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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1990-7-12
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pubmed:abstractText |
Considering the different localizations of malignant fibrous histiocytomas (MFH), that of the recto-vaginal septum is extremely rare. The present report describes a case, probably the first in literature, characterized by a storiform-pleomorphic histological type, treated with posterior exenteration and adjuvant chemotherapy. The Authors stress the still controversial histogenetic problem, as well as those related to a correct therapeutic approach.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:issn |
0392-2936
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
11
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
75-80
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pubmed:dateRevised |
2005-11-17
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pubmed:meshHeading |
pubmed-meshheading:2161339-Combined Modality Therapy,
pubmed-meshheading:2161339-Female,
pubmed-meshheading:2161339-Histiocytoma, Benign Fibrous,
pubmed-meshheading:2161339-Humans,
pubmed-meshheading:2161339-Middle Aged,
pubmed-meshheading:2161339-Neoplasm Recurrence, Local,
pubmed-meshheading:2161339-Rectal Neoplasms,
pubmed-meshheading:2161339-Vaginal Neoplasms
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pubmed:year |
1990
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pubmed:articleTitle |
Malignant fibrous primary histiocytoma of the recto-vaginal septum.
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pubmed:affiliation |
Department of Oncological Gynecology, Regina Elena National Cancer Institute, Rome, Italy.
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pubmed:publicationType |
Journal Article,
Case Reports
|