Pascualini María Florencia, Caballero Escuti Guadalupe, Valente Enrique, Kurpis María, Ruiz Lascano Alejandro
Servicio de Dermatología, Hospital Privado Centro Médico de Córdoba, Argentina.
Medicina (B Aires). 2013;73(3):252-4.
The scleromyxedema is a rare condition characterized by hyperproliferation of fibroblasts with increased dermal deposition of mucin and frequently associated with monoclonal gammopathy of undetermined significance. Various treatments have been reported, with inconsistent results. In addition, the rarity of the disease and the lack of randomized controlled trials results in treatment options derived from anecdotal reports. We describe the case of a 52 year-old female patient diagnosed with scleromyxedema who developed a monoclonal gammopathy, with adequate response to thalidomide. The follow up of these patients is important due to the risk of progression to multiple myeloma and complications related to systemic treatments.
硬化性黏液水肿是一种罕见病症,其特征为成纤维细胞过度增殖,伴有黏蛋白在真皮层的沉积增加,且常与意义未明的单克隆丙种球蛋白病相关。已有多种治疗方法的报道,但结果不一。此外,该疾病的罕见性以及缺乏随机对照试验,导致治疗方案多源于个案报道。我们描述了一例52岁女性硬化性黏液水肿患者的病例,该患者出现了单克隆丙种球蛋白病,对沙利度胺治疗反应良好。由于存在进展为多发性骨髓瘤的风险以及与全身治疗相关的并发症,对这些患者进行随访很重要。