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Annals of Thoracic Medicine. 2014; 9 (2): 124-126
em Inglês | IMEMR | ID: emr-142000

RESUMO

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.


Assuntos
Humanos , Feminino , Linfangioleiomiomatose , Transplante de Pulmão , Gerenciamento Clínico , Povidona-Iodo , Pleurodese , Sirolimo , Tomografia Computadorizada por Raios X , Radiografia Torácica
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