Source:http://linkedlifedata.com/resource/pubmed/id/14596351
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2003-11-4
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pubmed:abstractText |
Mucormycosis is a rare invasive mycotic infection treated by antifungini or amphotericin B. We describe the case of a patient with septic fever and a necrotic lesion, with phlegmon of medial left thigh. Surgery was performed to drain the abscess content and to remove the necrotic tissue; mucormycosis was diagnosized by histological and culture tests and treated by intravenous amphotericin B. Since the lesion worsened, liposomal amphotericin B was directly infused into the left common iliac artery, with progressive improvement, and treatment was continued until complete recovery. Therefore, the endoarterial infusion of liposomal amphotericin B was a safe and successful treatment of advanced lesions of mucormycosis. In such lesions, intravenous general antibiotic administration probably is not sufficient to reach the whole infected area.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1121-7138
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
26
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
395-8
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pubmed:dateRevised |
2011-2-25
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pubmed:meshHeading |
pubmed-meshheading:14596351-Adult,
pubmed-meshheading:14596351-Amphotericin B,
pubmed-meshheading:14596351-Antifungal Agents,
pubmed-meshheading:14596351-Diagnosis, Differential,
pubmed-meshheading:14596351-Humans,
pubmed-meshheading:14596351-Infusions, Intra-Arterial,
pubmed-meshheading:14596351-Liposomes,
pubmed-meshheading:14596351-Male,
pubmed-meshheading:14596351-Mucormycosis
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pubmed:year |
2003
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pubmed:articleTitle |
Safe and successful endoarterial infusion of liposomal amphotericin B in treatment of mucormycosis.
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pubmed:affiliation |
Department of Clinical Medicine and Emerging Diseases, University of Palermo, Italy.
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pubmed:publicationType |
Journal Article,
Case Reports
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