Premium
Cutaneous Lupus Erythematosus in Children: Experience from a Tertiary Care Pediatric Dermatology Clinic
Author(s) -
AlKharafi Najla N. A. H.,
Alsaeid Khaled,
AlSumait Anwar,
AlSabah Humoud,
AlAjmi Hejab,
Rahim Jasim Abdul,
AlEnezi Hamid,
Nanda Arti
Publication year - 2016
Publication title -
pediatric dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.542
H-Index - 73
eISSN - 1525-1470
pISSN - 0736-8046
DOI - 10.1111/pde.12788
Subject(s) - medicine , dermatology , tertiary care , disease , pediatrics , family history , systemic disease , presentation (obstetrics) , autoimmune disease , lupus erythematosus , connective tissue disease , surgery , immunology , antibody
Background/Objectives The manifestations of cutaneous lupus erythematosus (CLE) and their relevance to systemic disease are well characterized in adults, but data are limited in children. The objective of the current study was to examine the spectrum of CLE and its relationship to systemic disease in children from a tertiary care pediatric dermatology clinic. Materials and Methods An analysis of 26 children with CLE registered consecutively over 14 years was performed. Results Ninety‐six percent of the patients were of Arab ethnicity. They included seven (27%) cases with neonatal lupus erythematosus (LE) (71% females and 29% males). Of the other 19 children with CLE, 95% were female. The mean and median age at diagnosis was 11 years. Eighty‐nine percent of the patients fulfilled the criteria for systemic LE. All patients had LE‐specific lesions and 83% had LE‐nonspecific manifestations. Atypical initial presentations were recorded in 28% of the patients, and 22% of the patients had the rare LE variants. Of the LE‐specific manifestations, acute CLE was seen in 83%, subacute in 44%, and chronic in 22%. Autoimmune associations were recorded in 44% and a positive family history of autoimmune diseases in 61%. Conclusion This study highlights a striking female predominance, higher risk of systemic disease in children presenting with CLE, higher prevalence of atypical presentation and rare CLE variants, and underrepresentation of discoid LE in children and signifies the need for more surveys to delineate the spectrum of pediatric CLE in different parts of the world.