Suppr超能文献

妊娠性脓疱型银屑病:8 例患者的临床和遗传学特征及文献复习。

Pustular psoriasis of pregnancy: Clinical and genetic characteristics in a series of eight patients and review of the literature.

机构信息

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.

出版信息

Dermatol Ther. 2022 Aug;35(8):e15593. doi: 10.1111/dth.15593. Epub 2022 May 30.

Abstract

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.

摘要

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。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验