Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Hirasaki, Shoji, Kanzaki, Hiromitsu, Okuda, Masato, Suzuki, Seiyuu, Fukuhara, Tetsuji, Hanaoka, Toshihito
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
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
_version_ 1782174145229881344
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
work_keys_str_mv AT hirasakishoji compositeparagangliomaganglioneuromaintheretroperitoneum
AT kanzakihiromitsu compositeparagangliomaganglioneuromaintheretroperitoneum
AT okudamasato compositeparagangliomaganglioneuromaintheretroperitoneum
AT suzukiseiyuu compositeparagangliomaganglioneuromaintheretroperitoneum
AT fukuharatetsuji compositeparagangliomaganglioneuromaintheretroperitoneum
AT hanaokatoshihito compositeparagangliomaganglioneuromaintheretroperitoneum