Scleroderma as paraneoplastic disease: A new case of a rare association with renal cell carcinoma

2021 ◽  
pp. 239719832110508
Author(s):  
Francesca Ruffilli ◽  
Melissa Padovan ◽  
Giovanni Ciancio ◽  
Veronica Venturelli ◽  
Beatrice Maranini ◽  
...  
2015 ◽  
Vol 11 (4) ◽  
pp. 1033 ◽  
Author(s):  
Subhadip Khatua ◽  
Kousik Bose ◽  
Arghya Bandyopadhyay ◽  
Abhijit Banerjee

2020 ◽  
Vol 2 (2) ◽  
Author(s):  
Jideofor Okechukwu Ugwu ◽  
Okechukwu Hyginus Ekwunife ◽  
Chuka Abunike Ugwunne ◽  
Felix I. Menkiti ◽  
Andy Nwankwo Osuigwe

Renal cell carcinoma is the most common malignant renal tumour in adults but quite rare in children. Duplex renal collecting systems are relatively common congenital renal abnormalities. However, its coexistence with renal cell carcinoma is yet to be established beyond a mere coincidence. So far, there are only 2 cases of such coexistence in literature till date. We therefore report a case of a 13-year-old girl who was referred to us with a right flank mass. Abdominal computerized tomographic scan revealed a right renal tumour necessitating a laparotomy at which a duplex collecting system was discovered in the ipsilateral kidney and a nephrouterectomy was done with a histologic finding of renal cell carcinoma. We report this rare relationship and review of literature to stimulate further study into this rare association.


2016 ◽  
Vol 5 (3) ◽  
pp. 262
Author(s):  
AnkitKumar Jitani ◽  
Yookarin Khonglah ◽  
Nabanita Das ◽  
Amrita Saha

Author(s):  
Mariem Khadhar ◽  
hela jebali ◽  
ikram mami ◽  
fethi ben hamida ◽  
lamia rais ◽  
...  

Granulomatosis reaction associated with tumor has been designated as sarcoid-like reaction. Very few cases of association of systemic sarcoidosis and neoplasia have been reported. We reported two cases of sarcoidosis and renal cell carcinoma.


2011 ◽  
Vol 3 (02) ◽  
pp. 116-118 ◽  
Author(s):  
Sunil Kumar Yeshvanth ◽  
Harish S Permi ◽  
Kishan Prasad Hosapatna Laxminarayana ◽  
Teerthanath Shrinivas ◽  
Jayaprakash K Shetty

ABSTRACTChromophobe renal cell carcinoma is a relatively uncommon variant of renal cell carcinoma. Eosinophilic variant of chromophobe renal cell carcinoma (EVCRCC) is still less frequent and is composed predominantly of small to medium-sized cells with abundant granular eosinophilic cytoplasm. We report two cases of EVCRCC, with one having a rare association of right atrial myxoma. We present these cases, due to the rarity of EVCRCC and an unusual association of right atrial myxoma in one of them. Both patients recovered well after surgery, with no recurrence or metastasis after 2 years of follow-up.


2007 ◽  
Vol 177 (4S) ◽  
pp. 413-413
Author(s):  
Marco Roscigno ◽  
Roberto Bertini ◽  
Cesare Cozzarini ◽  
Alessandra Pasta ◽  
Mattia Sangalli ◽  
...  

2007 ◽  
Vol 177 (4S) ◽  
pp. 413-413
Author(s):  
Yu-Ning Wong ◽  
Brian L. Egleston ◽  
Ismail R. Saad ◽  
Robert G. Uzzo

2007 ◽  
Vol 177 (4S) ◽  
pp. 305-305
Author(s):  
Richard A. Ashley ◽  
Jonathan C. Routh ◽  
Sameer A. Siddiqui ◽  
Brant A. Inman ◽  
Thomas J. Sebo ◽  
...  

2007 ◽  
Vol 177 (4S) ◽  
pp. 303-304 ◽  
Author(s):  
Tobias Klatte ◽  
Heiko Wunderlich ◽  
Jean-Jacques Patard ◽  
Mark D. Kleid ◽  
John S. Lam ◽  
...  

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