Search Results for "Other rare kidney tumors"
Found 28 results
Inflammatory Myofibroblastoma
IMT: rare pediatric tumor, often in lungs. Treated surgically; may recur but rarely metastasizes. Targeted therapy effective for genetic mutations.
Langerhans Cell Histiocytosis
This article introduces LCH: rare childhood blood cancer (2-10/million kids). Affects organs; liver/spleen involvement high-risk. Treatment differs from adults.
Tumors of Liver
This article introduces Liver: largest regenerative organ, reddish-brown, upper right abdomen. Two main lobes (right larger), two smaller lobes. Weight ratio declines with age.
Symptom Management
This article introduces Child cancer symptom management: treats pain/discomfort promptly. Pain relief crucial for quality of life, immune function. Early reporting ensures effective care.
Chordo-Epithelioma
This article introduces Pediatric chordoma: rare spinal tumor, often skull-based. Linked to tuberous sclerosis. Challenging to fully resect surgically.
Multiple Endocrine Neoplasia Syndrome
This article introduces MEN syndrome: genetic disorder causing endocrine gland tumors/hyperplasia (benign/malignant). Affects hormone-producing glands via bloodstream hormone release.
Ovarian Tumor
This article introduces Pediatric ovarian tumors: rare malignancies in ovarian tissue. Ovaries produce eggs/hormones. Located beside uterus in pelvis.
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.
Yolk Sac Tumor
This article introduces Yolk sac tumor: aggressive germ cell malignancy, early treatment boosts >90% survival.
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