Meier Mark A, Rubenfire Melvyn
Division of Cardiology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Clin Cardiol. 2006 Mar;29(3):103-6. doi: 10.1002/clc.4960290304.
Severe thromboembolic pulmonary hypertension is an infrequent but potentially fatal complication of effort thrombosis (Paget-Schroetter syndrome) of the upper extremity. It has been sporadically reported in the literature, but in most cases has affected young, otherwise healthy athletes. Because this syndrome has been rarely described, it is likely underdiagnosed, and optimal evaluation and treatment has not been established. We describe three young athletic persons who developed thrombosis of the subclavian vein after repetitive motion of the upper extremity, and in whom life-threatening pulmonary hypertension resulted from acute and chronic pulmonary emboli. We then review the mechanism, clinical presentation, diagnosis, and available therapeutic modalities.
严重血栓栓塞性肺动脉高压是上肢劳力性血栓形成(佩吉特-施罗特综合征)的一种罕见但可能致命的并发症。文献中曾有零星报道,但大多数病例发生在年轻且原本健康的运动员身上。由于该综合征很少被描述,很可能存在诊断不足的情况,且尚未确立最佳的评估和治疗方法。我们描述了三名年轻运动员,他们在上肢反复运动后发生了锁骨下静脉血栓形成,并因急性和慢性肺栓塞导致了危及生命的肺动脉高压。然后我们回顾了其发病机制、临床表现、诊断及现有的治疗方式。