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タイトル: ACTH非依存性両側副腎皮質大結節性過形成(AIMAH)によるCushing症候群の1例
その他のタイトル: ACTH-independent bilateral macronodular adrenocortical hyperplasia (AIMAH): a case report
著者: 三木, 健史  KAKEN_name
中山, 治郎  KAKEN_name
志水, 清紀  KAKEN_name
細見, 昌弘  KAKEN_name
清原, 久和  KAKEN_name
竹田, 雅司  KAKEN_name
花田, 正人  KAKEN_name
著者名の別形: MIKI, Takeshi
NAKAYAMA, Jirou
SHIMIZU, Kiyonari
HOSOMI, Masahiro
KIYOHARA, Hisakazu
TAKEDA, Masashi
HANADA, Masato
キーワード: AIMAH
Cushing's syndrome
発行日: Apr-1999
出版者: 泌尿器科紀要刊行会
誌名: 泌尿器科紀要
巻: 45
号: 4
開始ページ: 245
終了ページ: 248
抄録: We report a case of adrenocorticotropic hormone (ACTH)-independent macronodular adrenocortical hyperplasia (AIMAH). A 54-year-old Japanese man was admitted to our hospital for further examination of obesity and hypertension. Endocrinological studies showed that plasma cortisol was high (22.5 micrograms/dl) without diurnal rhythm, and plasma ACTH was low. Two or 8 mg of dexamethasone did not suppress the plasma cortisol levels. Abdominal computed tomography revealed nodular hyperplasia of bilateral adrenal glands. Adrenal scintigraphy showed the positive uptake of 131I-adosterol to bilateral adrenal glands. Brain magnetic resonance imaging revealed no abnormalities. He was diagnosed as having Cushing's syndrome with bilateral adrenal hyperplasia, and bilateral adrenalectomy was performed. Left and right adrenal glands were 52 g and 35 g, respectively, and were occupied by yellow nodular lesions. Histologically, hyperplastic lesions were composed of clear cells. Finally he was diagnosed with AIMAH.
URI: http://hdl.handle.net/2433/114029
PubMed ID: 10363143
出現コレクション:Vol.45 No.4

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