Source:http://linkedlifedata.com/resource/pubmed/id/21941483
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
|
| pubmed:dateCreated |
2011-9-23
|
| pubmed:abstractText |
Infantile myofibromatosis is a rare fibrous tumor of infancy. The cutaneous solitary type has typically an excellent prognosis. However, histologically, it is important to rule out leiomyosarcoma, which has a poor prognosis. The low frequency of mitosis was definitive for a diagnosis of infantile myofibromatosis. We present a cutaneous solitary-type case of infantile myofibromatosis. Following incisional biopsy, the tumor remitted spontaneously.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:status |
PubMed-not-MEDLINE
|
| pubmed:month |
May
|
| pubmed:issn |
1662-6567
|
| pubmed:author |
pubmed-author:AbeRiichiroR,
pubmed-author:AbeYukikoY,
pubmed-author:AoyagiSatoruS,
pubmed-author:HamasakaErikaE,
pubmed-author:HataHirooH,
pubmed-author:KikuchiKazuhiroK,
pubmed-author:MukaiMakioM,
pubmed-author:NatsugaKenK,
pubmed-author:ShibataMasahikoM,
pubmed-author:ShimizuHiroshiH,
pubmed-author:ShinkumaSatoruS,
pubmed-author:TateishiYasukiY,
pubmed-author:TomitaYukiY
|
| pubmed:issnType |
Electronic
|
| pubmed:volume |
3
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
181-5
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| pubmed:year |
2011
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| pubmed:articleTitle |
Spontaneous remission of solitary-type infantile myofibromatosis.
|
| pubmed:affiliation |
Department of Dermatology, Hokkaido University Graduate School of Medicine, Sapporo, Tokyo, Japan.
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| pubmed:publicationType |
Journal Article
|