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Congenital Malformations of the Head and Neck pp 67–85Cite as

Congenital Malformations of the Nose and Nasopharynx

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Abstract

This chapter provides embryologic and clinical descriptions, photographs, and illustrations of the more common congenital anomalies of the nose and nasopharynx. The authors present the topics in sections based on the underlying pathology. These sections include malformations that occur because the nose failed to form properly (such as arhinia, polyrhinia, and nasal colomboma), those that resulted in midline nasal and nasopharyngeal malformations (such as choanal atresia and craniopharyngioma), and those that resulted in congenital nasopharyngeal or nasal midline masses (such as epignathi, Thornwaldt cysts, dermoids, gliomas, and encephaloceles).

Keywords

  • Arhinia
  • Bifid nose
  • Proboscis
  • Choanal atresia
  • Epignathis
  • Nasal pyriform stenosis
  • Dermoid
  • Glioma
  • Encephalocele

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  • DOI: 10.1007/978-1-4419-1714-0_3
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Author information

Authors and Affiliations

  1. Division of Pediatric Otolaryngology, The Children’s Hospital of Philadelphia, 3400 Civic Center Boulevard, Wood Building, 1st Floor, Philadelphia, PA, 19104, USA

    Mark D. Rizzi M.D. & Brian P. Dunham M.D.

  2. Department of Otolaryngology: Head and Neck Surgery, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA

    Mark D. Rizzi M.D. & Brian P. Dunham M.D.

Authors
  1. Mark D. Rizzi M.D.
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  2. Brian P. Dunham M.D.
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Correspondence to Mark D. Rizzi M.D. .

Editor information

Editors and Affiliations

  1. Pediatric Otolaryngology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA

    Lisa M. Elden

  2. Pediatric Otolaryngology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA

    Karen B. Zur

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Rizzi, M.D., Dunham, B.P. (2014). Congenital Malformations of the Nose and Nasopharynx. In: Elden, L., Zur, K. (eds) Congenital Malformations of the Head and Neck. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-1714-0_3

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  • DOI: https://doi.org/10.1007/978-1-4419-1714-0_3

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