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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
1991-11-14
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pubmed:abstractText |
Purpura fulminans is a rare disease characterized by purpura ecchymosis, hypotension, and fever associated with disseminated intravascular coagulation. It often begins as a benign infectious process and subsequently progresses to a severe, catastrophic outcome. It is recognized to originate from congenital or acquired protein C deficiency. We present an unusual case of an adult with Xanthomonas maltophilia sepsis that subsequently developed into purpura fulminans with involvement of the four extremities. We discuss the importance of the protein C system in coagulation homeostasis and its relationship to purpura fulminans.
|
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
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pubmed:month |
Apr
|
pubmed:issn |
0385-2407
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
18
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
225-9
|
pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:1918597-Anemia, Aplastic,
pubmed-meshheading:1918597-Extremities,
pubmed-meshheading:1918597-Gangrene,
pubmed-meshheading:1918597-Humans,
pubmed-meshheading:1918597-Male,
pubmed-meshheading:1918597-Middle Aged,
pubmed-meshheading:1918597-Protein C Deficiency,
pubmed-meshheading:1918597-Purpura,
pubmed-meshheading:1918597-Sepsis,
pubmed-meshheading:1918597-Xanthomatosis,
pubmed-meshheading:1918597-Xanthomonas
|
pubmed:year |
1991
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pubmed:articleTitle |
Purpura fulminans secondary to Xanthomonas maltophilia sepsis in an adult with aplastic anemia.
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pubmed:affiliation |
Department of Dermatology, Otaru City General Hospital, Japan.
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pubmed:publicationType |
Journal Article,
Case Reports
|