Unilateral Primary Pigmented Nodular Adrenocortical Disease: Report of a Rare Case
Author(s) -
Sanjay D. Deshmukh,
Vandana L. Gaopande,
Snehal Purandare,
Shreepad Bhat
Publication year - 2015
Publication title -
turkish journal of endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.111
H-Index - 5
ISSN - 1301-2193
DOI - 10.4274/tjem.2509
Subject(s) - medicine , dermatology , rare disease , disease , pathology
Primary pigmented adrenocortical disease is a rare disorder usually affecting both adrenals. It causes Cushing’s syndrome that is adrenocorticotropic hormone independent. It is treated by bilateral adrenalectomy. We present an unusual case where this condition was unilateral and was diagnosed as adenoma on imaging. The patient was subsequently treated by unilateral adrenalectomy, and had no signs of recurrence in 5-year postoperative follow-up. This case emphasizes the importance of histopathology and immunohistochemistry in diagnosis of this condition
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