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五叶舌：一种新的实体。

Pentafid tongue: A new entity.

作者信息

Senan Manesh, Menon Varun P

机构信息

Departments of Plastic Surgery and Oral and Maxillofacial surgery, Kerala Institute of Medical Sciences (KIMS), Trivandrum, Kerala, India.

出版信息

Indian J Plast Surg. 2015 Sep-Dec;48(3):301-4. doi: 10.4103/0970-0358.173130.

DOI:10.4103/0970-0358.173130
PMID:26933286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4750265/
Abstract

Tongue plays a pivotal role in both physiological and functional life of human beings. Structural and developmental abnormalities of the tongue in various forms have been reported in isolation or in combination with various syndromes. Though cases of bifid tongues have been mentioned in literature, no reports of pentafid tongue have been reported till date. Here we describe a unique case of congenital pentafid tongue along with bilateral polydactyly and its surgical management.

摘要

舌头在人类的生理和功能生活中都起着关键作用。已经有各种形式的舌头结构和发育异常被单独或与各种综合征一起报道。尽管文献中提到过分叉舌的病例，但迄今为止尚未有五叉舌的报道。在此，我们描述了一例伴有双侧多指畸形的先天性五叉舌的独特病例及其手术治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/4750265/4916fbec5dc3/IJPS-48-301-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/4750265/7abafe2746ea/IJPS-48-301-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/4750265/89282fbd5aa1/IJPS-48-301-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/4750265/f14c9fa7d02e/IJPS-48-301-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/4750265/ae99809acb6f/IJPS-48-301-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/4750265/3d21f1680f97/IJPS-48-301-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/4750265/6614515d9540/IJPS-48-301-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/4750265/67f199049217/IJPS-48-301-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/4750265/20db67064e94/IJPS-48-301-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/4750265/4916fbec5dc3/IJPS-48-301-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/4750265/7abafe2746ea/IJPS-48-301-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/4750265/89282fbd5aa1/IJPS-48-301-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/4750265/f14c9fa7d02e/IJPS-48-301-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/4750265/ae99809acb6f/IJPS-48-301-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/4750265/3d21f1680f97/IJPS-48-301-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/4750265/6614515d9540/IJPS-48-301-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/4750265/67f199049217/IJPS-48-301-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/4750265/20db67064e94/IJPS-48-301-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/4750265/4916fbec5dc3/IJPS-48-301-g009.jpg

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Midline defects of the orofaciodigital syndrome type VI (Váradi syndrome).口面指综合征VI型（瓦拉迪综合征）的中线缺陷。
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Syndrome of polydactyly, cleft lip, lingual hamartomas, renal hypoplasia, hearing loss, and psychomotor retardation: variant of the Mohr syndrome or a new syndrome?多指畸形、唇裂、舌错构瘤、肾发育不全、听力丧失和精神运动发育迟缓综合征：莫尔综合征的变异型还是一种新综合征？
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Congenital syndromes connected with tongue malformations.
Bull Assoc Anat (Nancy). 1992 Dec;76(235):67-72.