Kchouk M, Gouider R, Ben Romdhane M H, Touibi S
Service de Neuroradiologie, Institut National de Neurologie, La Rabta, Tunis, Tunisie.
Ann Pediatr (Paris). 1993 Mar;40(3):145-8.
Lipoma of the corpus callosum is a rare congenital intracranial tumor. Although only 153 cases had been reported as of March 1992, the incidence of this tumor is underestimated (some cases are unpublished and others are asymptomatic). Three cases of lipoma of the corpus callosum diagnosed in children are reported herein. These tumors may be either discovered fortuitously in an asymptomatic patient or responsible for manifestations of which the most common are seizures, headache, and mental disorders. Diagnosis rests on imaging techniques. The main investigation is computed tomography which discloses a mass composed of fat, with or without peripheral calcifications, and also identifies any other malformations such as dysgenesis of the corpus callosum.
胼胝体脂肪瘤是一种罕见的先天性颅内肿瘤。虽然截至1992年3月仅报告了153例,但该肿瘤的发病率被低估了(一些病例未发表,另一些病例无症状)。本文报告了3例儿童胼胝体脂肪瘤。这些肿瘤可能在无症状患者中偶然发现,也可能导致一些症状,其中最常见的是癫痫、头痛和精神障碍。诊断依赖于影像学技术。主要检查是计算机断层扫描,它可显示由脂肪组成的肿块,有无周边钙化,还能识别任何其他畸形,如胼胝体发育不全。