Yuichi Hirata, Masafumi Hiramatsu, Kenji Sugiu, Juntaro Fujita, Yuta Sotome, Masato Kawakami, Ryu Kimura, Yuki Ebisudani, Jun Haruma, Shota Tanaka
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引用次数: 0
摘要
背景:血友病 A 的特征是缺乏第八因子,从而导致严重的出血性疾病。血液凝固异常会使脑动脉瘤的治疗复杂化:一名患有先天性血友病 A 的 20 岁男子因巨大颈动脉海绵状动脉瘤(CCA)而出现外展神经麻痹。由于凝血功能障碍,他选择了颈内动脉简单结扎术,治疗后动脉瘤开始缩小。然而,由于来自后交通动脉和颈外动脉分支的侧支动脉,动脉瘤再次复发。使用血管内技术闭塞了这些动脉,结果动脉瘤完全闭塞:据作者所知,这是首例治疗与血友病 A 相关的巨大 CCA 的病例。对于有凝血功能障碍的患者,外科手术的选择有限,标准治疗可能无法实现完全治愈。在治疗伴有凝血障碍的巨大 CCA 时,仔细考虑治疗策略至关重要。https://thejns.org/doi/10.3171/CASE24693。
Challenges in the treatment of giant cavernous carotid aneurysm associated with hemophilia A: illustrative case.
Background: Hemophilia A is characterized by a deficiency of factor VIII, leading to severe bleeding disorders. Abnormal blood coagulation can complicate the treatment of cerebral aneurysms.
Observations: A 20-year-old man with congenital hemophilia A presented with abducens nerve palsy caused by a giant cavernous carotid aneurysm (CCA). Because of the coagulopathy, simple internal carotid artery ligation was chosen, and the aneurysm initially shrank following treatment. However, it recurred due to collateral arteries from the posterior communicating artery and branches of the external carotid artery. These arteries were occluded using endovascular techniques, resulting in complete obliteration of the aneurysm.
Lessons: To the best of the authors' knowledge, this is the first reported case of treating a giant CCA associated with hemophilia A. In patients with coagulopathy, surgical options are limited, and standard treatments may not achieve a complete cure. Careful consideration of treatment strategies is crucial when managing giant CCA in the context of a coagulation disorder. https://thejns.org/doi/10.3171/CASE24693.