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首页> 外文期刊>Heart, lung & circulation >Massive pulmonary embolism and acute limb ischaemia in a patient of hereditary spherocytosis and patent foramen ovale.
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Massive pulmonary embolism and acute limb ischaemia in a patient of hereditary spherocytosis and patent foramen ovale.

机译:遗传性球囊增多和卵圆孔未闭的患者发生大规模肺栓塞和急性肢体缺血。

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摘要

Paradoxical embolism accounts for 2% of patients who present with acute arterial embolism of extremities. We report a case of a 41 year-old male with hereditary spherocytosis who presented to the emergency department with acute limb ischaemia and pulmonary embolism. On further evaluation, he was found to have patent foramen ovale (PFO) and deep vein thrombosis (DVT), leading to paradoxical embolism. The purpose of this report is to emphasise that in a patient presenting with acute limb ischaemia without an obvious systemic arterial embolic source, an evaluation for a right-to-left shunting lesion, especially PFO, should be performed.
机译:矛盾性栓塞占四肢急性动脉栓塞的2%。我们报告了一例41岁的男性,患有遗传性球血红细胞增多症,他因急性肢体缺血和肺栓塞而向急诊科就诊。经过进一步评估,他被发现患有卵圆孔未闭(PFO)和深静脉血栓形成(DVT),从而导致矛盾性栓塞。本报告的目的是强调,对于没有明显全身性动脉栓塞源的急性肢体缺血患者,应进行从右向左分流病变,尤其是PFO的评估。

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