Home contents
2019
   N# 1 |
2018
   N# 1 | 2 | 3 | 4 | 5 |
2017
   N# 1 | 2 | 3 | 4 | 5 |
2016
   N# 1 | 2 | 3 | 4 | 5 |
2015
   N# 1 | 2 | 3 | 4 | 5 |
2014
   N# 1 | 2 | 3 | 4 | 5 |
2013
   N# 1 | 2 | 3 | 4 | 5 |
2012
   N# 1 | 2 | 3 | 4 | 5 |
2011
   N# 1 | 2 | 3 | 4 | 5 |
2010
   N# 1 | 2 | 3 | 4 | 5 |
2009
   N# 1 | 2 | 3 | 4 | 5 |
2008
   N# 1 | 2 | 3 | 4 | 5 |
2007
   N# 1 | 2 | 3 | 4 | 5 |
2006
   N# 1 | 2 | 3 | 4 | 5 |
2005
   N# | 1 | 2 | 3 | 4 | 5 |
2004
   N# 1 | 2 | 3 | 4 | 5 |
2003
   N# 1 | 2 | 3 | 4 | 5 |
2002
   N# 1 | 2 | 3 | 4 | 5 |
2001
   N# 1 | 2 | 3 | 4 | 5 |
2000
   N# | 1 | 2 | 3 | 4 | 5 |
1999
   N# 1 | 2 | 3 | 4 | 5 |
1998
   N# 1 | 2 | 3 | 5 |
1997
   N# 1 | 2 | 3 | 4 | 5 |
1996
   N# 4 | 5 |

Click on the number of the review to see the content
Teaching bulletin CME
List of all teaching bulletins CME.
Editor reading committee
Editor reading committee.
To publish...
Instructions for authors
Archives Press and Books
Select of books and press articles.
Mailing list
News information letter.
Subscription prices


If you wish to adjust the size of the displayed characters, click in the high menu on "Your account" and choose the desired size.



  Contents > Previous page > Article detail print Order
o Issue N# 3 - 2018 o

GENETIC

Cowden syndrome: Otolaryngology approach


Authors : Ahumada F, Encinas A, Sánchez A, Villacampa JM, Cenjor C. (Casablanca)

Ref. : Rev Laryngol Otol Rhinol. 2018;139,3:59-61.

Article published in english
Downloadable PDF document english



Summary : Background: Cowden syndrome (CS) is a rare autosomal dominant geno­der­ma­­tosis. Inheritance with variable expression that is at increased risk of breast, thyroid, endo­metrial, and renal cancers. Case report: Patient with pharyngeal involvement, with previous clinical and genetic diagnosis of Cowden syndrome. Nasofibrolaryngoscopy revealed multiple pharyngeal masses confirmed by MRI. Excision surgery was performed and malignancy was not observed in the patho­logical study. Results: This treatment was effective decreasing size of the bulky lesions. Conclusion: We believe head and neck surgeons need to balance their decisions between individual risk assessment, potential psychological benefits and accepted guidelines. We believe that need more studies describing the head and neck manifestations on this rare syndrome.

Price : 12.00 €      order
|


Subscribe online - Pay by credit card!


© Copyright 1999-2024 - Revue de Laryngologie   Réalisation - Hébergement ELIDEE