Elsevier

Urology

Volume 61, Issue 4, April 2003, Page 838
Urology

Case report
Metastatic renal carcinoid: case report and review of the literature

https://doi.org/10.1016/S0090-4295(02)02560-8Get rights and content

Abstract

Primary renal carcinoid tumor is a rare tumor of the kidney. Metastatic renal carcinoid tumor has not been described in the medical literature. We report a case of renal metastasis of a primary bronchial carcinoid tumor and review the literature about renal carcinoid tumors.

Section snippets

Case report

A 64-year-old woman was referred to our department with a solid mass in the right kidney. The patient had sought medical attention for a cervical mass she first noted 2 months before admission. Abdominal ultrasonography was performed in search of a metastatic mass and revealed the renal lesion.

The patient’s medical history documented upper lobectomy of the left lung to remove a mass 2 years before the present admission. Histologically, it was a bronchial carcinoid tumor. The physical

Comment

Carcinoid tumors are thought to arise from neuroendocrine cells. Histologically, they stain positively to markers of neuroendocrine tissue, including neuron-specific enolase, synaptophysin, and chromogranin. Carcinoid tumors secrete a variety of hormones and biogenic amines, including serotonin, corticotropin, histamine, dopamine, substance P, neurotensin, prostaglandins, and kallikrein.1 The release of serotonin and other vasoactive substances into the systemic circulation is thought to cause

Conclusions

We report on a solid lesion of the kidney found to be a bronchial carcinoid metastasis. Our review of published studies on bladder and renal carcinoid tumors yielded descriptions of only primary tumors. Carcinoid tumors, both primary and secondary, might be elusive and difficult to diagnose. Their detection is facilitated by the highly sensitive radiolabeled octreotide scan.

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