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- Nobumasa Ohara, Takashi Tani, Kenshi Terajima, Tetsutaro Ozawa, Yuichiro Yoneoka, Hiroki Shimada, Yasuhiro Nakamura, Go Hasegawa, and Tsutomu Nishiyama.
- Department of Endocrinology and Metabolism, Uonuma Kikan Hospital, Japan.
- Intern. Med. 2024 Aug 10.
AbstractMany cases of primary aldosteronism (PA) in patients who developed hypokalemia-induced rhabdomyolysis and underwent adrenalectomy for aldosterone-producing adenoma (APA) have been reported; however, the immunohistopathological and molecular features remain unknown. We herein report the case of a 28-year-old woman with PA who presented with hypokalemia-induced rhabdomyolysis and underwent adrenalectomy for unilateral APA. An immunohistochemical analysis revealed that most adenoma cells were positive for steroidogenic enzymes, including CYP11B2. A genetic analysis revealed a somatic mutation in the KCNJ5. These findings suggest a strong aldosterone production capacity in our patient's adenoma, which was presumably related to her severe hyperaldosteronism and the resultant hypokalemia-induced rhabdomyolysis.
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