Erden Fatma, Borlu Murat, Simsek Yasin, Kelestemur Hasan Fahrettin
Department of Dermatology and Venereology, Ankara Occupational Diseases Hospital, Ankara, Turkey.
Department of Dermatology and Venereology, Faculty of Medicine, Erciyes University, Kayseri, Turkey.
Postepy Dermatol Alergol. 2019 Jun;36(3):272-275. doi: 10.5114/ada.2018.74639. Epub 2018 Mar 21.
Cushing's syndrome is a rare condition characterized by increased glucocorticoid levels. Dermatologically, it causes a variety of skin conditions such as atrophy, striae, acne, plethora, hypertrichosis, hirsutism, acanthosis nigricans, hyperpigmentation, alopecia, purpura and fragile skin. Although skin lesions of Cushing's syndrome have been described, exogenous and endogenous types have not been studied in detail.
To determine differences in possible skin lesions depending on the cause of Cushing's syndrome.
A total of 35 patients - 16 iatrogenic Cushing's syndrome patients and 19 endogenous Cushing's syndrome patients - who were diagnosed in Erciyes University and 15 healthy individuals were included in this study.
There was at least one skin finding in 34 (97.1%) of the patients with Cushing's syndrome and 9 (60%) in the control group ( = 0.001). Comparison regarding skin findings in patient and control groups revealed that hypertrichosis, hyperpigmentation, and fungal infections were significantly more frequent in the patient group than the control group. Hirsutism was found more frequently in the endogenous group whereas stria, hypertrichosis and fungal infections were more frequent in the exogenous group.
Since Cushing's syndrome is a rare disease and it is often diagnosed later in life, data on the frequency of skin findings are limited and sparse in the literature. In the comparison of endogenous Cushing's and exogenous Cushing's groups, acne, hypertrichosis, and fungal infections were found more frequently in the exogenous Cushing's group and hirsutism more frequently in the endogenous Cushing's group.
库欣综合征是一种罕见疾病,其特征为糖皮质激素水平升高。在皮肤科方面,它会引发多种皮肤问题,如萎缩、萎缩纹、痤疮、多血质、多毛症、毛发过多、黑棘皮病、色素沉着、脱发、紫癜以及皮肤脆弱。尽管已有关于库欣综合征皮肤病变的描述,但外源性和内源性类型尚未得到详细研究。
确定取决于库欣综合征病因的可能皮肤病变差异。
本研究纳入了在埃尔西耶斯大学确诊的35例患者——16例医源性库欣综合征患者和19例内源性库欣综合征患者——以及15名健康个体。
库欣综合征患者中有34例(97.1%)至少有一项皮肤表现,而对照组中有9例(60%)(P = 0.001)。患者组和对照组皮肤表现的比较显示,患者组的多毛症、色素沉着和真菌感染明显比对照组更常见。内源性组中毛发过多更常见,而外源性组中萎缩纹、多毛症和真菌感染更常见。
由于库欣综合征是一种罕见疾病,且通常在生命后期才被诊断出来,文献中关于皮肤表现频率的数据有限且稀少。在内源性库欣综合征组和外源性库欣综合征组的比较中,外源性库欣综合征组中痤疮、多毛症和真菌感染更常见,而内源性库欣综合征组中毛发过多更常见。