Krishnan Prasad, Chattopadhyay Arijit, Saha Manash
Department of Neurosurgery, National Neurosciences Centre, Peerless Hospital Complex, Panchasayar, Kolkata, West Bengal, India.
Department of Neurology, National Neurosciences Centre, Peerless Hospital Complex, Panchasayar, Kolkata, West Bengal, India.
J Pediatr Neurosci. 2014 Sep-Dec;9(3):273-5. doi: 10.4103/1817-1745.147591.
A 7-year-old male child presented with poorly controlled generalized tonic-clonic seizures. On examination, he was mentally retarded, deaf and had a swelling at the root on the nose. Computed tomography scan done previously revealed a left temporal arachnoid cyst (AC) due to which he was referred for surgery. However, magnetic resonance imaging revealed a constellation of abnormalities - all of which could be responsible for his seizures. The combination of periventricular nodular heterotopias with encepaholcele is rarely described in the literature, and more infrequently so its combination with AC and callosal dysgenesis - the Chudley-Mccullough syndrome. We describe the case and review relevant literature on this subject.
一名7岁男童出现全身性强直阵挛性癫痫发作,控制不佳。检查发现,他智力发育迟缓、失聪,鼻根部有肿胀。此前进行的计算机断层扫描显示左侧颞叶蛛网膜囊肿(AC),因此他被转诊接受手术。然而,磁共振成像显示出一系列异常——所有这些都可能是其癫痫发作的原因。脑室周围结节性异位合并脑膨出的情况在文献中很少被描述,而其与AC和胼胝体发育不全的合并情况则更少见——即Chudley-Mccullough综合征。我们描述了该病例并回顾了关于这一主题的相关文献。