Search Results for "Ewing sarcoma"
Found 18 results
Rare Childhood Tumour
This article introduces Pediatric cancers rare; mortality halved since 1975. Ultra-rare cases lack data, treated via limited case reports and shared clinical experience.
Musculoskeletal System
This article introduces Childhood cancer survivors risk bone/joint issues post-treatment (surgery/chemo/radiation). Requires monitoring for symptoms and diagnostic tests for long-term health.
Alimentary System
This article introduces Child cancer survivors under 5 face higher dental/jaw risks as permanent teeth undeveloped during treatment, increasing long-term complications.
The Second Type of Cancer
This article introduces Childhood cancer survivors risk second cancers (post 2+ months). Genetic factors/treatment type influence risk. Requires lifelong monitoring with tailored screenings.
Langerhans Cell Histiocytosis
This article introduces LCH: rare childhood disorder (peak 1-4yrs), ranges from mild to fatal. Treatment varies. Prognosis better in adults/single-system cases.
Hepatoblastoma
This article introduces Hepatoblastoma: top pediatric liver cancer (90% under age 5). Presents as abdominal mass. Treated with chemo/surgery. 80% survival rate.
Osteosarcoma (benign tumor composed of bone-like material)
This article introduces Osteosarcoma: most common pediatric bone cancer (5% childhood tumors), typically affects teens' long bones (knee area). Aggressive, requires prompt treatment.
Ewing sarcoma
This article introduces Ewing sarcoma: rare pediatric bone/soft tissue tumor. Treat with chemo/surgery/radiation. Highly aggressive, poor prognosis, often recurs.
Other rare kidney tumors
Other rare kidney tumors
Synovial sarcoma
This article introduces Synovial sarcoma: common in youth near joints. SYT-SSX gene fusion. Surgery + chemo/radiation. 50-60% 5-year survival.
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