LOGO
PL

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

Monika Leończyk-Spórna, Anna Ankudowicz, Agnieszka Lewecka

Affiliation and address for correspondence
Pediatr Med Rodz 2023, 19 (2), p. 140–143
DOI: 10.15557/PiMR.2023.0025
PlumX metrics:
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.

Keywords
linear scleroderma, saber cut, morphea en coup de sabre

Oświadczam, że posiadam prawo wykonywania zawodu lekarza i jestem uprawniony do otrzymywania specjalistycznych informacji medycznych. Chcę zapoznać się z informacją z serwisu.