Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/27245
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dc.contributor.authorTemnithikul B.
dc.contributor.authorRungrunanghiranya S.
dc.contributor.authorLimtanyakul P.
dc.contributor.authorAngkananard T.
dc.contributor.authorWessagowit V.
dc.date.accessioned2022-12-14T03:17:01Z-
dc.date.available2022-12-14T03:17:01Z-
dc.date.issued2022
dc.identifier.issn2690442X
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85141485366&doi=10.1002%2fski2.186&partnerID=40&md5=29db2dbd9430a61a9785121eaa8b371e
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/27245-
dc.description.abstractPurpura fulminans (PF) is an uncommon syndrome of acute purplish skin eruption characterized by coagulation of the microvasculature, which leads to purplish lesions and skin necrosis. There are three subtypes; idiopathic PF, neonatal PF and, the most common subtype, acute infectious PF (AIPF). Acute infectious PF is related to the thrombotic subtype of disseminated intravascular coagulation (DIC) and usually is superimposed on sepsis. This can rapidly lead to multi-organ failure from thrombotic occlusion of small and medium-sized blood vessels. We report a case of Klebsiella-induced AIPF in a 78-year-old Thai woman and also review other published cases. © 2022 The Authors. Skin Health and Disease published by John Wiley & Sons Ltd on behalf of British Association of Dermatologists.
dc.languageen
dc.publisherJohn Wiley and Sons Inc
dc.titleKlebsiella-induced acute infectious purpura fulminans in a Thai woman: Case report and review of literature
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationDiscrete Dynamics in Nature and Society. Vol 2022, No. (2022), p.-
dc.identifier.doi10.1002/ski2.186
Appears in Collections:Scopus 2022

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