Could this Child have Cancer Flashcards
Risk to having a childhood cancer
neurofibromastosis, immune defs, chromosomal instability (Fanconi anemia, ataxia
telangiectasia) genetic syndromes (Down syndrome, Turner’s Syndrome, overgrowth
syndrome)
Epi: most common (40% of all childhood cancers)
acute lymphoblastic leukemia
what symptoms of ALL are due to mass effect in the bone marrow?
Mass effect in bone marrow: ¯RBC (pallor, fatigue), ¯plt (bleeding, petechia, ecchymoses), ¯WBC
(fever, infection)
• Mass effect elsewhere: hepatosplenomegaly, lymphadenopathy, bone pain
investigations when a kid comes in with pallor, fatigue, petechiae, and lymphpenia
• CBC: WBC may or may not be elevated, anemia, thrombocytopenia
• Smear: atypical lymphocyte, leukemic blast cells
• Lymph Node Biopsy: indicated when continues to enlarge after 2-3wk or with Abx, symptoms,
supraclavicular LN
• Bone Marrow Aspiration: homogenous population, fewer normal populations, cellularity
Lymphoma
Epi: 3rd most common
Subtypes: Hodgkin’s (typically __); Non-Hodgkin’s Lymphoma (__more frequently, __ + __ defs common)
Symptoms: painless __, __ mass, pleural effusions, abdo mass, B symptoms (fever, __ __, wt loss)
Epi: 3rd most common
Subtypes: Hodgkin’s (typically teens); Non-Hodgkin’s Lymphoma (males more frequently, celiac + immune defs common)
Symptoms: painless lymphadenopathy, mediastinal mass, pleural effusions, abdo mass, B symptoms (fever, night sweats, wt loss)
most common brain tumour
medulloblastoma
headache features that are worrisome
- diminishes over the course of the day
- worse when lying down/recumbent
- worsen over time
- worsen with valsalva
- not laterallized (often front or back)
- focal neuro findings
when to image an aching head
- Presence or onset of neurologic abnormality
- Ocular findings, such as papilledema, decrease in vision
- Vomiting that is persistent, increasing in frequency, or preceded by headache
- Change in character of a headache
- Recurrent morning headaches or headaches that repeatedly wake a child
- Short stature or deceleration of linear growth
- Diabetes insipidus
- Age of three years of less
- Neurofibromatosis
- Macrocephaly in infants/toddlers
osteo vs ewing sarcoma
Bo ne Tumours Subtypes: osteosarcoma (long bones, older teens), Ewing Sarcoma (more prone to diaphysis of long bones or axial skeleton) Investigations: X-ray (low threshold) Management: refer to ortho/onco
Wilms’ tumours are located in the ___<
kidney
When to Biopsy a Lymph Node
With no laboratory or radiographic data to explain the large nodes:
Nodes that remain enlarged or continue to enlarge after ____weeks, particularly after a course of ___
Nodes that have not diminished in size after ___weeks or have not returned to normal by ___ weeks
When to Biopsy a Lymph Node
With no laboratory or radiographic data to explain the large nodes:
Nodes that remain enlarged or continue to enlarge after 2-3 weeks, particularly after a course of antibiotics
Nodes that have not diminished in size after 5-6 weeks or have not returned to normal by 10-12 weeks