Misra B K, Shaw J F, Gordon A
University Department of Surgical Neurology, Edinburgh University, Western General Hospital, UK.
Childs Nerv Syst. 1987;3(5):297-300. doi: 10.1007/BF00271828.
The case of a newborn boy with a congenital cystic neck mass causing respiratory distress is reported. This lesion extended from the submandibular region through a bone defect to the middle cranial fossa but remained totally extradural. There was no underlying brain abnormality. The cyst was composed mainly of mature neuroglial tissue, with some ependymal and choroid plexus elements, and was diagnosed as heterotopic brain. After 8 years' follow-up, the child still has no deficits.
报告了一例患有先天性颈部囊性肿块并导致呼吸窘迫的男婴病例。该病变从下颌下区域通过骨缺损延伸至中颅窝,但完全位于硬膜外。未发现潜在的脑部异常。囊肿主要由成熟的神经胶质组织组成,伴有一些室管膜和脉络丛成分,被诊断为异位脑。经过8年的随访,该患儿仍无功能缺损。