scholarly journals Renal Cell Carcinoma in A Patient with Kartagener Syndrome: First Case Report in English Language

2015 ◽  
Vol 1 (1) ◽  
pp. 33-35
Author(s):  
Erkin Sağlam ◽  
Akif Türk ◽  
Ahmet Selimoğlu ◽  
Mehmet Kutlu Demirkol ◽  
Nertila Poci Sağlam ◽  
...  
2020 ◽  
Vol 4 (3) ◽  
pp. 124-127
Author(s):  
Bruno Nogueira Cesar ◽  
Nilo Eduardo Delboni Nunes ◽  
Maria Amelia Aguiar Hazin ◽  
Renato Demarchi Foresto ◽  
Gianna Mastroianni Kirsztajn ◽  
...  

Spontaneous tumor lysis syndrome is a rare emergency in onco-nephrology that results from extensive cancer cell lysis independent of antitumoral therapy. It is common among hematological tumors and can be rarely seen with solid tumors. In medical literature, there is only one case report with spontaneous tumor lysis syndrome in renal cell carcinoma and it was associated with metastases. To the best of our knowledge, this is the first report of spontaneous tumor lysis syndrome in non-metastatic renal cell carcinoma.


Author(s):  
Fatih Temel Yilmaz ◽  
Lutfullah Sari ◽  
Mahmut Esat Aykan ◽  
Mehmet Gultekin ◽  
Ilker Oz

Introduction: Nephrocolic fistula is a pathological connection between the kidney and colon. Percutaneous tumour ablation therapy is a rare cause of iatrogenic nephrocolic fistula in the literature. Case Presentation: Interventional radiologists should be careful, especially in patients with repeated ablation. Granulation of tissue may lead to unexpected results secondary to tissue fragility and impedance changes. Conclusion: In addition, we should keep in mind that there is decreasing hydro dissection benefit in cases with the previous ablation. As far as we know, this is the first case report of an iatrogenic ephrocolic fistula after microwave ablation for recurrence renal cell carcinoma.


2015 ◽  
Vol 9 (9-10) ◽  
pp. 651 ◽  
Author(s):  
Kyung Hwa Choi ◽  
Young Dong Yu ◽  
Moon Hyung Kang ◽  
Dong Soo Park

Renal cell carcinoma (RCC) with Von Hippel-Lindau (VHL) syndrome is associated with multiple recurrences and a young age at diagnosis. Therefore the primary goal of treatment is to stabilize the disease, minimizing the surgical resection and preserving the renal function in the patients with VHL who have developing RCC nodules after initial treatment. This is the first case report of VHL disease, with long-term stable disease, treated with a half dose of sorafenib after surgical resection and radiofrequency ablation for multiple recurrent stage T1 masses. We discuss the efficacy and safety of low-dose sorafenib treatment and review RCC in a patient with VHL disease.


2001 ◽  
Vol 115 (1) ◽  
pp. 65-67 ◽  
Author(s):  
J. Yiotakis ◽  
A. Hantzakos ◽  
A. Kostakopoulos ◽  
G. Adamopoulos

In this case report, we present a solitary metastasis of renal cell carcinoma inside the masseter muscle. To our knowledge, it is the very first case ever encountered.


2015 ◽  
Vol 2015 ◽  
pp. 1-3
Author(s):  
Kallappan Senthil ◽  
Manickam Ramalingam ◽  
Karpagam Janardhan ◽  
Anandan Murugesan ◽  
Mizar Ganapathy Pai

Introduction. Adrenal myelolipomas are uncommon nonfunctioning tumors of the adrenal. Synchronous renal cell carcinomas with adrenal myelolipomas are very rare. We present the case report of adrenal myelolipoma with synchronous RCC managed laparoscopically.Case Report. A 60-year-old old gentleman presented with incidental right upper polar mass with right adrenal mass. Metastatic work-up was negative. Laparoscopic radical nephrectomy with adrenalectomy was done under general anesthesia. The biopsy report was right kidney clear cell adenocarcinoma (T1b) with right adrenal myelolipoma.Conclusion. This is the first case report of laparoscopic adrenalectomy with nephrectomy for ipsilateral synchronous renal cell carcinoma with adrenal myelolipoma.


2015 ◽  
Vol 7 (3) ◽  
pp. 245-248 ◽  
Author(s):  
Dietrich Barth ◽  
Silvio Puhlmann ◽  
Joachim Barth

Seborrheic keratoses can often be found in elderly people. In general, they appear gradually. In cases of a sudden eruption with itching it might be paraneoplastic. Although some authors doubt the existence of the paraneoplastic Leser-Trélat syndrome, we present a case of sudden eruption of seborrheic keratoses connected with a newly diagnosed renal cell carcinoma. As far as we know, this is the first case report of a Leser-Trélat syndrome with a malignancy of the kidney.


2010 ◽  
Vol 63 (2) ◽  
pp. 174-176 ◽  
Author(s):  
A. Bressenot ◽  
C. Delaunay ◽  
G. Gauchotte ◽  
A. Oliver ◽  
G. Boudrant ◽  
...  

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