医学
间质性肺病
结缔组织病
贝里穆马布
寻常性间质性肺炎
纤维化
病理
硬皮病(真菌)
肺
结缔组织
肺纤维化
特发性肺纤维化
疾病
免疫学
内科学
自身免疫性疾病
抗体
B细胞
B细胞激活因子
接种
作者
John Mwangi,Chase Litteken,Ramya Gorthi,Yeswanth Attoti,Rama Atluri
出处
期刊:Cureus
[Cureus, Inc.]
日期:2021-11-02
被引量:6
摘要
Interstitial lung disease or ILD can be described as inflammation, fibrosis, or scarring of the lung’s interstitial, resulting in dyspnea. ILD represents a group of heterogeneous parenchymal lung disorders with complex pathophysiology, differentiated by the clinical and radiological patterns. ILD is one of the most serious pulmonary complications associated with connective tissue diseases (CTDs), resulting in significant morbidity and mortality. Nonspecific interstitial pneumonia is the most common morphological and pathological pattern of ILD seen in CTDs. There are limitations in the therapeutic options resulting in significant morbidity. Certain biologic therapies are being evaluated for the various forms of ILD. The ILD, in this case, is associated with systemic lupus erythematosus (SLE) and scleroderma overlap that was effectively treated with belimumab, a recombinant monoclonal antibody against the B-cell activating factor (B-lymphocyte stimulator).
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