Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association)
Online ISSN : 1882-5133
Print ISSN : 1345-2843
ISSN-L : 1345-2843
Case Reports
Two patients with adrenocorticotropic hormone-independent macronodular hyperplasia successfully treated using laparoscopic hemiadrenalectomy
Kento KURATA, Naoyoshi ONODA, Tetsuro ISHIKAWA, Hidemi KAWAJIRI, Tsutomu TAKASHIMA, Atsushi SHIOI, Kenichi WAKASA, Kosei HIRAKAWA
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2012 Volume 73 Issue 2 Pages 460-465

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Abstract
Here, we report the cases of 2 patients with adrenocorticotropic hormone (ACTH) -independent macronodular adrenocortical hyperplasia (AIMAH) successfully treated with laparoscopic unilateral adrenalectomy. Case 1 : A 51-year-old man with treatment-resistant hypertension was diagnosed with AIMAH. Further examination revealed that the patient had preclinical Cushing's syndrome (PC), and unilateral right adrenalectomy was performed. Case 2 : A 61-year-old woman with early-onset hypertension from the age of 40 years was incidentally found to have AIMAH with PC, and unilateral right adrenalectomy was performed. The blood-pressure levels of the 2 patients improved, and serum levels of ACTH and cortisol became normalized after the operation. Conventionally, bilateral total adrenalectomy is the treatment of choice for a patient with AIMAH, although life-time steroid supplementation is required. The outcomes observed in our cases and in recent reports show that hemi-adrenalectomy is a safe and feasible alternative and should be considered as the standard surgical treatment for AIMAH patients to compensate for the critical demerit of bilateral total adrenalectomy.
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© 2012 Japan Surgical Association
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