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Proboscis lateralis: A case report of a rare giant craniofacial teratoma in an infant

  • Al-Shaqsi, Sultan (Department of Plastic and Reconstructive and Craniofacial Surgery, Khoula Hospital) ;
  • Al-Bulushi, Taimoor (Department of Plastic and Reconstructive and Craniofacial Surgery, Khoula Hospital) ;
  • Al-Hinai, Qasim (Department of Neurosurgery, Khoula Hospital)
  • 투고 : 2017.12.01
  • 심사 : 2018.06.07
  • 발행 : 2018.11.15

초록

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.

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참고문헌

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