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DCフィールド | 値 | 言語 |
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dc.contributor.author | 池田, 純一 | ja |
dc.contributor.author | 六車, 光英 | ja |
dc.contributor.author | 井上, 貴昭 | ja |
dc.contributor.author | 西田, 晃久 | ja |
dc.contributor.author | 川喜多, 繁誠 | ja |
dc.contributor.author | 室田, 卓之 | ja |
dc.contributor.author | 大杉, 治之 | ja |
dc.contributor.author | 滝澤, 奈恵 | ja |
dc.contributor.author | 木下, 秀文 | ja |
dc.contributor.author | 松田, 公志 | ja |
dc.contributor.author | 野田, 亜未香 | ja |
dc.contributor.author | 宇都宮, 啓太 | ja |
dc.contributor.alternative | Ikeda, Junichi | en |
dc.contributor.alternative | Muguruma, Kouei | en |
dc.contributor.alternative | Inoue, Takaaki | en |
dc.contributor.alternative | Nishida, Teruhisa | en |
dc.contributor.alternative | Kawakita, Shigenari | en |
dc.contributor.alternative | Murota, Takashi | en |
dc.contributor.alternative | Ohsugi, Haruyuki | en |
dc.contributor.alternative | Takizawa, Nae | en |
dc.contributor.alternative | Kinoshita, Hidefumi | en |
dc.contributor.alternative | Matsuda, Tadashi | en |
dc.contributor.alternative | Noda, Amika | en |
dc.contributor.alternative | Utsunomiya, Keita | en |
dc.date.accessioned | 2017-03-01T01:29:18Z | - |
dc.date.available | 2017-03-01T01:29:18Z | - |
dc.date.issued | 2017-01-31 | - |
dc.identifier.issn | 0018-1994 | - |
dc.identifier.uri | http://hdl.handle.net/2433/218502 | - |
dc.description.abstract | Adrenal corticotropin (ACTH) -independent macronodular adrenal hyperplasia (AIMAH) is a rare cause of Cushing’s syndrome. Bilateral adrenalectomy is the treatment of choice, but lifetime steroid replacement is essential. Here we report a case of AIMAH whose hyperglycemia was improved following unilateral adrenalectomy. A 42-year-old woman with serious intellectual disability and intractable epilepsy presented with polydipsia. Casual blood glucose and hemoglobin A1c (HbA1c) were 322 mg/dl and 8.5%, respectively. The cortisol level was high and ACTH level was low. Abdominal computed tomography and magnetic resonance imaging revealed unsuspected macronodular enlargement of bilateral adrenal glands (left 8 cm, right 4 cm in maximal diameter) and she was diagnosed with AIMAH. Both adrenal glands showed intense 131 I-adosterol accumulation predominantly in the left side and left-unilateral laparoscopic adrenalectomy was performed. Both insulin and oral antidiabetic drugs could be cancelled postoperatively, and HbA1c decreased to 5.7%. Steroid was not replaced but she never experienced adrenal crisis. We conclude that unilateral adrenalectomy is a safe and effective treatment for certain cases of AIMAH. | en |
dc.format.mimetype | application/pdf | - |
dc.language.iso | jpn | - |
dc.publisher | 泌尿器科紀要刊行会 | ja |
dc.rights | 許諾条件により本文は2018/02/01に公開 | ja |
dc.subject | ACTH-independent macronodular adrenal hyperplasia (AIMAH) | en |
dc.subject | Unilateral adrenalectomy | en |
dc.subject | Laparoscopic surgery | en |
dc.subject | Cushing’ssyndrome | en |
dc.subject.ndc | 494.9 | - |
dc.title | 片側副腎摘除にて高血糖が改善したACTH 非依存性大結節性副腎皮質過形成(AIMAH)の1例 | ja |
dc.title.alternative | Improvement in Hyperglysemia Following Unilateral Adrenalectomy for ACTH-Independent Macronodular Adrenal Hyperplasia (AIMAH) : A Case Report | en |
dc.type | departmental bulletin paper | - |
dc.type.niitype | Departmental Bulletin Paper | - |
dc.identifier.ncid | AN00208315 | - |
dc.identifier.jtitle | 泌尿器科紀要 | ja |
dc.identifier.volume | 63 | - |
dc.identifier.issue | 1 | - |
dc.identifier.spage | 7 | - |
dc.identifier.epage | 10 | - |
dc.textversion | publisher | - |
dc.sortkey | 02 | - |
dc.address | 関西医科大学総合医療センター腎泌尿器外科 | ja |
dc.address | 関西医科大学総合医療センター腎泌尿器外科 | ja |
dc.address | 関西医科大学総合医療センター腎泌尿器外科 | ja |
dc.address | 関西医科大学総合医療センター腎泌尿器外科 | ja |
dc.address | 関西医科大学総合医療センター腎泌尿器外科 | ja |
dc.address | 関西医科大学総合医療センター腎泌尿器外科 | ja |
dc.address | 関西医科大学附属病院腎泌尿器外科 | ja |
dc.address | 関西医科大学附属病院腎泌尿器外科 | ja |
dc.address | 関西医科大学附属病院腎泌尿器外科 | ja |
dc.address | 関西医科大学附属病院腎泌尿器外科 | ja |
dc.address | 関西医科大学内科学第二講座 | ja |
dc.address | 関西医科大学放射線科学講座 | ja |
dc.address.alternative | The Department of Urology and Andrology, Kansai Medical University Medical Center | en |
dc.address.alternative | The Department of Urology and Andrology, Kansai Medical University Medical Center | en |
dc.address.alternative | The Department of Urology and Andrology, Kansai Medical University Medical Center | en |
dc.address.alternative | The Department of Urology and Andrology, Kansai Medical University Medical Center | en |
dc.address.alternative | The Department of Urology and Andrology, Kansai Medical University Medical Center | en |
dc.address.alternative | The Department of Urology and Andrology, Kansai Medical University Medical Center | en |
dc.address.alternative | The Department of Urology and Andrology, Kansai Medical University Hospital | en |
dc.address.alternative | The Department of Urology and Andrology, Kansai Medical University Hospital | en |
dc.address.alternative | The Department of Urology and Andrology, Kansai Medical University Hospital | en |
dc.address.alternative | The Department of Urology and Andrology, Kansai Medical University Hospital | en |
dc.address.alternative | The Department of Medicine II, Kansai Medical University | en |
dc.address.alternative | The Department of Radiology, Kansai Medecal University | en |
dc.identifier.pmid | 28245538 | - |
dc.identifier.selfDOI | 10.14989/ActaUrolJap_63_1_7 | - |
dcterms.accessRights | open access | - |
datacite.date.available | 2018-02-01 | - |
dc.identifier.pissn | 0018-1994 | - |
dc.identifier.jtitle-alternative | Acta urologica Japonica | la |
dc.identifier.jtitle-alternative | Hinyokika Kiyo | en |
出現コレクション: | Vol.63 No.1 |

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