一名患有血管痉挛性心绞痛的绝经前中年妇女的双侧孤立性冠状动脉口狭窄:病例报告

Koji Takahashi, Akihiro Kodama, Shigeki Uemura, Takafumi Okura
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摘要

血管痉挛性心绞痛(VSA)在绝经前妇女中并不常见,因为绝经前妇女的慢性内皮损伤较少,导致血管重塑被认为是冠状动脉血管痉挛的主要发病机制。此外,血管痉挛很少发生在双侧冠状动脉口。孤立性冠状动脉管腔狭窄(ICOS)通常会导致严重的劳力性心绞痛,需要进行手术干预,中年女性更常出现这种情况,其病因包括纤维肌发育不良(FMD)和大血管炎。然而,与 VSA 相关的 ICOS 却极为罕见。 一名 50 岁的绝经前日本妇女主诉,自 3 年前以来,每天清晨轻微用力时都会出现典型的心绞痛胸痛。冠状动脉造影检查发现双侧轻度至中度 ICOS,此外,使用冠状动脉内注射乙酰胆碱进行的血管痉挛激发试验证实,双侧冠状动脉大动脉多支血管痉挛。确定 ICOS 病因的检查没有发现 FMD 或任何其他疾病。自首次发病以来的 24 年中,在未对双侧 ICOS 进行干预的情况下,服用钙通道阻滞剂(CCB)后心绞痛发作有所缓解。此外,在首次发病 24 年后进行的冠状动脉计算机断层扫描(CTA)显示没有 ICOS。 我们的患者具有典型且频繁的 VSA 症状,冠状动脉造影显示其双侧冠状动脉口均存在轻度至中度 ICOS 和血管痉挛。ICOS 的病因排除了 FMD 或大血管炎。在使用 CCB 后很少出现 VSA,在首次发病 24 年后的冠状动脉 CTA 显示没有 ICOS。我们患者的双侧 ICOS 可能与 VSA 有关。
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Bilateral Isolated Coronary Ostial Stenosis in a Middle-Aged Premenopausal Woman with Vasospastic Angina: A Case Report
Vasospastic angina (VSA) is uncommon in premenopausal women who have less chronic endothelial injury causing vascular remodelling considered a primary role in the pathogenesis for coronary vasospasms. Furthermore, vasospasms rarely occur in the bilateral coronary ostia. Isolated coronary ostial stenosis (ICOS), which often causes severe effort angina and requires surgical intervention, is more commonly reported in middle-aged women, with causes including fibromuscular dysplasia (FMD) and large-vessel vasculitis. However, ICOS associated with VSA is extremely rare. A 50-year-old premenopausal Japanese woman presented with a complaint of typical chest pain due to angina during light exertion daily in the early morning hours since 3 years. Coronary angiography revealed bilateral mild-to-moderate ICOS in addition to multivessel spasms involving the bilateral coronary ostia confirmed by the vasospasm provocation test using intracoronary acetylcholine injection. Tests to determine the cause of ICOS did not identify FMD or any other disease. The angina attacks alleviated after calcium channel blocker (CCB) administration without intervention for bilateral ICOS for 24 years since the first presentation. Moreover, coronary computed tomography angiography (CTA) performed 24 years after the first presentation showed no ICOS. In our patient with typical and frequent VSA symptoms, coronary angiography revealed both mild-to-moderate ICOS and the vasospasms in the bilateral coronary ostia. FMD or large-vessel vasculitis were ruled out as the causes of ICOS. VSA rarely occurred after the prescription of CCB, and coronary CTA 24 years after the first presentation showed no ICOS. Bilateral ICOS in our patient might be VSA-related.
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