Vol. 28 - Num. 112
Clinical Reviews
Cristina M.ª Copado Mozosa, M.ª del Carmen Salazar Garcíaa, Elena Reyzabal Ereñob
aMIR-Pediatría. Hospital General Universitario de Ciudad Real. España.
bServicio de Pediatría. Hospital General Universitario de Ciudad Real. España.
Correspondence: CM Copado. E-mail: ccopado@sescam.jccm.es
Reference of this article: Copado Mozos CM, Salazar García MC, Reyzabal Ereño E. Schönlein-Henoch purpura (immunoglobulin A vasculitis): a case report . Rev Pediatr Aten Primaria. 2026;28:[en prensa].
Published in Internet: 13-10-2026 - Visits: 95
Abstract
Immunoglobulin A (IgA) vasculitis, classically known as Schönlein-Henoch purpura, is the most common systemic vasculitis in childhood. Diagnosis is clinical, and the primary care paediatrician plays a central role both in the initial suspicion and in follow-up, since renal involvement ─the main determinant of prognosis─ may appear weeks after onset. We present the case of a seven-year-old girl with palpable purpura on the lower limbs and arthralgia three weeks after an episode of streptococcal pharyngotonsillitis confirmed by a rapid antigen detection test. She had no renal or gastrointestinal involvement at diagnosis and progressed favourably with symptomatic treatment, remaining under follow-up with blood pressure and urinalysis monitoring.
Keywords
● Arthralgia ● Case reports ● Henoch-Schönlein purpura ● IgA vasculitis