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Laparoscopic excision of a large Adrenal Ganglioneuroma masquerading as Pheochromocytoma- A case report & review of literature

Adrenal Ganglioneuromas are rare. Evaluation for hormone secretion followed by complete excision is the treatment of choice for such masses. We present our experience of a symptomatic large Adrenal Ganglioneuroma, which was removed with laparoscopic procedure. A 44-year gentleman presented with a sy...

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Autores principales: Santosh, K., Das, Manoj K., Ayyanar, Pavithra, Mandal, Swarnendu, Nayak, Prasant, Kumar, Sumit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7262088/
https://www.ncbi.nlm.nih.gov/pubmed/32489900
http://dx.doi.org/10.1016/j.eucr.2020.101276
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author Santosh, K.
Das, Manoj K.
Ayyanar, Pavithra
Mandal, Swarnendu
Nayak, Prasant
Kumar, Sumit
author_facet Santosh, K.
Das, Manoj K.
Ayyanar, Pavithra
Mandal, Swarnendu
Nayak, Prasant
Kumar, Sumit
author_sort Santosh, K.
collection PubMed
description Adrenal Ganglioneuromas are rare. Evaluation for hormone secretion followed by complete excision is the treatment of choice for such masses. We present our experience of a symptomatic large Adrenal Ganglioneuroma, which was removed with laparoscopic procedure. A 44-year gentleman presented with a symptomatic adrenal tumor. Under the impression of Adrenal Pheochromocytoma, tumor was excised laparoscopically without any untoward event. And to our surprise Adrenal Ganglioneuroma was detected in biopsy. Hence, Ganglioneuromas should be considered as a differential for a functional or symptomatic adrenal mass. And by following proper technique even such large functional adrenal masses can be removedlaparoscopically.
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spelling pubmed-72620882020-06-01 Laparoscopic excision of a large Adrenal Ganglioneuroma masquerading as Pheochromocytoma- A case report & review of literature Santosh, K. Das, Manoj K. Ayyanar, Pavithra Mandal, Swarnendu Nayak, Prasant Kumar, Sumit Urol Case Rep Oncology Adrenal Ganglioneuromas are rare. Evaluation for hormone secretion followed by complete excision is the treatment of choice for such masses. We present our experience of a symptomatic large Adrenal Ganglioneuroma, which was removed with laparoscopic procedure. A 44-year gentleman presented with a symptomatic adrenal tumor. Under the impression of Adrenal Pheochromocytoma, tumor was excised laparoscopically without any untoward event. And to our surprise Adrenal Ganglioneuroma was detected in biopsy. Hence, Ganglioneuromas should be considered as a differential for a functional or symptomatic adrenal mass. And by following proper technique even such large functional adrenal masses can be removedlaparoscopically. Elsevier 2020-05-22 /pmc/articles/PMC7262088/ /pubmed/32489900 http://dx.doi.org/10.1016/j.eucr.2020.101276 Text en © 2020 Published by Elsevier Inc. 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 Oncology
Santosh, K.
Das, Manoj K.
Ayyanar, Pavithra
Mandal, Swarnendu
Nayak, Prasant
Kumar, Sumit
Laparoscopic excision of a large Adrenal Ganglioneuroma masquerading as Pheochromocytoma- A case report & review of literature
title Laparoscopic excision of a large Adrenal Ganglioneuroma masquerading as Pheochromocytoma- A case report & review of literature
title_full Laparoscopic excision of a large Adrenal Ganglioneuroma masquerading as Pheochromocytoma- A case report & review of literature
title_fullStr Laparoscopic excision of a large Adrenal Ganglioneuroma masquerading as Pheochromocytoma- A case report & review of literature
title_full_unstemmed Laparoscopic excision of a large Adrenal Ganglioneuroma masquerading as Pheochromocytoma- A case report & review of literature
title_short Laparoscopic excision of a large Adrenal Ganglioneuroma masquerading as Pheochromocytoma- A case report & review of literature
title_sort laparoscopic excision of a large adrenal ganglioneuroma masquerading as pheochromocytoma- a case report & review of literature
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7262088/
https://www.ncbi.nlm.nih.gov/pubmed/32489900
http://dx.doi.org/10.1016/j.eucr.2020.101276
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