Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1994-7-6
pubmed:abstractText
Extracardiac rhabdomyomas are divided into three subtypes: adult rhabdomyomas (ARs), fetal rhabdomyomas (FRs) and genital rhabdomyomas (GRs), each of which has characteristic clinicopathologic features that facilitate their diagnosis. Rhabdomyomas are invariably benign and show varying degrees of skeletal muscle differentiation by electron microscopy and immunohistochemistry. The etiology of these lesions is not understood; however, there is cytogenetic evidence to indicate that ARs are probably neoplastic in origin. The differential diagnosis of rhabdomyomas includes granular cell tumors and hibernomas for ARs, rhabdomyosarcomas and fibromatosis for FRs, and sarcoma botryoides and vaginal polyps for GRs. Identification and investigation of these lesions provide opportunity for gaining insight into skeletal muscle tumor differentiation and skeletal-muscle tumors in general.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0740-2570
pubmed:author
pubmed:issnType
Print
pubmed:volume
11
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
15-25
pubmed:dateRevised
2007-5-16
pubmed:meshHeading
pubmed:year
1994
pubmed:articleTitle
Extracardiac rhabdomyomas.
pubmed:affiliation
Institute of Pathology, Case Western Reserve University, Cleveland, OH 44106.
pubmed:publicationType
Journal Article, Review