Literature DB >> 16543680

A case of adrenocorticotropin-independent bilateral adrenal macronodular hyperplasia (AIMAH) with primary hyperparathyroidism (PHPT).

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.

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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


  5 in total

1.  The role of unilateral adrenalectomy in ACTH-independent macronodular adrenal hyperplasia (AIMAH).

Authors:  Maurizio Iacobone; Nora Albiger; Carla Scaroni; Franco Mantero; Ambrogio Fassina; Giovanni Viel; Mauro Frego; Gennaro Favia
Journal:  World J Surg       Date:  2008-05       Impact factor: 3.352

2.  Classification, diagnosis and treatment of ACTH-independent macronodular adrenal hyperplasia.

Authors:  Heng-Chuan Su; Jun Dai; Xin Huang; Wen-Long Zhou; Bao-Xing Huang; Wan-Li Cao; Fu-Kang Sun
Journal:  Can Urol Assoc J       Date:  2013 Sep-Oct       Impact factor: 1.862

3.  The role of unilateral adrenalectomy in corticotropin-independent bilateral adrenocortical hyperplasias.

Authors:  Yunze Xu; Wenbin Rui; Yicheng Qi; Chongyu Zhang; Juping Zhao; Xiaojing Wang; Yuxuan Wu; Qi Zhu; Zhoujun Shen; Guang Ning; Yu Zhu
Journal:  World J Surg       Date:  2013-07       Impact factor: 3.352

Review 4.  Long delay in diagnosis of a case with MEN1 due to concomitant presence of AIMAH with insulinoma: a case report and literature review.

Authors:  Vajihe Chavoshi; Seyed Saeed Tamehri Zadeh; Shayesteh Khalili; Amirhassan Rabbani; Seyed Amir Hassan Matini; Zhaleh Mohsenifar; Farzad Hadaegh
Journal:  BMC Endocr Disord       Date:  2022-04-21       Impact factor: 3.263

5.  A novel nonsense mutation in ARMC5 causes primary bilateral macronodular adrenocortical hyperplasia.

Authors:  Wen-Tao He; Xiong Wang; Wen Song; Xiao-Dong Song; Yan-Jun Lu; Yan-Kai Lv; Ting He; Xue-Feng Yu; Shu-Hong Hu
Journal:  BMC Med Genomics       Date:  2021-05-10       Impact factor: 3.063

  5 in total

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