A case of Degos disease with intestinal microperforation
10.3760/cma.j.cn101480-20190605-00082
- VernacularTitle:Degos病合并肠道微穿孔一例
- Author:
Weiwei ZHENG
1
;
Mi WANG
;
Yijuan LIN
;
Xunru HUANG
;
Zehao ZHUANG
;
Chengdang WANG
Author Information
1. 福建医科大学附属第一医院消化内科 福建医科大学消化系病研究室 福建医科大学第一临床医学院，福州 350005
- Publication Type:Journal Article
- Keywords:
Degos disease;
Malignant atrophic papulosis;
Intestinal perforation;
Micro
- From:
Chinese Journal of Inflammatory Bowel Diseases
2020;04(2):168-170
- CountryChina
- Language:Chinese
-
Abstract:
Degos disease is a rare multi-system necrotic vasculitis disease. Autoimmune abnormality, heredity, infection and coagulation abnormality may be involved in the disease. Usually skin manifestations would be the first manifestation of this disease. However, intestinal perforation and hemorrhage are the main causes of death, which are not easy to be recognized or diagnosed by gastroenterologist. A case of this rare disease with intestinal microperforation is reported for reference.
