Aldosterone-producing adenoma with a somatic KCNJ5 mutation revealing APC-dependent familial adenomatous polyposis

36Citations
Citations of this article
42Readers
Mendeley users who have this article in their library.

Abstract

Context: Recurrent somatic mutations in KCNJ5, CACNA1D, ATP1A1, and ATP2B3 have been identified in aldosterone-producing adenomas (APAs). The question as to whether they are responsible for both nodulation and aldosterone production is not solved. Case Description: We describe the case of a young patient who was diagnosed with severe arterial hypertension due to primary aldosteronism at age 26 years, followed by hemorrhagic stroke 4 years later. Abdominal computed tomography showed bilateral macronodular adrenal hyperplasia. Identification of lateralized aldosterone secretion led to right adrenalectomy, followed by normalization of biochemical and hormonal parameters and amelioration of blood pressure. The resected adrenal showed three nodules, one of them expressing aldosterone synthase and harboring a somatic KNCJ5 mutation. A Weiss revisited index of 3 of the APA prompted us to perform a second 18F-2-fluoro-2-deoxy-D-glucose-positron emission tomography after surgery, which revealed abnormal rectal activity despite the absence of clinical symptoms. Gastrointestinal exploration showed multiple polyps with severe dysplasia, and the diagnosis of familial adenomatous polyposis was established in the presence of a germline heterozygous APC gene mutation. Sequencing of somatic DNA from the APA and a secondadrenalnodulerevealed biallelicAPCinactivationdueto loss of heterozygosity inbothnodules. Conclusions: This case report underlines the need for establishing the frequency of germline APC variants in patients with primary aldosteronismandbilateral macronodular adrenal hyperplasia because their presence may predispose to APA development and severe hypertension well before the first familial adenomatous polyposissymptomsappear.Froma mechanistic point of view, it supports a two-hitmodelforAPA development, whereby the first hit drives increased cell proliferation whereas the second hit specifies the pattern of hormonal secretion. (J Clin Endocrinol Metab 101: 3874-3878, 2016).

Cite

CITATION STYLE

APA

Vouillarmet, J., Fernandes-Rosa, F., Graeppi-Dulac, J., Lantelme, P., Decaussin-Petrucci, M., Thivolet, C., … Zennaro, M. C. (2016). Aldosterone-producing adenoma with a somatic KCNJ5 mutation revealing APC-dependent familial adenomatous polyposis. Journal of Clinical Endocrinology and Metabolism, 101(11), 3874–3878. https://doi.org/10.1210/jc.2016-1874

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free