Medved Fabian, Seiz Marcel, Baur Marc-Oliver, Neumaier-Probst Eva, Tuettenberg Jochen
Department of Neurosurgery, University Children's Hospital, and Department of Neuroradiology, Mannheim Medical Faculty, University of Heidelberg, Mannheim, Germany.
J Neurosurg Pediatr. 2009 Feb;3(2):132-6. doi: 10.3171/2008.10.PEDS08202.
Symptomatic intramedullary arachnoid cysts are rare, especially in children; these lesions are rarely described as a cause of spinal cord compression in this age group. The authors report on an 18-month-old boy who experienced a sudden loss of his ability to stand and walk due to a paraparesis. Magnetic resonance imaging of the spine exhibited a cystic intramedullary lesion at the level of T5-6. A hemilaminectomy was performed, and after myelotomy the cystic lesion was decompressed by fenestration to the subarachnoid space. The histopathological examination verified the diagnosis of an arachnoid cyst. In the postoperative course the boy experienced complete resolution of the initial paraparesis.
有症状的髓内蛛网膜囊肿很罕见,在儿童中尤为如此;在这个年龄组中,这些病变很少被描述为脊髓压迫的原因。作者报告了一名18个月大的男孩,他因双下肢轻瘫突然失去站立和行走能力。脊柱磁共振成像显示T5-6水平有一个囊性髓内病变。进行了半椎板切除术,在脊髓切开术后,通过向蛛网膜下腔开窗引流对囊性病变进行了减压。组织病理学检查证实了蛛网膜囊肿的诊断。在术后过程中,男孩最初的双下肢轻瘫完全恢复。