Hutchinson J C
Am J Otolaryngol. 1981 Feb;2(1):54-8. doi: 10.1016/s0196-0709(81)80010-5.
A rare case of acinic cell carcinoma of minor salivary gland origin is reported and the literature regarding this type of tumor is reviewed. These tumors arise from either an intercalated duct stem cell or the reserve cell of the salivary gland terminal tubule but not from both simultaneously. Rarely these neoplasms arise from more mature acinar cells. It is clear that these tumors behave ominously. The 25 year determinate survival rate is 50 per cent, with a 20 per cent incidence of metastasis. Surgical excision is the treatment of choice. Radiotherapy, especially neutron therapy, has a place in the treatment of this tumor. The role of chemotherapy is not known at this time.
报告了1例罕见的起源于小唾液腺的腺泡细胞癌，并复习了关于此类肿瘤的文献。这些肿瘤起源于闰管干细胞或唾液腺终末小管的储备细胞，但不同时起源于两者。这些肿瘤很少起源于更成熟的腺泡细胞。显然，这些肿瘤预后不佳。25年的确定生存率为50%，转移发生率为20%。手术切除是首选治疗方法。放射治疗，尤其是中子治疗，在该肿瘤的治疗中占有一席之地。目前化疗的作用尚不清楚。
