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作 者:Tamás Erdélyi Aniko Bohács Krisztina Vincze Zsuzsanna Kováts Veronika Sárosi András Sinkovicz Gyorgy Balázs Veronika Müller
机构地区:[1]Department of Pulmonology,Semmelweis University,Budapest,Hungary [2]1st Department of Internal Medicine,Medical School,University of Pécs,Pécs,Hungary [3]Department of Radiology,The Heart and Vascular Center,Semmelweis University,Budapest,Hungary
出 处:《Case Reports in Clinical Medicine》2014年第12期636-638,共3页临床医学病理报告(英文)
摘 要:Lymphangioleiomyomatosis (LAM) is a rare disease that affects women, especially in child-bearing age. Clinical manifestations include angiomyolipoma, pneumothorax, chylothorax, cystic changes of lungs and progressive pulmonary failure. In this article, we report a case of lung transplantation (LuTX) for end stage pulmonary LAM and the treatment of angiomyolipoma showing growth after LuTX resulting in complete remission with combination therapy of everolimus and tacrolimus.Lymphangioleiomyomatosis (LAM) is a rare disease that affects women, especially in child-bearing age. Clinical manifestations include angiomyolipoma, pneumothorax, chylothorax, cystic changes of lungs and progressive pulmonary failure. In this article, we report a case of lung transplantation (LuTX) for end stage pulmonary LAM and the treatment of angiomyolipoma showing growth after LuTX resulting in complete remission with combination therapy of everolimus and tacrolimus.
关 键 词:LYMPHANGIOLEIOMYOMATOSIS EVEROLIMUS ANGIOMYOLIPOMA Lung Transplant
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