En coup de sabre linear scleroderma – diagnostic difficulties. Case report

IF 0.1 Q4 PEDIATRICS
Monika Leończyk-Spórna, Anna Ankudowicz, Agnieszka Lewecka
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引用次数: 0

Abstract

Frontal linear scleroderma (morphea en coup de sabre) is a rare disease from the group of limited connective tissue diseases, most often affecting children. Due to the fact that it is not a common dermatosis, diagnosis and treatment may be difficult. Therefore, we believe it is advisable to present the diagnostic difficulties in a patient of the Provincial Integrated Hospital in Elbląg. It is also noteworthy that the patient’s neurological symptoms preceded the appearance of skin lesions. Clinical symptoms and imaging studies led us to observe progressive hemifacial atrophy. The patient requires interdisciplinary specialist care and diagnosis in the field of neurology, dermatology, rheumatology and ophthalmology.
线性硬皮病的诊断困难。病例报告
额线状硬皮病(morphea en coup de sabre)是一种罕见的疾病,来自有限结缔组织疾病组,最常影响儿童。由于它不是一种常见的皮肤病,诊断和治疗可能很困难。因此,我们认为建议在Elbląg中呈现省级综合医院患者的诊断困难。同样值得注意的是,患者的神经系统症状先于皮肤病变的出现。临床症状和影像学检查使我们观察到进行性面瘫萎缩。患者需要神经病学、皮肤病学、风湿病学和眼科领域的跨学科专家护理和诊断。
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来源期刊
CiteScore
0.50
自引率
0.00%
发文量
33
审稿时长
20 weeks
期刊介绍: PEDIATRIA I MEDYCYNA RODZINNA is a peer-reviewed scientific journal publishing original articles that constitute significant contributions to the advancements of paediatrics and family medicine. In addition, PEDIATRIA I MEDYCYNA RODZINNA, publishes information from the medical associations, reports and materials from international congresses, letters to the Editor, information on new medical products as well as abstracts and discussions on papers published in other scientific journals, reviews of books and other publications.
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