Abdominal Manifestations of IgG4-Related Disease

Jeffrey D. Olpin, Akram M. Shaaban, Neel Patel

Research output: Contribution to journalReview articlepeer-review

Abstract

IgG4-related disease is a recently recognized systemic disorder involving multiple organs throughout the body. The multi-organ involvement of this disease was previously thought to occur as isolated, unrelated autoimmune disorders. Although virtually any part of the body may be involved in IgG4-related disease, abdominal manifestations tend to predominate in most affected individuals. While autoimmune pancreatitis is the most commonly encountered abdominal disorder in the setting of IgG4-related disease, the liver, kidneys, gastrointestinal tract, retroperitoneum, and mesentery may likewise be involved. Various diagnostic criteria for IgG4-related disease have been proposed based on physical exam, serology, and histopathologic confirmation. However, imaging plays an essential role in the diagnosis of this disorder, not only to establish the presence of IgG4-related disease, but to assess the severity and extent of systemic disease involvement.

Original languageEnglish (US)
Article number23
JournalCurrent Radiology Reports
Volume4
Issue number5
DOIs
StatePublished - May 1 2016
Externally publishedYes

Keywords

  • Autoimmune pancreatitis
  • IgG4
  • Immunoglobulin
  • Plasma cell
  • Sclerosing cholangitis
  • Sclerosing mesenteritis

ASJC Scopus subject areas

  • Radiology Nuclear Medicine and imaging

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