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孤立性先天性双裂舌。

Isolated congenital bifid tongue.

作者信息

Surej Kumar L K, Kurien Nikhil M, Sivan Madhu P

机构信息

Department of Oral and Maxillofacial Surgery, PMS College of Dental Science and Research, Golden Hills, Vattappara, Trivandrum, Kerala, India.

出版信息

Natl J Maxillofac Surg. 2010 Jul;1(2):187-9. doi: 10.4103/0975-5950.79228.

DOI:10.4103/0975-5950.79228
PMID:22442597
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3304211/
Abstract

Human growth and development is a meticulously planned and precisely executed process. Even a mild disturbance can have clinically significant manifestations later on. Even today, ancient beliefs and practices override/delay patient's aspiration for seeking treatment as seen in the case report presented here. Congenital bifid tongue in association with various other orofacial abnormalities has been reported, many of which have been linked to various syndromes. But congenital bifid tongue occurring in the absence of other orofacial abnormalities is very rare. Here, we discuss a case of bifid tongue involving the anterior one-third of tongue, reported in a 45-year-old male patient unusually with no other intraoral abnormalities.

摘要

人类生长发育是一个精心规划且精确执行的过程。即使是轻微的干扰,日后也可能出现具有临床意义的表现。即便在今天,如本病例报告所示,古老的观念和做法仍会凌驾于/延迟患者寻求治疗的意愿。已有先天性双裂舌与各种其他口面部异常相关的报道,其中许多与各种综合征有关。但在没有其他口面部异常的情况下出现先天性双裂舌非常罕见。在此,我们讨论一例发生在一名45岁男性患者身上的双裂舌病例,该双裂舌累及舌前三分之一,且该患者无其他口腔内异常,情况较为特殊。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a9e/3304211/742b028dc4e0/NJMS-1-187-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a9e/3304211/8e2869155fbf/NJMS-1-187-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a9e/3304211/6fafbb6dd141/NJMS-1-187-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a9e/3304211/742b028dc4e0/NJMS-1-187-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a9e/3304211/8e2869155fbf/NJMS-1-187-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a9e/3304211/6fafbb6dd141/NJMS-1-187-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a9e/3304211/742b028dc4e0/NJMS-1-187-g003.jpg

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引用本文的文献

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本文引用的文献

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Prenatally diagnosed lethal type Larsen-like syndrome associated with bifid tongue.产前诊断的致死型类拉森综合征伴双舌畸形。
Turk J Pediatr. 2008 Jul-Aug;50(4):395-9.
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Oral-facial digital syndrome type 1.口面指综合征 1 型。
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Bifid tongue: a rare feature associated with infants of diabetic mother syndrome.
Am J Med Genet A. 2007 Sep 1;143A(17):2035-9. doi: 10.1002/ajmg.a.31877.
双侧舌底与多种鳃裂异常相关。
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Traumatic bifid tongue: A rare presentation in a child. Case report.创伤性裂舌:儿童中的罕见表现。病例报告。
Ann Med Surg (Lond). 2020 Jul 11;57:11-13. doi: 10.1016/j.amsu.2020.06.040. eCollection 2020 Sep.
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Salivary hamartoma with a bifid tongue in an adult patient.一名成年患者患有唾液腺错构瘤并伴有双裂舌。
Natl J Maxillofac Surg. 2018 Jan-Jun;9(1):61-63. doi: 10.4103/njms.NJMS_28_17.
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Multidisciplinary management of Opitz G BBB syndrome.奥皮茨G BBB综合征的多学科管理。
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Bifid tongue - a complication of tongue piercing.分叉舌——舌穿刺的一种并发症。
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Seventeen-year follow-up of a patient with median cleft of the lower lip, mandible, and tongue with flexion contracture: a case report.下唇、下颌骨及舌正中裂合并屈曲挛缩患者的17年随访:病例报告
Cleft Palate Craniofac J. 2002 Sep;39(5):555-9. doi: 10.1597/1545-1569_2002_039_0555_syfuoa_2.0.co_2.
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Tassier cleft no 30 (median cleft from lower lip to manubrium).第30号塔西埃裂(从下唇至胸骨柄的正中裂)
Indian J Pediatr. 2001 Dec;68(12):1163-4. doi: 10.1007/BF02722937.
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Congenital midline palatomandibular bony fusion with a mandibular cleft and a bifid tongue.
Br J Plast Surg. 1997 Feb;50(2):139-41. doi: 10.1016/s0007-1226(97)91328-x.
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Orodigitofacial syndromes type I and II: clinical and surgical studies.I型和II型口指面部综合征:临床与外科研究
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