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The Rare Togetherness of Bladder Leiomyoma and Neurofibromatosis

Neurofibromatosis Type 1 (Von Recklinghausen disease) is a common, autosomal dominant hereditary disorder characterized by involvement of multiple tissues derived from the neural crest. Urinary system involvement in neurofibromatosis is a rare condition. Leiomyoma of the bladder is a rare benign mes...

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Autores principales: Yucel, Cem, Budak, Salih, Kisa, Erdem, Celik, Orcun, Kozacioglu, Zafer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5904780/
https://www.ncbi.nlm.nih.gov/pubmed/29736289
http://dx.doi.org/10.1155/2018/2302918
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author Yucel, Cem
Budak, Salih
Kisa, Erdem
Celik, Orcun
Kozacioglu, Zafer
author_facet Yucel, Cem
Budak, Salih
Kisa, Erdem
Celik, Orcun
Kozacioglu, Zafer
author_sort Yucel, Cem
collection PubMed
description Neurofibromatosis Type 1 (Von Recklinghausen disease) is a common, autosomal dominant hereditary disorder characterized by involvement of multiple tissues derived from the neural crest. Urinary system involvement in neurofibromatosis is a rare condition. Leiomyoma of the bladder is a rare benign mesenchymal tumor. In this case, our experience and approach regarding the bladder leiomyoma development in a patient diagnosed with neurofibromatosis are presented and the literature data has been reviewed.
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spelling pubmed-59047802018-05-07 The Rare Togetherness of Bladder Leiomyoma and Neurofibromatosis Yucel, Cem Budak, Salih Kisa, Erdem Celik, Orcun Kozacioglu, Zafer Case Rep Urol Case Report Neurofibromatosis Type 1 (Von Recklinghausen disease) is a common, autosomal dominant hereditary disorder characterized by involvement of multiple tissues derived from the neural crest. Urinary system involvement in neurofibromatosis is a rare condition. Leiomyoma of the bladder is a rare benign mesenchymal tumor. In this case, our experience and approach regarding the bladder leiomyoma development in a patient diagnosed with neurofibromatosis are presented and the literature data has been reviewed. Hindawi 2018-01-08 /pmc/articles/PMC5904780/ /pubmed/29736289 http://dx.doi.org/10.1155/2018/2302918 Text en Copyright © 2018 Cem Yucel et al. 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
Yucel, Cem
Budak, Salih
Kisa, Erdem
Celik, Orcun
Kozacioglu, Zafer
The Rare Togetherness of Bladder Leiomyoma and Neurofibromatosis
title The Rare Togetherness of Bladder Leiomyoma and Neurofibromatosis
title_full The Rare Togetherness of Bladder Leiomyoma and Neurofibromatosis
title_fullStr The Rare Togetherness of Bladder Leiomyoma and Neurofibromatosis
title_full_unstemmed The Rare Togetherness of Bladder Leiomyoma and Neurofibromatosis
title_short The Rare Togetherness of Bladder Leiomyoma and Neurofibromatosis
title_sort rare togetherness of bladder leiomyoma and neurofibromatosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5904780/
https://www.ncbi.nlm.nih.gov/pubmed/29736289
http://dx.doi.org/10.1155/2018/2302918
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