Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
1987-1-5
|
pubmed:abstractText |
We studied a rare case of congenital myofibromatosis of the orbit as part of a generalized multicentric disease in a 5-month-old boy. The ultrasonographic and computed tomographic findings were those of a low-reflective, firm, vascularized, lesion with heterogeneous internal structure. The histopathologic findings showed vascular channels with large polygonal cells and transition toward myofibroblasts with interwoven collagen fiber bundles.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
0002-9394
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
102
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
779-87
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:3538883-Follow-Up Studies,
pubmed-meshheading:3538883-Humans,
pubmed-meshheading:3538883-Infant,
pubmed-meshheading:3538883-Leiomyoma,
pubmed-meshheading:3538883-Male,
pubmed-meshheading:3538883-Orbital Neoplasms,
pubmed-meshheading:3538883-Soft Tissue Neoplasms,
pubmed-meshheading:3538883-Tomography, X-Ray Computed,
pubmed-meshheading:3538883-Ultrasonography
|
pubmed:year |
1986
|
pubmed:articleTitle |
Congenital generalized multicentric myofibromatosis with orbital involvement.
|
pubmed:publicationType |
Journal Article,
Case Reports
|