The Rare Togetherness of Bladder Leiomyoma and Neurofibromatosis

Joint Authors

Celik, Orcun
Yucel, Cem
Kisa, Erdem
Kozacioglu, Zafer
Budak, Salih

Source

Case Reports in Urology

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

Medicine

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