Burrascano Davide, Verro Barbara, Ottoveggio Gaetano, Florena Ada Maria, Saraniti Carmelo
Unit of Otorhinolaryngology, Department of Biomedicine, Neuroscience and Advanced Diagnostic, University of Palermo, 90127 Palermo, Italy.
Unit of Anesthesia, Intensive Care, and Emergency, Department of Precision Medicine in Medical, Surgical and Critical Care (Me.Pre.C.C.), University of Palermo, Italy.
Iran J Otorhinolaryngol. 2025;37(2):95-98. doi: 10.22038/ijorl.2024.81617.3746.
Granulomatosis with Polyangiitis (GPA), also known as Wegener's Granulomatosis, is an ANCA-associated vasculitis that primarily affects small vessels, leading to necrotizing granulomatous reactions in the airways and small vessels. The etiology remains uncertain.
We report the case of a woman in her 70s, who was previously tracheostomized at another facility and was presented to our attention with glottic-subglottic stenosis. We performed a lysis of glottic synechia and subglottic debulking via transoral laser microsurgery, yielding satisfactory results over the short term. However, a relapse occurred within two months, along with ulcerative lesions on the nasal septum. Biopsies revealed multinucleated giant cells and inflammation suggestive of vasculitis. Based on the histological and clinical features, a diagnosis of vasculitis was considered. Anti-Neutrophil Cytoplasmic Antibodies testing was positive. A rheumatological examination confirmed the hypothesis of Granulomatosis with Polyangiitis. The lack of typical symptoms was the main reason for the delayed diagnosis.
Involvement of the subglottic region and the upper portion of the trachea is a rare but severe complication of GPA. The current literature reports only few cases of laryngeal stenosis, with poor prognosis. Histological examinations of biopsied laryngeal tissue showed significant but non-specific inflammation, contributing to the delay in diagnosis. There are still no precise guidelines for the surgical treatment of subglottic stenosis. This case underscores the importance of considering laryngeal involvement in GPA for early diagnosis and timely intervention to prevent serious complications in order to improve patient outcomes.
肉芽肿性多血管炎(GPA),又称韦格纳肉芽肿,是一种与抗中性粒细胞胞浆抗体(ANCA)相关的血管炎,主要累及小血管,导致气道和小血管出现坏死性肉芽肿反应。其病因仍不确定。
我们报告了一例70多岁的女性病例,该患者此前在另一家机构接受了气管造口术,因声门-声门下狭窄前来我院就诊。我们通过经口激光显微手术进行了声门粘连松解和声门下减容,短期内取得了满意的效果。然而,两个月内病情复发,同时鼻中隔出现溃疡性病变。活检显示有多核巨细胞和提示血管炎的炎症。根据组织学和临床特征,考虑诊断为血管炎。抗中性粒细胞胞浆抗体检测呈阳性。风湿科检查证实了肉芽肿性多血管炎的诊断假设。缺乏典型症状是诊断延迟的主要原因。
声门下区域和气管上部受累是GPA一种罕见但严重的并发症。目前文献仅报道了少数喉狭窄病例,预后较差。对活检的喉部组织进行组织学检查显示有明显但非特异性的炎症,这导致了诊断延迟。对于声门下狭窄的外科治疗仍没有精确的指南。该病例强调了在GPA中考虑喉部受累以进行早期诊断和及时干预以预防严重并发症从而改善患者预后的重要性。