| Literature DB >> 16543680 |
Mikano Sato1, Masayoshi Soma, Tomohiro Nakayama, Kotoko Kosuge, Ryou Suzuki, Kazuyoshi Okada, Kazutoshi Komatsu, Masahiko Sugitani, Koichi Matsumoto.
Abstract
We report a rare case of ACTH-independent macronodular adrenal hyperplasia (AIMAH) with primary hyperparathyroidism (PHPT). A 57-year-old woman was admitted to our hospital for further examination of secondary hypertension and bilateral adrenal macrotumors. Midnight serum cortisol elevation with undetectable plasma ACTH, increased 24-hour urinary free cortisol excretion, and loss of the normal circadian rhythm in cortisol secretion established the diagnosis of Cushing's syndrome. Total resection of the enlarged left adrenal gland was performed with subsequent steroid replacement. Her general condition improved but serum calcium level increased 3 weeks after surgery. PHPT was diagnosed on the basis of endocrinological examination, although imaging studies failed to detect parathyroid lesion. In summary, we believe this to be the first report of a case of AIMAH with PHPT.Entities:
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Year: 2006 PMID: 16543680 DOI: 10.1507/endocrj.53.111
Source DB: PubMed Journal: Endocr J ISSN: 0918-8959 Impact factor: 2.349