并存的斯-韦综合征、面部婴幼儿血管瘤和先天性大理石样皮肤毛细血管扩张症。
Concurrent Sturge-Weber syndrome, facial infantile hemangioma, and cutis marmorata telangiectatica congenita.
作者信息
Poliak Nina, Rainey Anthony
机构信息
Wright Center of Graduate Medical Education, Scranton, and Lehigh Valley Health Network, Children's Clinic, Allentown, Pennsylvania; and Geisinger Commonwealth School of Medicine, Scranton, Pennsylvania, USA.
Geisinger Commonwealth School of Medicine, Scranton, Pennsylvania, USA.
出版信息
Cutis. 2017 Oct;100(4):252-254.
We present a unique case of 3 vascular malformations-Sturge-Weber syndrome (SWS), facial infantile hemangioma (IH), and cutis marmorata telangiectatica congenita (CMTC)-with dermatologic manifestations presenting in the same patient. This case highlights the possibility of occurrence of multiple vascular malformations in the same patient; the potential role of epigenetic factors; and the importance of a multidisciplinary approach to diagnose, treat, and manage this complicated interplay of vascular abnormalities to achieve the best outcome.
我们报告了一例独特的病例，一名患者同时出现了三种血管畸形——斯特奇-韦伯综合征（SWS）、面部婴儿血管瘤（IH）和先天性大理石样皮肤毛细血管扩张症（CMTC），伴有皮肤表现。该病例凸显了同一患者发生多种血管畸形的可能性；表观遗传因素的潜在作用；以及采用多学科方法来诊断、治疗和管理这种复杂的血管异常相互作用以实现最佳结果的重要性。
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