Gardner's syndrome associated fibromas
Language English Country Australia Media print
Document type Journal Article
PubMed
15189507
DOI
10.1111/j.1440-1827.2004.01660.x
PII: PIN1660
Knihovny.cz E-resources
- MeSH
- Adult MeSH
- Fibroma chemistry pathology surgery MeSH
- Gardner Syndrome chemistry pathology surgery MeSH
- Immunoenzyme Techniques MeSH
- Humans MeSH
- Neoplasms, Multiple Primary chemistry pathology surgery MeSH
- Biomarkers, Tumor analysis MeSH
- Soft Tissue Neoplasms chemistry pathology surgery MeSH
- Terminology as Topic MeSH
- Treatment Outcome MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Male MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Biomarkers, Tumor MeSH
Three patients with Gardner's syndrome having benign fibrous proliferations in the soft tissues and the oral cavity are presented. Lesions in all three patients were morphologically different. Two excised lesions in Case 1 were histologically identical to nuchal-type fibroma (NTF) and one lesion in this patient was an epidermal cyst. Case 2 had a lesion located in the soft tissues of the shoulder, which was morphologically similar to NTF and, in addition, contained mildly atypical and multinucleated fibroblastic cells. The oral lesion in Case 3 looked like a fibroma and was morphologically different from all fibrous lesions that have ever been described in Gardner's syndrome. The cases in the present report show that the term Gardner's fibroma is just a descriptive name encompassing a spectrum of morphologically different benign fibrous proliferations associated with this syndrome. Therefore, the term Gardner's fibroma should not be used as a specific name for NTF arising in patients with Gardner's syndrome as suggested in the most recent WHO classification of soft tissue and bone tumors.
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