Abstract

Primary small-cell neuroendocrine carcinoma of the kidney with urothelial carcinoma is very rare, and it has a unique pathomorphology and immunohistochemical phenotype. Since it is easily missed diagnosed or misdiagnosed, it needs to be differentiated from a variety of other tumors. In addition to poor prognosis, the carcinoma also has strong invasive ability. The clinicopathological characteristics, immunohistochemical phenotype, and diagnosis and differential diagnosis of four patients with primary small-cell neuroendocrine carcinoma with urothelial carcinoma were retrospectively analyzed, and the relevant literature was reviewed. Three cases occurred in the left kidney and one case occurred in the right kidney. The main clinical symptoms were gross hematuria and waist pain. Tumor histological morphology and immunohistochemical markers support small-cell neuroendocrine carcinoma with urothelial carcinoma.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.