白塞氏病的心内血栓:美国罕见病例

Swapna Gopathi , Ryan T. Hurt , Juan Guardiola
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引用次数: 6

摘要

白塞氏病是一种罕见的系统性疾病,与潜在的血管炎有关。大多数双相障碍病例发生在亚洲和北美,病例很少。患者通常表现为口腔溃疡,并有许多其他临床表现,包括生殖器病变、皮肤病变(毛囊炎、结节性红斑和痤疮)和葡萄膜炎。BD的咯血和咳嗽可能是肺部累及包括肺动脉动脉瘤(PAA)的征兆。心内血栓是另一种罕见的BD,但如果在影像学上发现右心肿块,则应怀疑。我们提出一个怀疑BD的病例,他表现为咯血,并被诊断为PAA和心内血栓。他的口疮直到后来因咯血住院才被诊断出来。由于相关的高死亡率,临床医生应注意双相障碍的不寻常表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intracardiac thrombus in Behcet’s disease: A rare case in the United States

Behcet’s disease is a rare systemic disorder which is associated with an underlying vasculitis. Most cases of BD occur in Asia and North American cases are rare. Patients often present with aphthous ulcers and have a number of other clinical findings including genital lesions, skin lesions (folliculitis, erythema nodosum, and acne), and uveitis. Hemoptysis and cough in BD may be a sign of pulmonary involvement with include pulmonary artery aneurysms (PAA). Intracardiac thrombus is another rare occurrence in BD but should be suspected if there is a right heart mass detected on imaging. We present a case of suspected BD who presented with hemoptysis and was diagnosed with PAA and intracardiac thrombus. His aphthous ulcers were not diagnoses until subsequent hospitalization for hemoptysis. Clinicians should be aware of unusual presentations of BD because of the associated high mortality.

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