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Pheochromocytoma of the organ of Zuckerkandl

Paragangliomas are uncommon neuroendocrine neoplasms that occur in characteristic locations. While parasympathetic paragangliomas are mainly located at the head and neck, sympathetic paragangliomas are mostly located below the neck. Among parasympathetic paragangliomas, pheochromocytomas are the mos...

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Autores principales: Le, Hoang Di Thu, Nguyen, Thai Thi My Hanh, Pham, Anh Vu, Dang, Cong Thuan, Nguyen, Thanh Thao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708655/
https://www.ncbi.nlm.nih.gov/pubmed/33299507
http://dx.doi.org/10.1016/j.radcr.2020.11.024
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author Le, Hoang Di Thu
Nguyen, Thai Thi My Hanh
Pham, Anh Vu
Dang, Cong Thuan
Nguyen, Thanh Thao
author_facet Le, Hoang Di Thu
Nguyen, Thai Thi My Hanh
Pham, Anh Vu
Dang, Cong Thuan
Nguyen, Thanh Thao
author_sort Le, Hoang Di Thu
collection PubMed
description Paragangliomas are uncommon neuroendocrine neoplasms that occur in characteristic locations. While parasympathetic paragangliomas are mainly located at the head and neck, sympathetic paragangliomas are mostly located below the neck. Among parasympathetic paragangliomas, pheochromocytomas are the most common. Ninety percent of cases of pheochromocytomas arise within the adrenal gland. We report a case of a 63-year-old woman with an extra-adrenal pheochromocytoma of the organ of Zuckerkandl detected by CT and MRI and subsequently confirmed by postoperative histology and immunohistochemistry.
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spelling pubmed-77086552020-12-08 Pheochromocytoma of the organ of Zuckerkandl Le, Hoang Di Thu Nguyen, Thai Thi My Hanh Pham, Anh Vu Dang, Cong Thuan Nguyen, Thanh Thao Radiol Case Rep Case Report Paragangliomas are uncommon neuroendocrine neoplasms that occur in characteristic locations. While parasympathetic paragangliomas are mainly located at the head and neck, sympathetic paragangliomas are mostly located below the neck. Among parasympathetic paragangliomas, pheochromocytomas are the most common. Ninety percent of cases of pheochromocytomas arise within the adrenal gland. We report a case of a 63-year-old woman with an extra-adrenal pheochromocytoma of the organ of Zuckerkandl detected by CT and MRI and subsequently confirmed by postoperative histology and immunohistochemistry. Elsevier 2020-11-28 /pmc/articles/PMC7708655/ /pubmed/33299507 http://dx.doi.org/10.1016/j.radcr.2020.11.024 Text en © 2020 The Authors. Published by Elsevier Inc. on behalf of University of Washington. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Le, Hoang Di Thu
Nguyen, Thai Thi My Hanh
Pham, Anh Vu
Dang, Cong Thuan
Nguyen, Thanh Thao
Pheochromocytoma of the organ of Zuckerkandl
title Pheochromocytoma of the organ of Zuckerkandl
title_full Pheochromocytoma of the organ of Zuckerkandl
title_fullStr Pheochromocytoma of the organ of Zuckerkandl
title_full_unstemmed Pheochromocytoma of the organ of Zuckerkandl
title_short Pheochromocytoma of the organ of Zuckerkandl
title_sort pheochromocytoma of the organ of zuckerkandl
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708655/
https://www.ncbi.nlm.nih.gov/pubmed/33299507
http://dx.doi.org/10.1016/j.radcr.2020.11.024
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