Abstract

Results Sixty six cases (71,2% female) met the inclusion criteria. Average age of RP onset was 12,5y with median duration of 3,6y. RP was associated to: erythema pernio (34,8%), inter-phalangeal joints pain (30.3%), hands edema (28,8%), acrocyanosis (18,2%), profuse sweating (12,1% ) and trophic changes of fingers pulp (10,6%.). Antinuclear antibodies (ANA) were titled in 64 patients (97%), being positive (>1/80) in ten (15.6%). Capillaroscopy was performed on 43 (65.2%): 32 (74,4%) minor changes (tortuosity and segmental enlargement), four (9,3%) significant changes (giant capillaries, hemorrhagic and avascular areas), seven (16,3%) normal. Of 43 patients with complete study, five (11,6%) had secondary RP: two with juvenile systemic sclerosis, two in characterization and a probable case of mixed connective tissue disease. Secondary RP occurred mostly in less that 12-yearsold child. ANA ≥ 1/320 and significant changes on capillaroscopy had a significant statistic relationship with secondary RP.

Highlights

  • Raynaud’s phenomenon (RP) is characterized by changes in the color of extremities: pallor, cyanosis and erythema

  • RP can occur in children and, as in adults, in most cases is primary

  • Retrospective analysis of clinical files of children and adolescents in which RP was the reason for consultation

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Summary

Introduction

Raynaud’s phenomenon (RP) is characterized by changes in the color of extremities: pallor, cyanosis and erythema. M Tavares1*, A Novo1, H Sousa1, I Silva2, I Almeida3, M Guedes1 From 18th Pediatric Rheumatology European Society (PReS) Congress Bruges, Belgium. Background Raynaud’s phenomenon (RP) is characterized by changes in the color of extremities: pallor, cyanosis and erythema. It’s prevalence in adults ranges between 320% but there are few studies in pediatric age.

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Conclusion

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