英夫利昔单抗治疗特发性难治性儿童坏疽性脓皮病(PG)。

IF 5.3 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Biologics : Targets & Therapy Pub Date : 2019-05-27 eCollection Date: 2019-01-01 DOI:10.2147/BTT.S203753
Farhad Salehzadeh, Yusef Mohammadikebar, Afsaneh Enteshary, Omid Ghanbarpour, Mehrdad Mirzarahimi
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引用次数: 0

摘要

我们报告一个顽固性特发性儿童坏疽性脓皮病的病例在一个年轻的男孩谁遭受了这种疾病,因为3岁。在不同的细胞毒和类固醇治疗组合下,他有不良反应和间歇性复发。虽然关于英夫利昔单抗用于生物学和儿童坏疽性脓皮病的信息不多,但最终我们决定在该患者中使用英夫利昔单抗。英夫利昔单抗表现出显著的疗效,并在2年的随访中完全恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Infliximab in treatment of idiopathic refractory childhood pyoderma gangrenosum (PG).

We report a case of refractory idiopathic childhood pyoderma gangrenosum in a young boy who had suffered from this disease since 3 years of age. He had unfavorable responses and intermittent relapses under different combinations of cytotoxic and steroid therapies. Although there was not much information available about infliximab use for biologic and childhood pyoderma gangrenosum, eventually we decided to use infliximab in this patient. Infliximab showed a dramatic response and resulted in full recovery during 2 years' follow-up.

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来源期刊
Biologics : Targets & Therapy
Biologics : Targets & Therapy MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
8.30
自引率
0.00%
发文量
22
审稿时长
16 weeks
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