Carney Complex Complicated with Primary Pigmented Nodular Adrenocortical Disease without Cushing's Syndrome Recurrence for Five Years after Unilateral Adrenalectomy

Intern Med. 2022;61(2):205-211. doi: 10.2169/internalmedicine.7418-21. Epub 2022 Jan 15.

Abstract

We herein report a case of Carney complex (CNC) complicated with primary pigmented nodular adrenocortical disease (PPNAD) after unilateral adrenalectomy. A 44-year-old woman was admitted to our hospital for PPNAD surgery. She had previously undergone surgery for cardiac myxoma and had a PRKAR1A mutation with no family history of CNC. She had Cushing's signs, but her metabolic abnormalities were mild. Adrenal insufficiency due to poor medication adherence was a concern, so she underwent unilateral adrenalectomy. Cushing's signs improved postoperatively and without recurrence for five years. Treatment plans for PPNAD should be determined based on the patient's condition, medication adherence, and wishes.

Keywords: Carney complex; Cushing's syndrome; primary pigmented nodular adrenocortical disease; unilateral adrenalectomy.

Publication types

  • Case Reports

MeSH terms

  • Adrenal Cortex Diseases* / genetics
  • Adrenal Cortex Diseases* / surgery
  • Adrenalectomy
  • Adult
  • Carney Complex* / genetics
  • Carney Complex* / surgery
  • Cushing Syndrome* / etiology
  • Cushing Syndrome* / surgery
  • Cyclic AMP-Dependent Protein Kinase RIalpha Subunit / genetics
  • Female
  • Humans

Substances

  • Cyclic AMP-Dependent Protein Kinase RIalpha Subunit