TY - JOUR
T1 - Mucoepidermoid carcinoma of salivary glands in the pediatrics age group
T2 - 18 Clinical cases, including 11 second malignant neoplasms
AU - Védrine, Pierre Olivier
AU - Coffinet, Laurent
AU - Temam, Stéphane
AU - Montagne, Karine
AU - Lapeyre, Michel
AU - Oberlin, Odile
AU - Orbach, Daniel
AU - Simon, Claude
AU - Sommelet, Danièle
PY - 2006/9/1
Y1 - 2006/9/1
N2 - Background. Salivary gland tumors represent 1% of head and neck tumors, with only 5% of these occurring in patients younger than 20 years. Mucoepidermoid carcinoma (MEC) is one of the most frequent salivary gland cancers among adults and children. Methods. This survey was conducted among 34 French pediatric oncology departments. From 1980 to 2000, 18 cases were reported. Results. Treatment included surgery or radiotherapy, or both. The 5-year survival rate was 93.7%. Eleven patients had been previously treated by radiotherapy and/or chemotherapy for a first malignant tumor, specifically, lymphoid leukemia (n = 4), lymphoma (n = 3), brain tumor (n = 2), sarcoma (n = 1), and retinoblastoma (n = 1). Conclusions. MEC is very rare in the pediatric age group. Treatment involves surgical removal of the tumor plus radiotherapy, according to histologic staging. MEC has a good prognosis in young patients. The survival rate does not differ in the subgroup of patients with MEC as a secondary tumor.
AB - Background. Salivary gland tumors represent 1% of head and neck tumors, with only 5% of these occurring in patients younger than 20 years. Mucoepidermoid carcinoma (MEC) is one of the most frequent salivary gland cancers among adults and children. Methods. This survey was conducted among 34 French pediatric oncology departments. From 1980 to 2000, 18 cases were reported. Results. Treatment included surgery or radiotherapy, or both. The 5-year survival rate was 93.7%. Eleven patients had been previously treated by radiotherapy and/or chemotherapy for a first malignant tumor, specifically, lymphoid leukemia (n = 4), lymphoma (n = 3), brain tumor (n = 2), sarcoma (n = 1), and retinoblastoma (n = 1). Conclusions. MEC is very rare in the pediatric age group. Treatment involves surgical removal of the tumor plus radiotherapy, according to histologic staging. MEC has a good prognosis in young patients. The survival rate does not differ in the subgroup of patients with MEC as a secondary tumor.
KW - Adolescent
KW - Child
KW - Mucoepidermoid carcinoma
KW - Salivary gland neoplasms
KW - Second primary neoplasms
UR - http://www.scopus.com/inward/record.url?scp=33748249689&partnerID=8YFLogxK
U2 - 10.1002/hed.20429
DO - 10.1002/hed.20429
M3 - Article
C2 - 16783829
AN - SCOPUS:33748249689
SN - 1043-3074
VL - 28
SP - 827
EP - 833
JO - Head and Neck
JF - Head and Neck
IS - 9
ER -