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环孢素和霉酚酸酯治疗一名难治性伊文氏综合征患儿的疗效

Effectiveness of cyclosporine and mycophenolate mofetil in a child with refractory evans syndrome.

作者信息

Farruggia Piero, Macaluso Alessandra, Tropia Serena, Genova Selene, Paolicchi Olivia, Di Marco Floriana, D'Angelo Paolo

机构信息

Pediatric Hematology and Oncology Unit, G. Di Cristina Children's Hospital, Palermo;

出版信息

Pediatr Rep. 2011 Jun 16;3(2):e15. doi: 10.4081/pr.2011.e15.

Abstract

Evans Syndrome is a rare autoimmune disease consisting of hemolytic anemia, thrombocytopenia and/or neutropenia. It may be associated with other autoimmune or lymphoproliferative diseases. Its course can be extremely serious and, rarely, even life-threatening; thus it represents a excellent treatment challenge for the pediatric hematologist. First line treatment consists of steroids and/or immunoglobulin; further therapy with rituximab, vincristine, cyclophosphamide and other immunosuppressive drugs can be considered in unresponsive patients. We describe a baby with refractory Evans Syndrome that was cured by prolonged administration of mycophenolate mofetil and remained disease-free for 4 years after the discontinuation of treatment.

摘要

伊文氏综合征是一种罕见的自身免疫性疾病,包括溶血性贫血、血小板减少和/或中性粒细胞减少。它可能与其他自身免疫性或淋巴增殖性疾病有关。其病程可能极其严重,极少数情况下甚至会危及生命;因此,对于儿科血液科医生来说,它是一个极具挑战性的治疗难题。一线治疗包括使用类固醇和/或免疫球蛋白;对于无反应的患者,可以考虑使用利妥昔单抗、长春新碱、环磷酰胺和其他免疫抑制药物进行进一步治疗。我们描述了一名患有难治性伊文氏综合征的婴儿,通过长期服用霉酚酸酯治愈,停药后4年无疾病复发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d391/3133497/ea83b26dca61/pr-2011-2-e15-g001.jpg

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