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Mucoepidermoid Carcinoma Arising in a Background of Sialadenoma Papilliferum: A Case Report
Sialadenoma papilliferum is a rare tumor, primarily of minor salivary gland origin, first described by Abrams and Finck (Cancer 24:1057–63, 1969). It is both an exophytic and endophytic papillary lesion histologically resembling syringocystadenoma papilliferum of sweat gland. The tumor is considered...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Humana Press Inc
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2807533/ https://www.ncbi.nlm.nih.gov/pubmed/20596992 http://dx.doi.org/10.1007/s12105-009-0106-5 |
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author | Liu, Wei Gnepp, Douglas R. de Vries, Egbert Bibawy, Haidy Solomon, Marshall Gloster, Elizabeth S. |
author_facet | Liu, Wei Gnepp, Douglas R. de Vries, Egbert Bibawy, Haidy Solomon, Marshall Gloster, Elizabeth S. |
author_sort | Liu, Wei |
collection | PubMed |
description | Sialadenoma papilliferum is a rare tumor, primarily of minor salivary gland origin, first described by Abrams and Finck (Cancer 24:1057–63, 1969). It is both an exophytic and endophytic papillary lesion histologically resembling syringocystadenoma papilliferum of sweat gland. The tumor is considered benign although rare recurrent cases have been reported. Three cases of malignant transformation of sialadenoma papilliferum have been described in the literature. We report a high grade mucoepidermoid carcinoma arising in a background of sialadenoma papilliferum, at the base of the tongue, an unusual location for minor salivary gland neoplasms. Eleven months after excision and nodal dissection, there is no evidence of recurrence or metastasis. |
format | Text |
id | pubmed-2807533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Humana Press Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-28075332010-02-16 Mucoepidermoid Carcinoma Arising in a Background of Sialadenoma Papilliferum: A Case Report Liu, Wei Gnepp, Douglas R. de Vries, Egbert Bibawy, Haidy Solomon, Marshall Gloster, Elizabeth S. Head Neck Pathol Case Report Sialadenoma papilliferum is a rare tumor, primarily of minor salivary gland origin, first described by Abrams and Finck (Cancer 24:1057–63, 1969). It is both an exophytic and endophytic papillary lesion histologically resembling syringocystadenoma papilliferum of sweat gland. The tumor is considered benign although rare recurrent cases have been reported. Three cases of malignant transformation of sialadenoma papilliferum have been described in the literature. We report a high grade mucoepidermoid carcinoma arising in a background of sialadenoma papilliferum, at the base of the tongue, an unusual location for minor salivary gland neoplasms. Eleven months after excision and nodal dissection, there is no evidence of recurrence or metastasis. Humana Press Inc 2009-02-15 /pmc/articles/PMC2807533/ /pubmed/20596992 http://dx.doi.org/10.1007/s12105-009-0106-5 Text en © Humana 2009 |
spellingShingle | Case Report Liu, Wei Gnepp, Douglas R. de Vries, Egbert Bibawy, Haidy Solomon, Marshall Gloster, Elizabeth S. Mucoepidermoid Carcinoma Arising in a Background of Sialadenoma Papilliferum: A Case Report |
title | Mucoepidermoid Carcinoma Arising in a Background of Sialadenoma Papilliferum: A Case Report |
title_full | Mucoepidermoid Carcinoma Arising in a Background of Sialadenoma Papilliferum: A Case Report |
title_fullStr | Mucoepidermoid Carcinoma Arising in a Background of Sialadenoma Papilliferum: A Case Report |
title_full_unstemmed | Mucoepidermoid Carcinoma Arising in a Background of Sialadenoma Papilliferum: A Case Report |
title_short | Mucoepidermoid Carcinoma Arising in a Background of Sialadenoma Papilliferum: A Case Report |
title_sort | mucoepidermoid carcinoma arising in a background of sialadenoma papilliferum: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2807533/ https://www.ncbi.nlm.nih.gov/pubmed/20596992 http://dx.doi.org/10.1007/s12105-009-0106-5 |
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