Manganaris Argyrios, Kiziridou Anastasia, Manganaris Theodoros
E.N.T. Department, THEAGENIO Anticancer Hospital, 2 Alexandrou Simeonidi Str., Thessaloniki- Greece.
J Craniofac Surg. 2007 Jan;18(1):231-5. doi: 10.1097/01.scs.0000246740.84471.4e.
Adenoid cystic carcinoma of the parotid gland is relatively rare. According to a retrospective study of the medical records and histopathology files of 514 cases of parotid tumors operated at our hospital over a period of 18 years, adenoid cystic carcinoma represented only 2.3% of all parotid gland neoplasms, a total of 12 cases. In our records we retrieved only one documented case of adenoid cystic carcinoma that originated in the parotid gland subsequent to superficial parotidectomy for a benign lesion (pleomorphic adenoma). An even more exceptional presentation of adenoid cystic carcinoma is as a bilobed tumor extending from the post auricular to the temporal and zygomatic region. The management of this case is presented along with a brief review of the literature concerning the evaluation and management of this rare entity.
腮腺腺样囊性癌相对少见。根据对我院18年间514例腮腺肿瘤手术病例的病历及组织病理学档案的回顾性研究,腺样囊性癌仅占所有腮腺肿瘤的2.3%,共12例。在我们的记录中,仅检索到1例有记录的病例,该腺样囊性癌起源于因良性病变(多形性腺瘤)行腮腺浅叶切除术后的腮腺。腺样囊性癌更罕见的表现是呈双叶状肿瘤,从耳后延伸至颞部和颧部区域。本文介绍了该病例的处理方法,并对有关这种罕见疾病的评估和处理的文献进行了简要回顾。