Primary renal neuroendocrine tumor: A case report with computed tomography findings.

Autor: Takahata K; Department of Radiology, Aichi Prefectural Welfare Federation of Agricultural Cooperatives Kainan Hospital, 396 Minami Honda, Maegasu Cho, Yatomi City, Aichi, Japan., Kamei S; Department of Radiology, Aichi Prefectural Welfare Federation of Agricultural Cooperatives Kainan Hospital, 396 Minami Honda, Maegasu Cho, Yatomi City, Aichi, Japan., Yamamoto T; Department of Radiology, Aichi Medical University, 1-1 Yazako Karimata, Nagakute City, Aichi, Japan., Hirose Y; Department of Urology, Aichi Prefectural Welfare Federation of Agricultural Cooperatives Kainan Hospital, 396 Minami Honda, Maegasu Cho, Yatomi City, Aichi, Japan., Yamamto Y; Department of Pathology, Aichi Medical University, 1-1 Yazako Karimata, Nagakute City, Aichi, Japan., Suzuki K; Department of Radiology, Aichi Medical University, 1-1 Yazako Karimata, Nagakute City, Aichi, Japan.
Jazyk: angličtina
Zdroj: Radiology case reports [Radiol Case Rep] 2023 Nov 23; Vol. 19 (2), pp. 586-590. Date of Electronic Publication: 2023 Nov 23 (Print Publication: 2024).
DOI: 10.1016/j.radcr.2023.10.069
Abstrakt: 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.
(© 2023 The Authors. Published by Elsevier Inc. on behalf of University of Washington.)
Databáze: MEDLINE