- Author:
Sangjoon CHOI
1
;
Sujin PARK
;
Man Pyo CHUNG
;
Tae Sung KIM
;
Jong Ho CHO
;
Joungho HAN
Author Information
- Publication Type:Case Report
- Keywords: Lung; Neoplasm; IgG4-related disease; Autoimmune
- MeSH: Aged; Carcinoma, Adenosquamous; Fibrosis; Humans; Immunoglobulin G; Lung Diseases; Lung Diseases, Interstitial; Lung Neoplasms; Lung; Phlebitis; Plasma Cells; Respiratory System
- From:Journal of Pathology and Translational Medicine 2019;53(3):188-191
- CountryRepublic of Korea
- Language:English
- Abstract: IgG4-related disease is a systemic inflammatory disease and is known as IgG4-related lung disease (IgG4-RLD) when it involves the respiratory system. Primary lung cancer arising from a background of IgG4-RLD is very rare. Herein, we report a case of adenosquamous carcinoma arising from the background of IgG4-RLD and presenting as an interstitial lung disease pattern. A 66-year-old man underwent lobectomy under the impression of primary lung cancer. Grossly, the mass was ill-defined and gray-tan colored, and the background lung was fibrotic. Microscopically, tumor cells showed both squamous and glandular differentiation. Dense lymphoplasmacytic infiltration with fibrosis and obliterative phlebitis were seen in the background lung. IgG4 immunohistochemical stain showed diffuse positivity in infiltrating plasma cells. Primary lung adenosquamous carcinoma has not been reported in a background of IgG4-RLD. Due to the rarity of IgG4-RLD, physicians must follow patients with IgG4-RLD over long periods of time to accurately predict the risk of lung cancer.