Source:http://linkedlifedata.com/resource/pubmed/id/10414510
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
|
pubmed:dateCreated |
1999-8-3
|
pubmed:abstractText |
The number of opportunistic infections in the central nervous system (CNS) has been steadily increasing because of a rising number of immunocompromised patients. A rare form of CNS infection can be caused by Chaetomium species, one of the largest genera of saprophytic ascomycetes. The CNS lesions in the present case were caused by Chaetomium atrobrunneum. The main characteristic of almost all Chaetomium species is presence of hairs or setae covering the ascomata. Microbiological studies are the only definitive way to correctly identify this fungal organism. The rapid evolvement of the cerebral infection suggests that the brain tissue provides a favorable environment for growth and proliferation of these fungi. This is the second documented case of a fatal brain abscess caused by Chaetomium atrobrunneum, and the first case report in a bone marrow transplant patient.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
0046-8177
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
30
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
874-9
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:10414510-Adult,
pubmed-meshheading:10414510-Bone Marrow Transplantation,
pubmed-meshheading:10414510-Brain Diseases,
pubmed-meshheading:10414510-Chaetomium,
pubmed-meshheading:10414510-Fatal Outcome,
pubmed-meshheading:10414510-Humans,
pubmed-meshheading:10414510-Male,
pubmed-meshheading:10414510-Microscopy, Electron, Scanning,
pubmed-meshheading:10414510-Tomography, X-Ray Computed
|
pubmed:year |
1999
|
pubmed:articleTitle |
Fatal Chaetomium cerebritis in a bone marrow transplant patient.
|
pubmed:affiliation |
Department of Pathology, Loyola University Medical Center, Maywood, IL 60153, USA.
|
pubmed:publicationType |
Journal Article,
Case Reports
|