Eosinophilic fasciitis difficult to differentiate from scleroderma: A case report

被引:1
作者
Lan, Tian-Yi [1 ]
Wang, Zi-Han [1 ]
Kong, Wei-Ping [2 ]
Wang, Jin-Ping [2 ]
Zhang, Nan [2 ]
Jin, Di-Er [2 ]
Luo, Jing [2 ]
Tao, Qing-Wen [2 ]
Yan, Ze-Ran [2 ,3 ]
机构
[1] Beijing Univ Chinese Med, Grad Coll, Beijing 100029, Peoples R China
[2] China Japan Friendship Hosp, Tradit Chinese Med Dept Rheumatism, Beijing 100029, Peoples R China
[3] China Japan Friendship Hosp, Tradit Chinese Med Dept Rheumatism, 2 Yinghua St East, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
Eosinophilic fasciitis; Scleroderma; Biopsy; Diagnose; Prognosis; Case report;
D O I
10.12998/wjcc.v11.i13.3092
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Eosinophilic fasciitis (EF) is a rare connective tissue disease that can cause swelling and sclerosis of the extremities, and special attention is needed to differentiate EF from systemic sclerosis. Misdiagnosis or omission markedly delays treatment of EF, and severe skin sclerosis in advanced stages can cause joint contracture and tendon retraction, worsening the patient's prognosis and quality of life. CASE SUMMARY We report a case of EF in a young woman diagnosed by tissue biopsy, confirming the difficulty of differential diagnosis with scleroderma. CONCLUSION Focusing on skin manifestations, completing tissue biopsy and radiography can help diagnose EF effectively. Clinicians should enhance their understanding of the differences between EF and scleroderma, and early diagnosis and standardized treatment can improve the prognosis of patients with EF.
引用
收藏
页码:3092 / 3098
页数:7
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