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|a jpn
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|a Kubota, Y
|e verfasserin
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|a A case report of primary renal carcinoid tumor
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|c 1996
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|a Text
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|a ohne Hilfsmittel zu benutzen
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|a Date Completed 21.01.1997
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|a Date Revised 19.11.2015
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|a published: Print
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|a Citation Status MEDLINE
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|a 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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|a Case Reports
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|a Biomarkers, Tumor
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|a Hibi, H
|e verfasserin
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|a Yanaoka, M
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|a Kasahara, M
|e verfasserin
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|a Naide, Y
|e verfasserin
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773 |
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|i Enthalten in
|t Hinyokika kiyo. Acta urologica Japonica
|d 1962
|g 42(1996), 9 vom: 01. Sept., Seite 671-5
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