Literature DB >> 30844071

Long-Term Outcome of Primary Bilateral Macronodular Adrenocortical Hyperplasia After Unilateral Adrenalectomy.

Andrea Osswald1, Marcus Quinkler2, Guido Di Dalmazi3, Timo Deutschbein4, German Rubinstein1, Katrin Ritzel1, Stephanie Zopp1, Jerome Bertherat5, Felix Beuschlein1,6, Martin Reincke1.   

Abstract

CONTEXT: Unilateral adrenalectomy has been proposed in selected patients with primary bilateral macronodular adrenocortical hyperplasia (PBMAH), but its long-term outcome is unclear.
OBJECTIVE: The aim of this study was to analyze long-term clinical and biochemical outcomes of unilateral adrenalectomy vs bilateral adrenalectomy in patients with PBMAH in comparison with the outcome of cortisol-producing adenoma (CPA) treated with unilateral adrenalectomy.
DESIGN: Retrospective observational study in three German and one Italian academic tertiary care center. PATIENTS AND METHODS: Twenty-five patients with PBMAH after unilateral adrenalectomy (unilat-ADX-PBMAH), nine patients with PBMAH and bilateral adrenalectomy (bilat-ADX-PBMAH), and 39 patients with CPA and unilateral adrenalectomy (unilat-ADX-CPA) were included.
RESULTS: Baseline clinical and biochemical parameters were comparable in patients with unilat-ADX-PBMAH, bilat-ADX-PBMAH, and unilat-ADX-CPA. Directly after surgery, 84% of the patients with unilat-ADX-PBMAH experienced initial remission of Cushing syndrome (CS). In contrast, at last follow-up (median, 50 months), 32% of the patients with unilat-ADX-PBMAH were biochemically controlled compared with nearly all patients in the other two groups (P = 0.000). Adrenalectomy of the contralateral side had to be performed in 12% of the initial patients with unilat-ADX-PBMAH. Three of 20 patients with unilat-ADX-PBMAH (15%) died during follow-up, presumably of CS-related causes; no deaths occurred in the other two groups (P = 0.008). Deaths occurred exclusively in patients who were not biochemically controlled after unilateral ADX.
CONCLUSIONS: Our data suggest that unilateral adrenalectomy of patients with PBMAH leads to clinical remission and a lower incidence of adrenal crisis but in less sufficient biochemical control of hypercortisolism, potentially leading to higher mortality.
Copyright © 2019 Endocrine Society.

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Year:  2019        PMID: 30844071     DOI: 10.1210/jc.2018-02204

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  14 in total

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Review 2.  Update on primary bilateral macronodular adrenal hyperplasia (PBMAH).

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Journal:  J Endocr Soc       Date:  2020-10-29

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6.  Unilateral Adrenalectomy for Primary Aldosteronism Due to Bilateral Adrenal Disease Can Result in Resolution of Hypokalemia and Amelioration of Hypertension.

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8.  A New Insight into the Surgical Treatment of Primary Macronodular Adrenal Hyperplasia.

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Journal:  J Endocr Soc       Date:  2020-07-22

9.  A novel nonsense mutation in ARMC5 causes primary bilateral macronodular adrenocortical hyperplasia.

Authors:  Wen-Tao He; Xiong Wang; Wen Song; Xiao-Dong Song; Yan-Jun Lu; Yan-Kai Lv; Ting He; Xue-Feng Yu; Shu-Hong Hu
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Review 10.  Adrenal Incidentaloma.

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