A spontaneous paraganglioma–pheochromocytoma syndrome

We present a case of a 40–year old woman diagnosed with a four–place spontaneous paraganglioma–pheochromocytoma syndrome, which was treated surgically. The presence of the succinate dehydrogenase complex subunit D (SDHD) mutation that causes the pheochromocytoma was confirmed but no mutations in the...

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Autores principales: Toutounchi, Sadegh, Pogorzelski, Ryszard, Siński, Maciej, Łoń, Izabela, Zapała, Łukasz, Fiszer, Patryk, Krajewska, Ewa, Skórski, Maciej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Polish Urological Association 2013
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992452/
https://www.ncbi.nlm.nih.gov/pubmed/24757537
http://dx.doi.org/10.5173/ceju.2013.04.art12
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author Toutounchi, Sadegh
Pogorzelski, Ryszard
Siński, Maciej
Łoń, Izabela
Zapała, Łukasz
Fiszer, Patryk
Krajewska, Ewa
Skórski, Maciej
author_facet Toutounchi, Sadegh
Pogorzelski, Ryszard
Siński, Maciej
Łoń, Izabela
Zapała, Łukasz
Fiszer, Patryk
Krajewska, Ewa
Skórski, Maciej
author_sort Toutounchi, Sadegh
collection PubMed
description We present a case of a 40–year old woman diagnosed with a four–place spontaneous paraganglioma–pheochromocytoma syndrome, which was treated surgically. The presence of the succinate dehydrogenase complex subunit D (SDHD) mutation that causes the pheochromocytoma was confirmed but no mutations in the family members were found. After the excision of the paragangliomas located in the areas of the division of carotid arteries, and mediastinum, as well as a tumor on the left site of the celiac trunk, the patient remains asymptomatic and is regularly followed–up.
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spelling pubmed-39924522014-04-28 A spontaneous paraganglioma–pheochromocytoma syndrome Toutounchi, Sadegh Pogorzelski, Ryszard Siński, Maciej Łoń, Izabela Zapała, Łukasz Fiszer, Patryk Krajewska, Ewa Skórski, Maciej Cent European J Urol Original Paper We present a case of a 40–year old woman diagnosed with a four–place spontaneous paraganglioma–pheochromocytoma syndrome, which was treated surgically. The presence of the succinate dehydrogenase complex subunit D (SDHD) mutation that causes the pheochromocytoma was confirmed but no mutations in the family members were found. After the excision of the paragangliomas located in the areas of the division of carotid arteries, and mediastinum, as well as a tumor on the left site of the celiac trunk, the patient remains asymptomatic and is regularly followed–up. Polish Urological Association 2013-12-19 2013 /pmc/articles/PMC3992452/ /pubmed/24757537 http://dx.doi.org/10.5173/ceju.2013.04.art12 Text en Copyright by Polish Urological Association http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Toutounchi, Sadegh
Pogorzelski, Ryszard
Siński, Maciej
Łoń, Izabela
Zapała, Łukasz
Fiszer, Patryk
Krajewska, Ewa
Skórski, Maciej
A spontaneous paraganglioma–pheochromocytoma syndrome
title A spontaneous paraganglioma–pheochromocytoma syndrome
title_full A spontaneous paraganglioma–pheochromocytoma syndrome
title_fullStr A spontaneous paraganglioma–pheochromocytoma syndrome
title_full_unstemmed A spontaneous paraganglioma–pheochromocytoma syndrome
title_short A spontaneous paraganglioma–pheochromocytoma syndrome
title_sort spontaneous paraganglioma–pheochromocytoma syndrome
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992452/
https://www.ncbi.nlm.nih.gov/pubmed/24757537
http://dx.doi.org/10.5173/ceju.2013.04.art12
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