Primary Localized Cutaneous Amyloidosis: A Retrospective Study of an Uncommon Skin Disease in the Largest Tertiary Care Center in Switzerland.

Dermatology (Basel, Switzerland) Pub Date : 2022-01-01 Epub Date: 2021-09-15 DOI:10.1159/000518948
Carole Guillet, Simona Steinmann, Julia-Tatjana Maul, Isabel Kolm
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引用次数: 7

Abstract

Background: Primary localized cutaneous amyloidosis (PLCA) is defined by the deposition of amyloid protein in the skin without systemic involvement. There are four subtypes of PLCA: lichen amyloidosis (LA), macular amyloidosis (MA), biphasic amyloidosis (BA), and nodular amyloidosis (NA). PLCA occurs most frequently in Latin Americans and Asians. Treatment is not standardized.

Objectives: To identify subtypes, demographic and clinical features and treatment efficacy in patients with histopathologically confirmed PLCA.

Materials and methods: Data of PLCA patients were extracted from the electronic hospital database and included if diagnosis of PLCA was histopathologically confirmed and if sufficient information regarding treatment and follow-up was available. The evaluation of the treatment efficacy was based on a novel score to assess the reduction of itch and skin lesions.

Results: In this retrospective, monocentric study, 37 cases of PLCA diagnosed between 2000 and 2020 were included (21 females) with a mean age of 52 years. LA was the most frequent subtype found in 21 patients (56.8%), followed by MA in 10 patients (28%) and BA in 6 patients (16.2%). No cases of NA were included. 22 patients (59.4%) had skin phototype II or III. Regarding treatment, a combination of UVA1 phototherapy with high-potency topical corticosteroids seemed to show the highest efficacy with complete clearance of symptoms in 4 patients (10.8%). A substantial improvement of symptoms was found in 5 patients (12.7%) treated with high-potency topical corticosteroids alone or in combination either with UVA1 or bath PUVA or monotherapy with UVA1 phototherapy or capsaicin (0.075%) cream. Low-/medium-potency topical corticosteroids alone or in combination with UVBnb (311 nm) phototherapy showed a lower efficacy.

Conclusion: Our data show that PCLA is a rare disease in central Europe but can also be expected in a predominantly Caucasian population. The best treatment response was achieved with a combination of UVA1 phototherapy and high-potency topical corticosteroids.

Abstract Image

原发性局部皮肤淀粉样变性:瑞士最大的三级保健中心一种罕见皮肤病的回顾性研究。
背景:原发性局限性皮肤淀粉样变性(PLCA)是指淀粉样蛋白在皮肤中沉积而无全身累及。PLCA有四种亚型:地衣淀粉样变性(LA)、黄斑淀粉样变性(MA)、双期淀粉样变性(BA)和结节淀粉样变性(NA)。PLCA最常见于拉丁美洲和亚洲。治疗不规范。目的:探讨经组织病理学证实的PLCA患者的亚型、人口学特征、临床特征及治疗效果。材料和方法:从医院电子数据库中提取PLCA患者的数据,如果PLCA的诊断经组织病理学证实,并且有足够的治疗和随访信息,则纳入数据。治疗效果的评估是基于一种新的评分来评估瘙痒和皮肤病变的减少。结果:在这项回顾性的单中心研究中,纳入了2000年至2020年间诊断的37例PLCA(21例女性),平均年龄为52岁。LA是最常见的亚型,21例(56.8%),其次是MA(10例)(28%)和BA(6例)(16.2%)。未包括NA病例。22例(59.4%)为皮肤光型II或III型。在治疗方面,UVA1光疗联合高效外用皮质类固醇似乎显示出最高的疗效,4例患者(10.8%)的症状完全消除。5例患者(12.7%)单独使用高效外用皮质类固醇或联合UVA1或沐浴PUVA或单独使用UVA1光疗或辣椒素(0.075%)乳膏治疗,症状明显改善。低/中效外用皮质类固醇单独或联合UVBnb (311 nm)光疗显示出较低的疗效。结论:我们的数据显示PCLA在中欧是一种罕见的疾病,但也可能在主要的高加索人群中出现。最佳的治疗反应是UVA1光疗和高效外用皮质类固醇的结合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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