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A case of co-existing paraganglioma and thymoma

BACKGROUND: Head and neck paragangliomas are rare tumours and can arise as a part of inherited syndromes. Their association with thymic tumour is not well known. CASE DESCRIPTION: This report describes a female patient who presented with right sided neck paragangliomas. The histology of the tumour w...

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Autores principales: Bano, G., Sennik, D., Kenchaiah, M., Kyaw, Ye, Snape, Katie, Tripathi, V., Wilson, P., Vlahos, I., Hunt, I., Hodgson, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4628025/
https://www.ncbi.nlm.nih.gov/pubmed/26543766
http://dx.doi.org/10.1186/s40064-015-1269-z
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author Bano, G.
Sennik, D.
Kenchaiah, M.
Kyaw, Ye
Snape, Katie
Tripathi, V.
Wilson, P.
Vlahos, I.
Hunt, I.
Hodgson, S.
author_facet Bano, G.
Sennik, D.
Kenchaiah, M.
Kyaw, Ye
Snape, Katie
Tripathi, V.
Wilson, P.
Vlahos, I.
Hunt, I.
Hodgson, S.
author_sort Bano, G.
collection PubMed
description BACKGROUND: Head and neck paragangliomas are rare tumours and can arise as a part of inherited syndromes. Their association with thymic tumour is not well known. CASE DESCRIPTION: This report describes a female patient who presented with right sided neck paragangliomas. The histology of the tumour was consistent with paraganlioma. Few years later her MRI scan of the chest revealed presence of an anterior mediastinal mass that corresponded to the location of the thymus. Review of her previous scans showed that the mass was present all along and had gradually increased in size. Patient developed symptoms including fatigue, dyspnoea, migratory polyarthritis, Raynaud’s phenomenon and erythema nodosum. She had sternotomy and excision of mediastinal mass. The histology was consistent with cortical thymoma (WHO type B2) and she had radiotherapy. After treatment her constitutional symptoms improved. Her paraganglioma susceptibility genes are negative. DISCUSSION AND EVALUATION: To our knowledge this is only the second case report in the literature of coexistence of carotid body tumour and thymoma. The first case reported was bilateral carotid body tumour, thyroid gland adenoma and thymoma. This case also highlights the importance of long term surveillance, multidisciplinary management and being aware of associated pathologies in patients with isolated paraganglioma.
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spelling pubmed-46280252015-11-05 A case of co-existing paraganglioma and thymoma Bano, G. Sennik, D. Kenchaiah, M. Kyaw, Ye Snape, Katie Tripathi, V. Wilson, P. Vlahos, I. Hunt, I. Hodgson, S. Springerplus Case Study BACKGROUND: Head and neck paragangliomas are rare tumours and can arise as a part of inherited syndromes. Their association with thymic tumour is not well known. CASE DESCRIPTION: This report describes a female patient who presented with right sided neck paragangliomas. The histology of the tumour was consistent with paraganlioma. Few years later her MRI scan of the chest revealed presence of an anterior mediastinal mass that corresponded to the location of the thymus. Review of her previous scans showed that the mass was present all along and had gradually increased in size. Patient developed symptoms including fatigue, dyspnoea, migratory polyarthritis, Raynaud’s phenomenon and erythema nodosum. She had sternotomy and excision of mediastinal mass. The histology was consistent with cortical thymoma (WHO type B2) and she had radiotherapy. After treatment her constitutional symptoms improved. Her paraganglioma susceptibility genes are negative. DISCUSSION AND EVALUATION: To our knowledge this is only the second case report in the literature of coexistence of carotid body tumour and thymoma. The first case reported was bilateral carotid body tumour, thyroid gland adenoma and thymoma. This case also highlights the importance of long term surveillance, multidisciplinary management and being aware of associated pathologies in patients with isolated paraganglioma. Springer International Publishing 2015-10-21 /pmc/articles/PMC4628025/ /pubmed/26543766 http://dx.doi.org/10.1186/s40064-015-1269-z Text en © Bano 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.
spellingShingle Case Study
Bano, G.
Sennik, D.
Kenchaiah, M.
Kyaw, Ye
Snape, Katie
Tripathi, V.
Wilson, P.
Vlahos, I.
Hunt, I.
Hodgson, S.
A case of co-existing paraganglioma and thymoma
title A case of co-existing paraganglioma and thymoma
title_full A case of co-existing paraganglioma and thymoma
title_fullStr A case of co-existing paraganglioma and thymoma
title_full_unstemmed A case of co-existing paraganglioma and thymoma
title_short A case of co-existing paraganglioma and thymoma
title_sort case of co-existing paraganglioma and thymoma
topic Case Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4628025/
https://www.ncbi.nlm.nih.gov/pubmed/26543766
http://dx.doi.org/10.1186/s40064-015-1269-z
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