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Case Report: IgG4-related disease with atypical laryngeal presentation and Behçet/granulomatous polyangiitis mimicking features

机译:病例报告:与IgG4相关的疾病,具有非典型的喉部表现和Behçet/肉芽肿性多血管炎的模仿特征

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摘要

The following report describes two male patients with an ongoing medical history with a predominant laryngeal focus, who were finally diagnosed with IgG4-related disease (IgG4-RD). Their primary symptoms included hoarseness and pain of the throat, and they had undergone multiple laryngeal surgeries and laser treatments due to tumorous growth with limited success. Due to the onset of additional symptoms, they initially received the diagnoses granulomatous polyangiitis (GPA) and Behçet's disease. However, further analysis showed elevated IgG4 levels in serum and infiltration of IgG4-positive plasma cells upon biopsy of laryngeal and pulmonary tissue. Treatment was started with moderate doses of prednisone, leading to a rapid resolution of symptoms.
机译:以下报告描述了两名具有持续喉病史的男性患者,他们最终被诊断出患有IgG4相关疾病(IgG4-RD)。他们的主要症状包括声音嘶哑和喉咙痛,由于肿瘤的生长,他们接受了多次喉外科手术和激光治疗,但收效甚微。由于出现其他症状,他们最初接受了肉芽肿性多血管炎(GPA)和白塞病的诊断。但是,进一步的分析显示,在对喉和肺组织进行活检后,血清中的IgG4水平升高并且IgG4阳性浆细胞浸润。用中等剂量的泼尼松开始治疗,可迅速缓解症状。

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