cancer is second most common cause of death in children after 1 year of age (1st=injuries) usually occur sporadically, but increas...
- cancer is second most common cause of death in children after 1 year of age (1st=injuries)
- usually occur sporadically, but increased risk with
- neurocutaneous syndromes
- chromosomal syndromes
- immunodeficiency syndromes
- prior malignancy
- family history
- exposure to radiation, chemicals, biologic agents
- leukemia (25-35%) and brain tumours (20%) most common
- some malignancies may be more prevalent in certain age groups
- newborns: neuroblastoma, congenital leukemia
- infancy and childhood: leukemia, neuroblastoma, Wilms’, retinoblastoma
- adolescence: lymphoma, gonadal tumours, bone
LEUKEMIA
- most common childhood malignancy
- heterogenous group of diseases; types: ALL (80%), AML (15%) and CML (5%)
- etiology unknown; EBV associated with African Burkitt lymphoma,
retrovirus with T cell leukemia - signs and symptoms due to infiltration of leukemic cells
- into bone marrow (bone pain, anemia, neutropenia, thrombocytopenia)
- into tissues(lymphadenopathy, hepatosplenomegaly, CNS, testes)
- prognosis: low-risk - 90% long-term remission, high-risk - 70% long-term remission
- see also Hematology Notes
| Good | Poor |
age | 2-10 years | <2 or >10 years |
ethnicity | white | black |
sex | female | male |
lymphadenopathy | no | yes |
hepatosplenome galy | no | yes |
mediastinal mass | no | yes |
initial WBC | <20x 109/L | >20x 109/L |
hemoglobin | > 100 g/L | < 100 x g/L |
IDH | low | high |
lymphoblasts | typical | undifferentiated |
hyperploidy | yes | no |
translocation | no | yes |
LYMPHOMA
- third most common childhood tumour
HodgkinÃs lymphoma
- older children (age > 15), similar to adult HodgkinÃs
- presents with painless, firm lymphadenopathy
- B symptoms only in 30% of children
Non-HodgkinÃs lymphoma
- younger children (7-11 years)
- rapidly growing tumour with distant metastases
- signs and symptoms related to disease site, most commonlyabdomen, chest (mediastinal mass), head and neck region
- see also Hematology Notes
BRAIN TUMOURS
- predominantly infratentorial involving cerebellum, midbrain, brainstem
- glial (astrocytomas most common) or primitive neuroectodermal
(medulloblastoma, germ cell tumours, ependymothera)
signs and symptoms
- infratentorial: vomiting, morning headache, increased head circumference, ataxia, diplopia, nystagmus, papilledema
- supratentorial: focal deficits, seizure, long tract signs
Evaluation
- history, physical exam including complete neurological exam
- CT and/or MRI of head as indicated
- see also Neurosurgery Notes