Systemic Lupus Erythematosus and Antiphospholipid Antibody Syndrome

被引:13
作者
Kokosi, Maria [1 ,2 ,3 ]
Lams, Boris [3 ]
Agarwal, Sangita [3 ,4 ]
机构
[1] Royal Brompton Hosp, Interstitial Lung Dis Unit, Sydney St, London SW3 6NP, England
[2] Harefield NHS Fdn Trust, Sydney St, London SW3 6NP, England
[3] Guys & St Thomas Hosp NHS Fdn Trust, Interstitial Lung Dis Unit, London SE1 9RT, England
[4] Guys & St Thomas Hosp NHS Fdn Trust, Rheumatol Dept, London SE1 9RT, England
关键词
Systemic lupus erythematosus; Antiphospholipid syndrome; Interstitial lung disease; Pulmonary hypertension; Airways; Pleuritis; Alveolar hemorrhage; Pulmonary embolism; PULMONARY ARTERIAL-HYPERTENSION; SHRINKING LUNG SYNDROME; DIFFUSE ALVEOLAR HEMORRHAGE; CONNECTIVE-TISSUE DISEASES; LONG-TERM; VENOUS THROMBOEMBOLISM; ANTICARDIOLIPIN ANTIBODIES; VASODILATOR THERAPY; PROGNOSTIC-FACTORS; PLEURAL EFFUSIONS;
D O I
10.1016/j.ccm.2019.06.001
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Systemic lupus erythematosus (SLE) is a systemic inflammatory disease, characterized by an antibody response to nucleic antigens and involvement of any organ system. Pulmonary manifestations are frequent and include pleuritis, acute lupus pneumonitis, chronic interstitial lung disease, alveolar hemorrhage, shrinking lung syndrome, airway disease, pulmonary hypertension (PH), and thromboembolic disease. The antiphospholipid antibody syndrome (APLAS) is a systemic autoimmune disorder where different prothrombotic factors interact to induce arterial and venous thrombosis. The most common pulmonary manifestations are pulmonary thromboembolism and PH. This review will focus on the clinical presentation, diagnosis, and management of the SLE- and APLAS-associated pulmonary conditions.
引用
收藏
页码:519 / +
页数:12
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