Middle meningeal artery embolization and tranexamic acid therapy for subdural hematoma in a patient with hereditary hemorrhagic telangiectasia: illustrative case.

Robert Kushmakov, Ilona Cazorla-Morales, Keith Brenner, David Araten, Maksim Shapiro, Eytan Raz, Dimitris G Placantonakis
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Abstract

Background: Subdural hematoma is a rare manifestation of hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu disease. Here, the authors present a patient with HHT and a large chronic subdural hematoma, for whom nonsurgical management was pursued.

Observations: A 49-year-old right-handed male with a history of hypertension and familial HHT presented with complaints of mild confusion and left hemiparesis over several days. Noncontrast head computed tomography images demonstrated a large chronic right hemisphere subdural hematoma compressing the right cerebral hemisphere and causing a 1.3-cm midline shift. Due to concerns about surgical complications arising from hemorrhages of cryptic telangiectasias, the patient was treated conservatively with middle meningeal artery embolization and adjuvant tranexamic acid. There was clinical and radiological resolution several months later.

Lessons: This case highlights the rarity of a subdural hematoma as a manifestation of HHT and the nonsurgical treatment strategy as a mechanism to avoid hemorrhagic complications of surgical evacuation. https://thejns.org/doi/10.3171/CASE24483.

脑膜中动脉栓塞和氨甲环酸治疗遗传性出血性毛细血管扩张症患者硬膜下血肿:示例病例。
背景:硬膜下血肿是遗传性出血性毛细血管扩张症(HHT)(又称 Osler-Weber-Rendu 病)的一种罕见表现。在此,作者介绍了一名患有 HHT 并伴有巨大慢性硬膜下血肿的患者,对其采取了非手术治疗:一名 49 岁的右撇子男性患者,有高血压和家族性 HHT 病史,主诉几天来出现轻度意识模糊和左侧偏瘫。非对比头部计算机断层扫描图像显示,一个巨大的慢性右侧大脑半球硬膜下血肿压迫右侧大脑半球,导致中线移位 1.3 厘米。由于担心隐匿性毛细血管瘤出血引起手术并发症,患者接受了脑膜中动脉栓塞和氨甲环酸辅助治疗。几个月后,患者的临床和影像学症状得到缓解:本病例强调了硬膜下血肿作为HHT表现的罕见性,以及非手术治疗策略作为避免手术排空出血并发症的机制。https://thejns.org/doi/10.3171/CASE24483。
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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