Malignancy Flashcards

1
Q

Common cancers before 6yrs old

A

Neuroblastoma

Wilm’s tumour

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2
Q

Common cancers in adolescence

A

Hodgkin lymphoma

Bone

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3
Q

Most common childhood cancer

A

Leukaemia

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4
Q

Side effects of chemotherapy

A
Bone marrow suppression = anaemia
Immunosuppression = infections
Nausea and vomiting
Anorexia = malnutrition
Alopecia
Headache
Muscle atrophy
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5
Q

Most common childhood leukaemia

A

Acute lymphoblastic leukaemia

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6
Q

2 types of Acute lymphoblastic leukaemia

A

B and T lymphoblastic leukaemia

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7
Q

Clinical features of acute lymphoblastic leukaemia

A
Pancytopenia = pallor, anaemia, bleeding, bruising, nose bleeds, infections.
Fatigue, malaise, anorexia
Bone pain
Painless lumps in neck, axilla and groin
Hepatosplenomegaly
Headaches
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8
Q

Investigations for acute lymphoblastic leukaemia

A

FBC = normocytic normochromic anaemia. Thrombocytopenia/Low platelets, can get low WWC.
High lactate dehydrogenase, high urate.
Bone marrow biopsy diagnostic, shows blast nucleated cells.
LP = CSF high protein, low glucose, pleocytosis (high lymphocytes)
CXR = mediastinal mass in T cell type.

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9
Q

Onset of symptoms of ALL and age

A

Within 4 weeks, 2-6yrs.

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10
Q

Complication of ALL

A

Febrile neutropenic sepsis
Metastasis to CNS
Poor growth

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11
Q

Management of ALL

A

Chemotherapy in 3 stages:
Induction treatment - aim to achieve remission, vincristine, dexamethasone + asparaginase.
Consolidation treatment - exterminate residual disease.
Maintenance treatment - extend remission, methotrexate and mercaptopurine.

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12
Q

2 main types of brain tumours in kids

A

Astrocytoma

Medulloblastoma

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13
Q

CFx of lymphoma

A

Painless lymphadenopathy (mostly neck)
Longer history of symptoms than leukaemia.
Cough

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14
Q

Febrile neutropenic sepsis

A

Septicaemia

Piptazobactam and gentamicin.

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15
Q

Risk factors for ALL

A

Down syndrome
Philedelphia chromosome
Radiation exposure

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16
Q

High risk ALL

A

Age less than 1yr or greater than 10yrs
WCC greater than 50,000
CNS or testicular involvement
Genetics such as philedelphia chromosome.

17
Q

Name 3 types of brain cancers

A

Astrocytoma from glial cells
Craniopharyngioma (cause bilateral homonymous hemianopia)
Medulloblastoma.

18
Q

Presentation of brain tumour

A
Headache - worse on lying down
Early morning vomiting.
Squint, nystagmus, papilloedema
Ataxia
Personality and behaviour changes.
19
Q

Investigations for brain tumour

20
Q

Management of a brain tumour

A

Surgical resection if appropriate location (not brainstem!)

Radio +/- chemotherapy depending on age.

21
Q

Name of a neuroendocrine tumour

A

Neuroblastoma

22
Q

Origins of a neuroblastoma

A

adrenal medulla or sympathetic nervous system Rea e.g. sympathetic chain.

23
Q

Age of neuroblastoma

24
Q

Clinical features of a neuroblastoma

A
Englarged abdomen
Abdominal mass
Weight loss
Hepatomegaly
Limp and bone pain
Symptoms of compression of local structure or spinal root.
25
Investigations for neuroblastoma
CT and check for metastasis High urine catecholamine Biopsy
26
Management of neuroblastoma
Surgery +/- chemotherapy | If severe stem cell transplant
27
Name 2 types of bone tumours
Osteogenic sarcoma (most common, esp in older children). Ewing's sarcoma (more common in younger)
28
Age and gender of bone tumour
POST or during puberty! male
29
Presentation of bone tumour
limp and bain
30
Investigations and features of bone tumour
x-ray = nidus with central high density area, sclerosis or periosteal reaction, moth-eaten appearance. MRI Bone scan
31
Management of bone tumour
Chemotherapy before surgery (endo-prosthetic resection)
32
Name a kidney tumour
Nephroblastima/Wilm's
33
Clinical features of a kidney tumour
Painless, abdominal mass Haematuria Hypertension Anorexia
34
Investigations for a nephroblastoma
US/CT/MRI | Show distorted renal structure
35
Management of a nephroblastoma
Chemo before and after nephrectomy or resection. | Radiotherapy if advanced/high-grade.