Treatment of Kimura Disease With Intravenous Immunoglobulin

被引：19

作者：

Hernandez-Bautista, Victor ^{[1
]}

Antonio Yamazaki-Nakashimada, Marco ^{[1
]}

Vazquez-Garcia, Ruben ^{[1
]}

Stamatelos-Albarran, Daniela ^{[1
]}

Carrasco-Daza, Daniel ^{[2
]}

Luisa Rodriguez-Lozano, Ana ^{[1
]}

机构：

[1] Inst Nacl Pediat, Dept Clin Immunol, Mexico City 04530, DF, Mexico

[2] Inst Nacl Pediat, Dept Pathol, Mexico City 04530, DF, Mexico

来源：

PEDIATRICS | 2011年 / 128卷 / 06期

关键词：

intravenous immunoglobulin; Kimura disease; corticosteroids; children; ANGIOLYMPHOID HYPERPLASIA; SPONTANEOUS REGRESSION; IGE PRODUCTION; EOSINOPHILIA; TUMOR;

D O I：

10.1542/peds.2010-1623

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Kimura disease is an uncommon chronic inflammatory condition of unknown etiology and is characterized by painless subcutaneous nodules, usually affecting the head and neck, eosinophilia, and markedly elevated immunoglobulin E levels. Several reports have described the main modalities of treatment; both corticosteroids and surgery have provided good results, but occasionally corticosteroids cannot be tapered as the disease flares up. We report here the case of an 8-year-old boy diagnosed with Kimura disease who was successfully treated with 1 dose of intravenous immunoglobulin as a steroid-sparing agent. Pediatrics 2011; 128:e1633-e1635

引用

页码：E1633 / E1635

页数：3

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