Retroperitoneal Fibrosis Diagnosed as IgG4-related Disease after 35 Years

Intern Med. 2019 Feb 15;58(4):609-613. doi: 10.2169/internalmedicine.1241-18. Epub 2018 Oct 17.

Abstract

In 1982, we reported a case of retroperitoneal fibrosis (RPF) exhibiting various clinical manifestations. Our current understanding of immunoglobulin G4 (IgG4)-related disease led us to consider it as a possible diagnosis because all of the patient's clinical features could be explained by this disease entity. To confirm our hypothesis, were investigated the histopathological findings of resected specimens that had been stored for 35 years postoperatively. Typical pathological findings together with predominant IgG4+ plasma cell infiltration confirmed a potential diagnosis of IgG4-related RPF. Furthermore, we observed positive immunohistochemical staining for several molecules associated with T regulatory and T follicular helper cells.

Keywords: IgG4-related disease; T follicular helper (Tfh) cells; T regulatory (Treg) cells; retroperitoneal fibrosis.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Follow-Up Studies
  • Humans
  • Immunoglobulin G / blood*
  • Immunoglobulin G4-Related Disease / complications*
  • Immunoglobulin G4-Related Disease / diagnosis*
  • Immunohistochemistry
  • Male
  • Retroperitoneal Fibrosis / diagnosis*
  • Retroperitoneal Fibrosis / etiology*
  • Time Factors

Substances

  • Immunoglobulin G