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Metanephric Stromal Tumor: An Unusual Presentation of a Rare Paediatric Renal Neoplasm

A 2-year-old boy with prenatal diagnosis of a malformation uropathy was referred to paediatric surgery department. On systemic examination, there were no palpable masses. An ultrasonography of abdomen with color Doppler, a renal artery angiographic and scintigraphy revealed a preostial aneurysm at t...

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Autores principales: Abdeljelil, Nouha Ben, Hadhri, Rim, Njima, Manel, Sghaier, Yosra, Sahnoun, Lassaad, Zakhama, Abdelfatah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419545/
https://www.ncbi.nlm.nih.gov/pubmed/30829310
http://dx.doi.org/10.4103/ajps.AJPS_56_17
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author Abdeljelil, Nouha Ben
Hadhri, Rim
Njima, Manel
Sghaier, Yosra
Sahnoun, Lassaad
Zakhama, Abdelfatah
author_facet Abdeljelil, Nouha Ben
Hadhri, Rim
Njima, Manel
Sghaier, Yosra
Sahnoun, Lassaad
Zakhama, Abdelfatah
author_sort Abdeljelil, Nouha Ben
collection PubMed
description A 2-year-old boy with prenatal diagnosis of a malformation uropathy was referred to paediatric surgery department. On systemic examination, there were no palpable masses. An ultrasonography of abdomen with color Doppler, a renal artery angiographic and scintigraphy revealed a preostial aneurysm at the left renal artery. The patient had a left nephrectomy. Grossly, the specimen measured 75 mm × mm 50 × 20 mm with renal artery aneurysm measuring 30 mm × 35 mm. On cut section, the renal parenchyma contained a whitish tumor that measured 35 mm × 10 mm. Histopathologically, this tumor was diagnosed as metanephric stromal tumor.
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spelling pubmed-64195452019-04-17 Metanephric Stromal Tumor: An Unusual Presentation of a Rare Paediatric Renal Neoplasm Abdeljelil, Nouha Ben Hadhri, Rim Njima, Manel Sghaier, Yosra Sahnoun, Lassaad Zakhama, Abdelfatah Afr J Paediatr Surg Case Report A 2-year-old boy with prenatal diagnosis of a malformation uropathy was referred to paediatric surgery department. On systemic examination, there were no palpable masses. An ultrasonography of abdomen with color Doppler, a renal artery angiographic and scintigraphy revealed a preostial aneurysm at the left renal artery. The patient had a left nephrectomy. Grossly, the specimen measured 75 mm × mm 50 × 20 mm with renal artery aneurysm measuring 30 mm × 35 mm. On cut section, the renal parenchyma contained a whitish tumor that measured 35 mm × 10 mm. Histopathologically, this tumor was diagnosed as metanephric stromal tumor. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6419545/ /pubmed/30829310 http://dx.doi.org/10.4103/ajps.AJPS_56_17 Text en Copyright: © 2019 African Journal of Paediatric Surgery http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Abdeljelil, Nouha Ben
Hadhri, Rim
Njima, Manel
Sghaier, Yosra
Sahnoun, Lassaad
Zakhama, Abdelfatah
Metanephric Stromal Tumor: An Unusual Presentation of a Rare Paediatric Renal Neoplasm
title Metanephric Stromal Tumor: An Unusual Presentation of a Rare Paediatric Renal Neoplasm
title_full Metanephric Stromal Tumor: An Unusual Presentation of a Rare Paediatric Renal Neoplasm
title_fullStr Metanephric Stromal Tumor: An Unusual Presentation of a Rare Paediatric Renal Neoplasm
title_full_unstemmed Metanephric Stromal Tumor: An Unusual Presentation of a Rare Paediatric Renal Neoplasm
title_short Metanephric Stromal Tumor: An Unusual Presentation of a Rare Paediatric Renal Neoplasm
title_sort metanephric stromal tumor: an unusual presentation of a rare paediatric renal neoplasm
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419545/
https://www.ncbi.nlm.nih.gov/pubmed/30829310
http://dx.doi.org/10.4103/ajps.AJPS_56_17
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