Literature DB >> 28764308

Familial Cancers of Head and Neck Region.

Reshma Venugopal1, Radhika Manoj Bavle2, Paremala Konda3, Sudhakara Muniswamappa3, Soumya Makarla3.   

Abstract

Cancers that occur in families more often than would be expected by chance are termed as familial cancers. They occur due to an inherited genetic mutation and account for 5%-10% of all cancers. This review article presents some of the common Familial Cancer Syndromes (FCS) such as MEN 2B, hyperparathyroidism-jaw tumour syndrome, familial oral squamous cell carcinoma, melanoma, nasopharyngeal carcinoma, paraganglioma, neurofibroma and other syndromes associated with head and neck region.

Entities:  

Keywords:  Genetic susceptibility; Germline mutation; Multiple abnormalities; Oral manifestations

Year:  2017        PMID： 28764308      PMCID： PMC5535495          DOI： 10.7860/JCDR/2017/25920.9967

Source DB:  PubMed          Journal:  J Clin Diagn Res        ISSN： 0973-709X


  32 in total

Review 1.  Dyskeratosis congenita.

Authors:  T P B Handley; J A McCaul; G R Ogden
Journal:  Oral Oncol       Date:  2005-09-02       Impact factor: 5.337

2.  Neurofibromatosis type 2 (NF 2) or schwannomatosis?--Case report study and diagnostic criteria.

Authors:  Maciej Radek; Bartłomiej Tomasik; Maciej Wojdyn; Dorota Snopkowska-Wiaderna; Maciej Błaszczyk; Andrzej Radek
Journal:  Neurol Neurochir Pol       Date:  2016-02-23       Impact factor: 1.621

3.  Multiple endocrine neoplasia type 2B: maxillofacial significance in 5 cases.

Authors:  Robert Bruce MacIntosh; Prasanna-Kumar Shivapuja; Michael Brady Krzemien; Michael Lee
Journal:  J Oral Maxillofac Surg       Date:  2014-09-10       Impact factor: 1.895

4.  Contiguous bilateral head and neck paragangliomas in a carrier of the SDHB germline mutation.

Authors:  Nicole Collins; Alan Dietzek
Journal:  J Vasc Surg       Date:  2011-08-06       Impact factor: 4.268

5.  Rapid mutation scanning of genes associated with familial cancer syndromes using denaturing high-performance liquid chromatography.

Authors:  D J Marsh; G Theodosopoulos; V Howell; A L Richardson; D E Benn; A L Proos; C Eng; B G Robinson
Journal:  Neoplasia       Date:  2001 May-Jun       Impact factor: 5.715

Review 6.  Tumours of familial origin in the head and neck.

Authors:  Carlos Suárez; Juan Pablo Rodrigo; Alfio Ferlito; Rubén Cabanillas; Ashok R Shaha; Alessandra Rinaldo
Journal:  Oral Oncol       Date:  2006-07-20       Impact factor: 5.337

7.  Hyperparathyroidism-jaw tumour syndrome.

Authors:  J D Chen; C Morrison; C Zhang; K Kahnoski; J D Carpten; B T Teh
Journal:  J Intern Med       Date:  2003-06       Impact factor: 8.989

8.  Familial melanoma-associated mutations in p16 uncouple its tumor-suppressor functions.

Authors:  Noah C Jenkins; Jae Jung; Tong Liu; Megan Wilde; Sheri L Holmen; Douglas Grossman
Journal:  J Invest Dermatol       Date:  2012-11-29       Impact factor: 8.551

Review 9.  Multiple endocrine neoplasia type 1 (MEN1) and type 4 (MEN4).

Authors:  Rajesh V Thakker
Journal:  Mol Cell Endocrinol       Date:  2013-08-08       Impact factor: 4.102

Review 10.  Role of human papillomavirus and tumor suppressor genes in oral cancer.

Authors:  Vardendra Manvikar; Rama Kulkarni; Anila Koneru; M Vanishree
Journal:  J Oral Maxillofac Pathol       Date:  2016 Jan-Apr
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  1 in total

Review 1.  Epigenetic editing and tumor-dependent immunosuppressive signaling in head and neck malignancies.

Authors:  Spyridon Gougousis; Savvas Petanidis; Alexandros Poutoglidis; Nikolaos Tsetsos; Paraskevas Vrochidis; Ioannis Skoumpas; Nektarios Argyriou; Theodora Katopodi; Kalliopi Domvri
Journal:  Oncol Lett       Date:  2022-05-04       Impact factor: 3.111
  1 in total

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