Cannady Steven B, Batra Pete S, Koening Curry, Lorenz Robert R, Citardi Martin J, Langford Carol, Hoffman Gary S
Head and Neck Institute, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.
Laryngoscope. 2009 Apr;119(4):757-61. doi: 10.1002/lary.20161.
OBJECTIVES/HYPOTHESIS: Wegener granulomatosis (WG) is intimately associated with the sinonasal tract, with involvement reported in 85% of patients during the course of the disease process. The objectives of the study were: 1) to describe sinonasal symptoms and signs at the time of initial otolaryngologic evaluation; and 2) to review indications and outcomes for rhinologic surgery in WG at our institution.
A retrospective analysis of 120 patients presenting with WG and referred for otolaryngology consultation at a tertiary care center was performed.
Eighty-nine percent of patients exhibited sinonasal involvement including nasal crusting (69%), chronic rhinosinusitis (CRS) (61%), nasal obstruction (58%), bloody nasal discharge (52%), septal perforation (33%), saddle-nose deformity (23%), epiphora (13%), and mucocele formation (3.3%). Thirty-nine (33%) patients underwent primary functional endoscopic sinus surgery or dacryocystorhinotomy (DCR) prior to referral. Nineteen (16%) patients underwent noncosmetic, functional sinonasal procedures at our institution. These included endoscopic sinus surgery for CRS or mucocele decompression in 14 patients, DCR for chronic epiphora in seven patients, and orbital decompression for pseudotumor in three patients. Individual symptom recurrence within the first year was greatest for visual impairment from pseudotumor (50%), followed by CRS (14%) and nasolacrimal duct obstruction (11%).
The majority of patients with WG are referred to otolaryngology because of involvement of the sinonasal tract. Noncosmetic functional sinonasal procedures are indicated in a minority of patients. Sinonasal morbidity remains significant even after surgery. It is greatest for orbital pseudotumor, but also common for CRS and nasolacrimal duct obstruction.
目的/假设:韦格纳肉芽肿(WG)与鼻窦密切相关,据报道85%的患者在疾病过程中会累及鼻窦。本研究的目的是:1)描述初次耳鼻喉科评估时的鼻窦症状和体征;2)回顾我们机构中WG患者鼻科手术的适应证和结局。
对一家三级医疗中心收治的120例WG患者并转诊至耳鼻喉科咨询的病例进行回顾性分析。
89%的患者出现鼻窦受累,包括鼻痂(69%)、慢性鼻窦炎(CRS)(61%)、鼻塞(58%)、鼻出血(52%)、鼻中隔穿孔(33%)、鞍鼻畸形(23%)、溢泪(13%)和黏液囊肿形成(3.3%)。39例(33%)患者在转诊前接受了初次功能性鼻内镜鼻窦手术或泪囊鼻腔造口术(DCR)。19例(16%)患者在我们机构接受了非美容性的功能性鼻窦手术。其中包括14例因CRS或黏液囊肿减压而行的鼻内镜鼻窦手术,7例因慢性溢泪而行的DCR,以及3例因假瘤而行的眼眶减压术。第一年个体症状复发率最高的是假瘤导致的视力障碍(50%),其次是CRS(14%)和鼻泪管阻塞(11%)。
大多数WG患者因鼻窦受累而转诊至耳鼻喉科。少数患者需要进行非美容性的功能性鼻窦手术。即使手术后鼻窦发病率仍然很高。眼眶假瘤的发病率最高,但CRS和鼻泪管阻塞也很常见。