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|a Kimura, T
|e verfasserin
|4 aut
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|a A case of Sipple syndrome whose bilateral pheochromocytomas were resected separately after a 3-year interval
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|c 2000
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|a Text
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|a ohne Hilfsmittel zu benutzen
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|a Date Completed 04.08.2000
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|a Date Revised 15.11.2006
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|a published: Print
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|a Citation Status MEDLINE
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|a A 23-year-old woman who had undergone total thyroidectomy and parabronchial lymphadenectomy at the Department of Otolaryngology in our hospital was suspected to have a thyroid carcinoma. Histological examination revealed a medullary carcinoma of the thyroid and normal parathyroid glands. Because a computed tomographic scan after surgery revealed a tumor of the left adrenal gland, the patient was examined at our department two months after the thyroidectomy, 1994. Endocrinic examinations and 123I-MIBG scintigraphy revealed a left adrenal pheochromocytoma of Sipple syndrome. She then underwent left adrenalectomy. Histological diagnosis was pheochromocytoma of the left adrenal gland. Three years after the surgery, a right adrenal tumor was detected by computed tomography. Although results of endocrine examinations were normal, 131I-MIBG scintigraphy showed a hot spot in the right adrenal gland. Right adrenal pheochromocytoma was diagnosed 3 years after surgery for a contralateral adrenal pheochromocytoma. Although surgery was recommended, the patient consented to right adrenalectomy, 1 year later after marriage and before becoming pregnant. Histological examination of the resected specimen revealed pheochromocytoma of the right adrenal gland
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|a Case Reports
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|a English Abstract
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|a Journal Article
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|a Ikemoto, I
|e verfasserin
|4 aut
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|a Furuta, N
|e verfasserin
|4 aut
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|a Ohishi, Y
|e verfasserin
|4 aut
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773 |
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|i Enthalten in
|t Hinyokika kiyo. Acta urologica Japonica
|d 1962
|g 46(2000), 4 vom: 01. Apr., Seite 251-3
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