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作 者:Ling Chen Ting Ma Liang Wang Lixin Wang Minmin Li Rong Zhu
机构地区:[1]The Huai'an Clinical College of Xuzhou Medical University,Huai'an,Jiangsu 223300,China [2]Department of Respiratory Medicine,Huai'an First People's Hospital,Huai'an,Jiangsu 223300,China
出 处:《The Journal of Biomedical Research》2022年第2期141-144,共4页生物医学研究杂志(英文版)
摘 要:Takayasu arteritis (TA) is a chronic, nonspecific inflammatory disease of large and medium-sized vessels that primarily involves the aorta and its branches. TA involving the pulmonary arteries has a prevalence ranging from 14% to 86%, which can lead to pulmonary hypertension, a progressive increase in pulmonary artery pressure, and eventually death from right heart failure. The presentation of pulmonary arteritis (PA) is very nonspecific, with a reported misdiagnosis rate of up to 60% and a diagnosis time ranging from 1 month to more than 10 years. The clinical manifestation of pleural effusion is very rare in both TA and PA cases. Based on our literature review, this is the 6th reported case of TA with pleural effusion, and the specific mechanism of TA with pleural effusion is still unclear. The characteristics of this case and the previously reported cases are summarized in this article to improve the understanding of TA and PA and reduce the misdiagnosis rate.
关 键 词:Takayasu arteritis pulmonary arteritis pleural effusion case report literature review
分 类 号:R543.5[医药卫生—心血管疾病]
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