The Rare Togetherness of Bladder Leiomyoma and Neurofibromatosis
Joint Authors
Celik, Orcun
Yucel, Cem
Kisa, Erdem
Kozacioglu, Zafer
Budak, Salih
Source
Issue
Vol. 2018, Issue 2018 (31 Dec. 2018), pp.1-3, 3 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2018-01-08
Country of Publication
Egypt
No. of Pages
3
Main Subjects
Abstract EN
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.
American Psychological Association (APA)
Yucel, Cem& Budak, Salih& Kisa, Erdem& Celik, Orcun& Kozacioglu, Zafer. 2018. The Rare Togetherness of Bladder Leiomyoma and Neurofibromatosis. Case Reports in Urology،Vol. 2018, no. 2018, pp.1-3.
https://search.emarefa.net/detail/BIM-1151326
Modern Language Association (MLA)
Yucel, Cem…[et al.]. The Rare Togetherness of Bladder Leiomyoma and Neurofibromatosis. Case Reports in Urology No. 2018 (2018), pp.1-3.
https://search.emarefa.net/detail/BIM-1151326
American Medical Association (AMA)
Yucel, Cem& Budak, Salih& Kisa, Erdem& Celik, Orcun& Kozacioglu, Zafer. The Rare Togetherness of Bladder Leiomyoma and Neurofibromatosis. Case Reports in Urology. 2018. Vol. 2018, no. 2018, pp.1-3.
https://search.emarefa.net/detail/BIM-1151326
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-1151326