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作 者:Yuebo Jin Linqing Hou Hao Li Liyun Zhang Yuanhong Peng Naidi Wang Jing He
机构地区:[1]Department of Rheumatology and Immunology,Beijing Key Laboratory for Rheumatism Mechanism and Immune Diagnosis,Peking University People’s Hospital,Beijing 100044,China [2]Department of Rheumatology and Immunology,Linfen Third People’s Hospital,Linfen,Shanxi 041000,China [3]Department of Rheumatology and Immunology,Huabei Petroleum Administration Bureau General Hospital,Cangzhou,Hebei 062552,China [4]Affiliated Hospital of North Sichuan Medical College,Nanchong,Sichuan 637000,China
出 处:《Chinese Medical Journal》2024年第10期1252-1254,共3页中华医学杂志(英文版)
基 金:National Natural Science Foundation of China and by the Beijing Sci-Tech Program(No.Z191100006619114);Natural Science Foundation of China(No.81701607);Peking University People’s Hospital Scientific Research Development Funds(No.RDZH2022-03)
摘 要:To the Editor:Primary Sjögren’s syndrome(pSS)is a multi-systemic autoimmune disease characterized by the exocrine gland(mainly salivary and lacrimal glands)involvement,leading to xerostomia and xerophthalmia.[1]The course of pSS is relatively slow,but patients with pSS had higher risk of overall cancer,including malignant lymphoma(ML).[2]It is widely known that all-cause mortality rates were not increased in pSS patients as compared with healthy controls.Nonetheless,secondary lymphoproliferative disease was an important cause of excess mortality.
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