Leukaemia Flashcards
Presentation of leukaemia (8)
Fatigue
Fever
Failure to thrive (children)
Pallor due to anaemia
Petechiae and abnormal bruising due to thrombocytopenia
Abnormal bleeding
Lymphadenopathy
Hepatosplenomegaly
avg ages of different leukaemias
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)
Differential Diagnosis of Petechiae
Leukaemia
Meningococcal septicaemia
Vasculitis
Henoch-Schonlein Purpura (HSP)
Idiopathic Thrombocytopenia Purpura (ITP)
Non-accidental injury
Investigations for leukaemia (8)
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
Acute Lymphoblastic Leukaemia
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
Chronic Lymphocytic Leukaemia
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
Three typical phases of Chronic Myeloid Leukaemia
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
What translocation is associated with CML
Philadelphia chromosome
Translocation of genes between chromosome 9 and 22
t(9:22) translocation
Acute Myeloid Leukaemia
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
Management of leukaemia
Usually trteated with chemotherapy and steroids
Other therapies include:
Radiotherapy
Bone marrow transplant
Surgery
Complications of Chemotherapy
Failure
Stunted growth and development in children
Infections due to immunodeficiency
Neurotoxicity
Infertility
Secondary malignancy
Cardiotoxicity
Tumour lysis syndrome
Tumour Lysis Syndrome
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