A Rare Case of Neuroendocrine Tumor Following Radical Nephrectomy

Muhammad Rozaqy Ishaq, - and Nafis Audrey Febriansyah, - and Soetojo, - (2022) A Rare Case of Neuroendocrine Tumor Following Radical Nephrectomy. Folia Medica Indonesiana, 58 (2). pp. 192-194. ISSN 2355-8393

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Official URL: https://e-journal.unair.ac.id/FMI/article/view/332...


Neuroendocrine Tumors (NETs) are a diverse range of neoplasms with various biological and histologic features and therapeutic responses. The prevalence of primary renal carcinoids is scarce worldwide. At the moment, complete surgical resection is the primary treatment against primary neuroendocrine tumors of the kidney. Nephrectomy followed by the lymph node dissection is a standard procedure for localized primary renal NETs. Since renal carcinoid tumor is extremely rare, we decided to present a unique case of a 25-years-old male with neuroendocrine renal carcinoid tumor following radical nephrectomy. The results indicated a solid, solitary tumor verified on the frozen section because a postoperative CT–scan showed a recurring mass in the renal fossa following radical nephrectomy. The case emphasized the need to investigate primary renal NET in the workup and histological examination of renal tumors and also contributed to our understanding of this infrequent clinical entity.

Item Type: Article
Uncontrolled Keywords: Neuroendocrine Tumors, NETs, Carcinoid Tumor, Radical Nephrectomy, Case Report
Subjects: R Medicine > R Medicine (General)
R Medicine > RC Internal medicine > RC870-923 Diseases of the genitourinary system. Urology
Divisions: 01. Fakultas Kedokteran > Urologi
Muhammad Rozaqy Ishaq, -UNSPECIFIED
Nafis Audrey Febriansyah, -UNSPECIFIED
Soetojo, -NIDN0008065604
Depositing User: arys fk
Date Deposited: 29 Jan 2023 23:37
Last Modified: 29 Jan 2023 23:37
URI: http://repository.unair.ac.id/id/eprint/119752
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