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Urothelial neoplasm of the bladder in childhood and adolescence: a rare disease
PURPOSE: Bladder tumors are rare in children and adolescents. For this reason, the diagnosis is sometimes delayed in pediatric patients. We aimed to describe the diagnosis, treatment, and follow-up methods of bladder urothelial neoplasms in children and adolescents. MATERIALS AND METHODS: We carried...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Urologia
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871383/ https://www.ncbi.nlm.nih.gov/pubmed/27256177 http://dx.doi.org/10.1590/S1677-5538.IBJU.2015.0200 |
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author | Polat, Haci Utangac, Mehmet M. Gulpinar, Murat T. Cift, Ali Erdogdu, Ibrahim Halil Turkcu, Gul |
author_facet | Polat, Haci Utangac, Mehmet M. Gulpinar, Murat T. Cift, Ali Erdogdu, Ibrahim Halil Turkcu, Gul |
author_sort | Polat, Haci |
collection | PubMed |
description | PURPOSE: Bladder tumors are rare in children and adolescents. For this reason, the diagnosis is sometimes delayed in pediatric patients. We aimed to describe the diagnosis, treatment, and follow-up methods of bladder urothelial neoplasms in children and adolescents. MATERIALS AND METHODS: We carried out a retrospective multicenter study involving patients who were treated between 2008 and 2014. Eleven patients aged younger than 18 years were enrolled in the study. In all the patients, a bladder tumor was diagnosed using ultrasonography and was treated through transurethral resection of the bladder (TURBT). RESULTS: Nine of the 11 patients (82%) were admitted with gross hematuria. The average delay in diagnosis was 3 months (range, 0–16 months) until the ultrasonographic diagnosis was performed from the first episodes of macroscopic hematuria. A single exophytic tumor (1–4cm) was present in each patient. The pathology of all patients was reported as superficial urothelial neoplasm: two with papilloma, one with papillary urothelial neoplasm of low malignant potential (PUNLMP), four with low grade pTa, and four with low grade pT1. No recurrence was observed during regular cystoscopic and ultrasonographic follow-up. CONCLUSIONS: Regardless of the presence of hematuria, bladder tumors in children are usually not considered because urothelial carcinoma in this population is extremely rare, which causes a delay in diagnosis. Fortunately, the disease has a good prognosis and recurrences are infrequent. Cystoscopy may be unnecessary in the follow-up of children with bladder tumors. We believe that ultrasonography is sufficient in follow-up. |
format | Online Article Text |
id | pubmed-4871383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Sociedade Brasileira de Urologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-48713832016-05-19 Urothelial neoplasm of the bladder in childhood and adolescence: a rare disease Polat, Haci Utangac, Mehmet M. Gulpinar, Murat T. Cift, Ali Erdogdu, Ibrahim Halil Turkcu, Gul Int Braz J Urol Original Article PURPOSE: Bladder tumors are rare in children and adolescents. For this reason, the diagnosis is sometimes delayed in pediatric patients. We aimed to describe the diagnosis, treatment, and follow-up methods of bladder urothelial neoplasms in children and adolescents. MATERIALS AND METHODS: We carried out a retrospective multicenter study involving patients who were treated between 2008 and 2014. Eleven patients aged younger than 18 years were enrolled in the study. In all the patients, a bladder tumor was diagnosed using ultrasonography and was treated through transurethral resection of the bladder (TURBT). RESULTS: Nine of the 11 patients (82%) were admitted with gross hematuria. The average delay in diagnosis was 3 months (range, 0–16 months) until the ultrasonographic diagnosis was performed from the first episodes of macroscopic hematuria. A single exophytic tumor (1–4cm) was present in each patient. The pathology of all patients was reported as superficial urothelial neoplasm: two with papilloma, one with papillary urothelial neoplasm of low malignant potential (PUNLMP), four with low grade pTa, and four with low grade pT1. No recurrence was observed during regular cystoscopic and ultrasonographic follow-up. CONCLUSIONS: Regardless of the presence of hematuria, bladder tumors in children are usually not considered because urothelial carcinoma in this population is extremely rare, which causes a delay in diagnosis. Fortunately, the disease has a good prognosis and recurrences are infrequent. Cystoscopy may be unnecessary in the follow-up of children with bladder tumors. We believe that ultrasonography is sufficient in follow-up. Sociedade Brasileira de Urologia 2016 /pmc/articles/PMC4871383/ /pubmed/27256177 http://dx.doi.org/10.1590/S1677-5538.IBJU.2015.0200 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Polat, Haci Utangac, Mehmet M. Gulpinar, Murat T. Cift, Ali Erdogdu, Ibrahim Halil Turkcu, Gul Urothelial neoplasm of the bladder in childhood and adolescence: a rare disease |
title | Urothelial neoplasm of the bladder in childhood and adolescence: a rare disease |
title_full | Urothelial neoplasm of the bladder in childhood and adolescence: a rare disease |
title_fullStr | Urothelial neoplasm of the bladder in childhood and adolescence: a rare disease |
title_full_unstemmed | Urothelial neoplasm of the bladder in childhood and adolescence: a rare disease |
title_short | Urothelial neoplasm of the bladder in childhood and adolescence: a rare disease |
title_sort | urothelial neoplasm of the bladder in childhood and adolescence: a rare disease |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871383/ https://www.ncbi.nlm.nih.gov/pubmed/27256177 http://dx.doi.org/10.1590/S1677-5538.IBJU.2015.0200 |
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