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Complete Response of Rare Sarcomatoid Upper Tract Urothelial Carcinoma Variant: Case Report and Literature Review

Infiltrating urothelial carcinoma sarcomatoid variant is a rare variant of urothelial carcinoma. We report a case of a 68-year-old female with a history of hematuria. CT scan with contrast showed a mass in the 1/3 distal of the right ureter. The biopsy result showed a high-grade infiltrating urothel...

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Autores principales: Warli, Syah Mirsya, Laksmi, Lidya Imelda, Lubis, Nova Sabrina, Wijaya, William Saputra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10176196/
https://www.ncbi.nlm.nih.gov/pubmed/37187682
http://dx.doi.org/10.1159/000530264
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author Warli, Syah Mirsya
Laksmi, Lidya Imelda
Lubis, Nova Sabrina
Wijaya, William Saputra
author_facet Warli, Syah Mirsya
Laksmi, Lidya Imelda
Lubis, Nova Sabrina
Wijaya, William Saputra
author_sort Warli, Syah Mirsya
collection PubMed
description Infiltrating urothelial carcinoma sarcomatoid variant is a rare variant of urothelial carcinoma. We report a case of a 68-year-old female with a history of hematuria. CT scan with contrast showed a mass in the 1/3 distal of the right ureter. The biopsy result showed a high-grade infiltrating urothelial carcinoma. A radical nephroureterectomy was performed but at the follow-up after 3 months, there was a recurrent mass and gemcitabine-cisplatin chemotherapy was given. Since a high-grade infiltrating urothelial carcinoma sarcomatoid variant was an aggressive tumor, we need to give more attention to evaluating this tumor.
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spelling pubmed-101761962023-05-13 Complete Response of Rare Sarcomatoid Upper Tract Urothelial Carcinoma Variant: Case Report and Literature Review Warli, Syah Mirsya Laksmi, Lidya Imelda Lubis, Nova Sabrina Wijaya, William Saputra Case Rep Oncol Case Report Infiltrating urothelial carcinoma sarcomatoid variant is a rare variant of urothelial carcinoma. We report a case of a 68-year-old female with a history of hematuria. CT scan with contrast showed a mass in the 1/3 distal of the right ureter. The biopsy result showed a high-grade infiltrating urothelial carcinoma. A radical nephroureterectomy was performed but at the follow-up after 3 months, there was a recurrent mass and gemcitabine-cisplatin chemotherapy was given. Since a high-grade infiltrating urothelial carcinoma sarcomatoid variant was an aggressive tumor, we need to give more attention to evaluating this tumor. S. Karger AG 2023-05-12 /pmc/articles/PMC10176196/ /pubmed/37187682 http://dx.doi.org/10.1159/000530264 Text en © 2023 The Author(s). Published by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Case Report
Warli, Syah Mirsya
Laksmi, Lidya Imelda
Lubis, Nova Sabrina
Wijaya, William Saputra
Complete Response of Rare Sarcomatoid Upper Tract Urothelial Carcinoma Variant: Case Report and Literature Review
title Complete Response of Rare Sarcomatoid Upper Tract Urothelial Carcinoma Variant: Case Report and Literature Review
title_full Complete Response of Rare Sarcomatoid Upper Tract Urothelial Carcinoma Variant: Case Report and Literature Review
title_fullStr Complete Response of Rare Sarcomatoid Upper Tract Urothelial Carcinoma Variant: Case Report and Literature Review
title_full_unstemmed Complete Response of Rare Sarcomatoid Upper Tract Urothelial Carcinoma Variant: Case Report and Literature Review
title_short Complete Response of Rare Sarcomatoid Upper Tract Urothelial Carcinoma Variant: Case Report and Literature Review
title_sort complete response of rare sarcomatoid upper tract urothelial carcinoma variant: case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10176196/
https://www.ncbi.nlm.nih.gov/pubmed/37187682
http://dx.doi.org/10.1159/000530264
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