肺动脉高压是MCTD患者死亡的最常见原因: 相较其他结缔组织病相关肺动脉高压,进展更快,生存时间更短。 治疗 一般认为对糖皮质激素有反应,但未进行MCTD治疗的随机对照试验。 治疗基于其他相关结缔组织病的治疗经验。 诊断要点 对年轻女性出现肺动脉高压、间质性肺病和/或张开扩张的食管,应考虑MCTD。
Mixed connective tissue disease(MCTD) is a rare autoimmune disorder characterized by certain symptoms shared bylupus,scleroderma,polymyositisordermatomyositis, andrheumatoid arthritis. However, in MCTD, the symptoms are not as severe or extensive as with a specific one of these disorders. ...
Mixed connective tissue disease (MCTD) refers to one of a number of conditions in which patients have symptoms or signs that suggest a number of different disease entities within the spectrum of the connective tissue diseases (CTDs). The original MCTD, Sharp syndrome, was associated with a ...
Related to Mixed connective tissue disease: polymyositis, Undifferentiated Connective Tissue Diseasedis·ease (dĭ-zēz′) n. 1. An abnormal condition of a part, organ, or system of an organism resulting from various causes, such as infection, inflammation, environmental factors, or genetic defect...
例句 释义: 全部,混合性结缔组织病,混合结缔组织病 更多例句筛选 1. The authors report a rare case of a female patient diagnosed with mixed connective tissue disease (MCTD). 作者报告一例罕见的一名女患者诊断为混合性结缔组织病(MCTD)。 www.syyxw.com©...
Currently, there is no cure for rheumatoid arthritis, but there are several medications that can ease its symptoms. Most treatments are aimed at remission, where the patient has few or no symptoms of RA. When treatment is started early in the disease process, this can help minimize or slow ...
We are aware of reports on only two chil- dren with this disease. Six children with MCTD have been seen by us, four females and two males between 7 and 19 (mean-13) years of age. All six patients had symptoms or laboratory values sug- gestive of myositis indistinguishable from ...
We are aware of reports on only two chil- dren with this disease. Six children with MCTD have been seen by us, four females and two males between 7 and 19 (mean-13) years of age. All six patients had symptoms or laboratory values sug- gestive of myositis indistinguishable from ...
Mixed Connective Tissue Disease (MCTD) is relatively rare in children and typically presents with constitutional symptoms, rash, Raynaud’s phenomenon, and musculoskeletal symptoms. Cardiac involvement is an infrequent complication of MCTD usually occurr
Mixed connective tissue disease (MCDT) is a rare condition characterised by the presence of high titres of anti-U1 ribonucleoprotein antibodies and selected clinical features of systemic lupus erythematosus, systemic sclerosis and polymyositis/dermatomyositis. Early symptoms are non-specific, including easy...