagnosed by CT scans and angiographic examinations, later confirmed on autopsy. Clinical findings in cerebellar hypoplasia/aplasia are discussed here, along with the pathogenesis of cerebellar hypoplasia. In this case, several grand mal seizures and persistent headache were the only neurological symptoms. Repeated neurologic explorations did not reveal any abnormality. The clear demonstration of cerebellar hypoplasia associated with ipsilateral hypoplasia of the vertebral artery favors the concept of a vascular genesis of cerebellar hypoplasia/aplasia.
在一名48岁男性中，通过CT扫描和血管造影检查诊断出明显的单侧小脑发育不全，尸检后来得以证实。本文讨论了小脑发育不全/发育不全的临床发现，以及小脑发育不全的发病机制。在这个病例中，几次癫痫大发作和持续性头痛是仅有的神经症状。反复的神经检查未发现任何异常。与同侧椎动脉发育不全相关的小脑发育不全的明确显示支持小脑发育不全/发育不全的血管起源概念。
