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  • Title: [A case report of primary renal carcinoid tumor].
    Author: Kubota Y, Hibi H, Yanaoka M, Okishio N, Kasahara M, Naide Y.
    Journal: Hinyokika Kiyo; 1996 Sep; 42(9):671-5. PubMed ID: 8918667.
    Abstract:
    A 54-year-old woman was referred to our institute because of abdominal pain and constipation. The computed tomography of the abdomen revealed a 3 x 3 cm of low density tumor at the upper pole of the left kidney and para-aortic lymphadenopathy. Gastrointestinal investigation revealed no particular findings suggesting a carcinoid syndrome associated with the left kidney tumor. The specimen of the resected tumor showed staining pattern specific to carcinoid tumor; positive staining for chromogranin A and neuron-specific-enolase. Electron microscopy confirmed the presence of dense-core granules in the tumor cells. No evidence of metastasis or recurrence was noted for 13 months after the operation. This was a very rare case of primary renal carcinoid, representing the 26th case in the literature.
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