Jones A O, Lam A H, Martin H C
Department of Radiology, St Vincent's Hospital, Darlinghurst, Australia.
Australas Radiol. 1997 Feb;41(1):44-8. doi: 10.1111/j.1440-1673.1997.tb00468.x.
The imaging findings of two children with acinic cell carcinoma of the parotid gland are presented. Ultrasonic features are emphasized. One of these children, a 6-year-old boy, suffers from the oculocerebrorenal syndrome of Lowe, a rare congenital, inherited condition manifested by defects of the nervous system (mental retardation, hypotonia), eyes (cataracts, glaucoma) and kidneys. To date, no known association exists between these two rare entities. The other child, a 10-year-old girl, was otherwise well. The ultrasound findings of both cases demonstrate features more classic for a benign intraparotid mass than for a potentially malignant lesion. The possibility of acinic cell carcinoma should be considered if a well-defined, relatively homogenously hypo-echoic intraparotid mass is encountered in a child, especially if cystic spaces are present.
本文报告了两名腮腺腺泡细胞癌患儿的影像学表现,重点强调了超声特征。其中一名患儿为6岁男孩,患有Lowe眼脑肾综合征,这是一种罕见的先天性遗传性疾病,表现为神经系统(智力发育迟缓、肌张力减退)、眼睛(白内障、青光眼)和肾脏的缺陷。迄今为止,这两种罕见疾病之间尚无已知关联。另一名患儿为10岁女孩,其他方面健康。两例病例的超声表现显示,其特征更符合腮腺内良性肿块而非潜在恶性病变。如果在儿童中发现腮腺内边界清晰、相对均匀低回声的肿块,尤其是存在囊性间隙时,应考虑腺泡细胞癌的可能性。