Besekar Smruti M, Jogdand Sangita D, Naqvi Waqar M
Pharmacology, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, IND.
Research, Humen Edutech, Nagpur, IND.
Cureus. 2023 Jun 12;15(6):e40296. doi: 10.7759/cureus.40296. eCollection 2023 Jun.
A systematic review was carried out on a rare dermatological condition affecting papillary dermal tissue fibers of the skin known as elastosis perforans serpiginosa (EPS). The aim of this review was to highlight this skin disease, its association with other medical conditions, and its management. The search was conducted by using the keywords "elastosis perforans serpiginosa" and "case reports" in the databases. A total of 10 case reports were analyzed and presented by the parameters like age, gender, chief complaints, and medical history. The most common causes of EPS were drug-induced and occurred along with the Wilson disease. The study concluded that as EPS is an uncommon disease with few instances, there is a need for further research to analyze randomized controlled trials that have been conducted in relation to the condition.
对一种影响皮肤乳头真皮组织纤维的罕见皮肤病——匐行性穿通性弹力纤维病(EPS)进行了系统评价。本评价的目的是突出这种皮肤病、其与其他疾病的关联及其治疗方法。通过在数据库中使用关键词“匐行性穿通性弹力纤维病”和“病例报告”进行检索。共分析了10例病例报告,并根据年龄、性别、主要症状和病史等参数进行呈现。EPS最常见的病因是药物性的,且与威尔逊病同时发生。该研究得出结论,由于EPS是一种罕见疾病,病例较少,因此需要进一步研究以分析针对该疾病进行的随机对照试验。