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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Veröffentlicht in:Case reports in urology 2018, Vol.2018 (2018), p.1-3
Hauptverfasser: Celik, Orcun, Kisa, Erdem, Budak, Salih, Yucel, Cem, Kozacioglu, Zafer
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Sprache:eng
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Zusammenfassung: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.
ISSN:2090-696X
2090-6978
DOI:10.1155/2018/2302918