Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2016 Jun;36(3):218-21.
doi: 10.1016/j.annpat.2016.02.001. Epub 2016 May 24.

[Immunoglobulin G4-related lung disease: Case report and literature review]

[Article in French]
Affiliations
Case Reports

[Immunoglobulin G4-related lung disease: Case report and literature review]

[Article in French]
Clémence Delteil et al. Ann Pathol. 2016 Jun.

Abstract

We report the case of a 61-year-old man with a pulmonary nodule discovered while staging the metastasis of a squamous cell carcinoma. No primary cancer was found. Histological examination of the resected specimen (lingula) was in favor of IgG4-related inflammatory pseudotumor. Histological criteria were described in 2012, combining a dense lymphoplasmacitic infiltrate rich in IgG4-positive plasma cell, storiform fibrosis and obliterative phlebitis. IgG4/IgG plama cell ratio>40 % is mandatory for histological diagnosis of IgG4-related disease. This is a rare and often underdiagnosed disease. Diagnostic criteria are now defined and consensual, combining clinical signs, biology and histology.

Keywords: Characteristic histopathological features; Critères diagnostiques histologiques; Forme pseudotumorale pulmonaire; IgG4-related disease (IgG4-RD); Inflammatory pulmonary pseudotumor; Maladie à IgG4.

PubMed Disclaimer

Publication types

Substances

LinkOut - more resources