Gelabert-González Miguel, Pita-Buezas Lara, Santín-Amo José María, Román-Pena Paula, Serramito-García Ramón, García-Allut Alfredo
Servicio de Neurocirugía, Hospital Clínico Universitario, Santiago de Compostela, La Coruña, España; Departamento de Cirugía, Universidad de Santiago de Compostela, Santiago de Compostela, La Coruña, España.
Servicio de Neurocirugía, Hospital Clínico Universitario, Santiago de Compostela, La Coruña, España; Departamento de Cirugía, Universidad de Santiago de Compostela, Santiago de Compostela, La Coruña, España.
Neurocirugia (Astur). 2015 Mar-Apr;26(2):100-4. doi: 10.1016/j.neucir.2014.09.007. Epub 2015 Feb 2.
Intracranial arachnoid cysts are fluid-filled cavities that arise within the cranial arachnoid, representing approximately 1%-2% of all intracranial lesions among the paediatric population. We present the case of a 2-year-old boy who presented with instability and episodes of ocular deviation. A computed tomography scan (CT scan) and magnetic resonance imaging (MRI) of the brain revealed a suprasellar cyst and obstructive hydrocephalus. At birth a transfontanellar ultrasound was normal. The cyst underwent endoscopic fenestration with complete remission of symptoms. In the review of the literature, we found only 6 previous cases of an intracranial arachnoid cyst whose origin was not clearly congenital or traumatic, and ours is the second case of a suprasellar arachnoid cyst to arise de novo. The clinical features, imaging characteristics and treatment of the previously reported cases are discussed.
颅内蛛网膜囊肿是发生于颅蛛网膜内的充满液体的腔隙,在儿科人群的所有颅内病变中约占1%-2%。我们报告一例2岁男孩,表现为不稳和眼球偏斜发作。脑部计算机断层扫描(CT扫描)和磁共振成像(MRI)显示鞍上囊肿和梗阻性脑积水。出生时经囟门超声检查正常。该囊肿接受了内镜开窗术,症状完全缓解。在文献回顾中,我们仅发现6例颅内蛛网膜囊肿起源不明(非先天性或外伤性)的病例,我们的病例是第二例新发的鞍上蛛网膜囊肿。文中讨论了先前报道病例的临床特征、影像学特点及治疗情况。