Maiuri F, Cirillo S, Simonetti L, De Simone M R, Gangemi M
Institute of Neurosurgery, 2nd School of Medicine, University of Naples, Italy.
J Neurosurg Sci. 1988 Oct-Dec;32(4):161-7.
Fourteen cases of intracranial lipomas are reported and 200 cases from the literature are reviewed. Intracranial lipomas are rare lesions of developmental origin, which mainly occur in the region of the corpus callosum, more rarely in the ambient, interpeduncular, cerebellopontine angle and sylvian cisterns. Although they are usually asymptomatic, they can sometimes show neurological symptoms, mainly epileptic seizures. Computerized tomography and magnetic resonance imaging usually lead to the diagnosis, because of the very low-density attenuation values of lipomas on CT scan and the short T1 and T2 on magnetic resonance. A direct surgical approach is only rarely indicated, whereas cases associated to hydrocephalus require a CSF shunt. The anticonvulsivant therapy usually results in remission of the seizures.
报告了14例颅内脂肪瘤,并对文献中的200例病例进行了回顾。颅内脂肪瘤是一种罕见的发育性病变,主要发生在胼胝体区域,较少发生在脑池、脚间池、桥小脑角和外侧裂池。虽然它们通常无症状,但有时可出现神经症状,主要是癫痫发作。计算机断层扫描和磁共振成像通常可作出诊断,因为脂肪瘤在CT扫描上的密度衰减值很低,在磁共振上T1和T2很短。很少需要直接手术治疗,而与脑积水相关的病例则需要脑脊液分流。抗惊厥治疗通常可使癫痫发作缓解。