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Masson’s tumor of the kidney: a case report
BACKGROUND: Intravascular papillary endothelial hyperplasia (known also as Masson’s tumor) is a benign vascular lesion that commonly occurs in the skin and is rarely found in solid organs, especially in the kidney. In what follows, we will look into the first case of an unexpectedly diagnosed Masson...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303989/ https://www.ncbi.nlm.nih.gov/pubmed/30577814 http://dx.doi.org/10.1186/s13256-018-1898-2 |
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author | Essid, Mohamed Ali Bouzouita, Abderrazak Blel, Ahlem Gharbi, Maroua Chakroun, Marouen Ben Miled, Aycha Ayed, Haroun Cherif, Mohamed Ben Slama, Mohamed Riadh Derouiche, Amine Chebil, Mohamed |
author_facet | Essid, Mohamed Ali Bouzouita, Abderrazak Blel, Ahlem Gharbi, Maroua Chakroun, Marouen Ben Miled, Aycha Ayed, Haroun Cherif, Mohamed Ben Slama, Mohamed Riadh Derouiche, Amine Chebil, Mohamed |
author_sort | Essid, Mohamed Ali |
collection | PubMed |
description | BACKGROUND: Intravascular papillary endothelial hyperplasia (known also as Masson’s tumor) is a benign vascular lesion that commonly occurs in the skin and is rarely found in solid organs, especially in the kidney. In what follows, we will look into the first case of an unexpectedly diagnosed Masson’s tumor of the kidney presenting as a suspicious renal cyst. CASE PRESENTATION: A 61-year-old Arab man presented with a left renal cyst, incidentally revealed by ultrasonography. The laboratory values were unremarkable. Computed tomography and magnetic resonance imaging demonstrated a 38 mm left renal midportion Bosniak IV cyst. Our patient underwent a radical nephrectomy. Histopathology revealed the diagnosis of intravascular papillary endothelial hyperplasia. There was no recurrence detected after 9 years of follow-up. CONCLUSIONS: Renal intravascular papillary endothelial hyperplasia is a rare benign tumor which can mimic a suspicious renal mass on radiological findings. Thus, this entity should be considered more often in the thick of the diagnostic possibilities in order to avoid unnecessary nephrectomies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13256-018-1898-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6303989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63039892019-01-03 Masson’s tumor of the kidney: a case report Essid, Mohamed Ali Bouzouita, Abderrazak Blel, Ahlem Gharbi, Maroua Chakroun, Marouen Ben Miled, Aycha Ayed, Haroun Cherif, Mohamed Ben Slama, Mohamed Riadh Derouiche, Amine Chebil, Mohamed J Med Case Rep Case Report BACKGROUND: Intravascular papillary endothelial hyperplasia (known also as Masson’s tumor) is a benign vascular lesion that commonly occurs in the skin and is rarely found in solid organs, especially in the kidney. In what follows, we will look into the first case of an unexpectedly diagnosed Masson’s tumor of the kidney presenting as a suspicious renal cyst. CASE PRESENTATION: A 61-year-old Arab man presented with a left renal cyst, incidentally revealed by ultrasonography. The laboratory values were unremarkable. Computed tomography and magnetic resonance imaging demonstrated a 38 mm left renal midportion Bosniak IV cyst. Our patient underwent a radical nephrectomy. Histopathology revealed the diagnosis of intravascular papillary endothelial hyperplasia. There was no recurrence detected after 9 years of follow-up. CONCLUSIONS: Renal intravascular papillary endothelial hyperplasia is a rare benign tumor which can mimic a suspicious renal mass on radiological findings. Thus, this entity should be considered more often in the thick of the diagnostic possibilities in order to avoid unnecessary nephrectomies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13256-018-1898-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-22 /pmc/articles/PMC6303989/ /pubmed/30577814 http://dx.doi.org/10.1186/s13256-018-1898-2 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Essid, Mohamed Ali Bouzouita, Abderrazak Blel, Ahlem Gharbi, Maroua Chakroun, Marouen Ben Miled, Aycha Ayed, Haroun Cherif, Mohamed Ben Slama, Mohamed Riadh Derouiche, Amine Chebil, Mohamed Masson’s tumor of the kidney: a case report |
title | Masson’s tumor of the kidney: a case report |
title_full | Masson’s tumor of the kidney: a case report |
title_fullStr | Masson’s tumor of the kidney: a case report |
title_full_unstemmed | Masson’s tumor of the kidney: a case report |
title_short | Masson’s tumor of the kidney: a case report |
title_sort | masson’s tumor of the kidney: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303989/ https://www.ncbi.nlm.nih.gov/pubmed/30577814 http://dx.doi.org/10.1186/s13256-018-1898-2 |
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