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AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
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 Key Takeaways
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Objective & Hypothesis: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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Key Findings & Data:Generally, radiotherapy (RT) is not a part of treatment in infantsdue to the risk of severe late side effects.
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Conclusion & Impact: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.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
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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Cite This Article
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