Primary renal neuroendocrine tumor: A case report with computed tomography findings
Radiology Case Reports, ISSN: 1930-0433, Vol: 19, Issue: 2, Page: 586-590
2024
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
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Case Description
We report a rare case of a primary renal neuroendocrine tumor. The patient was a 64-year-old woman. The patient's chief complaint was gross hematuria. Dynamic contrast-enhanced computed tomography (CT) revealed a hypovascular mass 13 cm in diameter in the right kidney. The border of the mass was clear. A grossly contrast-impaired area and internal granular calcification were observed. A right radical nephrectomy was performed. Macroscopically, the mass was hemorrhaged and necrotic. It was diagnosed as a neuroendocrine tumor (NET) (Grade 2) histologically. Findings, such as hypovascularity, calcification, and necrosis, in our case were similar to those in previous reports. These findings are considered relatively characteristic of primary renal NETs.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1930043323008117; http://dx.doi.org/10.1016/j.radcr.2023.10.069; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85183764876&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/38074443; https://linkinghub.elsevier.com/retrieve/pii/S1930043323008117; https://dx.doi.org/10.1016/j.radcr.2023.10.069
Elsevier BV
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