Mahajan Vikram K, Sharma Neeraj, Sharma Vikas, Verma Rohit, Chandel Monika, Singh Ravinder
Department of Dermatology, Venereology and Leprosy, Dr. Radhakrishnan Government Medical College, Hamirpur, Himachal Pradesh, India.
Indian Dermatol Online J. 2024 Oct 28;15(6):920-929. doi: 10.4103/idoj.idoj_111_24. eCollection 2024 Nov-Dec.
Topical sunscreens decrease the quantity of ultraviolet (UV) light from the sun reaching the skin by either blocking or scattering it and help protect the skin from dyspigmentation, photoaging, DNA damage, and photocarcinogenesis, especially in photosensitive individuals. The significant role played by visible light and infrared light in skin pigmentation and photoaging has been recognized in recent years. The majority of broad-spectrum sunscreens protect against UV-B (290-320nm) and UV-A (320-400nm) radiation. Allergic reactions to sunscreens were relatively uncommon compared to their widespread use in the last more than four decades. With growing awareness of problems associated with excessive sunlight exposure, their use has increased exponentially, especially that of cosmetics and other personal grooming products containing UV filters. In recent years, sunscreen agents have been commonly identified as causing allergic contact dermatitis and photodermatitis. Thus, allergic contact dermatitis, photo-irritation, photo-allergenicity, and photo-toxicity (acute/subacute effects) are of immediate concern in the assessment of topical sunscreens for their optimal use. Sunscreen chemicals such as p-aminobenzoic acid (PABA) and PABA esters, the cinnamates, benzophenones, oxybenzone, and dibenzoylmethane that absorb UV radiation are common contact sensitizers capable of producing both allergic contact dermatitis and photodermatitis. The excipients in sunscreen formulations by themselves may also cause allergic reactions. Herein, we review potential allergens, clinical evaluation, and management aspects of topical sunscreen contact sensitivity for their optimal use in clinical practice.
外用防晒霜通过阻挡或散射阳光中的紫外线(UV),减少到达皮肤的紫外线量,有助于保护皮肤免受色素沉着、光老化、DNA损伤和光致癌作用,尤其是对光敏感个体。近年来,可见光和红外光在皮肤色素沉着和光老化中的重要作用已得到认可。大多数广谱防晒霜可抵御UV-B(290-320nm)和UV-A(320-400nm)辐射。与过去四十多年来广泛使用相比,对防晒霜的过敏反应相对较少见。随着人们对过度阳光照射相关问题的认识不断提高,其使用量呈指数级增长,尤其是含有紫外线过滤剂的化妆品和其他个人护理产品。近年来,防晒剂通常被认为会引起过敏性接触性皮炎和光皮炎。因此,在评估外用防晒霜的最佳使用时,过敏性接触性皮炎、光刺激、光致敏性和光毒性(急性/亚急性效应)是直接关注的问题。吸收紫外线的防晒化学品,如对氨基苯甲酸(PABA)及其酯类、肉桂酸盐、二苯甲酮、氧苯酮和二苯甲酰甲烷,是常见的接触致敏原,能够引起过敏性接触性皮炎和光皮炎。防晒霜配方中的辅料本身也可能引起过敏反应。在此,我们综述外用防晒霜接触敏感性的潜在过敏原、临床评估和管理方面,以便在临床实践中实现其最佳使用。