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A rare case of adrenocorticotropic hormone (ACTH)-independent macroadrenal hyperplasia showing ectopic production of ACTH.

Abstract
A 57-year-old Japanese man presented with drug-resistant hypertension without Cushingoid features. Endocrinological tests revealed autonomous secretion of cortisol with suppressed plasma adrenocorticotropic hormone (ACTH). Imaging examinations showed multiple macronodules in the bilateral adrenal gland. These findings were consistent with subclinical Cushing's syndrome caused by ACTH-independent macronodular adrenal hyperplasia (AIMAH). Left adrenalectomy was performed and the resected adrenal lesion was consistent with the pathological diagnosis of AIMAH. Furthermore, in resected tissue, we demonstrated intraadrenal production of ACTH by immunohistochemical analysis and RIA. This is a very rare case of AIMAH showing ectopic production of ACTH, which may be associated with autonomous cortisol secretion.
AuthorsMinoru Iwata, Yutaka Oki, Teruyo Okazawa, Shin Ishizawa, Chihiro Taka, Katsuya Yamazaki, Kazuyuki Tobe, Junya Fukuoka, Hironobu Sasano, Tetsuo Nishikawa
JournalInternal medicine (Tokyo, Japan) (Intern Med) Vol. 51 Issue 16 Pg. 2181-7 ( 2012) ISSN: 1349-7235 [Electronic] Japan
PMID22892500 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Adrenocorticotropic Hormone
Topics
  • Adrenal Cortex (pathology)
  • Adrenal Cortex Function Tests
  • Adrenal Glands (diagnostic imaging, metabolism)
  • Adrenalectomy
  • Adrenocorticotropic Hormone (blood, metabolism)
  • Cushing Syndrome (blood, metabolism)
  • Humans
  • Hyperplasia
  • Immunohistochemistry
  • Male
  • Middle Aged
  • Radioimmunoassay
  • Radionuclide Imaging

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