Ferraù Francesco, Alessi Ylenia, Nista Federica, Roux Anna, Ferone Diego, Arvat Emanuela
Department of Human Pathology of Adulthood and Childhood "G. Barresi", University of Messina, Messina, Italy.
Endocrinology Unit, "G. Martino" University Hospital, University of Messina, Messina, Italy.
J Endocrinol Invest. 2025 Apr;48(Suppl 1):83-89. doi: 10.1007/s40618-025-02537-0. Epub 2025 Feb 21.
Endogenous Cushing's syndrome (CS) is rare, with an incidence of 0.7-2.4 per million population per year according to population-based studies. However, evaluation of patients presenting disorders potentially related to cortisol excess, and therefore with a 'high risk of clinical suspicion' profile, could bring out several unrecognized cases. CS represents one of the most challenging endocrine diseases, with clinical features overlapping with those of common conditions affecting general population, invariably resulting in potential mis- or delayed diagnosis with negative consequences in terms of morbidity and mortality. CS is remarkably prevalent among young females, variably presenting with menstrual irregularities and/or signs and symptoms of hyperandrogenism. Herein we briefly reviewed literature on prevalence and clinical impact of menses abnormalities, acne and hirsutism -also coexisting in the context of a polycystic ovary syndrome- in CS, aiming at clarifying if, when and how to screen for hypercortisolism young women with these disorders.
根据基于人群的研究,内源性库欣综合征(CS)较为罕见,每年每百万人口中的发病率为0.7 - 2.4例。然而,对表现出可能与皮质醇过多相关疾病的患者进行评估,即具有“临床怀疑高风险”特征的患者评估,可能会发现一些未被识别的病例。CS是最具挑战性的内分泌疾病之一,其临床特征与影响普通人群的常见疾病重叠,总是导致潜在的误诊或诊断延迟,对发病率和死亡率产生负面影响。CS在年轻女性中尤为普遍,常表现为月经不规律和/或高雄激素血症的体征和症状。在此,我们简要回顾了关于CS中月经异常、痤疮和多毛症(也并存于多囊卵巢综合征的背景下)的患病率和临床影响的文献,旨在阐明对于患有这些疾病的年轻女性,是否、何时以及如何筛查皮质醇增多症。