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Urothelial Carcinoma in a 22-Year-Old Female with Angelman Syndrome
A 22-year-old nulligravid white female with Angelman syndrome was noted to have a 4-month history of premenstrual nausea, vomiting, and abdominal pain. She had an echogenic focus in her bladder noted on ultrasound. She was diagnosed with low grade urothelial carcinoma after cystoscopic evaluation wi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405399/ https://www.ncbi.nlm.nih.gov/pubmed/28487808 http://dx.doi.org/10.1155/2017/9298565 |
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author | Pugh, Jessica Huffaker, R. Keith |
author_facet | Pugh, Jessica Huffaker, R. Keith |
author_sort | Pugh, Jessica |
collection | PubMed |
description | A 22-year-old nulligravid white female with Angelman syndrome was noted to have a 4-month history of premenstrual nausea, vomiting, and abdominal pain. She had an echogenic focus in her bladder noted on ultrasound. She was diagnosed with low grade urothelial carcinoma after cystoscopic evaluation with biopsy and was sent to urology for further treatment. Urothelial carcinoma is rare in individuals younger than age 40. Patients may present with gross hematuria. There is often a delay in diagnosis in younger individuals with different genetic mutations noted upon diagnosis. |
format | Online Article Text |
id | pubmed-5405399 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-54053992017-05-09 Urothelial Carcinoma in a 22-Year-Old Female with Angelman Syndrome Pugh, Jessica Huffaker, R. Keith Case Rep Urol Case Report A 22-year-old nulligravid white female with Angelman syndrome was noted to have a 4-month history of premenstrual nausea, vomiting, and abdominal pain. She had an echogenic focus in her bladder noted on ultrasound. She was diagnosed with low grade urothelial carcinoma after cystoscopic evaluation with biopsy and was sent to urology for further treatment. Urothelial carcinoma is rare in individuals younger than age 40. Patients may present with gross hematuria. There is often a delay in diagnosis in younger individuals with different genetic mutations noted upon diagnosis. Hindawi 2017 2017-04-11 /pmc/articles/PMC5405399/ /pubmed/28487808 http://dx.doi.org/10.1155/2017/9298565 Text en Copyright © 2017 Jessica Pugh and R. Keith Huffaker. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Pugh, Jessica Huffaker, R. Keith Urothelial Carcinoma in a 22-Year-Old Female with Angelman Syndrome |
title | Urothelial Carcinoma in a 22-Year-Old Female with Angelman Syndrome |
title_full | Urothelial Carcinoma in a 22-Year-Old Female with Angelman Syndrome |
title_fullStr | Urothelial Carcinoma in a 22-Year-Old Female with Angelman Syndrome |
title_full_unstemmed | Urothelial Carcinoma in a 22-Year-Old Female with Angelman Syndrome |
title_short | Urothelial Carcinoma in a 22-Year-Old Female with Angelman Syndrome |
title_sort | urothelial carcinoma in a 22-year-old female with angelman syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405399/ https://www.ncbi.nlm.nih.gov/pubmed/28487808 http://dx.doi.org/10.1155/2017/9298565 |
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