Inflamatorni miofibroblastični tumor kolena sedmogodišnjeg dečaka: prikaz slučaja

Ključne reči: inflamatorni miofibroblastični tumor, koleno, dete, ROS1, PDGFRα, ALK-negativan

Sažetak


Inflamatorni miofibroblastični tumor (IMT) predstavlja retku mezenhimalnu neoplazmu intermedijernog biološkog potencijala, koja češće zahvata decu i mlade. Najčešće je lo­ka­lizovan u plućima i abdominopelvičnom predelu, ali mo­že nastati u gotovo svakom organu. Prikazujemo slučaj sedmo­godišnjeg dečaka sa ekstraartikularnom tumoroznom masom medijalnog aspekta desnog kolena. Radiološki (MRI) je lezija bila dobro ograničena, intenzivno homogeno pojačana nakon aplikacije kontrasta, bez invazije zgloba ili kosti. Lezija je u celosti hirurški uklonjena. Histopatološki nalaz je pokazao proliferaciju miofibroblasta u miksodnoj stromi sa izraženim inflamatornim infiltratom. Imunohistohemijski tumor je bio SMA pozitivan, ALK negativan; molekularno je dokazan re­aranžman ROS1 i fuzija COL1A1–PDGFRα. Postoperativni tok protekao je bez komplikacija, bez recidiva na kontroli. Ovaj slučaj naglašava značaj sveobuhvatne molekularne di­jagno­stike u atipičnim lokalizacijama IMT-a i potencijal za ci­ljanu terapiju kod neresektabilnih ili rekurentnih formi. 

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Objavljeno
2025/09/18
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Rubrika
Case Report