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双侧下颌下腺发育不全:病例报告及文献复习。

Bilateral Submandibular Gland Aplasia: A Case Report and Review of the Literature.

机构信息

Department of Radiology, Elazig Fethi Sekin City Hospital, Elazig, Turkey.

Department of Otorhinolaryngology, Elazig Fethi Sekin City Hospital, Elazig, Turkey.

出版信息

P R Health Sci J. 2022 Sep;41(3):172-175.

Abstract

The congenital absence of major salivary glands, particularly the submandibular gland, is a rare condition. Although the etiology of aplasia is unknown, it is thought to occur owing to defects that emerge during early fetal development. Agenesis of 1 or more of the major salivary glands may occur alone or in association with other congenital anomalies. Very few cases of bilateral submandibular gland aplasia have been reported in the literature. Patients with this condition can be either symptomatic or asymptomatic. Due to the probability of there being additional anomalies, patients and their families should be carefully evaluated. We present the ultrasound and computed tomography findings for a case of bilateral submandibular gland aplasia that was detected incidentally. A review of the literature on major salivary gland aplasia was also conducted.

摘要

先天性大唾液腺缺失,特别是下颌下腺缺失,是一种罕见的情况。尽管病因不明,但据认为是由于早期胎儿发育过程中出现的缺陷所致。一种或多种大唾液腺的发育不全可能单独发生,也可能与其他先天性异常同时发生。文献中报道的双侧下颌下腺发育不全的病例非常少。患有这种疾病的患者可能有症状,也可能无症状。由于存在其他异常的可能性,应仔细评估患者及其家属。我们介绍了一例偶然发现的双侧下颌下腺发育不全的超声和 CT 表现。还对大唾液腺发育不全的文献进行了回顾。

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