与斯特奇-韦伯综合征相关的IIb型色素性血管肉瘤严重横纹肌溶解

Bongjin Lee, Hyung Joo Jeong, Yu Hyeon Choi, C. Choi, June-Dong Park
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引用次数: 1

摘要

摘要色素血管增生是一种罕见的综合征,其特征为并发火焰痣(毛细血管畸形)和色素痣。根据目前的研究,PPV的主要病理生理机制是静脉发育不良导致代偿性侧支通道和静脉高压。动脉受累是罕见的。我们在此报告一例伴有SWS的PPV IIb型患者的肾血管性高血压、间歇性跛行和多动脉弥漫性狭窄导致的严重横纹肌溶解。
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Severe Rhabdomyolysis in Phacomatosis Pigmentovascularis Type IIb associated with Sturge-Weber Syndrome
Phacomatosis pigmentovascularis (PPV) is a rare syndrome characterized by concurrent nevus flammeus (capillary malformation) and pigmentary nevus. According to current research, the major pathophysiologic mechanism in PPV is venous dysplasia with resultant compensatory collateral channels and venous hypertension. Arterial involvement is rare. We herein report our experience on renovascular hypertension, intermittent claudication, and severe rhabdomyolysis due to diffuse stenosis of multiple arteries in a patient with PPV type IIb associated with SWS.
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