Department of Dermatology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Department of Rheumatology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
J Dermatol. 2022 Dec;49(12):1278-1283. doi: 10.1111/1346-8138.16572. Epub 2022 Sep 12.
Little is known about pregnancy in women with morphea. We aimed to describe the clinical presentation, pregnancy outcomes, and medical management of morphea during pregnancy. We conducted a case series of female patients of reproductive age (18-49 years) who were part of the longitudinal MAC (Morphea in Adults and Children) cohort seen in the outpatient dermatology clinic at the University of Texas Southwestern from July 2007 to February 2022. Women who were pregnant during research visits and had at least 6 months of follow-up in the MAC cohort were included. Data collected included demographics, morphea characteristics, pregnancy outcomes, and medication history. Median clinical disease activity and damage scores using the Localized Scleroderma Cutaneous Assessment Tool were recorded. Ten patients were pregnant during the study period. Five patients had pediatric-onset morphea and five had adult-onset morphea. Eight patients had linear and two had plaque morphea. Six patients had at least one morphea lesion on their abdomen. Median age at first pregnancy was 31 years (interquartile range [IQR], 26.0-35.8 years) and median duration of morphea was 13.5 years (IQR, 4.8-19.0 years). In seven patients, damage scores were stable with no increased morphea activity. Three patients (30%) experienced reactivation of morphea activity during pregnancy with a median Localized Scleroderma Activity Index of 4 (IQR, 2.5-10). Only one patient required immunosuppressive therapy during pregnancy for her morphea diagnosis. Seven of 10 patients had cesarean deliveries and one adverse fetal outcome was reported. In this small series, most patients maintained stability of their morphea and there were no adverse pregnancy outcomes directly related to morphea.
关于硬斑病患者的妊娠情况知之甚少。我们旨在描述妊娠期间硬斑病的临床表现、妊娠结局和医学管理。我们对 2007 年 7 月至 2022 年 2 月期间在德克萨斯大学西南分校皮肤科门诊接受治疗的成年和儿童硬斑病(MAC)纵向队列中的育龄期(18-49 岁)女性患者进行了病例系列研究。纳入在研究期间妊娠且在 MAC 队列中至少有 6 个月随访的女性。收集的数据包括人口统计学、硬斑病特征、妊娠结局和用药史。记录使用局限性硬皮病皮肤评估工具(Localized Scleroderma Cutaneous Assessment Tool)记录的中位数临床疾病活动度和损害评分。研究期间有 10 名患者妊娠。5 名患者为儿童期起病的硬斑病,5 名患者为成人期起病的硬斑病。8 名患者为线状硬斑病,2 名患者为斑块状硬斑病。6 名患者腹部至少有 1 处硬斑病皮损。首次妊娠的中位年龄为 31 岁(四分位距 [IQR],26.0-35.8 岁),硬斑病的中位病程为 13.5 年(IQR,4.8-19.0 年)。7 名患者的损害评分稳定,无硬斑病活动度增加。3 名患者(30%)在妊娠期间硬斑病活动度再次出现,局限性硬皮病活动指数中位数为 4(IQR,2.5-10)。仅 1 名患者因硬斑病诊断在妊娠期间需要免疫抑制治疗。10 名患者中有 7 名行剖宫产分娩,报告了 1 例不良胎儿结局。在这项小系列研究中,大多数患者的硬斑病病情稳定,没有与硬斑病直接相关的不良妊娠结局。