A Clinical Case Report About an Intracranial Lipoma

Gonçalo Januário
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Abstract

: Intracranial lipoma is a uncommon congenital malformation, represent less than 0.1% of all intracranial tumors. Result from abnormal persistence and mal-differentiation of meninx primitiva, during embryogenesis. The cases in which the tumor presents an extracranial component are caused by a secondary dehiscence of the skull with evagination of a small tuft of primitive meninges. These lesions are frequently located in the inter-hemispheric fissure in the pericallosal region in 50% of cases, other locations as ambient or quadrigeminal cisterns present an incidence about 20-25%. In half of cases the patients present associate midline brain malformations of varying severity, the most frequent is the agenesia of the corpus callosus. The most accepted theory states that in embryonic phases, mesenchymal alterations at the level of the cranial sutures in the sagittal plane can cause anomalies of the SSS, sinus rectum, tentorium, and parietal bones that would explain the associated anomalies. Majority of intracranial lipomas are detected incidentally, being a third of the asymptomatic cases. As in all other pathologies certain localizations cause specific symptomatology of the involved area. The most common clinical manifestations are headache, epilepsy, mental dysfunctions and cranial nerve deficits. The clinical diagnosis is unclear and it is necessary release complementary exams in every suspected cases. Neuroimaging studies such as computed tomography (CT) or magnetic resonance imaging (MRI) make possible identify these lesions. We describe a clinical case about a 79-year-old woman with headache without any other symptoms. Was done CT and MRI that showed a inter-hemispheric lesion located in the pericallosal region, without any other abnormality associated. The development, during the last decades, of neuroimaging and histogenesis techniques increased the knowledge about this pathology and modified the management in recent times. The surgery is contraindicated in the majority of the cases, however still play a role in some cases especially in presence of hydrocephalus, uncontrollable seizures, and bony affectation with cosmetic influence. The medical control of the epilepsy is mandatory. We present a clinical case about pericallosal intracranial lipoma and review the current literature. Taking in account the clinical situation and the imaging findings, we decide for a conservative approach with clinical/neurological and radiological follow-up.
颅内脂肪瘤1例临床报告
颅内脂肪瘤是一种罕见的先天性畸形,在所有颅内肿瘤中所占比例不到0.1%。在胚胎发生过程中,由于原始脑膜的异常持续和分化。肿瘤呈现颅外成分的病例是由颅骨继发性裂开引起的,伴有一小簇原始脑膜外翻。这些病变通常位于胼胝体周围区域的半球间裂(50%),其他位置为周围池或四合体池的发生率约为20-25%。在一半的病例中,患者出现不同程度的脑中线畸形,最常见的是胼胝体缺失。最被接受的理论认为,在胚胎期,矢状面颅缝水平的间质改变可导致SSS、直肠窦、幕骨和顶骨的异常,这可以解释相关的异常。大多数颅内脂肪瘤是偶然发现的,占无症状病例的三分之一。与所有其他病理一样,某些部位引起受累区域的特定症状。最常见的临床表现为头痛、癫痫、精神功能障碍和颅神经缺损。临床诊断不明确,有必要对每一例疑似病例进行补充检查。神经影像学研究,如计算机断层扫描(CT)或磁共振成像(MRI)使识别这些病变成为可能。我们描述一个79岁女性的临床病例,头痛无其他症状。经CT和MRI检查,发现胼胝体周围有一半球间病变,未见其他异常。在过去的几十年里,神经成像和组织发生技术的发展增加了对这种病理的认识,并在最近改变了治疗方法。在大多数情况下,手术是禁忌的,但在某些情况下,特别是在存在脑积水,无法控制的癫痫发作和影响美容的骨畸形时,手术仍然发挥作用。对癫痫的医疗控制是强制性的。我们报告一例颅胼胝体周围脂肪瘤的临床病例,并复习目前的文献。考虑到临床情况和影像学表现,我们决定采用保守方法,并进行临床/神经学和放射学随访。
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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