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DOI: 10.5999/aps.2017.01739
Proboscis lateralis: A case report of a rare giant craniofacial teratoma in an infant
The publication of this report was supported by funds from Ibn Sina Pharmacy, Sultanate of Oman.![](https://www.thieme-connect.de/media/10.1055-s-00051611/201806/lookinside/thumbnails/10_5999_aps_2017_01739_578-1.jpg)
Teratomas can occur in almost any region of the body and are the most common extragonadal germ cell childhood tumors. However, craniofacial teratomas are rare. Craniofacial teratomas can present unique features and cause significant functional and aesthetic concerns. There are complex lesions that can have components intra-cranially and extra-cranially. Therefore, their management requires significant multi-stage multidisciplinary surgical procedures. Herein, we present a case of craniofacial teratoma in a child with the phenotype of proboscis lateralis that highlights some of the pertinent point of the diagnosis and management of congenital neonatal teratomas.
Publication History
Received: 01 December 2017
Accepted: 07 June 2018
Article published online:
03 April 2022
© 2018. The Korean Society of Plastic and Reconstructive Surgeons. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonCommercial License, permitting unrestricted noncommercial use, distribution, and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes. (https://creativecommons.org/licenses/by-nc/4.0/)
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