Search Results for "Bone tumor"

Childhood Hepatocellular Carcinoma

This article introduces Pediatric HCC: rare liver cancer in 10-14-year-olds. Presents with abdominal symptoms. Treated surgically. Poor prognosis (<30% survival).

Hepatoblastoma

This article introduces Hepatoblastoma: top pediatric liver cancer (90% under age 5). Presents as abdominal mass. Treated with chemo/surgery. 80% survival rate.

Dermoid Tumor

This article introduces Germ cell tumors arise from flawed germ cell development, forming teratomas with mixed tissues in wrong locations.

Yolk Sac Tumor

This article introduces Yolk sac tumor: aggressive germ cell malignancy, early treatment boosts >90% survival.

Seminoma

This article introduces Dysgerminoma: Seminoma: testicular germ cell tumor, curable with surgery/radiation/chemo, 5-year survival >90%.

Disgerminoma

This article introduces Dysgerminoma: ovarian germ cell tumor, treated with surgery/chemo, 5-year survival ~85%.

Bone tumor List of volunteers

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.

Interpretation of nouns

This article introduces Cancer treatments: radiation, chemo (systemic/local), surgery (total/partial nephrectomy), immunotherapy, targeted therapy. Diagnostics: imaging (CT/MRI/PET), biopsies, scans.