Özofagusun sinovyal sarkomu: Olgu sunumu
Sinovyal sarkom çocukluk yaş grubunda üçüncü sıklıkta görülen yumuşak doku tümörüdür. Olguların büyük bir kısmı ekstremite yerleşimlidir. Sinovyal sarkom son derece nadir olarak göğüs duvarı, abdomen ve retroperitoneai bölgede de izlenmektedir. Literatürde saptayabildiğimiz çocukluk yaş grubunda özofagus yerleşimli sinovyal sarkom olgusu iki tanedir. Üç aydır progresif disfaji ve solunum sıkıntısı ile başvuran 8 yaşındaki kız çocukta indirekt laringoskopi ile saptanan larenks ve hypofarenksi dolduran, polipoid yapıda sinovial sarkom olgusu nadir görülmesi nedeniyle sunulmuştur. Olguya kemoterapi, radyoterapi ve lokal rezeksiyon uygulanmıştır. Çocuk 60 aylık takipte hastalıksız yaşamaktadır.
Synovial sarcoma of the esophagus: Case report
Synoviai sarcoma represents the third soft tissue tumor of the pediatric age group. Most of these cases are located in the extremities. Synoviai sarcoma is very rarely located in thoracic wall, in abdominal and retroperitoneai regions. Only two cases of childhood synoviai sarcoma of the esophagus has been reported. An 8 year-old girl with a three-months history of progressive dysphagia and dyspnea is represented in this study. A polypoid mass was observed by indirect laryngoscopy filling the larynx and hypopharynx. She underwent chemotherapy, radiotherapy and incomplete resection. She is alive without disease in 60 months follow-up.
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