Cheng Hui Mei, Chuah Sai Yee, Gan Emily Yiping, Jhingan Anjali, Thng Steven Tien Guan
Department of Dermatology, National Skin Centre, Singapore City, Singapore.
Department of Material Science and Engineering, Nanyang Technological University, Singapore City, Singapore.
Australas J Dermatol. 2018 Nov;59(4):322-327. doi: 10.1111/ajd.12813. Epub 2018 Apr 10.
BACKGROUND/OBJECTIVES: Controversy persists as to whether lichen planus pigmentosus and ashy dermatosis are separate clinical entities. This study was conducted to examine the clinicopathological features and treatment outcome of the two conditions.
A retrospective medical chart review of all patients who were diagnosed with lichen planus pigmentosus or ashy dermatosis was conducted. The information collected included the participants' age at onset, site of onset, duration of disease, presence of precipitating factors, distribution of disease, pigmentation and presence of symptoms. In patients from whom a biopsy was taken the histopathological reports were included.
Altogether 26 patients with ashy dermatosis and 29 with lichen planus pigmentosus were included in the study. Compared with ashy dermatosis, lichen planus pigmentosus had a more localised distribution with a preponderance for facial involvement, compared with the truncal preponderance in ashy dermatosis. Ashy dermatosis tended to have a more stable clinical course than lichen planus pigmentosus, which was more likely to wax and wane. The utility of histopathology in differentiating between the two conditions is low.
Ashy dermatosis and lichen planus pigmentosus, as defined in this study, appear to be two separate clinical entities with distinguishable clinical features and natural histories.
背景/目的:扁平苔藓样色素沉着症和色素性紫癜性皮病是否为独立的临床实体仍存在争议。本研究旨在探讨这两种疾病的临床病理特征及治疗效果。
对所有诊断为扁平苔藓样色素沉着症或色素性紫癜性皮病的患者进行回顾性病历审查。收集的信息包括参与者的发病年龄、发病部位、病程、诱发因素、疾病分布、色素沉着及症状表现。对进行活检的患者纳入其组织病理学报告。
本研究共纳入26例色素性紫癜性皮病患者和29例扁平苔藓样色素沉着症患者。与色素性紫癜性皮病相比,扁平苔藓样色素沉着症分布更局限,以面部受累为主,而色素性紫癜性皮病以躯干受累为主。色素性紫癜性皮病的临床病程往往比扁平苔藓样色素沉着症更稳定,后者更容易反复。组织病理学在区分这两种疾病方面的作用不大。
本研究中定义的色素性紫癜性皮病和扁平苔藓样色素沉着症似乎是两种具有可区分临床特征和自然病史的独立临床实体。