营养不良大疱性表皮松解症患者的妇产科随访,一项前瞻性研究。

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
M Fournier, E Bourrat, J Rapp, D Vexiau, C Trastour, C Chiaverini
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引用次数: 0

摘要

背景:萎缩性表皮松解症(DEB)是一种罕见的遗传性皮肤脆性疾病,会导致皮肤和粘膜出现水疱和糜烂,并演变为萎缩性和牵拉性疤痕。本研究旨在描述患有 DEB 的妇女的生殖器受累情况及其妇产科生活:在这项由两个中心组成的前瞻性研究中,皮肤科和/或妇科调查人员通过问卷收集了 18 岁以上 DEB 女性患者的数据。这些数据来自患者的医疗记录,包括月经周期、避孕方法、产科病史、妇科癌症和性传播疾病筛查以及性生活。外阴检查是常规随访的一部分。研究共招募了 27 名妇女(中位年龄为 35 岁;年龄范围为 19 至 72 岁),并将她们在 2021 年 1 月至 12 月期间的数据纳入研究。据报告,27 名妇女中有 14 名(52%)定期接受了妇科随访;16/27(59%)名妇女提到月经来潮;13/24(51%)名妇女至少接受过一次避孕治疗;17/27(63%)名妇女声称至少有过一次性交,大多数情况下都有困难;10/27(37%)名妇女足月妊娠,每名妇女生育 1 至 4 个孩子(即 21 次分娩:8 次剖腹产和 13 次阴道分娩)。在随访期间进行过外阴检查的 21 名妇女中,有 11 人在检查时出现了病变。根据法国的建议,性传播疾病(STD)、宫颈癌和乳腺癌的筛查率分别为18%(均为25岁以上)、70%和100%:与所有患者一样,患有 DEB 的妇女在一生中都需要妇科随访。此外,我们还强烈建议进行性学咨询,以帮助患者了解 DEB 的性心理方面问题,并告知患者具体的预防措施,以避免性行为、避孕和性传播疾病筛查过程中出现病变。即使患有严重疾病的妇女也有可能怀孕和分娩,而且通常不会出现重大并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gynaeco-obstetrical follow-up of patients with dystrophic epidermolysis bullosa, a prospective study.

Background: Dystrophic epidermolysis bullosa (DEB) is a rare group of genetic skin-fragility conditions resulting in blisters and erosions of the skin and mucosa, evolving into dystrophic and retractile scars. This study objective is to describe the genital involvement in women with DEB and their gynaeco-obstetrical life.

Results: In this prospective two-centre study, data from women with DEB who were older than 18 years was gathered into a questionnaire by the dermatologist and/or gynaecologist investigators. This data was collected from patients' medical records with regard to menstrual cycles, contraception methods, the obstetrical history, screening for gynaecological cancers and sexually transmitted diseases, and the sexual life. Vulvar examinations were carried out as part of the usual follow-up. In total, 27 women (median age 35 years; range 19 to 72) were recruited and their data included in the study between January and December 2021. The gynaecological follow-up was reported as regular for 14 of the 27 (52%) women; 16/27 (59%) mentioned menstruating; 13/24 (51%) had already had at least one contraceptive treatment; 17/27 (63%) declared they had sexual intercourse at least once, most often with difficulties; and 10/27 (37%) had full-term pregnancies, with 1 to 4 children per woman (i.e., 21 deliveries: 8 caesarean sections and 13 vaginal deliveries). Eleven of the 21 women who had a vulvar examination during follow-up had a lesion at the time of the exam. According to French recommendations, the rate of screening for sexually transmitted diseases (STDs), cervical cancer, and breast cancer was 18% (all over 25 years old), 70%, and 100%, respectively.

Conclusion: As for all patients, women with DEB need gynaecological follow-up during their life. A sexology consultation is also highly recommended to help with the psychosexual aspect of DEB and to inform patients about specific preventive measures to avoid lesions during the sexual act, for contraception and for STDs screening. Pregnancies and deliveries are possible even in women with severe disease, most often without major complications.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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