Department of Dermatology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Department of Dermatology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland,
Dermatology. 2021;237(6):878-883. doi: 10.1159/000514026. Epub 2021 Feb 16.
Prurigo pigmentosa (PP) is an inflammatory dermatosis typically reported in young Asian women and characterized by recurrent papulovesicular lesions resolving with a postinflammatory reticulated hyperpigmentation.
We have included all consecutive patients with PP diagnosed in our tertiary center between 2013 and 2020. The clinical information was retrospectively collected from medical records.
We identified 14 patients with PP. The median age at the time of diagnosis was 29.5 years (range 17-43 years), while the female-to-male ratio was 13:1. Diagnostic delay varied from 10 days to 10 years (mean of 25 months). Light microscopy studies consistently showed presence of a lymphohistiocytic infiltrate in combination in 40% of cases with neutrophils. Interface changes were found in 60% of cases. In 6 (43%) of 14 cases, there was a chronological relationship between the starting of a new diet and the development of the first flares. Treatment with doxycycline in 9 patients resulted in a complete regression of the lesions.
This was a retrospective study in a tertiary referral hospital.
Our observations indicate that PP is not so rare in Europe as previously thought and is often diagnosed after a long delay. Demographics, clinical characteristics and triggering factors in Caucasian patients are similar to those described in the Asian population. Diagnosis is based on the peculiar recurrent course and distinctive clinicopathological features. Tetracyclines represent the first-line therapy in PP.
色素性痒疹(PP)是一种炎症性皮肤病,通常见于年轻的亚洲女性,其特征为反复出现的丘疹水疱性皮损,消退后遗留炎症后网状色素沉着。
我们纳入了 2013 年至 2020 年期间在我们的三级中心诊断为 PP 的所有连续患者。临床信息从病历中回顾性收集。
我们共确定了 14 例 PP 患者。诊断时的中位年龄为 29.5 岁(范围 17-43 岁),女性与男性的比例为 13:1。诊断延迟时间从 10 天到 10 年不等(平均 25 个月)。光镜研究一致显示,40%的病例存在淋巴组织细胞浸润,伴有中性粒细胞浸润。60%的病例存在界面改变。在 14 例中有 6 例(43%),新饮食开始与首次发作之间存在时间上的关联。9 例患者接受多西环素治疗后皮损完全消退。
这是一项在三级转诊医院进行的回顾性研究。
我们的观察表明,PP 在欧洲并不像以前认为的那样罕见,而且常常在很长一段时间后才被诊断出来。白种人患者的人口统计学、临床特征和触发因素与亚洲人群描述的相似。诊断基于独特的复发性病程和独特的临床病理特征。四环素类药物是 PP 的一线治疗药物。