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软腭右半侧完全缺如——病例报告

Complete Agenesis of Right Half of Soft Palate-A Case Report.

作者信息

Agnihotri Ishan, Nayak Bibhuti Bhusan

机构信息

Department of Plastic & Reconstructive Surgery, SCB Medical College, Cuttack, Odisha, India.

出版信息

Indian J Plast Surg. 2024 May 10;57(5):404-407. doi: 10.1055/s-0044-1786366. eCollection 2024 Oct.

DOI:10.1055/s-0044-1786366
PMID:39552796
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11567772/
Abstract

Agenesis of soft palate is an extremely rare occurrence and is usually seen in conjunction with other congenital anomalies like Nager syndrome, Treacher Collins syndrome, and multiple congenital anomalies. Only a handful of isolated complete agenesis of one half of the soft palate has been reported in literature. Despite extensive literature review, incidence of such a case is practically unheard of. We present to you a case checking all the above boxes. We present this case of agenesis of right half of soft palate that was managed by our technique.

摘要

软腭发育不全极为罕见，通常与其他先天性异常如纳格尔综合征、特雷彻·柯林斯综合征以及多种先天性异常同时出现。文献中仅报道过少数几例孤立的软腭一侧完全发育不全的病例。尽管进行了广泛的文献检索，但这种病例的发生率实际上闻所未闻。我们在此向您呈现一个符合上述所有情况的病例。我们展示这例右侧软腭发育不全的病例，该病例采用我们的技术进行了治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f7f/11567772/e3eaf63272ba/10-1055-s-0044-1786366-i2412568-8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f7f/11567772/1133701b33fd/10-1055-s-0044-1786366-i2412568-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f7f/11567772/a1a937fcd07a/10-1055-s-0044-1786366-i2412568-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f7f/11567772/c94fd707e4ec/10-1055-s-0044-1786366-i2412568-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f7f/11567772/af664b8b2ff0/10-1055-s-0044-1786366-i2412568-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f7f/11567772/992bb071ab8c/10-1055-s-0044-1786366-i2412568-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f7f/11567772/f5d7f7f5bb1d/10-1055-s-0044-1786366-i2412568-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f7f/11567772/748bd2923c22/10-1055-s-0044-1786366-i2412568-7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f7f/11567772/e3eaf63272ba/10-1055-s-0044-1786366-i2412568-8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f7f/11567772/1133701b33fd/10-1055-s-0044-1786366-i2412568-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f7f/11567772/a1a937fcd07a/10-1055-s-0044-1786366-i2412568-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f7f/11567772/c94fd707e4ec/10-1055-s-0044-1786366-i2412568-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f7f/11567772/af664b8b2ff0/10-1055-s-0044-1786366-i2412568-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f7f/11567772/992bb071ab8c/10-1055-s-0044-1786366-i2412568-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f7f/11567772/f5d7f7f5bb1d/10-1055-s-0044-1786366-i2412568-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f7f/11567772/748bd2923c22/10-1055-s-0044-1786366-i2412568-7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f7f/11567772/e3eaf63272ba/10-1055-s-0044-1786366-i2412568-8.jpg

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本文引用的文献

1
Surgical Management of Velopharyngeal Insufficiency Due to Unilateral Oropharyngeal Agenesis in a Patient With Stickler Syndrome.单侧后鼻孔闭锁患者斯蒂克勒综合征伴发软腭咽闭合不全的手术治疗
Cleft Palate Craniofac J. 2021 Sep;58(9):1190-1194. doi: 10.1177/1055665620977414. Epub 2020 Dec 7.
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Reconstruction of an idiopathic hemipalatal hypoplasia: report of a case.特发性半侧腭发育不全的重建：病例报告
Br J Oral Maxillofac Surg. 2020 Jan;58(1):79-82. doi: 10.1016/j.bjoms.2019.04.015. Epub 2019 Nov 11.
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A very rare cause of asymmetric velopharyngeal incompetence: unilateral palate hypoplasia.
Cleft Palate Craniofac J. 2012 Jul;49(4):494-7. doi: 10.1597/10-097. Epub 2011 Jul 8.
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Hemipalatal hypoplasia.
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Gross unilateral abnormalities of the velum and pharynx.软腭和咽部的单侧明显异常。
Cleft Palate Craniofac J. 2002 Jul;39(4):461-8. doi: 10.1597/1545-1569_2002_039_0461_guaotv_2.0.co_2.
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Unilateral absence of the soft palate: case report of reconstruction with a mucoperiosteal island flap.单侧软腭缺失：带蒂黏骨膜瓣修复的病例报告
Cleft Palate Craniofac J. 1993 Sep;30(5):497-9. doi: 10.1597/1545-1569_1993_030_0497_uaotsp_2.3.co_2.
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Atypical cleft of the palate: a report.腭部非典型腭裂：一份报告。
Cleft Palate Craniofac J. 1994 Jul;31(4):313-5. doi: 10.1597/1545-1569_1994_031_0313_acotpa_2.3.co_2.
8
A significant feature of Nager's syndrome: palatal agenesis.纳热尔综合征的一个显著特征：腭发育不全。
Plast Reconstr Surg. 1989 Aug;84(2):219-26. doi: 10.1097/00006534-198908000-00005.