Kara Medine, Güçlü Oğuz, Dereköy Fevzi Sefa, Resorlu Mustafa, Adam Gürhan
Department of Otolaryngology, Canakkale Onsekiz Mart University Medical Hospital, Canakkale, Turkey.
Department of Radiology, Canakkale Onsekiz Mart University Medical Hospital, Canakkale, Turkey.
Case Rep Otolaryngol. 2014;2014:569026. doi: 10.1155/2014/569026. Epub 2014 Sep 1.
Background. Congenital absence of the submandibular gland (SMG) is a rare condition. Although complaints such as dry mouth, dental problems, or difficulty in swallowing may be seen, the subjects may also be asymptomatic. The absence of the SMG may be associated with hypertrophy of the contralateral SMG. Case Report. We report the case of a 44-year-old woman with incidentally detected left SMG aplasia, with contralateral SMG hypertrophy mimicking a mass, and the case of a 46-year-old woman with incidentally detected bilateral SMG aplasia, demonstrated by computerized tomography (CT) and magnetic resonance imaging (MRI). Conclusion. It is important for the clinician to know that this very rare abnormality may exist. When such a case is encountered, symptoms and findings should be reevaluated and, if necessary, conservative therapy should be initiated. The possibility of observing additional deformities should be kept in mind and an evaluation should be done for other cases in the family.
背景。先天性下颌下腺缺如(SMG)是一种罕见的病症。尽管可能会出现口干、牙齿问题或吞咽困难等症状,但患者也可能没有症状。SMG缺如可能与对侧SMG肥大有关。病例报告。我们报告了一例44岁女性,偶然发现左侧SMG发育不全,对侧SMG肥大类似肿块;以及一例46岁女性,偶然发现双侧SMG发育不全,通过计算机断层扫描(CT)和磁共振成像(MRI)得以证实。结论。临床医生了解这种非常罕见的异常情况可能存在很重要。遇到此类病例时,应重新评估症状和检查结果,必要时应开始保守治疗。应牢记观察到其他畸形的可能性,并对家族中的其他病例进行评估。