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Neonatal Acute Compartment Syndrome as First Manifestation of Hematologic Disease: Case Report

dc.contributor.authorSacras, ML
dc.contributor.authorLadeira, C
dc.contributor.authorCarmo, S
dc.contributor.authorKjöllerström, P
dc.date.accessioned2022-09-14T12:21:00Z
dc.date.available2022-09-14T12:21:00Z
dc.date.issued2021
dc.description.abstractHemophilia A, characterized by deficiency of functional plasma clotting factor VIII, is an X-linked disorder. Signs and symptoms depend on factor VIII levels. Severe hemophilia A (factor levels less than 1%) is usually diagnosed in the first two years of life. Pediatric compartment syndrome is most associated with trauma, but infectious and vascular causes must also be considered. We report a case of a newborn who presented with a severe hand hematoma after venous puncture, complicated by compartment syndrome. An isolated prolonged partial thromboplastin time was found, and hemophilia was suspected. Factor VIII levels less than 1% were consistent with severe hemophilia A. The patient received recombinant factor VIII perioperatively. Fasciotomy was performed and the patient was kept on antibiotics until closure.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationPort J Pediatr 2021;52:193-6pt_PT
dc.identifier.doidoi.org/10.25754/pjp.2021.20470pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/4247
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherSociedade Portuguesa de Pediatriapt_PT
dc.subjectAcute Diseasept_PT
dc.subjectCompartment Syndromes/ diagnosispt_PT
dc.subjectCompartment Syndromes/etiologypt_PT
dc.subjectCompartment Syndromes/therapypt_PT
dc.subjectFasciotomy; Hemophilia A/complicationspt_PT
dc.subjectHemophilia A/diagnosispt_PT
dc.subjectInfant, Newbornpt_PT
dc.subjectCase Reportpt_PT
dc.subjectHDE CIR PEDpt_PT
dc.subjectHDE HEM PEDpt_PT
dc.titleNeonatal Acute Compartment Syndrome as First Manifestation of Hematologic Disease: Case Reportpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage196pt_PT
oaire.citation.startPage196pt_PT
oaire.citation.volume52pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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