| Literature DB >> 23095295 |
Makoto Odaka1, Shohei Mori, Hisatoshi Asano, Makoto Yamashita, Noriki Kamiya, Toshiaki Morikawa.
Abstract
This report describes a rare case of IgG4-related lung disease that was difficult to distinguish from lung cancer. CT revealed a well-demarcated round tumor in S10 of the right lung of a 56-year-old man suspected of having lung cancer. PET revealed high fluorodeoxyglucose uptake with a maximum standardized uptake value of 14.0. Because primary lung cancer was strongly suspected, lower lobectomy was performed via the thoracoscopic approach without mini-thoracotomy. Histopathology showed lymphoplasmacytic infiltration. Immunostaining revealed numerous IgG4-positive plasma cells diffusely infiltrating the tumor. Serum IgG4 levels increased, thereby confirming the diagnosis of IgG4-related lung disease.Entities:
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Year: 2012 PMID: 23095295 DOI: 10.1111/j.1758-5910.2012.00149.x
Source DB: PubMed Journal: Asian J Endosc Surg ISSN: 1758-5902