Literature DB >> 9161855

[A case of concurrent bilateral adrenocortical adenoma causing Cushing's syndrome].

F Koga1, S Sumi, H Umeda, S Maeda, M Honda, Y Hosoya, M Yano, A Konita, S Suzuki, K Yoshida.   

Abstract

A 43-year-old woman presented with obesity and lumbago. Endocrinological examinations revealed normal plasma cortisol levels and a suppressed serum adrenocorticotropic hormone (ACTH) level. On venous sampling, markedly elevated plasma cortisol levels were observed for bilateral adrenal veins (243 and 62.3 micrograms/dl on the right and left sides, respectively). Although the computed tomogram revealed bilaterally enlarged adrenal glands, 131I-adosterol scintigram showed a strong uptake only on the right side. Right adrenalectomy successfully relieved Cushing's syndrome. Pathological diagnosis was adrenocortical adenoma, 3.5 cm in diameter. Cushing's syndrome recurred in 9 years. At that time, she underwent left subtotal adrenalectomy including a 3-cm adrenocortical adenoma. Postoperative convalescence has been uneventful with oral steroid supplementation. All 14 previously reported cases of bilateral adrenocortical adenoma (BAA) causing Cushing's syndrome as well as the present case were concurrent and dominant in females of reproductive age. This suggests that some cofactors other than ACTH, such as estrogen, contribute to the pathogenesis of BAA.

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Year:  1997        PMID: 9161855

Source DB:  PubMed          Journal:  Hinyokika Kiyo        ISSN: 0018-1994


  1 in total

1.  The clinical conundrum of corticotropin-independent autonomous cortisol secretion in patients with bilateral adrenal masses.

Authors:  William F Young; Hendrick du Plessis; Geoffrey B Thompson; Clive S Grant; David R Farley; Melanie L Richards; Dana Erickson; Adrian Vella; Anthony W Stanson; J Aidan Carney; Charles F Abboud; Paul C Carpenter
Journal:  World J Surg       Date:  2008-05       Impact factor: 3.352

  1 in total

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