Mesenteric fibromatosis in a patient with Camurati-Engelmann disease. A case report and literature review.
Tumori
; 91(6): 552-4, 2005.
Article
em En
| MEDLINE
| ID: mdl-16457156
ABSTRACT
Mesenteric fibromatosis is a rare type of desmoid tumor characterized by local aggressiveness and a tendency to relapse. In view of these characteristics it may be considered a low-grade fibrosarcoma. Camurati-Engelmann disease is a very rare form of bone dysplasia characterized by osteosclerosis of the diaphyses of the long bones. Here we describe the case of a male patient affected by these two rare diseases in association with chronic inflammatory intestinal disease.
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Base de dados:
MEDLINE
Assunto principal:
Neoplasias Peritoneais
/
Síndrome de Camurati-Engelmann
/
Fibroma
/
Mesentério
Tipo de estudo:
Systematic_reviews
Limite:
Adult
/
Humans
/
Male
Idioma:
En
Revista:
Tumori
Ano de publicação:
2005
Tipo de documento:
Article
País de afiliação:
Itália