肉样瘤病、结核病和治疗肉芽肿性炎症的临床难题

K. Luthra, Jyoti Singh
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引用次数: 0

摘要

肉样瘤病的表现多种多样,包括与肺结核(TB)重叠。肉样瘤病可以先于结核病发生,也可以与结核病并存。某些特征如空洞性合并症、胸腔积液和树突状结节高度提示活动性肺结核。微小结节的淋巴管周围分布和离散淋巴结则提示肉样瘤病。鉴别这两种疾病的并存是至关重要的,因为这两种疾病的治疗都是自相矛盾的:肉样瘤病的免疫抑制和结核病的抗结核治疗。在某些情况下,结核病会使用免疫抑制,如结核性脑膜炎、眼结核和结核性心包炎。本文旨在让人们更好地了解肉芽肿性炎症治疗过程中面临的临床困境,并对肉芽肿病与结核病重叠的现有文献进行补充。
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Sarcoidosis, tuberculosis, and the clinical dilemma of treating granulomatous inflammation
Sarcoidosis can have a varied presentation, including an overlap with tuberculosis (TB). It can precede or coexist with TB. Certain features such as cavitary consolidation, pleural effusion, and tree-in-bud nodules are highly suggestive of active TB. The perilymphatic distribution of micronodules and discrete lymph nodes are features suggestive of sarcoidosis. Identifying the coexistence of the diseases is essential, as the treatment of either disease is a paradox: immunosuppression in sarcoidosis and antitubercular therapy in TB. There are certain conditions in which immunosuppression is used in TB, e.g., tubercular meningitis, ocular TB, and TB pericarditis. This article aims to provide a better understanding of the clinical dilemma faced during the treatment of granulomatous inflammation and adds to the existing literature regarding the overlap between sarcoidosis and TB.
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