scholarly journals Spontaneous regression of biopsy proven primary renal cell carcinoma: A case study

2012 ◽  
Vol 6 (5) ◽  
pp. E203-E205 ◽  
Author(s):  
Gurswinder Gary Jawanda ◽  
Darrel Drachenberg
2012 ◽  
Vol 6 (5) ◽  
Author(s):  
Gurswinder Gary Jawanda ◽  
Darrel Drachenberg

Spontaneous regression of renal cell carcinoma (RCC) is a wellrecognized and interesting phenomenon that is poorly understood and rarely documented. There are very few reported cases of spontaneously regressed primary RCC. We present a 63-year-old male with a biopsy-proven RCC that regressed with complete resolution of symptoms.


1986 ◽  
Vol 27 (4) ◽  
pp. 314 ◽  
Author(s):  
Seung Kang Choi ◽  
Soo Kee Chang ◽  
Jin Moo Lee ◽  
Woo Hee Jung ◽  
Chan Il Park

2002 ◽  
Vol 167 (1) ◽  
pp. 242-243 ◽  
Author(s):  
K.O. KOBAYASHI ◽  
TAKASHI SATO ◽  
KEN-ICHI SUNAOSHI ◽  
ATSUSHI TAKAHASHI ◽  
MITSUHARU TAMAKAWA

2007 ◽  
Vol 177 (4S) ◽  
pp. 167-168 ◽  
Author(s):  
Anil Thomas ◽  
Brian R. Lane ◽  
Brian I. Rini ◽  
Steven C. Campbell

2020 ◽  
Vol 15 (2) ◽  
pp. 56-58
Author(s):  
Shafiqur Rahman ◽  
B Ahmed ◽  
ATM Mowladad Chowdhury ◽  
Mirza M Hasan ◽  
Sayedul Islam

A forty eight year old woman with the clinical diagnosis of renal mass due to renal cell carcinoma was found to have renal tuberculosis. The clinical presentation and management are being discussed. Bangladesh Journal of Urology, Vol. 15, No. 2, July 2012 p.56-58


2021 ◽  
Vol 14 (6) ◽  
pp. e243058
Author(s):  
Cristian Solano ◽  
Shrinjaya Thapa ◽  
Mohammad Muhsin Chisti

Xp11.2 translocation renal cell carcinoma (TRCC) is a rare and aggressive variant of renal cell carcinoma (RCC) when presenting in adults. We report a case of a man in his early 40s who was diagnosed with stage III Xp11.2 TRCC and underwent radical nephrectomy. Seven months following the surgery, an adrenal nodule and bilateral pulmonary nodules were discovered. He underwent cryoablation of the adrenal nodule and systemic treatment with daily pazopanib. He displayed stable disease for approximately 6 years. Following this period, multiple hospitalisations interrupted daily pazopanib therapy resulting in progression of disease. His regimen was then changed to ipilimumab and nivolumab, followed by current daily therapy with axitinib. The patient now shows stable disease in his 10th year after diagnosis. This case study demonstrates the efficacy of pazopanib for metastatic Xp11.2 TRCC and warrants further investigation to supplement the guidelines regarding the use of targeted therapy for TRCC.


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