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dc.contributor.authorVelásquez-Rimachi, V.
dc.contributor.authorPalma-García, L.
dc.contributor.authorPacheco-Barrios, K.
dc.contributor.authorAlva-Díaz, C.
dc.date.accessioned2025-10-31T18:32:14Z
dc.date.available2025-10-31T18:32:14Z
dc.date.issued2020
dc.identifier.urihttps://hdl.handle.net/20.500.12805/4536
dc.description.abstractThe catastrophic antiphospholipid syndrome (CAPS) is an autoimmune disease associated with rapid failure of multiple organs and represents less than 1% of all cases of the antiphospholipid syndrome (APS). Antiphospholipid antibodies are present in approximately 9% of patients with pregnancy losses, 14% with stroke, 11% with myocardial infarction and 10% with deep vein thrombosis.1 The CAPS is considered a rare but devastating variant (30–50% mortality).2, 3 It is diagnosed according to the Asherson criteria that include: an involvement of three or more organs, a rapid progression (simultaneously or in less than one week), a laboratory demonstration of antiphospholipid antibodies and histologic evidence of small vessel occlusion (may involve one or more sites and may be accompanied by vasculitis)...en_US
dc.formatapplication/pdf
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofurn:issn:2531-1379
dc.rightshttps://purl.org/coar/access_right/c_abf2
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0/
dc.subjectPharmacotherapy and Antiphospholipid Antibody Insightsen_US
dc.subjectCatastrophic Antiphospholipid Syndrome Dynamicsen_US
dc.titleSuccessful treatment of catastrophic antiphospholipid syndrome with therapeutic plasma exchange: a case reporten_US
dc.typehttps://purl.org/coar/resource_type/c_0857
dc.identifier.doihttps://doi.org/10.1016/j.htct.2019.07.003
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#3.02.17
dc.type.otherCommunication letter o Case Report
dc.identifier.journalHematology, Transfusion and Cell Therapy
dc.type.versionhttps://purl.org/coar/version/c_970fb48d4fbd8a85


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