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孤立性肿块形成型IgG4相关性胆管炎作为系统性IgG4相关性疾病的初始临床表现

Isolated Mass-Forming IgG4-Related Cholangitis as an Initial Clinical Presentation of Systemic IgG4-Related Disease.

作者信息

Kim Seokhwi, Bae Hyunsik, Choi Misun, Kim Binnari, Heo Jin Seok, Kim Ho Seong, Choi Seung Hee, Jang Kee-Taek

机构信息

Department of Pathology and Translational Genomics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

出版信息

J Pathol Transl Med. 2016 Jul;50(4):300-5. doi: 10.4132/jptm.2015.12.01. Epub 2016 Jan 11.

Abstract

IgG4-related disease (IgG4-RD) may involve multiple organs. Although it usually presents as diffuse organ involvement, localized mass-forming lesions have been occasionally encountered in pancreas. However, the same pattern has been seldom reported in biliary tract. A 61-year-old male showed a hilar bile duct mass with multiple enlarged lymph nodes in imaging studies and he underwent trisectionectomy under impression of cholangiocarcinoma. Gross examination revealed a mass-like lesion around hilar bile duct. Histopathologically, dense lymphoplasmacytic infiltration and storiform fibrosis were identified without evidence of malignancy. Immunohistochemical stain demonstrated rich IgG4-positive plasma cell infiltration. Follow-up imaging studies disclosed multiple enlarged lymph nodes with involvement of pancreas and perisplenic soft tissue. The lesions have been significantly reduced after steroid treatment, which suggests multi-organ involvement of systemic IgG4-RD. Here, we report an unusual localized mass-forming IgG4-related cholangitis as an initial presentation of IgG4-RD, which was biliary manifestation of systemic IgG4-related autoimmune disease.

摘要

IgG4相关性疾病(IgG4-RD)可累及多个器官。虽然它通常表现为弥漫性器官受累,但胰腺偶尔也会出现局限性肿块形成性病变。然而,胆道出现相同模式的情况鲜有报道。一名61岁男性在影像学检查中显示肝门部胆管肿块伴多发肿大淋巴结,他在被诊断为胆管癌的情况下接受了肝三段切除术。大体检查发现肝门部胆管周围有一个肿块样病变。组织病理学检查显示有密集的淋巴浆细胞浸润和束状纤维化,未发现恶性证据。免疫组化染色显示有丰富的IgG4阳性浆细胞浸润。随访影像学检查发现多发肿大淋巴结,累及胰腺和脾周软组织。类固醇治疗后病变明显缩小,这提示全身性IgG4-RD有多器官受累。在此,我们报告一例罕见的局限性肿块形成性IgG4相关性胆管炎,作为IgG4-RD的初始表现,它是全身性IgG4相关自身免疫性疾病的胆道表现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5778/4963967/a68951e013da/jptm-2015-12-01f1.jpg

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