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淋巴增生性疾病中的免疫性血小板减少症。

Immune thrombocytopenia in lymphoproliferative disorders.

机构信息

Division of Hematology, Department of Cell Therapy and Hematology, San Bortolo Hospital, Via Rodolfi 37, Vicenza 36100, Italy.

出版信息

Hematol Oncol Clin North Am. 2009 Dec;23(6):1261-74. doi: 10.1016/j.hoc.2009.08.006.

Abstract

Lymphoproliferative disorders are recognized as a common cause of secondary immune thrombocytopenia (ITP). The mechanisms involved in the pathogenesis of ITP associated with lymphoproliferative disorders are heterogeneous and often linked to the presence and activity of the malignant clone. A better understanding of the responsible mechanisms leading to ITP in each disease may allow for targeted treatment decisions, avoiding unwarranted immunosuppression and bleeding complications.

摘要

淋巴增殖性疾病被认为是继发性免疫性血小板减少症(ITP)的常见原因。与淋巴增殖性疾病相关的 ITP 的发病机制中涉及的机制是异质的,并且通常与恶性克隆的存在和活性有关。更好地了解导致每种疾病 ITP 的相关机制可能有助于做出针对性的治疗决策,避免不必要的免疫抑制和出血并发症。

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