Literature DB >> 32653407

Thoracic duct embolization in kaposiform lymphangiomatosis.

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.
Copyright © 2020 Society for Vascular Surgery. Published by Elsevier Inc. All rights reserved.

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


  1 in total

1.  Treatment of severe Kaposiform lymphangiomatosis positive for NRAS mutation by MEK inhibition.

Authors:  Guy Chowers; Gadi Abebe-Campino; Hana Golan; Asaf Vivante; Shoshana Greenberger; Michalle Soudack; Galia Barkai; Ilana Fox-Fisher; Dong Li; Michael March; Mark R Battig; Hakon Hakonarson; Denise Adams; Yoav Dori; Adi Dagan
Journal:  Pediatr Res       Date:  2022-03-04       Impact factor: 3.953

  1 in total

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