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摘要:
Chronic immune thrombocytopenic purpura (ITP) is a condition based on an immune-mediated mechanism that determines the premature hyperdestruction of the thrombocytes in peripheral blood, as well as their deficient synthesis at the level of the bone marrow. The chronic immune purpura could be of primary, idiopathic cause, as well as of secondary cause, occurring in the context of other pathologies. The characteristic of the primary form of the disease is the presence of isolated thrombocytopenia, defined by a platelet count under 100,000/mm3 in peripheral blood, in the absence of supporting causes for thrombocytopenia. In the secondary form of the disease, the decreased platelet count is due to associated pathologies involving an immune mechanism, responsible for the occurrence of thrombocytopenia. This study aims to emphasize the involvement of autoimmune diseases, such as systemic lupus erythematosus (SLE), dermatomyositis, rheumatoid polyarthritis or antiphospholipid syndrome in the pathogenesis of secondary thrombocytopenia. Furthermore, the study was conducted on a sample of 40 patients, divided into two groups: The first group comprising asymptomatic patients diagnosed with thrombocytopenia following routine tests, and the second group comprising patients with hemorrhagiparous symptomatology (petechiae, ecchymoses, epistaxis, gingivorrhagia), who went to the doctor in order to determine the etiology of the hemorrhagiparous syndrome. The average value of the thrombocytopenia of the patients included in the study was of 60.20 ± 19.75 × 103/μL. Laboratory investigations performed in order to establish the etiology of thrombocytopenia showed that 80% of patients presented positive antiplatelet antibodies. Moreover, 20% of the patients in the study showed positive anti-double-stranded DNA, 20% were identified with IgG anticardiolipin antibodies, while antinuclear antibodies were present in 10% of the patients.
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篇名 Involvement of Autoimmune Diseases in the Pathogenesis of Chronic Immune Thrombocytopenic Purpura
来源期刊 生物医学工程(英文) 学科 医学
关键词 THROMBOCYTOPENIC PURPURA ANTIPLATELET Antibodies Systemic LUPUS ERYTHEMATOSUS ANTIPHOSPHOLIPID Syndrome
年,卷(期) swyxgcyw_2015,(3) 所属期刊栏目
研究方向 页码范围 142-148
页数 7页 分类号 R5
字数 语种
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研究主题发展历程
节点文献
THROMBOCYTOPENIC
PURPURA
ANTIPLATELET
Antibodies
Systemic
LUPUS
ERYTHEMATOSUS
ANTIPHOSPHOLIPID
Syndrome
研究起点
研究来源
研究分支
研究去脉
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相关学者/机构
期刊影响力
生物医学工程(英文)
月刊
1937-6871
武汉市江夏区汤逊湖北路38号光谷总部空间
出版文献量(篇)
252
总下载数(次)
1
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