Tylosis with oesophageal cancer: Diagnosis, management and [PDF]

Sep 29, 2015 - Definition. Tylosis with oesophageal cancer is characterised by thickening of the skin of the hands and f

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Orphanet J Rare Dis. 2015; 10: 126.

PMCID: PMC4589029

Published online 2015 Sep 29. doi: 10.1186/s13023-015-0346-2

Tylosis with oesophageal cancer: Diagnosis, management and molecular mechanisms Anthony Ellis, Janet M. Risk, Thiviyani Maruthappu, and David P. Kelsell Department of Gastroenterology, Royal Liverpool University Hospital, Prescot Street, Liverpool, L7 8XP UK Department of Molecular & Clinical Cancer Medicine, Institute of Translational Medicine, University of Liverpool, L69 3BX Liverpool, UK Centre for Cell Biology and Cutaneous Research, The Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, E1 4AT UK David P. Kelsell, Email: [email protected]. Corresponding author. Received 2014 Dec 18; Accepted 2015 Sep 24. Copyright © Ellis et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. This article has been cited by other articles in PMC.

Abstract

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Introduction

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Disease name/synonyms

Definition

Epidemiology

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Clinical description

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Aetiology

Diagnosis and diagnostic methods

Differential diagnosis

Genetic counselling

Management including treatment

Prognosis

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Unresolved questions

Conclusions

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Acknowledgements

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Abbreviations

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Footnotes

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Competing interests The author(s) declare that they have no competing interests. Authors’ contributions All four authors drafted, read and approved the final version of the manuscript.

References

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Articles from Orphanet Journal of Rare Diseases are provided here courtesy of BioMed Central

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