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Lipoma in the Corpus Callosum Presenting with Epileptic Seizures Associated with Expanding Perifocal Edema: A Case Report and Literature Review

机译:Call体脂肪瘤伴癫痫发作与扩大性周围水肿相关:一例报道并文献复习

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摘要

This report describes a rare case of a patient with lipoma presenting with epileptic seizures associated with expanding perifocal edema. The patient was a 48-year-old man who presented with loss of consciousness and convulsions. Magnetic resonance imaging (MRI) revealed a calcified mass in the corpus callosum with perifocal edema causing mass effect. An interhemispheric approach was used to biopsy the mass lesion. Histological examination revealed typical adipose cells, along with hamartomatous components. These components contained neurofilament and S-100-positive structures showing marked calcification. Fibrous cells immunoreactive for α-smooth muscle actin and epithelial membrane antigen proliferated with focal granulomatous inflammatory changes. MIB-1 index was approximately 5% in immature cells observed in granulomatous areas. We thus suspected a coexisting neoplastic component. The residual lesion persisted in a dormant state for 2 years following biopsy. Surgical resection of a lipoma is extremely difficult and potentially dangerous. However, in the present case, the lesion was accompanied by atypical, expanding, and perifocal edema. Surgical treatment was inevitable for the purpose of histological confirmation, considering differential diagnoses such as dermoid, epidermoid, and glioma. In the end, anticonvulsant therapy proved effective for controlling epileptic seizures.
机译:该报告描述了罕见的脂瘤患者出现伴发性局灶性水肿的癫痫发作。该患者为一名48岁男子,出现意识丧失和抽搐。磁共振成像(MRI)显示call体钙化肿块伴焦斑水肿,引起肿块效应。半球间方法用于对肿块进行活检。组织学检查发现典型的脂肪细胞以及错构成分。这些成分包含神经丝和S-100阳性结构,显示出明显的钙化。纤维细胞对α-平滑肌肌动蛋白和上皮膜抗原具有免疫反应性,并伴有局灶性肉芽肿性炎症改变。在肉芽肿区域观察到的未成熟细胞中,MIB-1指数约为5%。因此,我们怀疑肿瘤成分并存。活检后残留病灶在休眠状态持续2年。脂肪瘤的手术切除非常困难,并且有潜在的危险。但是,在本例中,病变伴有非典型性,扩大性和局灶性水肿。考虑到鉴别诊断,如皮肤样,表皮样和神经胶质瘤,为了进行组织学确认,手术治疗是不可避免的。最后,抗惊厥疗法被证明对控制癫痫发作有效。

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