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Henoch-Schönlein purpura in northern Spain: clinical spectrum of the disease in 417 patients from a single center

Abstract: The severity of clinical features and the outcomes in previous series of patients reported with Henoch-Schönlein purpura (HSP) vary greatly, probably due to selection bias. To establish the actual clinical spectrum of HSP in all age groups using an unselected and wide series of patients diagnosed at a single center, we performed a retrospective review of 417 patients classified as having HSP according to the criteria proposed by Michel et al. Of 417 patients, 240 were male and 177 female, with a median age at the time of disease diagnosis of 7.5 years (interquartile range [IQR], 5.3-20.1 yr). Three-quarters of the patients were children or young people aged 20 years or younger (n = 315), and one-quarter were adults (n = 102). The most frequent precipitating events were a previous infection (38%), usually an upper respiratory tract infection, and/or drug intake (18.5%) shortly before the onset of the vasculitis. At disease onset the most common manifestations were skin lesions (55.9%), nephropathy (24%), gastrointestinal involvement (13.7%), joint symptoms (9.1%), and fever (6.2%). Cutaneous involvement occurring in all patients, mainly purpuric skin lesion, was the most common manifestation when the vasculitis was fully established, followed by gastrointestinal (64.5%), joint (63.1%), and renal involvement (41.2%). The main laboratory findings were leukocytosis (36.7%), anemia (8.9%), and increased serum IgA levels (31.7%). The most frequent therapies used were corticosteroids (35%), nonsteroidal antiinflammatory drugs (14%), and cytotoxic agents (5%). After a median follow-up of 12 months (IQR, 2-38 mo), complete recovery was observed in most cases (n = 346; 83.2%), while persistent, usually mild, nephropathy was observed in only 32 (7.7%) cases. Relapses were observed in almost a third of patients (n = 133; 31.9%).In conclusion, although HSP is a typical vasculitis affecting children and young people, it is not uncommon in adults. The prognosis is favorable in most cases, depending largely on renal involvement.

Otras publicaciones de la misma revista o congreso con autores/as de la Universidad de Cantabria

 Fuente: Medicine (Baltimore). 2014 Mar;93(2):106-13

Editorial: Lippincott Williams & Wilkins

 Fecha de publicación: 01/03/2014

Nº de páginas: 8

Tipo de publicación: Artículo de Revista

 DOI: 10.1097/MD.0000000000000019.

ISSN: 0025-7974,1536-5964

 Proyecto español: RD08/ 0075 ; RD12/0009/0013

Autoría

CALVO RÍO, VANESA

LORICERA, JAVIER

MATA, CRISTINA

MARTÍN PENAGOS, LUIS

ORTIZ SANJUÁN, FRANCISCO

JESUS LINO ALVAREZ GRANDA

JAVIER RUEDA GOTOR

JOSE HECTOR FERNANDEZ LLACA

SUSANA ARMESTO ALONSO

PEIRÓ, ENRIQUETA