IgG4相关疾病胰胆受累的内镜治疗方法

José De Jesús Herrera-Esquivel, Carlos A. Zacaula-Aguilar, Enrique Cortinez-Encarnación, Ana Karen García-Ávila, José Rodrigo Muñoz-Gutiérrez, Miguel Ángel Domínguez-Varela, Manuel A. Pérez-Turrent
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引用次数: 0

摘要

导言免疫球蛋白 G4 相关疾病(IgG4-RD)是一种罕见的、影响胰胆管的全身性自身免疫性纤维炎性疾病,通常会模仿恶性肿瘤。病例系列两名 IgG4-RD 患者出现腹部症状和肝功能检查异常。影像学检查和内镜超声检查(EUS)发现胆管狭窄和胰腺异常。血清IgG4水平升高和组织病理学检查结果证实了诊断。这两名患者对泼尼松反应良好,临床症状有所改善,肝功能检查也趋于正常。准确诊断需要结合临床、放射学、血清学和组织病理学结果的多学科方法。结论诊断标准和先进影像学技术的建立改善了 IgG4-RD 的治疗。然而,将 IgG4-RD 与其他胆道疾病区分开来仍具有挑战性,这就需要医学专业人员不断进行研究和合作。
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Endoscopic approach for pancreatobiliary involvement in IgG4 related disease

Introduction

Immunoglobulin G4-related disease (IgG4-RD) is a rare, systemic autoimmune fibroinflammatory disorder affecting the pancreatobiliary tract, often mimicking malignancies. Diagnosis relies on clinical and histological features, using Mayo Clinic HISORt and Japan Biliary Association criteria.

Case series

Two patients with IgG4-RD presented with abdominal symptoms and abnormal liver function tests. Imaging and endoscopic ultrasound (EUS) revealed bile duct stenosis and pancreatic abnormalities. Elevated serum IgG4 levels and histopathological findings confirmed the diagnosis. Both patients responded well to prednisone, showing clinical improvement and normalization of liver function tests.

Discussion

IgG4-RD represents a diagnostic challenge due to its diverse manifestations. Accurate diagnosis requires a multidisciplinary approach, incorporating clinical, radiological, serological, and histopathological findings. Early recognition and corticosteroid therapy are crucial for achieving remission.

Conclusion

The establishment of diagnostic criteria and advanced imaging techniques has improved the management of IgG4-RD. However, distinguishing it from other biliary disorders remains challenging, necessitating ongoing research and collaboration among medical professionals.
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