一例罕见的急性动脉血栓显示未分化动脉平滑肌肉瘤

Masato Tsuchimochi , Shigeta Miyake , Taisuke Akimoto , Yuta Otomo , Yasunobu Nakai , Kotaro Oshio , Tetsuya Yamamoto
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引用次数: 0

摘要

摘要主动脉平滑肌肉瘤是一种罕见且难以捉摸的恶性肿瘤,由于其非特异性症状和病程的侵袭性,使其诊断和治疗陷入困境。我们报告一个独特的情况下,意外发现动脉平滑肌肉瘤发生在急性脑梗死的管理。一名先前健康的58岁女性,最初表现为急性缺血性中风的严重神经功能缺损,接受了及时的再通治疗,结果成功恢复。出乎意料的是,提取的血栓的组织病理学检查显示为动脉平滑肌肉瘤。诊断过程包括免疫组织化学和增强计算机断层扫描,确认存在起源于升主动脉的平滑肌肉瘤。鉴于患者的严重残疾,姑息治疗方法被选择优先考虑的舒适和生活质量。本病例强调了急性再通治疗对功能恢复和组织病理学检查的诊断潜力,揭示了罕见疾病。进一步的病例积累对于完善治疗策略和改善血管肉瘤的预后是必不可少的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rare case of acute arterial thrombosis revealing undifferentiated arterial leiomyosarcoma
Aortic leiomyosarcoma, a rare and elusive malignancy, presents diagnostic and therapeutic dilemmas due to its nonspecific symptoms and aggressive course. We report a unique case where the incidental discovery of arterial leiomyosarcoma occurred during acute cerebral infarction management. A previously healthy 58-year-old woman, initially presenting with severe neurological deficits indicative of acute ischemic stroke, underwent prompt recanalization therapy that resulted in successful restoration. Unexpectedly, a histopathological examination of the extracted thrombus revealed arterial leiomyosarcoma. The diagnostic process involved immunohistochemistry and contrast-enhanced computed tomography, confirming the presence of leiomyosarcoma originating from the ascending aorta. Given the patient's severe disability, a palliative care approach was chosen to prioritize comfort and quality of life. This case underscores the diagnostic potential of acute recanalization therapy for functional recovery as well as histopathological examination, shedding light on rare diseases. Further case accumulation is essential to refine treatment strategies and improve prognostic outcomes for vascular sarcomas.
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