1Division of Endocrinology and Molecular Medicine, Department of Medicine, University of Kentucky, Lexington, Kentucky
2Isfahan Endocrine and Metabolism Research Center, Isfahan University of Medical Sciences, Isfahan, Iran
3Department of Internal Medicine, School of Medicine, Bushehr University of Medical Sciences, Bushehr, IRAN
4Department of pathology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, IRAN
American Journal of Medical Case Reports.
2021,
Vol. 9 No. 10, 492-494
DOI: 10.12691/ajmcr-9-10-3
Copyright © 2021 Science and Education PublishingCite this paper: Kamyar Asadipooya, Roohollah Narimani, Ashraf Aminorroaya, Bijan Iraj, Mohammadreza Kalantarhormozi, Novin Afshar Moghadam, Elaheh Kavoussi, Mitra Dashtizadeh. Cushing Syndrome Due to Pigmented Nodular Adrenal Hyperplasia in an Iranian Patient: A Case Report and Review of the Literature.
American Journal of Medical Case Reports. 2021; 9(10):492-494. doi: 10.12691/ajmcr-9-10-3.
Correspondence to: Mohammadreza Kalantarhormozi, Department of Internal Medicine, School of Medicine, Bushehr University of Medical Sciences, Bushehr, IRAN. Email:
m.kalantraihormozi111@yahoo.comAbstract
Primary pigmented nodular adrenocortical disease (PPNAD) is a rare cause of Adrenocorticotropic hormone-independent Cushing syndrome. In this case, we present a case of PPNAD in 25 y/o women who presented with a 3 years history of weight gain, hirsutism, and abnormal menstruation. Our findings were suggestive of PPNAD in the pathological study of adrenal biopsy.
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