Künzel Julian, Agaimy Abbas, Hornung Joachim, Lell Michael, Ganslandt Oliver, Semrau Sabine, Zenk Johannes
Department of Otorhinolaryngology, Head & Neck Surgery, University Hospital of Erlangen-Nuremberg Erlangen, Germany.
Department of Pathology, University Hospital of Erlangen-Nuremberg Erlangen, Germany.
Int J Clin Exp Pathol. 2014 Apr 15;7(5):2641-6. eCollection 2014.
Endolymphatic sac tumor (ELST) is a rare low-grade locally aggressive neoplasm of the inner ear that may occur sporadically or in the setting of von Hippel-Lindau syndrome. We herein present a case of sporadic ELST in a 39-year-old man, treated using an interdisciplinary approach (surgery+radiotherapy), with a 10-year follow-up. The patient presented with hearing loss of sudden onset. The treatment of choice for ELST is radical tumor resection, which is associated with a good long-term prognosis. Remission may last for years, but there may be local recurrences, probably as a result of incomplete resection. Adjuvant radiotherapy is an option in case of recurrence and could be discussed after incomplete resection. The purpose of this report is to call attention to ELSTs, which are difficult to diagnose due to their rarity and variety of presentations.
内淋巴囊肿瘤(ELST)是一种罕见的低度局部侵袭性内耳肿瘤,可散发性发生或发生于冯·希佩尔-林道综合征背景下。我们在此报告一例39岁男性散发性ELST病例,采用多学科方法(手术+放疗)治疗,并进行了10年随访。患者表现为突发听力丧失。ELST的首选治疗方法是根治性肿瘤切除术,其长期预后良好。缓解可能持续数年,但可能会出现局部复发,这可能是由于切除不完全所致。复发时辅助放疗是一种选择,在切除不完全时可考虑进行讨论。本报告的目的是引起对ELST的关注,因其罕见性和多种表现形式而难以诊断。