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Successful management of bilateral refractory chylothorax after double lung transplantation for lymphangioleiomyomatosis

Lymphangioleiomyomatosis (LAM) is a rare disease that leads to airways and lymphatic channels obstruction due to abnormal smooth muscle proliferation. It presents with dyspnea, pneumothorax or chylothorax. Lung transplantation (LT) has emerged as a valuable therapeutic option with limited reports. W...

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Autores principales: Hussein, Mohammed, Aljehani, Yasser M., Nizami, Imran, Saleh, Waleed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4005159/
https://www.ncbi.nlm.nih.gov/pubmed/24791177
http://dx.doi.org/10.4103/1817-1737.128862
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author Hussein, Mohammed
Aljehani, Yasser M.
Nizami, Imran
Saleh, Waleed
author_facet Hussein, Mohammed
Aljehani, Yasser M.
Nizami, Imran
Saleh, Waleed
author_sort Hussein, Mohammed
collection PubMed
description Lymphangioleiomyomatosis (LAM) is a rare disease that leads to airways and lymphatic channels obstruction due to abnormal smooth muscle proliferation. It presents with dyspnea, pneumothorax or chylothorax. Lung transplantation (LT) has emerged as a valuable therapeutic option with limited reports. We report a case of LAM that underwent double LT and complicated by refractory bilateral chylothorax which was managed successfully by povidone-iodine pleurodesis and the addition of sirolimus to the post-transplantation immunosuppressive therapy. The patient has no recurrence with 24 months follow-up.
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spelling pubmed-40051592014-05-01 Successful management of bilateral refractory chylothorax after double lung transplantation for lymphangioleiomyomatosis Hussein, Mohammed Aljehani, Yasser M. Nizami, Imran Saleh, Waleed Ann Thorac Med Case Report Lymphangioleiomyomatosis (LAM) is a rare disease that leads to airways and lymphatic channels obstruction due to abnormal smooth muscle proliferation. It presents with dyspnea, pneumothorax or chylothorax. Lung transplantation (LT) has emerged as a valuable therapeutic option with limited reports. We report a case of LAM that underwent double LT and complicated by refractory bilateral chylothorax which was managed successfully by povidone-iodine pleurodesis and the addition of sirolimus to the post-transplantation immunosuppressive therapy. The patient has no recurrence with 24 months follow-up. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4005159/ /pubmed/24791177 http://dx.doi.org/10.4103/1817-1737.128862 Text en Copyright: © Annals of Thoracic Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Hussein, Mohammed
Aljehani, Yasser M.
Nizami, Imran
Saleh, Waleed
Successful management of bilateral refractory chylothorax after double lung transplantation for lymphangioleiomyomatosis
title Successful management of bilateral refractory chylothorax after double lung transplantation for lymphangioleiomyomatosis
title_full Successful management of bilateral refractory chylothorax after double lung transplantation for lymphangioleiomyomatosis
title_fullStr Successful management of bilateral refractory chylothorax after double lung transplantation for lymphangioleiomyomatosis
title_full_unstemmed Successful management of bilateral refractory chylothorax after double lung transplantation for lymphangioleiomyomatosis
title_short Successful management of bilateral refractory chylothorax after double lung transplantation for lymphangioleiomyomatosis
title_sort successful management of bilateral refractory chylothorax after double lung transplantation for lymphangioleiomyomatosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4005159/
https://www.ncbi.nlm.nih.gov/pubmed/24791177
http://dx.doi.org/10.4103/1817-1737.128862
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