Cerebral Lymphangioma: A Clinical Case History.

IF 1.3 Q3 MEDICINE, GENERAL & INTERNAL
Cureus Pub Date : 2025-06-20 eCollection Date: 2025-06-01 DOI:10.7759/cureus.86455
Fadwa Fliyou, Sidi Mamoun Louraoui, Youssef Ouboukhlik, Mounir Rghioui, Abdessamad El Azhari, Faycal Moufid
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Abstract

Cerebral lymphangioma is an extremely rare entity, especially in adults. We report the case of a 38-year-old male who presented with diabetic ketoacidosis (fasting glucose: 4.65 g/L; glycated hemoglobin (HbA1c): 9.5%; urinary ketones and glucose: 4+ (highly positive)), severe holocranial headache, left hemiparesis, and agitation. MRI revealed a 58×46.5 mm right parietal extra-axial lesion with cystic and hemorrhagic components, initially suggestive of a cystic meningioma. Gross total surgical resection was performed following metabolic stabilization. Histopathology confirmed the diagnosis of lymphangioma. Postoperatively, the patient experienced a marked reduction in headache intensity (from 8/10 to 2/10 on the visual analog scale) and improvement in motor strength. This case illustrates the diagnostic challenge posed by cerebral lymphangiomas, which may closely mimic other cystic extra-axial lesions on imaging, particularly hemorrhagic meningiomas. It also demonstrates that complete surgical resection can result in favorable clinical outcomes. To our knowledge, this is one of the very few documented cases of cerebral lymphangioma in an adult, underscoring the need for increased awareness and further case reports to guide diagnosis and management.

脑淋巴管瘤:一个临床病例。
脑淋巴管瘤是一种极为罕见的疾病,尤其是在成人中。我们报告一例38岁男性糖尿病酮症酸中毒(空腹血糖:4.65 g/L;糖化血红蛋白(HbA1c): 9.5%;尿酮和葡萄糖:4+(高度阳性)),严重颅脑头痛,左偏瘫,躁动。MRI显示58×46.5毫米右顶叶轴外病变伴囊性和出血成分,初步提示囊性脑膜瘤。代谢稳定后进行手术切除。组织病理学证实淋巴管瘤的诊断。术后,患者头痛强度明显减轻(视觉模拟评分从8/10降至2/10),运动强度得到改善。这个病例说明了脑淋巴管瘤的诊断挑战,它在影像学上可能与其他囊性轴外病变非常相似,特别是出血性脑膜瘤。它还表明,完全手术切除可获得良好的临床结果。据我们所知,这是少有的记录在案的成人脑淋巴管瘤病例之一,强调需要提高认识和进一步的病例报告来指导诊断和管理。
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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