Ritwik Priyanshi, Brannon Robert B
Department of Pediatric Dentistry, LSU School of Dentistry, 1100 Florida Avenue, New Orleans, LA, 70119, USA.
J Med Case Rep. 2012 Sep 11;6:287. doi: 10.1186/1752-1947-6-287.
Minor salivary gland neoplasms of epithelial origin are rare in children and adolescents and most are not well documented, except for a few small series and case reports. This study represents a retrospective clinical analysis of nine cases of benign epithelial salivary gland neoplasms accessioned over a 35-year period at the Louisiana State University School of Dentistry and combines the data with well-documented cases from the English-language literature.
A retrospective clinical analysis of nine cases of benign epithelial salivary gland neoplasms was performed over a 35-year period at the Louisiana State University School of Dentistry and combined with data of well-documented cases from the English-language literature.
The nine benign salivary gland neoplasms in patients aged 19 months to 18 years accounted for 2.3% of the Louisiana State University School of Dentistry accessioned salivary gland tumors. These nine cases comprised eight pleomorphic adenomas and one cystadenoma. There were 40 cases in the literature, of which 34 were pleomorphic adenomas. Combining the data for the 42 pleomorphic adenomas resulted in a mean age of 12 years with a 2.8:1 female predilection. The hard palate and/or soft palate were the most common site (69.1%). The average duration and size was 2.1 years and 2.4cm, respectively. Bone involvement occurred in seven cases. Wide local excision was the treatment most often employed. Cases followed for two years or more had a recurrence rate of 13.0%. The remaining seven neoplasms in the combined data comprised myoepithelioma, cystadenoma and sialadenoma papilliferum.
A relatively long duration (2 years) of a submucosal mass in a minor salivary gland-bearing area with or without bone involvement occurring in a child or adolescent should raise the question of a possible salivary gland neoplasm. A pleomorphic adenoma is the most common benign salivary gland neoplasm in the first and second decade of life. Complete surgical excision affords the best chance of preventing recurrence for pleomorphic adenomas. The recurrence rate of pleomorphic adenomas with two or more years follow-up is 13.0%. Other types of minor salivary gland neoplasms are exceedingly rare and therefore data is sparse, precluding any valid conclusions.
上皮来源的小唾液腺肿瘤在儿童和青少年中较为罕见,除了少数小样本系列研究和病例报告外,大多数病例的记录并不完善。本研究对路易斯安那州立大学牙科学院35年间收治的9例良性上皮性唾液腺肿瘤进行了回顾性临床分析,并将这些数据与英文文献中记录完善的病例数据相结合。
对路易斯安那州立大学牙科学院35年间收治的9例良性上皮性唾液腺肿瘤进行回顾性临床分析,并与英文文献中记录完善的病例数据相结合。
9例良性唾液腺肿瘤患者年龄在19个月至18岁之间,占路易斯安那州立大学牙科学院收治的唾液腺肿瘤的2.3%。这9例病例包括8例多形性腺瘤和1例囊腺瘤。文献中有40例病例,其中34例为多形性腺瘤。将42例多形性腺瘤的数据合并后,平均年龄为12岁,女性与男性的患病比例为2.8:1。硬腭和/或软腭是最常见的发病部位(69.1%)。平均病程和肿瘤大小分别为2.1年和2.4厘米。7例出现骨受累情况。广泛局部切除是最常采用的治疗方法。随访两年或更长时间的病例复发率为13.0%。合并数据中的其余7例肿瘤包括肌上皮瘤、囊腺瘤和乳头状唾液腺瘤。
儿童或青少年在小唾液腺所在区域出现持续时间相对较长(2年)的黏膜下肿物,无论有无骨受累,都应怀疑可能是唾液腺肿瘤。多形性腺瘤是10至20岁人群中最常见的良性唾液腺肿瘤。完整的手术切除为预防多形性腺瘤复发提供了最佳机会。随访两年或更长时间的多形性腺瘤复发率为13.0%。其他类型的小唾液腺肿瘤极为罕见,因此数据稀少,无法得出任何有效结论。