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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Park, Bong Soo Jin, Kyu Bok Kim, Yeon Mee Oh, Hee Taek Song, Seung Eon Lim, Tae Won Kim, Yang Wook |
| Description | Responsible library: WPRO |
| Abstract | Carcinoid tumors are low-grade malignant tumors arising from neuroendocrine cells. Primary renal carcinoid tumor is very rare due to the absence of neuroendocrine cells in the kidney and ureter. Therefore, little is known about the management and prognosis of renal carcinoid. Here, we report a case of a primary renal carcinoid tumor arising from a normal kidney in a 21-year-old man. He presented with a left renal mass, which was found accidentally. Abdominal computed tomography (CT) showed a 5.5 x 5.0-cm cystic mass with calcification. We suspected a cystic renal cell carcinoma and performed a laparoscopic radical nephrectomy. However, the histology revealed a well-differentiated neuroendocrine tumor. We concluded that it was a primary renal carcinoid tumor with no distant metastasis and did not administer chemotherapy or radiation therapy. He is recurrence-free after 8 months. |
| File Format | HTM / HTML |
| ISSN | 17389364 |
| e-ISSN | 22890769 |
| Journal | The Korean Journal of Medicine |
| Issue Number | 5 |
| Volume Number | 84 |
| Language | Korean |
| Publisher | The Korean Association of Internal Medicine |
| Publisher Date | 2013-01-01 |
| Publisher Place | Korea (South) |
| Access Restriction | Open |
| Subject Keyword | Discipline Medicine Carcinoid Tumor Carcinoma, Renal Cell Kidney Neoplasm Metastasis Nephrectomy Neuroendocrine Cells Neuroendocrine Tumors Prognosis Ureter |
| Content Type | Text |
| Resource Type | Article Case study |
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