Duymaz Ahmet, Karabekmez Furkan Erol, Tosun Zekeriya, Keskin Mustafa, Karamese Mehtap, Savaci Nedim
Department of Plastic and Reconstructive Surgery, Meram Medical School, Selcuk University, Konya, Turkey.
J Craniofac Surg. 2008 Jul;19(4):1104-6. doi: 10.1097/SCS.0b013e318176ac6c.
Parry-Romberg syndrome is characterized by progressive hemifacial atrophy that is the lack of tissue (generally soft tissue and rarely bone and muscle) in the atrophic area of the face. The etiology and the incidence of this pathologic process are uncertain, but it is relatively rare and self-limited. The objective of this study is to present 21-year-old female patient with progressive hemifacial atrophy who was reconstructed with composite galeal frontalis flap. Although many reconstructive methods have been described, reconstruction of both eyebrow deficiency and forehead atrophy with composite galeal frontalis flap was not described before.
帕里-罗姆伯格综合征的特征是进行性半侧面部萎缩，即面部萎缩区域缺乏组织（通常为软组织，骨骼和肌肉较少见）。这种病理过程的病因和发病率尚不确定，但相对罕见且具有自限性。本研究的目的是介绍一名21岁患有进行性半侧面部萎缩的女性患者，其采用复合颞肌筋膜额部皮瓣进行了重建。尽管已经描述了许多重建方法，但此前尚未有使用复合颞肌筋膜额部皮瓣同时修复眉毛缺失和额部萎缩的报道。
