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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2015
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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. |
format | Online Article Text |
id | pubmed-4628025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
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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