Myers Hannah, Ceci Francesca M, Rupley Katherine, Roberts Michael
Department of Dermatology, Medical College of Georgia, Augusta, GA, USA.
Department of Dermatology, Philadelphia College of Osteopathic Medicine, Atlanta, GA, USA.
Am J Case Rep. 2024 May 3;25:e942853. doi: 10.12659/AJCR.942853.
BACKGROUND Pigmented purpuric dermatosis (PPD) is a rare disease that is poorly understood but thought to result from inflammation of the capillaries causing extravasation of erythrocytes into the soft tissue. There are a variety of potential causes, including medications, such as acetaminophen and aspirin, abnormal humoral immunity, and excessive exercise. Although benign, PPD can be bothersome to patients due to associated pruritus, weeping, and poor cosmetic results. Treatment of this lesion is difficult, with no standardized regimen and a tendency for relapse once treatment is discontinued. CASE REPORT This case reports on a 77-year-old man who presented to an outpatient dermatology clinic with bilateral lower extremity edema with associated weeping and erythema for 1 year. A biopsy was conducted and resulted as PPD. He began treatment with excimer laser therapy after conservative and topical treatment options failed, with resolution of symptoms without recurrence for approximately 1 year. CONCLUSIONS PPD is notoriously difficult to treat, and historic treatment options include topical corticosteroids, oral supplements, and immunomodulators, all of which come with a range of adverse effects. However, new literature supports the use of phototherapy to treat PPD, with varying results. Previously implemented options include but are not limited to phototherapy with psoralen plus ultraviolet A, narrow band ultraviolet B, advanced fluorescence technology pulsed light, and fractional non-ablative 1540-nm erbium: glass laser, each with varying degrees of success. This case discusses the successful treatment of recalcitrant PPD with excimer laser therapy and maintenance of remission for approximately 1 year.
色素性紫癜性皮病(PPD)是一种罕见疾病,人们对其了解甚少,但认为是由毛细血管炎症导致红细胞外渗至软组织引起的。其潜在病因多种多样,包括药物,如对乙酰氨基酚和阿司匹林、体液免疫异常以及过度运动。尽管PPD是良性疾病,但由于伴有瘙痒、渗液以及不佳的外观效果,会给患者带来困扰。该病变的治疗困难,没有标准化方案,且一旦停止治疗有复发倾向。
本病例报告了一名77岁男性,因双侧下肢水肿伴渗液和红斑1年就诊于皮肤科门诊。进行活检后诊断为PPD。在保守治疗和局部治疗方案失败后,他开始接受准分子激光治疗,症状得以缓解,且约1年未复发。
PPD notoriously难以治疗,既往的治疗选择包括外用糖皮质激素、口服补充剂和免疫调节剂,所有这些都伴有一系列不良反应。然而,新的文献支持使用光疗来治疗PPD,但效果各异。先前实施的选择包括但不限于补骨脂素加紫外线A光疗、窄谱中波紫外线、先进荧光技术脉冲光以及非剥脱性1540纳米铒玻璃激光,每种方法的成功率各不相同。本病例讨论了准分子激光治疗顽固性PPD的成功经验以及约1年的缓解维持情况。