Oncology Flashcards

1
Q

What is leukaemia?

A

Cancer of a particular line of stem cells in the bone marrow → causing unregulated production of certain types of blood cells

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1
Q

How are types of leukaemia classified?

A
  • How rapidly they progress → acute (fast) or chronic (slow)
  • Cell line affected → myeloid or lymphoid
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2
Q

Types of leukaemia that affect children
(from most to least common)

A
  • Acute lymphoblastic leukaemia (ALL) = the most common in children
  • Acute myeloid leukaemia (AML) = the next most common
  • Chronic myeloid leukaemia (CML) = rare
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3
Q

Most common leukaemia type found in children?

A

Acute lymphoblastic leukaemia

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4
Q

At what age does ALL and AML peak in children?

A
  • ALL peaks aged 2 – 3 years
  • AML peaks aged under 2 years
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5
Q

What does leukaemia causes to the other blood cell types?

A

Pancytopenia

  • Red blood cells (anaemia),
  • White blood cells (leukopenia)
  • Platelets (thrombocytopenia)

(The excessive production of a abnormal WBC - due to genetic mutation in preursor cell = can lead to suppression of the other cell lines, causing underproduction of other cell types)

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6
Q

What is the main environmental risk factor for childhood leukaemia?

A

Radiation exposure (e.g. with an abdominal xray during pregnancy)

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7
Q

Name a condition that predisposes a child to leaukaemia

A
  • Down’s syndrome
  • Kleinfelter syndrome
  • Noonan syndrome
  • Fanconi’s anaemia
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8
Q

Presentation of leukaemia

A

Typically non-specific:

  • Persistent fatigue
  • Unexplained fever
  • Failure to thrive
  • Weight loss
  • Night sweats
  • Pallor (anaemia)
  • Petechiae and abnormal bruising (thrombocytopenia)
  • Unexplained bleeding (thrombocytopenia)
  • Abdominal pain
  • Generalised lymphadenopathy
  • Unexplained or persistent bone or joint pain
  • Hepatosplenomegaly
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9
Q

Investigations for childhood leukaemia

A
  • Unexplained petechiae or hepatomegaly → immediate specialist assessment + urgent FBC (within 48 hours)

Ix to establish diagnosis:
* FBCanaemia, leukopenia, thrombocytopenia + high numbers of the abnormal WBCs
* Blood film → can show blast cells
* Bone marrow biopsy
* Lymph node biopsy

Further staging tests:
* Chest xray
* CT scan
* Lumbar puncture
* Genetic analysis and immunophenotyping of the abnormal cells

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10
Q

Management of childhood leukaemia

A

Chemotherapy

Others:
* Radiotherapy
* Bone marrow transplant
* Surgery

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11
Q

Complications of chemotherapy

A
  • Failure to treat the leukaemia
  • Stunted growth and development
  • Immunodeficiency and infections
  • Neurotoxicity
  • Infertility
  • Secondary malignancy
  • Cardiotoxicity
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12
Q

Prognosis for ALL and AML

A
  • ALL → approx. 80% (depends on individual factors)
  • AML → less positive
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13
Q

Info: Hepatoblastoma

A
  • Malignant tumour of liver - usually occurs in young children
  • Hepatoblastoma = different from hepatocellular carcinoma - which usually occurs in adults + occasionally older children
  • (The blastomas are the paediatric ones e.g. retinoblastoma, neuroblastoma etc)
  • Rare - 10 kids in UK per year

Presentation: Abdominal distension or with mass, pain and jaundice is ually rare
Ix: Elevated alpha-fetoprotein
Management: Chemotherapy, surgery, inoperable cases - liver transplant needed
Prognosis: generally good + children will be cured

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14
Q
A
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