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本文引用的文献

1
Proboscis lateralis of nose-a case report.鼻侧长鼻畸形——病例报告
Indian J Surg. 2012 Apr;74(2):181-3. doi: 10.1007/s12262-011-0279-5. Epub 2011 Apr 27.
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Proboscis lateralis.侧鼻畸形
Indian J Otolaryngol Head Neck Surg. 1999 Jan;51(1):74-5. doi: 10.1007/BF02996854.
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New classification scheme of proboscis lateralis based on a review of 50 cases.基于50例病例回顾的侧鼻皮样囊肿新分类方案
Cleft Palate Craniofac J. 2012 Mar;49(2):201-7. doi: 10.1597/10-127.1. Epub 2011 Jan 10.
4
Proboscis lateralis-like appendage: description of a new facial anomaly.类鼻侧附器:一种新的面部异常的描述。
Ann Plast Surg. 2011 Apr;66(4):357-9. doi: 10.1097/SAP.0b013e3181dbc726.
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A preterm infant with semilobar holoprosencephaly and hydrocephalus: a case report.一名患有半侧叶全前脑畸形和脑积水的早产儿:病例报告。
Cases J. 2010 Jan 22;3:35. doi: 10.1186/1757-1626-3-35.
6
An unusual congenital facial anomaly: erectile proboscis-like structure.一种罕见的先天性面部异常:勃起样鼻状结构。
Ann Plast Surg. 2006 Jul;57(1):107-9. doi: 10.1097/01.sap.0000205773.52107.22.
7
Proboscis lateralis: clinical and radiological features.侧鼻畸形:临床及影像学特征
J Laryngol Otol. 2005 Feb;119(2):158-60. doi: 10.1258/0022215053420013.
8
Bilateral nasal proboscis associated with unilateral anophthalmia, unilateral diffuse pigmentation of the conjunctiva, and anomalies of the skull and brain.双侧鼻状畸形伴单侧无眼球、单侧结膜弥漫性色素沉着以及颅骨和脑部异常。
AMA Arch Otolaryngol. 1959 Nov;70:545-50. doi: 10.1001/archotol.1959.00730040557002.
9
THE FACE PREDICTS THE BRAIN: DIAGNOSTIC SIGNIFICANCE OF MEDIAN FACIAL ANOMALIES FOR HOLOPROSENCEPHALY (ARHINENCEPHALY).面部预示大脑:正中面部异常对全前脑畸形(无脑回畸形)的诊断意义。
Pediatrics. 1964 Aug;34:256-63.
10
Proboscis lateralis: radiological evaluation.侧鼻吻:影像学评估。
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侧鼻畸形:1例罕见的与前脑无裂畸形相关的双侧病例

Proboscis Lateralis : A Rare Bilateral Case in Association with Holoprosencephaly.

作者信息

Kolluru Vasavi, Coumary Sendhil

机构信息

Assistant Professor, Department of Obstetrics and Gynaecology, Mahatma Gandhi Medical college and Research Institute , Puducherry, India .

Professor, Department of Obstetrics and Gynaecology, Mahatma Gandhi Medical college and Research Institute , Puducherry, India .

出版信息

J Clin Diagn Res. 2015 Aug;9(8):QD03-4. doi: 10.7860/JCDR/2015/12950.6344. Epub 2015 Aug 1.

DOI:10.7860/JCDR/2015/12950.6344
PMID:26436002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4576595/
Abstract

Proboscis lateralis is a very rare congenital craniofacial malformation characterized by a trunk like tubular appendage arising commonly from roof of the orbit near medial canthus. It may be seen as an isolated defect with sporadic occurrence or it may be associated with a spectrum of anomalies. It is usually unilateral and very few bilateral cases of proboscis lateralis have been reported in the literature worldwide. Alobar holoprosencephaly is commonly associated with a single central proboscis and cyclopia. Here we report an unusual case of a bilateral proboscis lateralis seen in association with holoprosencephaly.

摘要

侧鼻畸形是一种非常罕见的先天性颅面畸形,其特征是通常从内眦附近的眶顶长出一个像躯干一样的管状附属物。它可能表现为孤立性缺陷,偶有发生,也可能与一系列异常情况相关。它通常是单侧的,全世界文献中报道的双侧侧鼻畸形病例非常少。叶状全前脑畸形通常与单个中央鼻畸形和独眼畸形相关。在此,我们报告一例与全前脑畸形相关的双侧侧鼻畸形的罕见病例。