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女性患者在性交过程中发生主动脉壁内血肿。

Aortic Intramural Hematoma in a Female Patient During Sexual Intercourse.

机构信息

Emergency Medicine Residency, Merit Health Wesley, Hattiesburg, MS, USA.

Department of Emergency Medicine, Merit Health Wesley, Hattiesburg, MS, USA.

出版信息

Am J Case Rep. 2022 Jul 28;23:e936167. doi: 10.12659/AJCR.936167.

Abstract

BACKGROUND Acute aortic syndrome (AAS) is a spectrum of severe life-threatening disease processes that are often initially encountered in the emergency department (ED) setting and require prompt recognition and treatment to prevent significant complications, including death. We describe an atypical presentation of aortic intramural hematoma in a female patient during sexual intercourse, a situation not previously described in the literature. CASE REPORT The patient was a 45-year-old woman who presented to the ED with a chief concern of chest pain. Just prior to the onset of her symptoms, the patient was having sexual intercourse with her husband, and during her orgasm she felt a "pop" in her chest with radiation to her back. The patient was diaphoretic and hypertensive on arrival, with a blood pressure of 220/140 mmHg. Computed tomography angiography of the chest was performed and showed an intramural hematoma (or thrombosed dissection) of the distal aortic arch and descending thoracic aorta. In the ED, the patient was started on intravenous antihypertensives, which were eventually switched to oral agents. Cardio-thoracic surgery staff was consulted and recommended medical management. As oral doses were increased, the intravenous antihypertensives were weaned, and the patient was eventually discharged home with scheduled outpatient follow-up. CONCLUSIONS Intramural aortic hematoma is a form of AAS with independent pathogenesis but similar progression, complications, and treatment as aortic dissection and thus demands efficient diagnosis and treatment. A high degree of suspicion, even in atypical situations, is paramount, as efficient recognition and treatment can be lifesaving.

摘要

背景

急性主动脉综合征(AAS)是一系列严重的危及生命的疾病过程,这些疾病过程通常最初在急诊科(ED)环境中遇到,需要及时识别和治疗,以防止出现重大并发症,包括死亡。我们描述了一名女性患者在性交过程中出现主动脉壁内血肿的非典型表现,这种情况在文献中以前没有描述过。

病例报告

患者是一名 45 岁女性,因胸痛就诊于 ED。在出现症状之前,患者正在与她的丈夫进行性行为,在她达到性高潮时,她感到胸部有“噗”的一声,同时辐射到背部。患者到达时出汗且高血压,血压为 220/140mmHg。进行了胸部计算机断层血管造影,显示降主动脉和胸主动脉远段的壁内血肿(或血栓性夹层)。在 ED,患者开始接受静脉降压治疗,最终改为口服药物。胸心血管外科医生会诊并建议进行药物治疗。随着口服剂量的增加,静脉降压药逐渐减少,患者最终在家中出院,并安排了门诊随访。

结论

壁内主动脉血肿是 AAS 的一种形式,具有独立的发病机制,但与主动脉夹层的进展、并发症和治疗相似,因此需要有效的诊断和治疗。即使在非典型情况下,也要高度怀疑,因为有效的识别和治疗可以挽救生命。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12fd/9344760/35361205ac3c/amjcaserep-23-e936167-g001.jpg

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