Shah J R, Juhász C, Kupsky W J, Asano E, Sood S, Fain D, Chugani H T
Department of Neurology, Harper University Hospital, Detroit Medical Center, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Neurology. 2003 Aug 12;61(3):395-7. doi: 10.1212/wnl.61.3.395.
Parry-Romberg syndrome is a rare disorder associated with unilateral facial atrophy involving skin, subcutaneous tissue, skeletal muscle, and bone. Occasionally, there is CNS involvement with epilepsy being the most common CNS manifestation. The authors report a child with Parry-Romberg syndrome with a course strongly suggestive of Rasmussen encephalitis. The boy underwent hemispherectomy, and pathology showed the typical findings of Rasmussen encephalitis, suggesting that these two conditions may share common etiologic factors.
帕里-罗姆伯格综合征是一种罕见疾病，与单侧面部萎缩有关，累及皮肤、皮下组织、骨骼肌和骨骼。偶尔会有中枢神经系统受累，癫痫是最常见的中枢神经系统表现。作者报告了一名患有帕里-罗姆伯格综合征的儿童，其病程强烈提示为拉斯穆森脑炎。该男孩接受了大脑半球切除术，病理显示出拉斯穆森脑炎的典型表现，提示这两种疾病可能有共同的病因。
