Kendereski A, Micić D, Sumarac M, Zorić S, Macut D, Colić M, Skaro-Milić A, Bogdanović Z
Institute of Endocrinology, Clinical Centre of Serbia, Military Medicine Academy, Belgrade, Yugoslavia.
J Endocrinol Invest. 1999 May;22(5):395-400. doi: 10.1007/BF03343579.
A case of chronic primary adrenal insufficiency without hyperpigmentation in a 64-year-old woman is reported. Due to the absence of hyperpigmentation the diagnosis was delayed and she became critically ill. During endocrine evaluation, in order to investigate the mechanism responsible for the absence of hyperpigmentation, skin biopsy was done and hormones responsible for the skin pigmentation were measured. Absence of hyperpigmentation is explained by high degree of melanosome degradation in secondary lysosomes called "compound melanosomes", which overwhelmed increased stimulation of the skin pigmentation. Melanocyte-stimulating hormones were elevated with a strikingly high beta-LPH/ACTH ratio. To our knowledge, this is the first study of pathogenic mechanisms responsible for the absence of hyperpigmentation in white Addison's disease.
报告了一例64岁女性慢性原发性肾上腺皮质功能减退且无色素沉着的病例。由于无色素沉着,诊断被延误,患者病情危重。在内分泌评估过程中,为研究无色素沉着的机制,进行了皮肤活检并检测了与皮肤色素沉着相关的激素。无色素沉着是由于在称为“复合黑素小体”的次级溶酶体中黑素小体高度降解,这超过了对皮肤色素沉着增加的刺激。促黑素细胞激素升高,β-促脂解素/促肾上腺皮质激素比值显著升高。据我们所知,这是首次对白种人艾迪生病中无色素沉着的致病机制进行研究。