Chronic catastrophic-like antiphospholipid syndrome: a “smoldering” variant?

dc.creatorAthanazio, Daniel Abensur
dc.creatorRocha, Maria Cristina
dc.creatorSouza, Túlio Geraldo de Souza e
dc.creatorSilva, Natália Oliveira e
dc.creatorJezler, Sérgio
dc.creatorSantiago, Mittermayer Barreto
dc.creatorAthanazio, Daniel Abensur
dc.creatorRocha, Maria Cristina
dc.creatorSouza, Túlio Geraldo de Souza e
dc.creatorSilva, Natália Oliveira e
dc.creatorJezler, Sérgio
dc.creatorSantiago, Mittermayer Barreto
dc.date.accessioned2022-10-07T15:30:30Z
dc.date.available2022-10-07T15:30:30Z
dc.date.issued2009
dc.identifier0172-8172
dc.identifierhttp://www.repositorio.ufba.br/ri/handle/ri/6216
dc.identifierv. 30, n. 1
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/4005174
dc.description.abstractCatastrophic antiphospholipid syndrome (CAPS) is characterized by life-threatening diVuse thrombotic manifestations involving particularly small vessels of kidney, lungs, brain and skin. We report a 20-year-old female with systemic lupus erythematosus and secondary antiphospholipid syndrome who presented typical organ and histological involvement as seen in CAPS but with protracted course suggesting a “smoldering” form of the disease.
dc.languageen
dc.publisherSpringer Verlag
dc.sourcehttp://www.springerlink.com.ez10.periodicos.capes.gov.br/content/h666h2n7j60g7r86/fulltext.pdf
dc.subjectCatastrophic antiphospholipid syndrome
dc.subjectThrombotic microangiopathy
dc.subjectCapillaritis
dc.titleChronic catastrophic-like antiphospholipid syndrome: a “smoldering” variant?
dc.typeArtigo de Periódico


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