| Literature DB >> 32653407 |
Jacob J Bundy1, Yoshio Ootaki2, Thomas W McLean3, Brandon S Hays4, Michael Miller5, Trevor Downing5.
Abstract
An 11-year-old girl with kaposiform lymphangiomatosis presented with recurrent chylous pericardial effusions that were refractory to pericardial drainage and medical therapy. Magnetic resonance imaging demonstrated a prominent lymphatic duct with anterior mediastinal extension into the left clavicular region and a region of high signal that was favored to represent a low-flow lymphatic malformation. The patient underwent direct access thoracic duct lymphangiography with thoracic duct embolization and sclerotherapy of the large left-sided neck and pericardial lymphatic malformation. After the procedure, her pericardial effusions resolved, and she has remained asymptomatic for 15 months.Entities:
Keywords: Lymphatic malformation; Sclerotherapy; Thoracic duct embolization; Vascular anomaly
Mesh:
Year: 2020 PMID: 32653407 DOI: 10.1016/j.jvsv.2020.03.013
Source DB: PubMed Journal: J Vasc Surg Venous Lymphat Disord