• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

全唾液腺完全性先天性发育不全:一例报告并文献复习

Complete congenital agenesis of all major salivary glands: a case report and review of the literature.

作者信息

Pham Dang N, Picard M, Mondié J M, Barthélémy I

机构信息

Stomatology and Maxillofacial Departement, Hopital Estaing, Centre Hospitalier Universitaire, Clermont-Ferrand, France.

出版信息

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2010 Oct;110(4):e23-7. doi: 10.1016/j.tripleo.2010.04.008. Epub 2010 Jul 24.

DOI:10.1016/j.tripleo.2010.04.008
PMID:20656534
Abstract

Congenital agenesis of the salivary glands is uncommon. There are documented cases of partial or unilateral aplasia of the major salivary glands associated with the lacrimal puncta, but very few reports of the absence of all major salivary glands. We report the case of a 10-year-old girl with xerostomia and extensive teeth caries. Physical examination and imaging showed total and bilateral aplasia of the parotid, submandibular, and sublingual glands, with no involvement of the minor salivary glands or the lacrimal puncta. We describe the clinical presentation, important aspects in diagnosing partial forms of the condition, and patient management.

摘要

唾液腺先天性发育不全并不常见。有文献记载了与泪点相关的主要唾液腺部分或单侧发育不全的病例,但关于所有主要唾液腺均缺失的报道极少。我们报告一例10岁患有口干症和广泛龋齿的女孩病例。体格检查和影像学检查显示腮腺、颌下腺和舌下腺完全双侧发育不全,小唾液腺和泪点未受累。我们描述了临床表现、诊断该疾病部分形式的重要方面以及患者管理。

相似文献

1
Complete congenital agenesis of all major salivary glands: a case report and review of the literature.全唾液腺完全性先天性发育不全:一例报告并文献复习
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2010 Oct;110(4):e23-7. doi: 10.1016/j.tripleo.2010.04.008. Epub 2010 Jul 24.
2
Congenital agenesis of all major salivary glands and absence of unilateral lacrimal puncta: a case report and review of the literature.所有主要唾液腺先天性发育不全及单侧泪点缺失:一例报告并文献复习
Acta Otolaryngol. 2012 Jun;132(6):671-5. doi: 10.3109/00016489.2011.648273. Epub 2012 Feb 16.
3
Aplasia of submandibular salivary glands associated with ectodermal dysplasia.下颌下涎腺发育不全伴外胚层发育不良。
J Oral Pathol Med. 2004 Nov;33(10):634-6. doi: 10.1111/j.1600-0714.2004.00250.x.
4
The investigation of major salivary gland agenesis: a case report.大唾液腺发育不全的调查:一例报告。
Pediatr Dent. 2001 Mar-Apr;23(2):131-4.
5
Congenital aplasia of the major salivary glands: literature review and case report.先天性大唾液腺发育不全:文献综述与病例报告
Pediatr Dent. 2011 Mar-Apr;33(2):113-8.
6
Bilateral aplasia of the major salivary glands and unilateral atresia of lacrimal duct.双侧大唾液腺发育不全及单侧泪管闭锁
J Craniofac Surg. 2013 Mar;24(2):e177-9. doi: 10.1097/SCS.0b013e318280187f.
7
Case report: aplasia of the lacrimal and major salivary glands (ALSG).病例报告:泪腺和主要唾液腺发育不全(ALSG)
Int J Pediatr Otorhinolaryngol. 2009 Jun;73(6):899-901. doi: 10.1016/j.ijporl.2009.03.004. Epub 2009 Apr 18.
8
Radiological evaluation of major salivary glands agenesis. A case report.大唾液腺发育不全的影像学评估。病例报告。
Minerva Stomatol. 2006 Apr;55(4):223-8.
9
A case of major salivary gland agenesis.一例大唾液腺发育不全病例。
Acta Otolaryngol. 2006 Feb;126(2):219-22. doi: 10.1080/00016480500314139.
10
Bilateral agenesis of parotid salivary glands, an extremely rare condition: report of a case and review of literature.双侧腮腺缺如,一种极为罕见的病症:病例报告及文献复习
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2008 Mar;105(3):e73-5. doi: 10.1016/j.tripleo.2007.10.013.

引用本文的文献

1
Current developments and opportunities of pluripotent stem cells-based therapies for salivary gland hypofunction.基于多能干细胞的唾液腺功能减退治疗的当前进展与机遇
Front Cell Dev Biol. 2024 Jan 19;12:1346996. doi: 10.3389/fcell.2024.1346996. eCollection 2024.
2
Aplasia of the Major and Minor Salivary Glands: Report of a Rare Case.大、小唾液腺发育不全:1例罕见病例报告。
J Oral Maxillofac Res. 2022 Dec 31;13(4):e5. doi: 10.5037/jomr.2022.13405. eCollection 2022 Oct-Dec.
3
Imaging of parotid anomalies in infants and children.
婴幼儿腮腺异常的影像学检查
Insights Imaging. 2022 Feb 24;13(1):27. doi: 10.1186/s13244-022-01166-y.
4
Unusual Conditions Impairing Saliva Secretion: Developmental Anomalies of Salivary Glands.影响唾液分泌的异常情况:唾液腺发育异常
Front Physiol. 2019 Jul 3;10:855. doi: 10.3389/fphys.2019.00855. eCollection 2019.
5
Aplasia of the lacrimal and major salivary glands (ALSG). First case report in spanish population and review of the literature.泪腺和主要唾液腺发育不全(ALSG)。西班牙人群中的首例病例报告及文献综述。
J Clin Exp Dent. 2018 Dec 1;10(12):e1238-e1241. doi: 10.4317/jced.55350. eCollection 2018 Dec.
6
Major salivary gland aplasia and hypoplasia in Down syndrome: review of the literature and report of a case.唐氏综合征中的大唾液腺发育不全和发育不良:文献综述及病例报告
Clin Case Rep. 2017 May 4;5(6):939-944. doi: 10.1002/ccr3.975. eCollection 2017 Jun.
7
Recurrent inflammation of accessory parotid tissue associated with unilateral parotid gland aplasia: diagnostic and therapeutic implications.单侧腮腺发育不全伴副腮腺组织反复炎症:诊断和治疗意义。
Eur Arch Otorhinolaryngol. 2012 May;269(5):1551-4. doi: 10.1007/s00405-011-1902-6. Epub 2012 Jan 5.