Sener R N
Department of Radiology, Ege University Hospital, Bornova, Izmir, Turkey.
Pediatr Radiol. 1993;23(6):489-90. doi: 10.1007/BF02012464.
The case is presented of a 1.5-year-old with the typical CT features of tuberous sclerosis and pachygyria, in combination. Tuberous sclerosis was evidenced by multiple subependymal calcifications, and pachygyria by the relevant CT appearances. Periventricular heterotopia and total callosal agenesis were associated findings. The findings in this patient convincingly suggest a close relationship between tuberous sclerosis and pachygyria, although the case is the first to be reported in the literature.
本文介绍了一名1.5岁儿童，其具有结节性硬化症和巨脑回畸形的典型CT特征。结节性硬化症通过多个室管膜下钙化得以证实，巨脑回畸形则通过相关的CT表现得以证实。室管膜下异位和胼胝体完全缺如是相关的伴随发现。该患者的这些发现令人信服地表明结节性硬化症与巨脑回畸形之间存在密切关系，尽管这是文献中首次报道的病例。
