Carcinosarcoma Arising From the Renal Pelvis: A Rare Case Report.

Autor: Hacıosmanoğlu T; Department of Urology, Sisli Hamidiye Etfal Training and Research Hospital, University of Health Sciences, Istanbul, TUR., Baloğlu İH; Department of Urology, Sisli Hamidiye Etfal Training and Research Hospital, University of Health Sciences, Istanbul, TUR., Türk S; Department of Urology, Sultan 1. Murat State Hospital, Edirne, TUR., Demirel HC; Department of Urology, Istanbul Aydin University VM Medical Park Florya Hospital, Istanbul, TUR., Özağarı AA; Department of Pathology, Sisli Hamidiye Etfal Training and Research Hospital, University of Health Sciences, Istanbul, TUR.
Jazyk: angličtina
Zdroj: Cureus [Cureus] 2023 Sep 20; Vol. 15 (9), pp. e45610. Date of Electronic Publication: 2023 Sep 20 (Print Publication: 2023).
DOI: 10.7759/cureus.45610
Abstrakt: Carcinosarcoma is a malignant tumor of biphasic character consisting of epithelial and mesenchymal components. This rarely-seen tumor has an exceedingly aggressive nature. While it is rare in the urinary system, it appears even more rarely in the renal pelvis. Thus, there are few publications in the literature on carcinosarcomas originating from the renal pelvis. This paper presents a 42-year-old male patient with carcinosarcoma of the renal pelvis (CSRP), kidney stone disease, and a nephrocutaneous fistula who underwent radical nephrectomy and eventually died of metastatic disease. The rarity of the disease is the main obstacle to conducting comprehensive clinical trials. Therefore, it is of great importance to publish the identified carcinosarcoma of the renal pelvis cases.
Competing Interests: The authors have declared that no competing interests exist.
(Copyright © 2023, Hacıosmanoğlu et al.)
Databáze: MEDLINE