Stefanko Nicole S, Cossio Maria-Laura, Powell Julie, Blei Francine, Davies Olivia M T, Frieden Ilona J, Garzon Maria C, Lauren Christine T, Maheshwari Mohit, McCuaig Catherine C, Metry Denise, Salman Sumaiya, Drolet Beth A, Siegel Dawn H
Medical College of Wisconsin, Milwaukee, Wisconsin.
Sainte-Justine University Hospital Center, Montreal, Québec, Canada.
Pediatr Dermatol. 2019 Sep;36(5):618-622. doi: 10.1111/pde.13871. Epub 2019 Jun 20.
Awareness of PHACE syndrome has increased; however, little information exists regarding its natural history, especially in patients over the age of 18. We aim to describe the natural history of PHACE to enhance clinical management and counseling of patients.
A cohort of patients ≥ 18 years was identified through the PHACE Syndrome Registry and a Vascular Anomalies Clinic Database. A cross-sectional survey was designed after a review of the literature by PHACE experts (IF, JP, DS). Questions were selected by consensus, and the survey was conducted using the Qualtrics platform and via in-person interviews. A 75% response rate was found.
Eighteen adults-17 females and one transgender male-completed the survey. Respondents ranged in age from 18 to 59, with 24 being the mean age. Eighty-nine percent reported experiencing headaches, and 17% reported experiencing acute but transient symptoms mimicking acute ischemic stroke, later diagnosed as atypical migraines. Thirty-three percent reported hearing loss, and 67% endorsed dental issues. One patient experienced two arterial dissections. Three-fourths who attempted conception were successful, and none of their children had clinical features of PHACE. Because results were based on a retrospective survey, data captured were prone to recall bias and not objective. Results were limited by a small sample size.
Health care providers should be aware of a possible increased risk of neurovascular complications, including atypical migraines mimicking transient ischemic attacks and arterial dissection, in adults with PHACE. Heritability has not been demonstrated, and future studies are needed to assess the risk of infertility.
PHACE综合征的知晓率有所提高;然而,关于其自然病史的信息却很少,尤其是在18岁以上的患者中。我们旨在描述PHACE的自然病史,以加强对患者的临床管理和咨询。
通过PHACE综合征登记处和血管异常诊所数据库确定了一组年龄≥18岁的患者。在PHACE专家(IF、JP、DS)对文献进行回顾后设计了一项横断面调查。通过共识选择问题,并使用Qualtrics平台和面对面访谈进行调查。发现回复率为75%。
18名成年人——17名女性和1名跨性别男性完成了调查。受访者年龄在18岁至59岁之间,平均年龄为24岁。89%的人报告有头痛症状,17%的人报告有类似急性缺血性中风的急性但短暂症状,后来被诊断为非典型偏头痛。33%的人报告有听力损失,67%的人认可存在牙齿问题。一名患者经历了两次动脉夹层。四分之三尝试怀孕的人成功了,他们的孩子都没有PHACE的临床特征。由于结果基于回顾性调查,所收集的数据容易出现回忆偏差且不客观。结果受样本量小的限制。
医疗保健提供者应意识到,患有PHACE的成年人可能有更高的神经血管并发症风险,包括类似短暂性脑缺血发作的非典型偏头痛和动脉夹层。尚未证实其遗传性,未来需要进行研究以评估不孕风险。