中国麻风皮肤病杂志 ›› 2021, Vol. 37 ›› Issue (12): 793-794.doi: 10.12144/zgmfskin202112793

• 病例报告 • 上一篇    下一篇

太藤丘疹性红皮病一例

王绍瑜1,何俊辰2,张宇2,马秀亮2,张理涛2   

  1. 1天津中医药大学研究生院，天津，301617；2天津市中医药研究院附属医院，天津，300120
  • 出版日期:2021-12-15 发布日期:2021-09-29
  • 通讯作者: 张理涛，E-mail: zhanglitao@medmail.com.cn

Papuloerythroderma of Ofuji: a case report

WANG Shaoyu1, HE Junchen2, ZHANG Yu2, MA Xiuliang2, ZHANG Litao2   

  1. 1 Tianjin University of Traditional Chinese Medicine Graduate School, Tianjin 301617, China;
    2 Tianjin Academy of Traditional Chinese Medicine Affiliated Hospital, Tianjin 300120, China 
  • Online:2021-12-15 Published:2021-09-29
  • Contact: ZHANG Litao, E-mail: zhanglitao@medmail.com.cn

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摘要： 太藤丘疹红皮病是一种较为罕见的皮肤疾病，由Ofuji等于1984年首次报道，本病诊断要点为融合成片的红褐色扁平丘疹、“帆布椅”征和剧烈瘙痒。实验室检查通常可见嗜酸粒细胞增多和血清IgE水平的升高。本文报道1例太藤丘疹性红皮病。

Abstract: Papuloerythroderma of Ofuji (PEO) is a rare skin condition first described in 1984 by Ofuji and characterized by diffuse erythroderma composed of papules coalescing into plaques, the deck-chair sign and intense itching. Common laboratory findings include peripheral and tissue eosinophilia, elevated levels of immunoglobulin E. In this artide, we report a case and review the literature.