Polish Journal of Pathology
eISSN: 2084-9869
ISSN: 1233-9687
Polish Journal of Pathology
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abstract:
Case report

Pulmonary granular cell tumor coexisting with interstitial lung disease – a rare case report

Zeynep Sagnak Yilmaz
1
,
Safak Ersoz
1
,
Elif Ozsagır
2
,
Kubra Ozturk Turker
3
,
Olcay Aycicek
4
,
Deha Cebi Ozturk
5

  1. Department of Pathology, Karadeniz Technical University Faculty of Medicine, Trabzon, Turkey
  2. Department of Pathology, Bingol State Hospital, Bingol, Turkey
  3. Department of Pathology, Kanuni Training and Research Hospital, Trabzon, Turkey
  4. Department of Chest Diseases, Karadeniz Technical University Faculty of Medicine, Trabzon, Turkey
  5. Department of Chest Diseases, Ahi Evren Chest Cardiovascular Surgery Training and Research Hospital, Trabzon, Turkey
Pol J Pathol 2025; 76 (4)
Online publish date: 2026/01/19
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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.
keywords:

granular cell tumor, interstitial lung disease, endobronchial tumor

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