胼胝体脂肪瘤。3例病例报告及文献综述]。

Annales de pediatrie Pub Date : 1993-03-01
M Kchouk, R Gouider, M H Ben Romdhane, S Touibi
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引用次数: 0

摘要

摘要胼胝体脂肪瘤是一种罕见的先天性颅内肿瘤。尽管截至1992年3月仅报告了153例,但这种肿瘤的发病率被低估了(一些病例未发表,其他病例无症状)。本文报告三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,也可能导致最常见的症状是癫痫、头痛和精神障碍。诊断依赖于影像技术。主要的检查是计算机断层扫描,它可以发现由脂肪组成的肿块,有或没有周围钙化,也可以识别任何其他畸形,如胼胝体发育不良。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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[Lipoma of the corpus callosum. 3 case reports and review of the literature].

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only 153 cases had been reported as of March 1992, the incidence of this tumor is underestimated (some cases are unpublished and others are asymptomatic).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.

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