scholarly journals The Rare Togetherness of Bladder Leiomyoma and Neurofibromatosis

2018 ◽  
Vol 2018 ◽  
pp. 1-3
Author(s):  
Cem Yucel ◽  
Salih Budak ◽  
Erdem Kisa ◽  
Orcun Celik ◽  
Zafer Kozacioglu

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.

2015 ◽  
Vol 5 (5) ◽  
pp. 309-311 ◽  
Author(s):  
Wahib Zafar ◽  
Benjamin Chaucer ◽  
Fidencio Davalos ◽  
Siddiqui Beenish ◽  
Marie Chevenon ◽  
...  

Author(s):  
Ioannis Karaitianos ◽  
Panagiotis Athanassiou ◽  
Christiana Tsomidou ◽  
Ifigenia Kostoglou-Athanassiou

2012 ◽  
Vol 33 (6) ◽  
pp. 1429-1433 ◽  
Author(s):  
Marica Eoli ◽  
Donata Bianchessi ◽  
Anna Luisa Di Stefano ◽  
Elena Prodi ◽  
Elena Anghileri ◽  
...  

2013 ◽  
Vol 2013 (oct16 1) ◽  
pp. bcr2013200033-bcr2013200033
Author(s):  
S. M. Rocha ◽  
M. B. Ferreira ◽  
R. Ribeiro ◽  
J. Correia

2021 ◽  
pp. 1-3
Author(s):  
El Azzouzi B ◽  
◽  
Zouita I ◽  
Benfaddoul O ◽  
Basraoui N ◽  
...  

Plexiform neurofibroma is a rare benign tumor of the peripheral nerves at the expense of perineural connective cells. It is pathognomonic of neurofibromatosis type 1 (NF1 or Von Recklinghausen disease). MRI is of great help in the diagnosis of this pathology. Anatomopathological confirmation is sometimes necessary, especially in the absence of a context suggestive of NF1. We report the observation of an oung boy with a cervical plexiform neurofibroma revealing a neurofibromatosis Type 1


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