Laboratory of Molecular and Functional Genetics, Faculty of Sciences of Sfax, Sfax University, Sfax, Tunisia.
Department of Dermatology, CHU Hedi Chaker, Sfax, Sfax University, Sfax, Tunisia.
Dermatol Ther. 2022 Aug;35(8):e15593. doi: 10.1111/dth.15593. Epub 2022 May 30.
Pustular psoriasis of pregnancy (PPP) can lead to life-threatening complications. The objective of this study is to report clinical and genetic spectrum, prognostic factors and management options. A retrospective study was designed including eight PPP patients. Clinical data were collected, and performed genetic and statistical analysis to identify factors associated with fetal complications, resistance to treatment and post-partum flare extension. A systematic review of the literature was also carried out. Eight Tunisian patients, with a mean age of 23 ± 3.3 years, were included. They presented 14 flares (F) during pregnancies and one flare after delivery. Additional GPP flares outside pregnancy periods were noted in 2/8 of patients. The mean duration of PPP flares was 16.66 ± 7.8 weeks. The first flare occurred at a gestational age of 26 ± 5 weeks. Only 2/8 studied patients presented a homozygous mutation c.80 T > C (p.L27P) in IL36RN gene. Used treatments were topical steroids (n = 12F), systemic steroids (n = 5F), ciclosporin (n = 1F), UVB (n = 1F) and acitretin (in post-partum n = 6F). Complications were oligoamnios (n = 2), intra-uterine growth retardation (n = 1), fetal death in utero (n = 1), prematurity (n = 3), low weight at birth (n = 2). A significant association was found between (i) occurrence of fetal complications and early gestational age at the onset (p = 0.036), (ii) resistance to topical steroids and body surface affected area (p = 0.008), (iii) presence of mutation c.80 T > C in PPP flares and low serum levels of calcium (p = 0.01). Our systematic review of the literature identified 39 patients with 41 flares of PPP. Only 7/39 patients presented a causative mutation in IL36RN and CARD14 genes. PPP is characterized by a phenotypic heterogeneity and can be associated to IL36RN mutations. Its early onset can be associated with fetal complications. Systemic steroids and cyclosporine remain the most used therapies.
妊娠性脓疱型银屑病(PPP)可导致危及生命的并发症。本研究旨在报告临床和遗传谱、预后因素和治疗选择。设计了一项回顾性研究,纳入了 8 例 PPP 患者。收集了临床数据,并进行了遗传和统计学分析,以确定与胎儿并发症、治疗耐药性和产后发作扩展相关的因素。还进行了系统的文献回顾。纳入了 8 名突尼斯患者,平均年龄为 23±3.3 岁。他们在怀孕期间出现了 14 次发作(F),分娩后出现了 1 次发作。2/8 例患者在妊娠期间外还出现了其他点滴状银屑病发作。PPP 发作的平均持续时间为 16.66±7.8 周。首次发作发生在妊娠 26±5 周。仅 2/8 例研究患者在 IL36RN 基因中存在 c.80T>C(p.L27P)纯合突变。所用治疗方法包括局部类固醇(n=12F)、全身类固醇(n=5F)、环孢素(n=1F)、UVB(n=1F)和阿维 A(n=6F)。并发症包括羊水过少(n=2)、宫内生长迟缓(n=1)、胎儿宫内死亡(n=1)、早产(n=3)、出生体重低(n=2)。在发病时的早期妊娠(p=0.036)、(ii)局部类固醇耐药与受影响的体表面积(p=0.008)、(iii)PPP 发作时存在 c.80T>C 突变与低血清钙水平(p=0.01)之间存在显著相关性。我们对文献的系统回顾确定了 39 名患者的 41 次 PPP 发作。只有 7/39 例患者在 IL36RN 和 CARD14 基因中存在致病突变。PPP 的特点是表型异质性,可与 IL36RN 突变相关。其早期发病可与胎儿并发症相关。全身类固醇和环孢素仍然是最常用的治疗方法。