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Renal hilar pheochromocytoma: a case report

Paraganglioma is a rare tumor arising from undifferentiated cells of the primitive neural crest. These tumors are most commonly found in the adrenal gland, other localisations are also possible. A 58-year-old woman who presented with history of left lumbar pain, headache, hypertension, palpitation a...

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Autores principales: Ahallal, Youness, Tazi, Mohammed Fadl, Elfatemi, Hind, Znati, Kaoutar, Tazi, Elmehdi, Amarti, Afaf, El Fassi, Mohammed Jamal, Moulay, Hassan Farih M H
Formato: Texto
Lenguaje:English
Publicado: Cases Network Ltd 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2740209/
https://www.ncbi.nlm.nih.gov/pubmed/19829802
http://dx.doi.org/10.4076/1757-1626-2-6416
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author Ahallal, Youness
Tazi, Mohammed Fadl
Elfatemi, Hind
Znati, Kaoutar
Tazi, Elmehdi
Amarti, Afaf
El Fassi, Mohammed Jamal
Moulay, Hassan Farih M H
author_facet Ahallal, Youness
Tazi, Mohammed Fadl
Elfatemi, Hind
Znati, Kaoutar
Tazi, Elmehdi
Amarti, Afaf
El Fassi, Mohammed Jamal
Moulay, Hassan Farih M H
author_sort Ahallal, Youness
collection PubMed
description Paraganglioma is a rare tumor arising from undifferentiated cells of the primitive neural crest. These tumors are most commonly found in the adrenal gland, other localisations are also possible. A 58-year-old woman who presented with history of left lumbar pain, headache, hypertension, palpitation and sweating was found to have a secreting left renal hilar pheochromocytoma. Radical excision of the tumor was therefore undertaken and her hypertension was controlled. From the case report and literature review, the authors suggest a diagnostic and therapeutic strategy for the management of ectopic localization of pheochromocytoma.
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spelling pubmed-27402092009-10-14 Renal hilar pheochromocytoma: a case report Ahallal, Youness Tazi, Mohammed Fadl Elfatemi, Hind Znati, Kaoutar Tazi, Elmehdi Amarti, Afaf El Fassi, Mohammed Jamal Moulay, Hassan Farih M H Cases J Case report Paraganglioma is a rare tumor arising from undifferentiated cells of the primitive neural crest. These tumors are most commonly found in the adrenal gland, other localisations are also possible. A 58-year-old woman who presented with history of left lumbar pain, headache, hypertension, palpitation and sweating was found to have a secreting left renal hilar pheochromocytoma. Radical excision of the tumor was therefore undertaken and her hypertension was controlled. From the case report and literature review, the authors suggest a diagnostic and therapeutic strategy for the management of ectopic localization of pheochromocytoma. Cases Network Ltd 2009-06-29 /pmc/articles/PMC2740209/ /pubmed/19829802 http://dx.doi.org/10.4076/1757-1626-2-6416 Text en © 2009 Ahallal et al.; licensee Cases Network Ltd. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case report
Ahallal, Youness
Tazi, Mohammed Fadl
Elfatemi, Hind
Znati, Kaoutar
Tazi, Elmehdi
Amarti, Afaf
El Fassi, Mohammed Jamal
Moulay, Hassan Farih M H
Renal hilar pheochromocytoma: a case report
title Renal hilar pheochromocytoma: a case report
title_full Renal hilar pheochromocytoma: a case report
title_fullStr Renal hilar pheochromocytoma: a case report
title_full_unstemmed Renal hilar pheochromocytoma: a case report
title_short Renal hilar pheochromocytoma: a case report
title_sort renal hilar pheochromocytoma: a case report
topic Case report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2740209/
https://www.ncbi.nlm.nih.gov/pubmed/19829802
http://dx.doi.org/10.4076/1757-1626-2-6416
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