Eghwrudjakpor P O, Kurisaka M, Fukuoka M, Mori K
Department of Neurosurgery, Kochi Medical School, Nankoku City, Japan.
Acta Neurochir (Wien). 1991;110(3-4):124-8. doi: 10.1007/BF01400679.
Intracranial lipomas are very rare, probably congenital lesions. Though they can occur anywhere in the intracranial space, a good proportion of cases tend to be located around the midline. Review of the literature as well as our own three cases--which forms the basis of this article--shows that they are mostly asymptomatic. When symptoms occur, they are frequently the result of coexisting general clinical conditions. Lipomas used to be reported mainly as incidental findings at autopsy. Advances in neuro-imaging techniques have vastly improved the likelihood of their being discovered during life. At present however, significant increase in the reported incidence of these tumours is yet to be seen. Surgical extirpation of the tumour is not considered necessary in the majority of patients, many of whom show remarkable clinical improvement following shunt procedures for obstructive hydrocephalus as well as treatment of coexisting conditions such as epilepsy.
颅内脂肪瘤非常罕见,可能是先天性病变。虽然它们可发生于颅内空间的任何部位,但相当一部分病例倾向于位于中线附近。文献回顾以及我们自己的三例病例——本文即以此为基础——表明它们大多无症状。当出现症状时,往往是并存的一般临床情况所致。脂肪瘤过去主要是在尸检时作为偶然发现被报告。神经成像技术的进步极大地提高了其在生前被发现的可能性。然而,目前这些肿瘤的报告发病率尚未见显著增加。大多数患者无需进行肿瘤手术切除,其中许多患者在针对梗阻性脑积水进行分流手术以及治疗并存疾病(如癫痫)后临床症状有显著改善。