Case Report
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World J Radiol. Aug 28, 2013; 5(8): 328-333
Published online Aug 28, 2013. doi: 10.4329/wjr.v5.i8.328
Primary renal carcinoid tumor: A rare cystic renal neoplasm
Jung-Hee Yoon
Jung-Hee Yoon, Department of Radiology, Haeundae Paik Hospital, Inje University College of Medicine, Busan 612-030, South Korea
Author contributions: Yoon JH solely contributed to this paper.
Correspondence to: Jung-Hee Yoon, MD, PhD, Associate Professor, Department of Radiology, Haeundae Paik Hospital, Inje University College of Medicine, 1435 Jwa-dong, Haeundae-gu, Busan 612-030, South Korea. radyjh@hanmail.net
Telephone: +82-51-7970355 Fax: +82-51-7970379
Received: April 10, 2013
Revised: June 22, 2013
Accepted: July 30, 2013
Published online: August 28, 2013
Abstract

We present the case of a 21-year-old man with an incidentally detected cystic renal mass. A well-defined, solid mass measuring approximately 8 cm x 6 cm with a cystic component was identified in the left kidney by abdominal multidetector computed tomography (CT) and ultrasonography. The mass was well-enhanced on the corticomedullary CT phase and washout of enhancement occurred on the nephrographic phase. The mass contained peripheral wall and septal calcifications in the cystic component. The lesion was resected and diagnosed as a primary renal carcinoid tumor. Primary carcinoid tumors of the kidney are extremely rare. This case is notable because of the rarity of this neoplasm and its unique radiologic and pathologic findings. A review of previously reported cases in the literature is also presented.

Keywords: Kidney, Kidney neoplasms, Carcinoid tumor, Neuroendocrine

Core tip: We present a rare confirmed case of primary carcinoid tumor developed at 21-year-old man with incidentally detected a mixed solid and cystic mass in the left kidney. This case is interesting because of the rarity of this neoplasm and its unique radiologic and pathologic findings.