IgG4-related respiratory disease

Shoko Matsui*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

38 Scopus citations

Abstract

IgG4-related diseases (IgG4-RDs), such as autoimmune pancreatitis and IgG4-related Mikulicz disease, are often accompanied by intrathoracic lesions, which are called IgG4-related respiratory disease (IgG4-RRD). IgG4-RRD has few subjective symptoms, and is usually detected during workup of patients with extra-thoracic lesions of IgG4-RD. IgG4-RRD is characterized by various conditions, including masses, nodules, thickening, and infiltration at numerous sites in the thorax through lymphatic routes. Although elevated serum IgG4 concentrations and pathologic evidence of lymphoplasmacytic infiltrates with abundant IgG4-positive plasma cells are characteristic findings of IgG4-RD, other intrathoracic diseases, such as multicentric Castleman disease and malignancy, may present with similar findings. Developing diagnostic criteria for IgG4-RRD, including clinicoradiological and pathological characteristics, is necessary for its appropriate diagnosis.

Original languageEnglish
Pages (from-to)251-256
Number of pages6
JournalModern Rheumatology
Volume29
Issue number2
DOIs
StatePublished - 2019/03/04

Keywords

  • IgG4-related disease
  • IgG4-related respiratory disease
  • diagnostic criteria
  • nonspecific interstitial pneumonia
  • pulmonary manifestations

ASJC Scopus subject areas

  • Rheumatology

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