需鉴别诊断的青少年慢性脑内包膜性血肿1例,经开颅及血肿清除成功治疗。

Surgical neurology international Pub Date : 2025-08-22 eCollection Date: 2025-01-01 DOI:10.25259/SNI_454_2025
Yodai Kikuchi, Shogo Dofuku, Rika Nakamura, Ken Kazama, Hideaki Imai
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摘要

背景:慢性脑内血肿(CEIH)是一种罕见的疾病,其发病机制尚不清楚。此外,尚未就其治疗办法达成共识。在这里,我们报告一例青少年皮质下CEIH成功治疗完全切除,包括包膜。病例描述:26岁女性,无明显病史,就诊前2个月零3周头痛,入院前1周拔除右侧第三磨牙。她到我们医院来,说是头痛。视野测试显示为左上象限视。头部CT示右侧颞叶5厘米环形高密度病灶,脑血管造影未见明显血管异常。在医院的第10天,她接受了开颅手术并切除了病变。术中发现血肿被包裹,实现了整体切除。组织病理学检查显示纤维结缔组织伴成纤维细胞增生,覆盖由纤维蛋白和红细胞组成的血肿,符合CEIH。术后过程顺利,无新的神经功能缺损,头痛和视野障碍均得到改善。术后2周出院。结论:尽管CEIH的发病机制尚不清楚,治疗方法也没有共识,但考虑到有复发和预后不良的报告,与残留的囊组织或与海绵状血管瘤共存有关,完全切除包括囊,被认为是本病例合适的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A case of juvenile chronic encapsulated intracerebral hematoma requiring differential diagnosis, successfully treated with craniotomy and hematoma evacuation.

Background: Chronic encapsulated intracerebral hematoma (CEIH) is a rare condition with an unclear pathogenesis. Moreover, no consensus has been established regarding its treatment. Here, we report a case of juvenile subcortical CEIH successfully treated with complete resection, including the capsule.

Case description: A 26-year-old woman with no notable medical history had experienced headaches for 2 months and 3 weeks before presentation and underwent extraction of the right third molar 1 week before admission. She presented to our hospital complaining of a headache. Visual field testing revealed left upper quadrantanopia. Head CT showed a 5 cm ring-shaped hyperdense lesion in the right temporal lobe, and cerebral angiography revealed no significant vascular abnormalities. On hospital day 10, she underwent craniotomy and removal of the lesion. Intraoperative findings revealed that the hematoma was encapsulated, and en bloc resection was achieved. Histopathological examination showed fibrous connective tissue with fibroblast proliferation covering a hematoma composed of fibrin and red blood cells, consistent with CEIH. The postoperative course was smooth, no new neurological deficits were observed, and both the headache and visual field disturbance improved. She was discharged home 2 weeks after surgery.

Conclusion: Although the pathogenesis of CEIH remains unclear and there is no consensus on treatment, complete resection, including the capsule, was considered the appropriate therapeutic approach in this case, given reports of recurrence and poor outcomes associated with residual capsule tissue or coexistence with cavernous malformations.

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