Severe Pulmonary Hypertension Secondary to Concomitant Mitral Stenosis with Veno-occlusive Disease in the Context of Systemic Sclerosis: Importance of Careful and Comprehensive Assessment

Mina Boutgourine, H. Nabawi, B. Maatof, Mohammed El-Jamili, Saloua El-Karimi, M. Hattaoui
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Abstract

Pulmonary Arterial Hypertension (PAH) is a clinical syndrome consisting of physiologic/ hemodynamic criteria that are a consequence of several etiologies. Confirmation of pulmonary hypertension is based on right heart catheterization. Pulmonary hypertension is a devastating condition that can lead to considerable morbidity and premature mortality. In the last few decades, significant advancement in the pharmacotherapy of pulmonary hypertension has resulted from better understanding of the complex pathogenesis and pathophysiology of this dreaded disease. Despite these accomplishments, pharmacotherapy of pulmonary hypertension is still far from perfect, and the mortality in this modern treatment era is still unacceptably high. We report a complex clinical presentation characterized by severe pulmonary hypertension secondary to concomitant mitral stenosis with veno-occlusive disease in the context of systemic sclerosis. Our case highlights the importance of a systematic and comprehensive diagnostic approach to avoid missing an underlying pathology.
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系统性硬化症并发二尖瓣狭窄伴静脉闭塞性疾病的严重肺动脉高压:仔细和全面评估的重要性
肺动脉高压(PAH)是一种由多种病因引起的生理/血流动力学标准组成的临床综合征。肺动脉高压的确认是基于右心导管检查。肺动脉高压是一种毁灭性的疾病,可导致相当高的发病率和过早死亡。在过去的几十年里,肺动脉高压的药物治疗取得了重大进展,这是由于对这一可怕疾病的复杂发病机制和病理生理有了更好的了解。尽管取得了这些成就,但肺动脉高压的药物治疗还远远不够完善,在这个现代治疗时代,死亡率仍然高得令人无法接受。我们报告了一个复杂的临床表现,其特点是在系统性硬化症的背景下,伴有二尖瓣狭窄和静脉闭塞性疾病的严重肺动脉高压。我们的病例强调了系统和全面的诊断方法的重要性,以避免遗漏潜在的病理。
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