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Composite paraganglioma-ganglioneuroma in the retroperitoneum
BACKGROUND: Paragangliomas occur most commonly in head and neck region and much less frequently, they are found in the retroperitoneum. Composite paraganglioma-ganglioneuroma of the retroperitoneum is very rare. CASE PRESENTATION: We present an unusual case of retroperitoneal composite paraganglioma...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2777156/ https://www.ncbi.nlm.nih.gov/pubmed/19889235 http://dx.doi.org/10.1186/1477-7819-7-81 |
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author | Hirasaki, Shoji Kanzaki, Hiromitsu Okuda, Masato Suzuki, Seiyuu Fukuhara, Tetsuji Hanaoka, Toshihito |
author_facet | Hirasaki, Shoji Kanzaki, Hiromitsu Okuda, Masato Suzuki, Seiyuu Fukuhara, Tetsuji Hanaoka, Toshihito |
author_sort | Hirasaki, Shoji |
collection | PubMed |
description | BACKGROUND: Paragangliomas occur most commonly in head and neck region and much less frequently, they are found in the retroperitoneum. Composite paraganglioma-ganglioneuroma of the retroperitoneum is very rare. CASE PRESENTATION: We present an unusual case of retroperitoneal composite paraganglioma-ganglioneuroma discovered on computed tomography in a 63-year-old female patient. Routine hematological examination and biochemical tests were within normal limits. Plasma adrenaline was 0.042 ng/ml, plasma noradrenaline 0.341 ng/ml, and plasma dopamine <0.01 ng/ml. An abdominal contrast-enhanced CT scan and magnetic resonance imaging revealed a 6.5 cm heterogeneous retroperitoneal mass with a cystic component. The retroperitoneal tumor accumulated (131)I-Metaiodobenzylguanidine ((131)I-MIBG) 48 hours after radioisotope injection. Under the diagnosis of paraganglioma in the retroperitoneum, the patient underwent surgery. The resected tumor (6.5 × 5 × 3 cm) was solid and easily removed en bloc. The cut surface of the tumor and histology revealed two different components in the tumor: paraganglioma centrally and ganglioneuroma on the periphery. She remains disease-free 18 months after surgery. CONCLUSION: This case reminds us that neuroendocrine tumor should be included in the differential diagnosis of a retroperitoneal mass although composite paraganglioma-ganglioneuroma in the retroperitoneum is very rare. |
format | Text |
id | pubmed-2777156 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27771562009-11-15 Composite paraganglioma-ganglioneuroma in the retroperitoneum Hirasaki, Shoji Kanzaki, Hiromitsu Okuda, Masato Suzuki, Seiyuu Fukuhara, Tetsuji Hanaoka, Toshihito World J Surg Oncol Case Report BACKGROUND: Paragangliomas occur most commonly in head and neck region and much less frequently, they are found in the retroperitoneum. Composite paraganglioma-ganglioneuroma of the retroperitoneum is very rare. CASE PRESENTATION: We present an unusual case of retroperitoneal composite paraganglioma-ganglioneuroma discovered on computed tomography in a 63-year-old female patient. Routine hematological examination and biochemical tests were within normal limits. Plasma adrenaline was 0.042 ng/ml, plasma noradrenaline 0.341 ng/ml, and plasma dopamine <0.01 ng/ml. An abdominal contrast-enhanced CT scan and magnetic resonance imaging revealed a 6.5 cm heterogeneous retroperitoneal mass with a cystic component. The retroperitoneal tumor accumulated (131)I-Metaiodobenzylguanidine ((131)I-MIBG) 48 hours after radioisotope injection. Under the diagnosis of paraganglioma in the retroperitoneum, the patient underwent surgery. The resected tumor (6.5 × 5 × 3 cm) was solid and easily removed en bloc. The cut surface of the tumor and histology revealed two different components in the tumor: paraganglioma centrally and ganglioneuroma on the periphery. She remains disease-free 18 months after surgery. CONCLUSION: This case reminds us that neuroendocrine tumor should be included in the differential diagnosis of a retroperitoneal mass although composite paraganglioma-ganglioneuroma in the retroperitoneum is very rare. BioMed Central 2009-11-05 /pmc/articles/PMC2777156/ /pubmed/19889235 http://dx.doi.org/10.1186/1477-7819-7-81 Text en Copyright © 2009 Hirasaki et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Hirasaki, Shoji Kanzaki, Hiromitsu Okuda, Masato Suzuki, Seiyuu Fukuhara, Tetsuji Hanaoka, Toshihito Composite paraganglioma-ganglioneuroma in the retroperitoneum |
title | Composite paraganglioma-ganglioneuroma in the retroperitoneum |
title_full | Composite paraganglioma-ganglioneuroma in the retroperitoneum |
title_fullStr | Composite paraganglioma-ganglioneuroma in the retroperitoneum |
title_full_unstemmed | Composite paraganglioma-ganglioneuroma in the retroperitoneum |
title_short | Composite paraganglioma-ganglioneuroma in the retroperitoneum |
title_sort | composite paraganglioma-ganglioneuroma in the retroperitoneum |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2777156/ https://www.ncbi.nlm.nih.gov/pubmed/19889235 http://dx.doi.org/10.1186/1477-7819-7-81 |
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