Nayak P K, Mahapatra A K
Department of Neurosurgery, All India Institute of Medical Sciences, New Delhi, India.
Pediatr Neurosurg. 2006;42(3):171-3. doi: 10.1159/000091862.
Associated cranial abnormalities with spinal dysraphism are not uncommon. We came across an unusual case of a 1-year-old male child with spinal dysraphism having lumbar meningomyelocele, who also had split cord malformation (hemicord with intervening bony spur) with lipoma of one of the hemicord and filum terminale. The patient also had communicating hydrocephalus without Chiari malformation and also near-total frontal bone agenesis. Single photon emission computed tomography scanning of brain revealed normal perfusion. In the first stage of repair, the patient had postoperative CSF leak for which ventriculo-peritoneal shunt was performed. This constitutes a rare anomaly associated with spinal dysraphism.
脊髓发育不良相关的颅骨异常并不罕见。我们遇到了一个不寻常的病例,一名1岁男童患有脊髓发育不良,伴有腰骶部脊髓脊膜膨出,同时还患有脊髓纵裂畸形(半脊髓伴中间骨嵴),其中一个半脊髓和终丝有脂肪瘤。该患者还患有交通性脑积水但无Chiari畸形,并且几乎完全没有额骨。脑部单光子发射计算机断层扫描显示灌注正常。在修复的第一阶段,患者术后出现脑脊液漏,为此进行了脑室-腹腔分流术。这是一种与脊髓发育不良相关的罕见异常。