逆行胸导管入路栓塞患有先天性心脏病和丛状胸导管变异的儿童淋巴畸形。

Lymphology Pub Date : 2024-01-01
A Saferite, B J Blair, A M Price, K A Fox, M D Seckeler
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引用次数: 0

摘要

先天性心脏病患者非典型血管的生理后遗症可能导致潜在的致命淋巴并发症,尤其是在心脏矫正手术后。经导管栓塞胸导管或淋巴络脉可降低这些患者的发病率和死亡率。虽然经导管栓塞术通常通过前向途径经腹进行,但在不可行的情况下(包括胸导管解剖结构的罕见变异),逆行栓塞术可能更为可取。我们介绍了一例先天性心脏手术后出现严重乳糜胸的患儿,该患儿被发现患有胸腔淋巴畸形和丛状胸导管变异,并成功接受了畸形栓塞术。
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Retrograde Thoracic Duct Access for Embolization of Lymphatic Malformations in a Child with Congenital Heart Disease and a Plexiform Thoracic Duct Variant.

The physiologic sequelae of the atypical vasculature in patients with congenital heart disease can result in potentially fatal lymphatic complications, especially after corrective cardiac surgery. Transcatheter embolization of the thoracic duct or lymphatic collaterals can reduce morbidity and mortality in these patients. While typically performed transabdominally via an antegrade approach, retrograde embolization may be preferable in cases where this is not feasible, including in rare variants of thoracic duct anatomy. We present a case of a child with severe chylothorax after congenital cardiac surgery who was found to have thoracic lymphatic malformations and a plexiform thoracic duct variant who underwent successful embolization of the malformations.

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