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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
|
pubmed:dateCreated |
1983-7-29
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pubmed:abstractText |
A patient with febrile ulceronecrotic Mucha-Habermann's disease manifested the characteristic features of this entity. These include a polymorphous eruption with histopathologic findings of Mucha-Habermann's disease, large ulceronecrotic skin lesions, intermittent high fever, and constitutional symptoms. The patient was unique in that he also had malabsorption and eosinophilia. This disease may represent a hypersensitivity reaction. To our knowledge, there are five previous cases of febrile ulceronecrotic Mucha-Habermann's disease reported in the world literature.
|
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0003-987X
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
119
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
597-601
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pubmed:dateRevised |
2008-3-17
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pubmed:meshHeading |
pubmed-meshheading:6859903-Eosinophilia,
pubmed-meshheading:6859903-Fever,
pubmed-meshheading:6859903-Humans,
pubmed-meshheading:6859903-Malabsorption Syndromes,
pubmed-meshheading:6859903-Male,
pubmed-meshheading:6859903-Middle Aged,
pubmed-meshheading:6859903-Necrosis,
pubmed-meshheading:6859903-Pityriasis,
pubmed-meshheading:6859903-Skin Ulcer
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pubmed:year |
1983
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pubmed:articleTitle |
Febrile ulceronecrotic Mucha-Habermann's disease.
|
pubmed:publicationType |
Journal Article,
Case Reports
|