Silent Mixed Ganglioneuroma/Pheochromocytoma which Produces a Vasoactive Intestinal Polypeptide
スポンサーリンク
概要
- 論文の詳細を見る
An unusual pheochromocytoma was incidentally discovered in a 48-year-old woman. The patient had a 3-year history of myasthenia gravis. At the time of examination in our hospital, the right adrenal tumor was incidentally discovered by ultrasonography of the abdomen. She had no history of headache, perspiration, palpitation or hypertension. Although blood catecholamine levels were within the normal limits, urinary secretion of catecholamine was elevated. Histologically, the tumor was diagnosed to be mixed ganglioneuroma/pheochromocytoma and histochemically confirmed to produce vasoactive intestinal polypeptide. Such a tumor is quite rare.(Internal Medicine 32: 63-66, 1993)
著者
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Inoue Junichi
The Department Of Internal Medicine Saga Medical School
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Hayashi Junichi
The Department Of Thoracic And Cardiovascular Surgery Niigata University School Of Medicine
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Nomura Masahiro
The Department of Digestive and Cardiovascular Medicine, The University of Tokushima
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MORICHIKA Yutaka
the Department of Internal Medicine, Hiroshima City Hospital
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NAGASHIMA Fujio
the Department of Internal Medicine, Hiroshima City Hospital
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ARAKI Yasuyuki
the Department of Internal Medicine, Hiroshima City Hospital
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SUGIHARA Tohru
the Department of Internal Medicine, Hiroshima City Hospital
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SHIBATA Susumu
the Department of Internal Medicine, Hiroshima City Hospital
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AKAGI Emiiru
the Department of Internal Medicine, Hiroshima City Hospital
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HAYASHI Junichi
the Department of Internal Medicine, Hiroshima City Hospital
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INOUE Junichi
the Department of Internal Medicine, Hiroshima City Hospital
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