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Idiopathic pulmonary artery dissection: a case report

机译:特发性肺动脉夹层:一例报告

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Introduction The occurrence of pulmonary artery dissection is extremely rare in patients without pulmonary hypertension, congenital cardiac abnormalities or cardiac intervention. A diagnosis of pulmonary artery dissection is rarely made during life because it generally leads to cardiogenic shock and sudden death. The progression or natural course of pulmonary artery dissection is not known and the optimum management is not defined because of the paucity of cases in the literature. Case presentation We report a rare case of a 51-year-old female patient, without pulmonary hypertension or other cardiac abnormalities, who presented with acute chest pain and was found to have a pulmonary artery dissection.. The diagnosis of pulmonary artery dissection was confirmed by computed tomography scan of the chest and cardiac magnetic resonance imaging. The patient declined surgical intervention and was followed up closely with medical therapy. At almost a year after her initial presentation, the patient is stable with no complications. Conclusions To our knowledge, there are no similar cases reported in the literature of people with pulmonary artery dissection who have been followed up and who have not had surgical intervention. We review the etiology, pathophysiology, clinical associations, diagnosis and management of patients with pulmonary artery dissection.
机译:简介在没有肺动脉高压,先天性心脏异常或心脏干预的患者中,发生肺动脉解剖的情况极为罕见。一生中很少诊断出肺动脉夹层,因为它通常会导致心源性休克和猝死。由于文献中病例很少,因此尚不清楚肺动脉解剖的进展或自然过程,也未定义最佳治疗方法。病例介绍我们报告了一位罕见的病例,其中一名51岁的女性患者没有肺动脉高压或其他心脏异常,表现出急性胸痛并被发现患有肺动脉夹层。确诊为肺动脉夹层通过胸部X线计算机断层扫描和心脏磁共振成像。该患者拒绝手术干预,并接受了药物治疗的密切随访。初次就诊后将近一年,患者病情稳定,无并发症。结论据我们所知,文献中没有报道类似的随访和未进行手术干预的肺动脉夹层患者的病例。我们回顾了肺动脉夹层患者的病因,病理生理,临床关联,诊断和管理。

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