Paediatric salivary gland cancer in Finland

被引:18
作者
Aro, Katri [1 ,2 ]
Leivo, Ilmo [3 ]
Grenman, Reidar [4 ]
Makitie, Antti A. [1 ,2 ]
机构
[1] Univ Helsinki, Cent Hosp, Dept Otorhinolaryngol Head & Neck Surg, FI-00029 Helsinki, Huch, Finland
[2] Univ Helsinki, FI-00029 Helsinki, Huch, Finland
[3] Univ Turku, Dept Pathol, Turku, Finland
[4] Turku Univ Hosp, Dept Otorhinolaryngol Head & Neck Surg, FIN-20520 Turku, Finland
关键词
Paediatric cancer; Salivary gland cancer; Survival; Tumour grade; EPSTEIN-BARR-VIRUS; MUCOEPIDERMOID CARCINOMA; CHILDHOOD-CANCER; PAROTID-GLAND; CHILDREN; TUMORS; NEOPLASMS; MALIGNANCIES; MANAGEMENT; SURVIVORS;
D O I
10.1016/j.ijporl.2012.05.024
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objectives: Worldwide, only 5% of all salivary gland tumours are reported in children and 35-50% of these are malignant. According to the Finnish Cancer Registry, 15 children were diagnosed with salivary gland cancer (SGC) during 1990-2009 in Finland. There are no previous studies available on the histopathology, treatment, and survival of patients with these rare malignancies in Finland. Methods: Retrospective patient and tumour data covering the past 20 years were retrieved from the five University Hospitals in Finland. Ten paediatric SGC patients with a median age of 14 years (range, 9-19 years) and with available adequate patient data were included. The series comprised four boys and six girls. Follow-up time varied from five months to 14 years. Results: Two patients had a history of a previous malignancy. The majority of cases had a parotid gland cancer (7/10), and mucoepidermoid carcinoma was the most common histological subtype (5/10). All patients presented with Stage I-II disease and were treated surgically with curative intent. One patient with a Stage I mucoepidermoid carcinoma of the parotid gland received postoperative radiotherapy. No recurrences were encountered and all patients were free of disease at the last follow up. Conclusions: The individual treatment design for paediatric SGC should follow consistent treatment strategies. All patients in the present study had low-grade tumours with a favourable prognosis. Since paediatric SGC is infrequent worldwide, the diagnostics, treatment, and follow up should be centralized in multidisciplinary Head and Neck Centres. (c) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1304 / 1307
页数:4
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