Kim Byungsoo, Seo Jung Wook
Taehan Yongsang Uihakhoe Chi. 2021 Mar;82(2):487-492. doi: 10.3348/jksr.2020.0025. Epub 2021 Jan 20.
Immunoglobulin G4 (IgG4)-related disease is a systemic disease characterized by dense lymphoplasmacytic infiltrates with abundant IgG4-positive plasma cells and fibroblast proliferation. The retroperitoneal involvement of IgG4-related disease usually appears as a soft-tissue mass covering the abdominal aorta or entrapping the ureters, resulting in hydronephrosis. Here, we present a case of IgG4-related disease with retroperitoneal involvement in a 75-year-old woman with an unusual manifestation. A preoperative computed tomography (CT) scan revealed an irregular infiltrative retroperitoneal mass invading the normal anatomic barriers, raising the suspicion of malignancy or inflammation. Contrast-enhanced CT revealed a homogeneous progressive enhancement of the mass.
免疫球蛋白G4(IgG4)相关疾病是一种全身性疾病,其特征为密集的淋巴浆细胞浸润,伴有大量IgG4阳性浆细胞和成纤维细胞增殖。IgG4相关疾病的腹膜后受累通常表现为覆盖腹主动脉或包绕输尿管的软组织肿块,导致肾盂积水。在此,我们报告一例75岁女性IgG4相关疾病腹膜后受累的病例,其表现不寻常。术前计算机断层扫描(CT)显示一个不规则浸润性腹膜后肿块侵犯正常解剖边界,引发了对恶性肿瘤或炎症的怀疑。增强CT显示肿块呈均匀渐进性强化。