Hereditary Cushing’s syndrome caused by primary bilateral macronodular adrenal hyperplasia due to ARMC5 mutation with concomitant primary hyperparathyroidism: the first known case in Russia

Primary bilateral macronodular adrenal hyperplasia (PBMAH), a genetically heterogeneous disease, is a rare cause of Cushing’s syndrome. Until recently, few cases were attributed to mutations in known genes. However, in 2013, ARMC5, a newly discovered tumor suppressor gene, was identified. Further studies have shown that mutations in the ARMC5 gene are found in 25–55% of all PBMAH cases.

This article describes a clinical case of hereditary Cushing’s syndrome caused by PBMAH in a 37-year old patient. The patient’s family history is remarkable for the presence of Cushing’s syndrome and PBMAH in the patient’s mother. Bilateral adrenalectomy was performed as the treatment of choice. Genetic analysis using whole-exome sequencing confirmed the hereditary cause of the disease, revealing a germline heterozygous mutation in the ARMC5 gene. The patient also had concomitant mild primary hyperparathyroidism, which had not been observed before in genetic carriers with the ARMC5 mutation.

Cushing’s syndrome, primary bilateral macronodular adrenal hyperplasia, ARMC5, whole-exome sequencing, primary hyperparathyroidism, case report

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