| Literature DB >> 2158506 |
P Limone1, M Maccario, R Vigliani, G Isaia, F Massara, G M Molinatti.
Abstract
Primary pigmented micronodular disease is a peculiar form of ACTH-independent Cushing's syndrome characterized by the familial occurrence, the frequent association with malformations and the pathological adrenocortical picture consisting in micronodules with cellular deposition of lipofuscinic pigment. We describe here a case occurring in a 14-year-old girl.Entities:
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Year: 1990 PMID: 2158506 DOI: 10.1007/BF03349532
Source DB: PubMed Journal: J Endocrinol Invest ISSN: 0391-4097 Impact factor: 4.256