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A Case Report of Hemophagocytic Syndrome

datacite.subject.fosCiências Médicas
dc.contributor.authorMendes, Tânia F.; Oliveira, Ana Isabel; Gomes, Carolina; Sousa, Nuno A.; Gonçalves Pereira, João
dc.date.accessioned2025-06-02T14:06:33Z
dc.date.available2025-06-02T14:06:33Z
dc.date.issued2025
dc.description.abstractAbstract Hemophagocytic syndrome (HPS) represents a critical and often overlooked hyperinflammatory condition that can lead to rapid multi-organ failure and high mortality rates, particularly in adults. This article presents a compelling case study of a 45-year-old male with a complex clinical presentation, highlighting the diagnostic challenges posed by HPS, including its nonspecific symptoms and the necessity for a high index of suspicion. We underscore the paramount importance of early recognition, thorough differential diagnosis, and prompt initiation of treatment to improve patient outcomes. This case not only illustrates the intricacies of diagnosing HPS but also advocates for increased awareness among healthcare providers to mitigate the risks associated with this life-threatening syndrome.por
dc.identifier.doi10.7759/cureus.79150
dc.identifier.urihttp://hdl.handle.net/10400.26/57916
dc.language.isoeng
dc.peerreviewedyes
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleA Case Report of Hemophagocytic Syndromepor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.titleCureus
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85

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