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dc.contributor.authorCalvo Río, Vanesa
dc.contributor.authorLoricera, Javier
dc.contributor.authorMata Arnaiz, María Cristina
dc.contributor.authorMartín Penagos, Luis
dc.contributor.authorOrtiz Sanjuán, Francisco Miguel
dc.contributor.authorÁlvarez Granda, Jesús Lino 
dc.contributor.authorGonzález Vela, María del Carmen 
dc.contributor.authorGonzález-Lamuño Leguina, Domingo 
dc.contributor.authorRueda Gotor, Javier
dc.contributor.authorFernández Llaca, José Héctor 
dc.contributor.authorGonzález López, Marcos Antonio 
dc.contributor.authorArmesto Alonso, Susana 
dc.contributor.authorPeiró, Enriqueta
dc.contributor.authorArias Rodríguez, Manuel 
dc.contributor.authorGonzález-Gay Mantecón, Miguel Ángel 
dc.contributor.authorBlanco Alonso, Ricardo 
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2017-02-06T15:58:20Z
dc.date.available2017-02-06T15:58:20Z
dc.date.issued2014-03
dc.identifier.issn0025-7974
dc.identifier.issn1536-5964
dc.identifier.otherRD08/0075
dc.identifier.otherRD12/0009/0013es_ES
dc.identifier.urihttp://hdl.handle.net/10902/10256
dc.description.abstractThe 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.es_ES
dc.format.extent8 p.es_ES
dc.language.isoenges_ES
dc.publisherLippincott Williams & Wilkinses_ES
dc.rightsAtribución 3.0 Españaes_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceMedicine (Baltimore). 2014 Mar;93(2):106-13es_ES
dc.titleHenoch-Schönlein purpura in northern Spain: clinical spectrum of the disease in 417 patients from a single centeres_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1097/MD.0000000000000019.
dc.type.versionpublishedVersiones_ES


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Atribución 3.0 EspañaExcepto si se señala otra cosa, la licencia del ítem se describe como Atribución 3.0 España