A Case of Sclerosing Pneumocytoma: A Rare Lung Tumor

Sclerosing pneumocytoma is a rare, benign neoplasm which may be in solid, papillary, sclerosing or hemorrhagic patterns histologically, and its papillary surfaces are covered with hyperplastic type 2 pneumocytes. It is often seen in middle-aged adults and women with no recurrence and no reported disease-related deaths. Herein, we present a 50-year-old female case of sclerosing pneumocytoma case who was diagnosed incidentally during acute bronchitis episode.

Nadir Bir Akciðer Tümörü olan Sklerozan Pnömositoma Olgusu

Sklerozan pnömositoma histolojik olarak solid, papiller, sklerotik, hemorajik paternlerde olabilen, papiller yüzeyleri hiperplastik tip 2 pnömositlerle döþeli çoðunlukla orta yaþ eriþkin ve kadýnlarda görülen benign, rekürrens yada hastalýða baðlý ölüm bildirilmeyen, nadir görülen bir neoplazidir. Biz 50 yaþýndaki kadýn hastada akut bronþit ataðý sýrasýnda insidental olarak saptanan sklerozan pnömositoma olgusunu sunduk

Image Slices of the Case