Tamás Tímea, Iszlai Zoltán, Szűcs Gabriella, Karosi Tamás
Fül-Orr-Gégészeti és Fej-Nyaksebészeti Osztály,Borsod-Abaúj-Zemplén Megyei Központi Kórház és Egyetemi Oktatókórház, Miskolc, Szentpéteri kapu 72-76., 3526.
Klinikai Központ, Belgyógyászati Klinika, Reumatológia Tanszék,Debreceni Egyetem, Debrecen.
Orv Hetil. 2020 Jul;161(28):1181-1185. doi: 10.1556/650.2020.31755.
Parry-Romberg syndrome is a rare, slowly progressive, autolimitated disease, characterized by unilateral facial atrophy. It is usually manifested in childhood and young adulthood. Because of the degree of atrophy and the variety of symptoms, the diagnosis, prognosis, and treatment of Parry-Romberg syndrome are a major challenge. The purpose of this case presentation is to highlight the difficulty of establishing the diagnosis, furthermore, to present the steps of examining the patient and to draw attention to the importance of proper timing of the surgery. Moreover, it wants to emphasize the importance of looking for diseases that often occur with the mentioned syndrome. Orv Hetil. 2020; 161(28): 1181-1185.
帕里-龙贝格综合征是一种罕见的、缓慢进展的、自限性疾病，其特征为单侧面部萎缩。它通常在儿童期和青年期出现。由于萎缩程度和症状的多样性，帕里-龙贝格综合征的诊断、预后和治疗是一项重大挑战。本病例报告的目的是突出诊断的困难，此外，展示检查患者的步骤，并提请注意手术时机恰当的重要性。此外，它想强调寻找常与上述综合征并发疾病的重要性。《匈牙利医学周报》。2020年；161(28): 1181 - 1185。
