Atopic dermatitis in skin of colour. Part 2: considerations in clinical presentation and treatment options

被引:3
|
作者
Gan, Christian [1 ,2 ]
Mahil, Satveer [3 ,4 ]
Pink, Andrew [3 ,4 ]
Rodrigues, Michelle [1 ,5 ,6 ]
机构
[1] Royal Childrens Hosp, Dept Dermatol, Melbourne, Vic, Australia
[2] St Vincents Hosp, Dept Dermatol, Melbourne, Vic, Australia
[3] Guys & St Thomas NHS Fdn Trust, St Johns Inst Dermatol, London, England
[4] Kings Coll London, London, England
[5] Univ Melbourne, Dept Paediat, Parkville, Vic, Australia
[6] Chroma Dermatol, Pigment & Skin Colour Ctr, Wheelers Hill, Vic, Australia
关键词
AFRICAN-AMERICAN; TACROLIMUS OINTMENT; LICHEN-PLANUS; UNMET NEEDS; PHOTOTHERAPY; CHILDREN; DERMATOLOGY; MANAGEMENT; DUPILUMAB; SECONDARY;
D O I
10.1093/ced/llad162
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Atopic dermatitis (AD) in people with skin of colour can appear psoriasiform, lichenoid, scaly or papular, with a violaceous colour and there is a higher prevalence of post-inflammatory dyspigmentation compared with affected individuals of White ethnicities, which can limit the use of current severity assessment tools. Greater participation from patients of different ethnicities in clinical trials is needed; with adequate representation, future studies may be able to better characterize potential differences in AD between different ethnic groups, as well as differences in treatment response. Recent advances in atopic dermatitis (AD) present the condition as a heterogeneous disease of distinct endotypes across ethnic groups. AD in people with skin of colour may appear psoriasiform, lichenoid, scaly or papular, with a violaceous colour and there is a higher prevalence of post-inflammatory dyspigmentation compared with affected individuals of White ethnicity. These differences in clinical presentation may limit the use of AD assessment tools in people with skin of colour, leading to the potential for misdiagnosis and underestimation of severity, particularly in relation to assessment of erythema. Recent targeted therapies for AD have been studied in multiple ethnic groups; however, ethnicity-based subgroup analysis is often not performed. Further research is required to understand whether treatment responses or safety may differ among ethnic groups.
引用
收藏
页码:1091 / 1101
页数:11
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