Fornwalt Brandon E, Altman Jerald S
Valley ENT, PC, Glendale, AZ 85308, USA.
Ear Nose Throat J. 2013 Jan;92(1):E1-3. doi: 10.1177/014556131309200115.
Parry-Romberg syndrome is an uncommon degenerative disorder characterized by a slow and progressive atrophy of the subcutaneous tissue on one side of the face. Its etiology is unknown, and there is no cure. It is usually seen in children. Surgical reconstruction is often the best treatment option, and a wide variety of techniques have been employed. It is often difficult to diagnose Parry-Romberg syndrome because its signs and symptoms overlap with those of several other disorders. We describe a case of Parry-Romberg syndrome in a 42-year-old woman, whose age at onset was the unusual feature of this case.
帕里-罗姆伯格综合征是一种罕见的退行性疾病,其特征为面部一侧皮下组织缓慢进行性萎缩。病因不明,无法治愈。多见于儿童。手术重建通常是最佳治疗选择,已采用了多种技术。帕里-罗姆伯格综合征的体征和症状与其他几种疾病重叠,因此常常难以诊断。我们描述了一例42岁女性的帕里-罗姆伯格综合征病例,该病例的发病年龄是其不寻常之处。