Campione Elena, Botta Annalisa, Di Prete Monia, Rastelli Emanuele, Gibellini Manuela, Petrucci Antonio, Bernardini Sergio, Novelli Giuseppe, Bianchi Luca, Orlandi Augusto, Massa Roberto, Terracciano Chiara
Department of Systems Medicine, Division of Dermatology, University of Rome Tor Vergata, Viale Oxford 81, 00133 Rome, Italy.
Department of Biomedicine and Prevention, Division of Medical Genetics, University of Rome Tor Vergata, Viale Oxford 81, 00133 Rome, Italy.
Neuromuscul Disord. 2017 Feb;27(2):163-169. doi: 10.1016/j.nmd.2016.11.004. Epub 2016 Nov 16.
Skin changes have been described in myotonic dystrophy type 1 (DM1). However, whether and in which way skin is a target of specific disease alterations in DM1 and DM2 has not been yet clarified. This study aims to explore cutaneous features of DM1 and DM2 patients. Skin examination was performed in 60 DM1, 15 DM2, and 103 control, unselected patients by means of dermoscopy. It revealed quantitative and qualitative abnormalities of nevi and typical signs of premature aging in both DM1 and DM2 patients, with a significantly higher frequency of dysplastic nevi, alopecia, xerosis and seborrheic dermatitis. Twenty-eight nevi were excised in DM patients and none showed histological features of melanoma, although 12 of them were diagnosed as dysplastic and the remaining 16 presented histological irregularity in melanin distribution. In DM1 patients, the number of nevi correlated with CTG expansion size, whereas the presence of dysplastic nevi and xerosis inversely correlated with vitamin D levels. DM1 and DM2 patients display a high frequency of skin abnormalities, the most common of which correlate with genotype severity and serum vitamin D levels. Skin examination is highly informative in these patients and reveals features suggestive of premature aging and impaired vitamin D homeostasis.
1型强直性肌营养不良(DM1)患者存在皮肤改变。然而,皮肤是否以及以何种方式成为DM1和DM2中特定疾病改变的靶点尚未明确。本研究旨在探索DM1和DM2患者的皮肤特征。通过皮肤镜对60例DM1患者、15例DM2患者和103例未经过挑选的对照患者进行了皮肤检查。结果显示,DM1和DM2患者均存在痣的数量和质量异常以及早衰的典型体征,发育异常痣、脱发、皮肤干燥和脂溢性皮炎的发生率显著更高。对DM患者的28颗痣进行了切除,尽管其中12颗被诊断为发育异常,其余16颗在黑色素分布上存在组织学不规则,但均未显示黑色素瘤的组织学特征。在DM1患者中,痣的数量与CTG重复序列扩增大小相关,而发育异常痣和皮肤干燥的存在与维生素D水平呈负相关。DM1和DM2患者皮肤异常的发生率较高,其中最常见的与基因型严重程度和血清维生素D水平相关。皮肤检查对这些患者具有很高的诊断价值,并揭示了提示早衰和维生素D内稳态受损的特征。