Literature DB >> 29394821

[A Case of an IgG4-Related Inflammatory Pseudotumor of the Liver Showing Enlargement That Was Difficult to Differentiate from Hepatic Cancer].

Kei Adachi1, Kazuhiko Hashimoto, Ryoji Nonaka, Jeong-Ho Moon, Yujiro Fujie, Shoichiro Fujita, Keiko Kojima, Jun Hanai, Shingi Imaoka, Tadashi Ohnishi.   

Abstract

A 60-year-old man was admitted for a liver mass(S3), which rapidly increased in size during intraductal papillary mucinous neoplasm(IPMN)follow-up. Although EOB-MRIwas performed, the mass could not be accurately diagnosed as hepatic cancer. Thus, we performed a lateral segmentectomy. In the resected specimen, a solid tumor mass was clearly bound in segment 3 of the liver. Since histopathology revealed no malignant cells and many IgG4-positive cells, we confirmed the diagnosis as IgG4-related inflammatory pseudotumor of the liver. IgG4-related diseases occur in various organs in the body, and they are known to associate with autoimmune pancreatitis and sclerosing cholangitis, but an IgG4-related inflammatory pseudotumor of the liver is a rare disease. It is often difficult to distinguish from hepatic cancer and surgical resection is performed.

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Year:  2017        PMID: 29394821

Source DB:  PubMed          Journal:  Gan To Kagaku Ryoho        ISSN: 0385-0684


  2 in total

1.  Untypical autoimmune pancreatitis and pancreatic cancer: differential diagnosis experiences extracted from misdiagnose of two cases.

Authors:  Gaopeng Li; Ting Liu; Jian Zheng; Wenqin Kang; Jun Xu; Zefeng Gao; Jinfeng Ma
Journal:  Orphanet J Rare Dis       Date:  2019-11-07       Impact factor: 4.123

2.  IgG4-Related Hepatic Pseudotumor Masquerading as a Klatskin Tumor.

Authors:  Jennifer Yoon; Steve Hu; Daniel Phillips; Amir Fathi; Adnan Ameer
Journal:  Case Reports Hepatol       Date:  2022-06-28
  2 in total

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