CTD-PAH的早期诊断困难,且患者往往病程进展迅速,导致右心功能逐渐恶化。尽管肺动脉高压的治疗已有多种药物可供选择,但针对CTD-PAH的临床数据仍然稀缺,治疗策略亟需优化。 2024年3月,Journal of Thoracic Disease杂志发表了一篇题为《Clini...
未分化结缔组织病是一种罕见的自身免疫性疾病,会导致全身多个器官受损,表现为疲劳、关节疼痛、皮疹等症状。治疗主要是控制症状和减轻炎症。 中文名: 未分化结缔组织病 英文名: Undifferentiated connective tissue disease 相关科室: 肿瘤内科、肿瘤外科、肿瘤康复科、肿瘤综合科、肿瘤妇科、肿瘤科、肿瘤外科 相关手术:...
小儿混合性结缔组织病是一种罕见的自身免疫性疾病,表现为关节疼痛、皮疹、发热等症状。治疗主要包括抗炎药物和免疫抑制剂。 中文名: 小儿混合性结缔组织病 英文名: Juvenile Mixed Connective Tissue Disease 相关科室: 小儿风湿免疫科,小儿心内科,小儿心外科,小儿神经内科,小儿呼吸科,小儿血液科,小儿消化科 相关手术...
PurposeUsual interstitial pneumonia (UIP) pattern of interstitial lung disease (ILD) can have varied etiology, with connective tissue disease (CTD) being a common known cause. The anterior upper lobe (AUL) sign, exuberant honeycombing (EHC), and straight edge (SE) sign are recently described ...
SDScleroderma(connective tissue disease) SDSnow Day SDShinedown(band) SDScience Data SDSalvia Divinorum(entheogenic spice) SDService Description SDSelf-Destruct SDSicherheitsdienst(German Security Department, WWII) SDShipping Date SDSystem Description ...
However, there is evidence that glucocorticoids influence the expression of such growth factors as vascular endothelial growth factor (VEGF), transforming growth factor-beta1 (TGF-beta1), and connective tissue growth factor (CTGF), which are known to influence the development or progression of renal...
Journal of Clinical Medicine Article In Systemic Sclerosis, a Unique Long Non Coding RNA Regulates Genes and Pathways Involved in the Three Main Features of the Disease (Vasculopathy, Fibrosis and Autoimmunity) and in Carcinogenesis Marzia Dolcino 1, Elisa Tinazzi 1, Antonio Puccetti 2,† and ...
October 01, 2023 [MEDLINE Abstract] Outcomes of aortic valve-sparing root replacement with cusp repair in connective tissue disease. October 01, 2023 [MEDLINE Abstract] Rationale and design of the ARAMIS trial: Anakinra versus placebo, a double blind randomized controlled trial for the treatment of...
excess of connective tissue and myxomatous degeneration, also named Barlow disease or thin elongated leaflets and chordae with fibroelastic and acid mucopolysaccharide deficiency [3]. Many patients with MVP show few clinical symptoms, if any. Nonetheless, MVP is the most common cause of isolate...
- 《Annals of the Rheumatic Diseases A Journal of Clinical Rheumatology & Connective Tissue Research》 被引量: 15发表: 2013年 Autoimmune disease risk variant of IFIH1 is associated with increased sensitivity to IFN-alpha and serologic autoimmunity in lupus patients Increased IFN-alpha signaling is ...