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作 者:Shuang Liu Chen Li Ming-Wei Tang Wen-Shuai Xu Ke-Qi Chen Xin Sui Xin-Lun Tian Kai-Feng Xu
机构地区:[1]School of Clinical Medicine,Chinese Academy of Medical Sciences&Peking Union Medical College,Beijing 100005,China [2]Department of Traditional Chinese Medicine,Chinese Academy of Medical Sciences&Peking Union Medical College Hospital,Beijing 100730,China [3]Department of Respiratory and Critical Care Medicine,Chinese Academy of Medical Sciences&Peking Union Medical College Hospital,Beijing 100730,China [4]Department of Radiology,Chinese Academy of Medical Sciences&Peking Union Medical College Hospital,Beijing 100730,China
出 处:《Chinese Medical Journal》2019年第19期2378-2379,共2页中华医学杂志(英文版)
摘 要:To the Editor:Lymphangioleiomyomatosis(LAM)is a rare multi-systemic disease that predominantly affects women and is associated with cystic lung destruction,chylous fluid accumulation,and abdominal tumors.[1]The lung function of LAM patients declines at two to four or more times faster rates than the typical age-related decline.Although the mammalian target of rapamycin(mTOR)inhibitor has shown certain benefits for patients with LAM,treatment options remain limited.[2]Synovitis,acne,pustulosis,hyperostosis,and osteitis(SAPHO)syndrome is a spectrum of heterogeneous diseases characterized by osteoarticular and dermatological manifestations.Nonsteroidal anti-inflammatory drugs(NSAIDs),disease-modifying anti-rheumatic drugs,bisphosphonates,and intra-articular steroids are frequently prescribed but are often insufficient to control disease progression.
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