@Article{Yilmaz2025,
journal="Polish Journal of Pathology",
issn="1233-9687",
volume="76",
number="4",
year="2025",
title="Pulmonary granular cell tumor coexisting with interstitial lung disease – a rare case report",
abstract="A granular cell tumor (GCT) is a soft tissue neoplasm of rare occurrence in the lung. A 44-year-old male asphalt worker had interstitial lung disease. Incidentally,  a 7 mm polypoid nodule was observed at the entrance of the right upper lobe bronchus. Tumor cells were characterized by a large granular eosinophilic cytoplasm and small, uniform nuclei. The neoplastic cells were diffuse positive for S-100, CD-68, NSE, vimentin, and SOX-10, and focal positive for calretinin and inhibin A. This case is unique in its distinction as the second literature case of pulmonary GCT coexisting with interstitial lung disease.",
author="Yilmaz, Zeynep Sagnak
and Ersoz, Safak
and Ozsagır, Elif
and Turker, Kubra
and Aycicek, Olcay
and Ozturk, Deha",
pages="338--342",
doi="10.5114/pjp.2025.158613",
url="http://dx.doi.org/10.5114/pjp.2025.158613"
}