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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。

Aplasia of the lacrimal and major salivary glands (ALSG). First case report in spanish population and review of the literature.

作者信息

Neagu David, Patiño-Seijas Beatriz, Luaces-Rey Ramón, Collado-López Javier, García-Rozado-González Álvaro, López-Cedrún-Cembranos José-Luis

机构信息

MD. Maxillofacial Surgery Department, University Hospital A Coruña, Spain.

MD. Maxillofacial Surgery Department, Private Practice Pontevedra, Spain.

出版信息

J Clin Exp Dent. 2018 Dec 1;10(12):e1238-e1241. doi: 10.4317/jced.55350. eCollection 2018 Dec.

DOI:10.4317/jced.55350
PMID:30697385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6343968/
Abstract

Aplasia of the lacrimal and the major salivary glands (ALSG) is a rare disorder with scarce cases described in the recent literature. The pattern of genetic inheritance is autosomal dominant with variable expressivity. A 40 years male patient was referred to the Oral and Maxillofacial Service at the Hospital Universitario de A Coruña diagnosed with complete agenesis of all salivary glands. Our case it is the first of ALSG syndrome in the Spanish literature. Imaging tests are necessary to confirm the lack of formation of salivary glands and alteration of lacrimal system. A mutation of FGF10 has been proposed as the responsible of the syndrome. The management of the lacrimal alteration depends of the clinical findings. Clinical suspicion remains the principal tool to diagnose the syndrome. ALSG, salivary glands aplasia.

摘要

泪腺和主要唾液腺发育不全(ALSG)是一种罕见疾病,近期文献中描述的病例很少。遗传模式为常染色体显性遗传,具有可变表达性。一名40岁男性患者被转诊至拉科鲁尼亚大学医院口腔颌面科,诊断为所有唾液腺完全缺如。我们的病例是西班牙文献中首例ALSG综合征。需要进行影像学检查以确认唾液腺未形成以及泪腺系统的改变。已提出FGF10突变是该综合征的病因。泪腺改变的治疗取决于临床检查结果。临床怀疑仍然是诊断该综合征的主要手段。ALSG,唾液腺发育不全。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb81/6343968/91ddfbf43c0c/jced-10-e1238-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb81/6343968/e01fdb220074/jced-10-e1238-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb81/6343968/bf255844ac01/jced-10-e1238-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb81/6343968/efb66da6c392/jced-10-e1238-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb81/6343968/91ddfbf43c0c/jced-10-e1238-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb81/6343968/e01fdb220074/jced-10-e1238-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb81/6343968/bf255844ac01/jced-10-e1238-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb81/6343968/efb66da6c392/jced-10-e1238-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb81/6343968/91ddfbf43c0c/jced-10-e1238-g004.jpg

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本文引用的文献

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Hyposalivation in a 16-year-old girl: a case of salivary gland aplasia.16 岁女孩唾液分泌减少:一例涎腺发育不全。
Aust Dent J. 2014 Mar;59(1):125-8. doi: 10.1111/adj.12136. Epub 2014 Feb 4.
2
Bilateral submandibular gland aplasia with hypertrophy of the sublingual glands of a patient with a cleft lip and palate: case report.唇腭裂患者双侧下颌下腺发育不全伴舌下腺肥大:病例报告
J Craniofac Surg. 2013;24(5):e532-3. doi: 10.1097/SCS.0b013e3182a2499e.
3
Complete agenesis of major salivary glands.主要唾液腺完全缺如。
Int J Pediatr Otorhinolaryngol. 2013 Oct;77(10):1782-5. doi: 10.1016/j.ijporl.2013.07.025. Epub 2013 Aug 28.
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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.
5
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.
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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.
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Dacryocystorhinostomy precipitating keratoconjunctivitis sicca in aplasia of lacrimal and major salivary glands (ALSG).因泪腺和大涎腺缺如而行的泪囊鼻腔吻合术诱发干燥性角结膜炎。
Ophthalmic Plast Reconstr Surg. 2012 Mar-Apr;28(2):e50-1. doi: 10.1097/IOP.0b013e318220863f.
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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
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Congenital bilateral parotid gland agenesis in Klinefelter syndrome.先天性双侧腮腺发育不全合并克氏综合征
J Craniomaxillofac Surg. 2010 Jun;38(4):248-50. doi: 10.1016/j.jcms.2009.09.006.
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