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脉冲地塞米松和来那度胺成功治疗儿童难治性脉络丛朗格汉斯细胞组织细胞增多症

Successful Treatment of Refractory Langerhans Cell Histiocytosis of the Choroid Plexus in a Child With Pulse Dexamethasone and Lenalidomide.

作者信息

Uppuluri Ramya, Ramachandrakurup Sreejith, Balaji Ravikanth, Subburaj Divya, Bakane Atish, Raj Revathi

机构信息

Departments of *Pediatric Hematology, Oncology and BMT †Radiology, Apollo Specialty Hospital, Chennai, Tamil Nadu, India.

出版信息

J Pediatr Hematol Oncol. 2017 Mar;39(2):e74-e78. doi: 10.1097/MPH.0000000000000735.

Abstract

Refractory/relapsed Langerhans cell histiocytosis (LCH) has a difficult course with a guarded prognosis. Salvage treatments available are both expensive and highly toxic. On the basis of the pathophysiology of LCH, we used a novel protocol including pulse dexamethasone and lenalidomide in a child with refractory LCH involving the choroid plexus, which resulted in durable remission with minimal toxicity. The protocol was extrapolated from the FIRST trial for patients with multiple myeloma. We present the clinical course, treatment protocol, and outcome in this child, who is at present disease free and in remission 18 months posttreatment.

摘要

难治性/复发性朗格汉斯细胞组织细胞增多症(LCH)病程艰难,预后不佳。现有的挽救性治疗既昂贵又毒性极大。基于LCH的病理生理学,我们对一名患有累及脉络丛的难治性LCH的儿童采用了一种新方案,包括脉冲地塞米松和来那度胺,该方案使患儿获得了持久缓解且毒性极小。该方案是从针对多发性骨髓瘤患者的FIRST试验中推断出来的。我们在此介绍该患儿的临床病程、治疗方案及结果,该患儿目前已无病生存,治疗后18个月处于缓解状态。

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