scholarly journals Recurrence of childhood nephrogenic adenoma in urinary bladder developed four years after previous surgery despite intravesical sodium hyaluronate therapy

2016 ◽  
Vol 42 (4) ◽  
pp. 303-306 ◽  
Author(s):  
Burak Ozcift ◽  
Ayper Kacar ◽  
Huseyin Tugrul Tiryaki
2001 ◽  
Vol 44 (3) ◽  
pp. 377
Author(s):  
Sun Hee Chung ◽  
Sun Wha Lee ◽  
Woon Seupp Han

2005 ◽  
Vol 37 (3) ◽  
pp. 477-481 ◽  
Author(s):  
Konstantinos Zougkas ◽  
Marinos Kalafatis ◽  
Panagiotis Kalafatis

2020 ◽  
Vol 2020 ◽  
pp. 1-3
Author(s):  
Iftikhar Khan ◽  
Mahmoud Obeid ◽  
Nasreen Hasan ◽  
Fayyad Jaradat ◽  
Bodhisatwa Sengupta ◽  
...  

Nephrogenic adenoma is a rare lesion that consists of epithelial cells arranged in tubular form, resembling tubules in the renal medulla, and is found usually in the urinary bladder although it can occur anywhere in the transitional epithelium of the lower urinary tract. The first case of nephrogenic adenoma of the urinary bladder was reported before the first kidney transplantation, and the lesion has been reported in patients with and without renal transplantation. The origin of cells in nephrogenic adenoma is debated and has been postulated to arise from cells of embryonic origin or from metaplasia secondary to chronic irritation or from implantation of allograft cells in patients with kidney transplantation. The long-term outcome and potential to convert into malignancy are not established, and therefore, there are no recommendations on how to follow up these patients. We present a case of a patient who was found to have nephrogenic adenoma of the urinary bladder during his second kidney transplantation from a cadaveric donor. He had undergone living donor kidney transplantation previously which subsequently failed. The patient did not manifest any symptoms of nephrogenic adenoma. During a follow-up period of 5 years, he has not manifested any symptoms related to nephrogenic metaplasia. Histopathological examination 5 years after the second transplantation did not show any malignant change. It can be concluded that nephrogenic adenoma is likely to behave in benign fashion post kidney transplantation.


1986 ◽  
Vol 10 (6) ◽  
pp. 979-982 ◽  
Author(s):  
A. P. Zingas ◽  
G. A. Kling ◽  
E. Crotte ◽  
E. Shumaker ◽  
P. M. Vazquez

2011 ◽  
Vol 14 (6) ◽  
pp. 438-444 ◽  
Author(s):  
Alison R. Huppmann ◽  
Bruce R. Pawel

Although not uncommon in adults, bladder tumors are rare in children. In addition, the histologic types of tumors seen in the pediatric population differ from those seen in adults. Although rhabdomyosarcoma is the most common pediatric bladder tumor, many other benign, malignant, and reactive lesions can be encountered. All may present clinically as a mass or polyp in the bladder. This study was designed to describe the pathology and patient demographics of pediatric bladder masses, because there are few studies describing these entities. Retrospectively reviewing our experience over a 21-year period, we identified 98 specimens from 65 patients with polyps or masses in the urinary bladder. As expected, the most frequent diagnosis was rhabdomyosarcoma. This was followed by fibroepithelial polyp and a variety of additional nonurothelial tumors. Only 7 urothelial tumors were identified, including 1 low-grade papillary urothelial carcinoma. Inflammatory lesions, such as cystitis cystica and nephrogenic adenoma, were invariably associated with an irritating factor when a history was provided. Our findings emphasize that diagnoses made in the pediatric urinary bladder are distinct from those in adults, although a wide variety of lesions may still be seen.


2020 ◽  
Vol 12 (2) ◽  
pp. 187
Author(s):  
Nicola Santoni ◽  
Lorna Cottrell ◽  
JenniferElizabeth Talia Jones ◽  
HollyJane Bekarma

2018 ◽  
Vol 32 (S1) ◽  
Author(s):  
Salvatore Cuzzocrea ◽  
Alessio Peritore ◽  
Rosalia Crupi ◽  
Michela Campolo ◽  
Rosalba Siracusa ◽  
...  

Urology ◽  
1980 ◽  
Vol 15 (2) ◽  
pp. 190-193 ◽  
Author(s):  
N.V. Raghavaiah ◽  
H. Norman Noe ◽  
David M. Parham ◽  
William M. Murphy

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