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Evaluation of UroVysion for Urachal Carcinoma Detection

Background: Patients with hematuria who are positive for urinary fluorescence in situ hybridization (FISH) are generally considered to have urothelial carcinoma. We determined whether UroVysion FISH could be used for the diagnosis of urachal carcinoma. Methods: Seven cases of urachal carcinoma with...

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Autores principales: Hu, Zhiquan, Ke, Chunjin, Liu, Zheng, Zeng, Xing, Li, Song, Xu, Hua, Yang, Chunguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482390/
https://www.ncbi.nlm.nih.gov/pubmed/32974362
http://dx.doi.org/10.3389/fmed.2020.00437
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author Hu, Zhiquan
Ke, Chunjin
Liu, Zheng
Zeng, Xing
Li, Song
Xu, Hua
Yang, Chunguang
author_facet Hu, Zhiquan
Ke, Chunjin
Liu, Zheng
Zeng, Xing
Li, Song
Xu, Hua
Yang, Chunguang
author_sort Hu, Zhiquan
collection PubMed
description Background: Patients with hematuria who are positive for urinary fluorescence in situ hybridization (FISH) are generally considered to have urothelial carcinoma. We determined whether UroVysion FISH could be used for the diagnosis of urachal carcinoma. Methods: Seven cases of urachal carcinoma with haematuria subjected to FISH analysis were retrospectively analyzed in our hospital from May 2012 to November 2019. Paraffin-embedded tissue sections from one FISH-positive and one FISH-negative urachal carcinoma were processed in strict accordance with the instructions of the UroVysion kit. Meanwhile, FISH data from the other 414 hematuria patients were collected as controls. Results: All 7 patients with urachal carcinoma were diagnosed with adenocarcinoma. According to Sheldon stage, six patients had stage IIIa and one patient had stage IVb. The sensitivity and specificity of urinary FISH for the diagnosis of urachal carcinoma were 71.43% (5/7) and 94.61% (281/297), respectively. The rates of polysomy for chromosomes 3 and 7 in positive patients were both 100% (5/5), whereas the rate of polysomy for chromosome 17 was 40% (2/5), and the chromosome 9p21 region (p16) gene deletion rate was 20% (1/5). Histological assessment and cytological FISH were consistent for urachal carcinoma. No significant difference was observed in the diagnostic efficacy between urachal carcinoma and urothelial carcinoma (71.43 vs. 87.18%, P = 0.245). Conclusions: Taken together, UroVysion FISH was found to be positive in a high proportion of pathologically confirmed urachal carcinoma of late stage with hematuria. Its chromosomal aberrations may be different from those of urothelial carcinoma, but more studies are needed to clarify their genetic background. Not all tumors showing abnormalities by FISH are urothelial carcinomas.
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spelling pubmed-74823902020-09-23 Evaluation of UroVysion for Urachal Carcinoma Detection Hu, Zhiquan Ke, Chunjin Liu, Zheng Zeng, Xing Li, Song Xu, Hua Yang, Chunguang Front Med (Lausanne) Medicine Background: Patients with hematuria who are positive for urinary fluorescence in situ hybridization (FISH) are generally considered to have urothelial carcinoma. We determined whether UroVysion FISH could be used for the diagnosis of urachal carcinoma. Methods: Seven cases of urachal carcinoma with haematuria subjected to FISH analysis were retrospectively analyzed in our hospital from May 2012 to November 2019. Paraffin-embedded tissue sections from one FISH-positive and one FISH-negative urachal carcinoma were processed in strict accordance with the instructions of the UroVysion kit. Meanwhile, FISH data from the other 414 hematuria patients were collected as controls. Results: All 7 patients with urachal carcinoma were diagnosed with adenocarcinoma. According to Sheldon stage, six patients had stage IIIa and one patient had stage IVb. The sensitivity and specificity of urinary FISH for the diagnosis of urachal carcinoma were 71.43% (5/7) and 94.61% (281/297), respectively. The rates of polysomy for chromosomes 3 and 7 in positive patients were both 100% (5/5), whereas the rate of polysomy for chromosome 17 was 40% (2/5), and the chromosome 9p21 region (p16) gene deletion rate was 20% (1/5). Histological assessment and cytological FISH were consistent for urachal carcinoma. No significant difference was observed in the diagnostic efficacy between urachal carcinoma and urothelial carcinoma (71.43 vs. 87.18%, P = 0.245). Conclusions: Taken together, UroVysion FISH was found to be positive in a high proportion of pathologically confirmed urachal carcinoma of late stage with hematuria. Its chromosomal aberrations may be different from those of urothelial carcinoma, but more studies are needed to clarify their genetic background. Not all tumors showing abnormalities by FISH are urothelial carcinomas. Frontiers Media S.A. 2020-08-27 /pmc/articles/PMC7482390/ /pubmed/32974362 http://dx.doi.org/10.3389/fmed.2020.00437 Text en Copyright © 2020 Hu, Ke, Liu, Zeng, Li, Xu and Yang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Hu, Zhiquan
Ke, Chunjin
Liu, Zheng
Zeng, Xing
Li, Song
Xu, Hua
Yang, Chunguang
Evaluation of UroVysion for Urachal Carcinoma Detection
title Evaluation of UroVysion for Urachal Carcinoma Detection
title_full Evaluation of UroVysion for Urachal Carcinoma Detection
title_fullStr Evaluation of UroVysion for Urachal Carcinoma Detection
title_full_unstemmed Evaluation of UroVysion for Urachal Carcinoma Detection
title_short Evaluation of UroVysion for Urachal Carcinoma Detection
title_sort evaluation of urovysion for urachal carcinoma detection
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482390/
https://www.ncbi.nlm.nih.gov/pubmed/32974362
http://dx.doi.org/10.3389/fmed.2020.00437
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