Leukaemia Flashcards

1
Q

Presentation of leukaemia (8)

A

Fatigue

Fever

Failure to thrive (children)

Pallor due to anaemia

Petechiae and abnormal bruising due to thrombocytopenia

Abnormal bleeding

Lymphadenopathy

Hepatosplenomegaly

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2
Q

avg ages of different leukaemias

A

Under 5 and over 45 – acute lymphoblastic leukaemia (ALL)

Over 55 – chronic lymphocytic leukaemia (CeLLmates)

Over 65 – chronic myeloid leukaemia (CoMmon)

Over 75 – acute myeloid leukaemia (AMbitions)

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3
Q

Differential Diagnosis of Petechiae

A

Leukaemia

Meningococcal septicaemia

Vasculitis

Henoch-Schonlein Purpura (HSP)

Idiopathic Thrombocytopenia Purpura (ITP)

Non-accidental injury

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4
Q

Investigations for leukaemia (8)

A

Full blood count

Blood film

Lactate dehydrogenase (LDH) - often raised in leukaemia

Bone marrow biopsy

CXR

Lymph node biopsy

Lumbar puncture

CT, MRI and PET

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5
Q

Acute Lymphoblastic Leukaemia

A

Malignant change in one of the lymphocyte precursor cells

Acute proliferation of a single type of lymphocyte (usually B-lymphocytes)

Often associated with Downs syndrome
Blood film shows blast cells
Associated with the Philadelphia chromosome (t(9:22) translocation) in 30% of adults

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6
Q

Chronic Lymphocytic Leukaemia

A

Chronic proliferation of a single type of well differentiated lymphocyte (usually B-lymphocytes)

Can cause warm autoimmune haemolytic anaemia
Can transform into high-grade lymphoma - Richter’s transformation

Blood film shows “smear” or “smudge” cells

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7
Q

Three typical phases of Chronic Myeloid Leukaemia

A

Chronic phase (5 years - often asymptomatic)

Accelerated phase (abnormal blast cells take up a high proportion of the cells in the bone marrow and blood - patients become symptomatic)

Blast phase (even higher proportion of blast cells and blood [>30%] severe symptoms and pancytopenia. It is often fatal

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8
Q

What translocation is associated with CML

A

Philadelphia chromosome

Translocation of genes between chromosome 9 and 22

t(9:22) translocation

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9
Q

Acute Myeloid Leukaemia

A

Most common acute leukaemia in adults

Can be the result of a transformation from a myeloproliferative disorder such as polycythaemia ruby vera or myelofibrosis

Blood film - blast cells. These blast cells can have rods inside their cytoplasm that are named Auer rods

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10
Q

Management of leukaemia

A

Usually trteated with chemotherapy and steroids

Other therapies include:

Radiotherapy
Bone marrow transplant
Surgery

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11
Q

Complications of Chemotherapy

A

Failure

Stunted growth and development in children

Infections due to immunodeficiency

Neurotoxicity

Infertility

Secondary malignancy

Cardiotoxicity

Tumour lysis syndrome

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12
Q

Tumour Lysis Syndrome

A

Caused by the release of uric acid from cells that are being destroyed by chemotherapy

Can form crystals in the interstitial tissue and tubules of the kidneys and causes acute kidney injury

Allopurinol or rasburicase are used to reduce the high uric acid levels

Potassium and phosphate are also released so these need to be monitored
High phosphate can lead to low calcium

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