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Yapay Zeka Hızlı Bakış & Çıkarımlar
AI Insight⚡ TL;DR(1 Cümlede Hızlı Çıkarım)
In this case report, we report a7-month-old boy with diagnosis of left mastoid bone ES with lung metastasesat diagnosis, showing a rapidly fatal outcome despite aggressive systemicchemotherapy and RT without surgery.
📌 3 Maddede Bu Makale
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Amaç & Hipotez:Ewing sarcoma (ES) is a rare tumor in infants and prognosis is controversial.There are no standard recommendations for treatment in such very youngpatients.
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Temel Bulgular & Veri:Generally, radiotherapy (RT) is not a part of treatment in infantsdue to the risk of severe late side effects.
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Sonuç & Katkı:In this case report, we report a7-month-old boy with diagnosis of left mastoid bone ES with lung metastasesat diagnosis, showing a rapidly fatal outcome despite aggressive systemicchemotherapy and RT without surgery.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri
Abstract
Ewing sarcoma (ES) is a rare tumor in infants and prognosis is controversial.There are no standard recommendations for treatment in such very youngpatients. Generally, radiotherapy (RT) is not a part of treatment in infantsdue to the risk of severe late side effects. In this case report, we report a7-month-old boy with diagnosis of left mastoid bone ES with lung metastasesat diagnosis, showing a rapidly fatal outcome despite aggressive systemicchemotherapy and RT without surgery.
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Bu Makaleye Atıf Yap
Yıldız, F., Orhan, D., Oğuz, K. K., Cengiz, M., Akyüz, C., Gürkaynak, M., Gültekin, M., Esen, Ç. S. B., Aydın, G. B. (2022). Ewing sarcoma in an infant and review of the literature. Turkish Journal of Pediatrics, Cilt: 61 - Sayı: 5, 760–764. https://ajindex.com/articles/613101