Abstract |
Primary immune thrombocytopenia ( ITP) is a complex autoimmune disorder in which the patient's immune system reacts with platelet autoantigens resulting in immune-mediated platelet destruction and/or suppression of platelet production. Corticosteroids can induce sustained remission rates in 50% to 75% of patients with active ITP. For these patients who are unresponsive to glucocorticoids, or relapsed after an initial response, multiple second-line treatment modalities can be chosen. However, how to make an optimal therapeutic strategy for a specific patient still remains a major challenge. As the pathogenetic heterogeneity of the ITP is increasingly identified, pathogenesis-oriented approach might offer an opportunity to improve the outcome of corticosteroid-resistant or relapsed ITP.
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Authors | Xin-Guang Liu, Ming Hou |
Journal | Open medicine (Warsaw, Poland)
(Open Med (Wars))
Vol. 11
Issue 1
Pg. 97-100
( 2016)
ISSN: 2391-5463 [Print] Poland |
PMID | 28352775
(Publication Type: Journal Article)
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