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Retroperitoneal pararenal isolated neurofibroma: report of a case and review of literature

The neurofibroma is a tumour of neural origin. This kind of neoplasm, though, is generally skin located. Rare cases in deep organs or in the peritoneal cavity are also reported in the literature. There are two types of neurofibromas, localized and diffuse; the latter is associated with von Recklingh...

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Autores principales: Corbellini, C, Vingiani, A, Maffini, F, Chiappa, A, Bertani, E, Andreoni, B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cancer Intelligence 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3357181/
https://www.ncbi.nlm.nih.gov/pubmed/22654960
http://dx.doi.org/10.3332/ecancer.2012.253
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author Corbellini, C
Vingiani, A
Maffini, F
Chiappa, A
Bertani, E
Andreoni, B
author_facet Corbellini, C
Vingiani, A
Maffini, F
Chiappa, A
Bertani, E
Andreoni, B
author_sort Corbellini, C
collection PubMed
description The neurofibroma is a tumour of neural origin. This kind of neoplasm, though, is generally skin located. Rare cases in deep organs or in the peritoneal cavity are also reported in the literature. There are two types of neurofibromas, localized and diffuse; the latter is associated with von Recklinghausen disease and always occurs together with skin neurofibromas. Here we report the case of a 47-year-old man affected by retroperitoneal neurofibroma, but not associated with von Recklinghausen disease. A computed tomography (CT) scan described a retroperitoneal pararenal lesion with no clear involvement of adjacent viscera. We describe the diagnostic modality, treatment planning and the timing of treatment of this neoplasm, reviewing also the literature.
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spelling pubmed-33571812012-05-31 Retroperitoneal pararenal isolated neurofibroma: report of a case and review of literature Corbellini, C Vingiani, A Maffini, F Chiappa, A Bertani, E Andreoni, B Ecancermedicalscience Case Report The neurofibroma is a tumour of neural origin. This kind of neoplasm, though, is generally skin located. Rare cases in deep organs or in the peritoneal cavity are also reported in the literature. There are two types of neurofibromas, localized and diffuse; the latter is associated with von Recklinghausen disease and always occurs together with skin neurofibromas. Here we report the case of a 47-year-old man affected by retroperitoneal neurofibroma, but not associated with von Recklinghausen disease. A computed tomography (CT) scan described a retroperitoneal pararenal lesion with no clear involvement of adjacent viscera. We describe the diagnostic modality, treatment planning and the timing of treatment of this neoplasm, reviewing also the literature. Cancer Intelligence 2012-05-15 /pmc/articles/PMC3357181/ /pubmed/22654960 http://dx.doi.org/10.3332/ecancer.2012.253 Text en © the authors; licensee ecancermedicalscience. 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
Corbellini, C
Vingiani, A
Maffini, F
Chiappa, A
Bertani, E
Andreoni, B
Retroperitoneal pararenal isolated neurofibroma: report of a case and review of literature
title Retroperitoneal pararenal isolated neurofibroma: report of a case and review of literature
title_full Retroperitoneal pararenal isolated neurofibroma: report of a case and review of literature
title_fullStr Retroperitoneal pararenal isolated neurofibroma: report of a case and review of literature
title_full_unstemmed Retroperitoneal pararenal isolated neurofibroma: report of a case and review of literature
title_short Retroperitoneal pararenal isolated neurofibroma: report of a case and review of literature
title_sort retroperitoneal pararenal isolated neurofibroma: report of a case and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3357181/
https://www.ncbi.nlm.nih.gov/pubmed/22654960
http://dx.doi.org/10.3332/ecancer.2012.253
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