Yang Jingpu, Jin Chengxun, Gao Yunhe, Wang Zonggui
Department of Otolaryngology, Head and Neck Surgery, Jilin University Second Hospital, Changchun, China.
Department of Pathology, Jilin University Second Hospital, Changchun, China.
Ear Nose Throat J. 2025 Mar;104(3):162-164. doi: 10.1177/01455613221077602. Epub 2022 May 20.
Immunoglobulin G4-related disease (IgG4-RD) is a novel clinical disease entity characterized by elevated serum IgG4 concentration and tumefaction or tissue infiltration by IgG4+ plasma cells. We report the case of a 56-year-old man who presented with nasal obstruction for 5 years. Rhinoscopy revealed hypertrophy and sclerosis of the inferior turbinate, whereas computed tomography revealed inflammation of the anterior ethmoid sinus and frontal sinuses. An endoscopic inferior turbinectomy was performed, and IgG4-RD was definitively diagnosed based on the histopathological features of the turbinate tissue. Prednisolone was administered postoperatively. IgG4-RD presenting with hypertrophy and sclerosis of the inferior turbinate is rare. Awareness of IgG4-RD originating in the sinonasal cavity is essential to avoid delayed diagnosis.
免疫球蛋白G4相关性疾病(IgG4-RD)是一种新型临床疾病实体,其特征为血清IgG4浓度升高以及IgG4+浆细胞引起的肿胀或组织浸润。我们报告一例56岁男性患者,其鼻塞症状持续5年。鼻镜检查显示下鼻甲肥大和硬化,而计算机断层扫描显示筛窦前部和额窦炎症。进行了内镜下下鼻甲切除术,并根据鼻甲组织的组织病理学特征确诊为IgG4-RD。术后给予泼尼松龙治疗。以下鼻甲肥大和硬化为表现的IgG4-RD较为罕见。认识到起源于鼻腔鼻窦的IgG4-RD对于避免延迟诊断至关重要。