Case 5 Leukemia Flashcards

1
Q

What is myeloid and lymphoid precursor?

A

Myeloid: platelets, RBC, macrophages, basophils/eosinophil/neutrophils
Lymphoid: T and B cells

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2
Q

What is the difference between acute and chronic leukemia?

A

acute: cells dont mature and remain in ‘blast’ form: monoblasts/myeloblasts…
chronic: similar appearance to mature cells but lack their functionality: monocytes, progranulocytes …

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3
Q

What is the symptoms for leukemia?

A
Anaemia
-	Fatigue
-	Dyspnoea
-	Palpitations
Thrombocytopenia
-	Easy bruising
-	Mucosal bleeding 
Leukopenia
-	Recurrent infection
Hepatomegaly, abdominal fullness
Blast cells infiltration of bone marrow
-	Pain and tenderness in bones
Lymphadenopathy 
-	More common in CLL and ALL as lymphoblasts settle more common in liver, spleen and lymph nodes
-	Mild and localised pain in lymph nodes
Swelling of gum 
-	Monocytic infiltration in AML
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4
Q

What is AML?

A
  • myeloidblasts
  • Common in older adults (average 65 yo)
  • Chromosomal translocation of 15 and 17
    associate with Down Syndrome (chromosome 21 trisomy)
  • Risk factor
    Exposure to radiation
    Alkylating chemotherapy
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5
Q

What is ALL?

A
Lymphoblasts
common in children 
-	Risk factor
Exposure to radiation
Alkylating chemotherapy
  • CNS/meninges involvement
  • Mediastinal involvement
  • Testicular involvement/enlargement
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6
Q

What is CML?

A
  • Caused by chromosomal translocation (Philadelphia chromosome 22)
    Chromosome 9 long arm and chromosome 22 long arm
  • BCR ABL gene
  • granulocytes
  • Retinal haemorrhage due to leukostaisis
  • GOUT due to purine breakdown from inc white cells
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7
Q

What are physical exams of leukemia?

A
  • Pallor
  • Fever due to infection
  • Petechiae, purpura
  • Bruising
  • Lymphadenopathy
  • Hepatosplenomegaly
  • Meningeal leukemia  infiltration of lymphocytes in meninges (ALL)
    Neck stiffness, purple rashes
    Brudzinski sign: hip and knee flex when neck is flexed
    Kernig sign: severe stiffness of hamstrings cause inability to straighten leg when hip is flexed at 90 degrees
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8
Q

What are some investigations for leukemia?

A
  • CBE
    Dec Hb/platelet, inc WBC
    EUC: inc uric acid, potassium and nitrates in cell lysis
  • Peripheral blood smear
    Myeloblasts: AML
    Lymphoblasts: ALL
  • Coagulation profile: do it for bleeding or petechiae
  • Bone marrow biopsy
    Inc blast cells to > 20% (normal is 1-2%)
    Inc lymphoblasts/myeloblasts
  • cytogenetics: philadelphia chromosomes

Differentiate AML and ALL

  • stained smear: myeloblasts are larger and finer chromatin, auer rods
  • immunophentotyping: express different CD receptors
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9
Q

What are some overall treatment options for leukemia?

A
	Chemotherapy
	Stem cell transplant
	Steroids
	TKI for CML
	Complication management
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10
Q

What is involved in leukemia chemo?

A
  • Cause apoptosis by initiating cellular stress pathways such as damaging DNA
  • Cell cycle will not continue  apoptosis caused by cellular checkpoints
  • Each dose kills a % of cells so repeating cycle eventually reduce tumour to 0

cytotoxic anti-neoplastic medication
- alkylating, antimetabolites, antimicrotubular, topoisomerase inhibitors, allopurinol

side effect of chemo
- nausea/vomiting, hair loss, easy bruising/bleeding

drugs treating nausea/vomiting
- ondansetron, dexamethasone, sedating anti-histamine, SP antagonists

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11
Q

What is involved in leukemia stem cell transplantation?

A
  • Transplantation of multipotent stem cells
  • Sources
    Bone marrow: pelvis, under general anaesthesia
    Peripheral blood stem cells: most common, donor’s blood pass through machine that removes WBC and RBC are returned to donor  blood stem cells lead to quicker recovery of marrow function following myeloblative chemotherapy
    Umbilical cord blood
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12
Q

What is involved in leukemia steroids?

A
dexamethasone
Short term adverse effect	
- Immunosuppression
- Mood changes (euphoria)
- Mood swings in between short term and long term
- Insomnia
- High blood glucose level	

Long term adverse effect

  • Significant immunosuppression
  • Mood changes (depression)
  • Osteoporosis
  • Weight gain
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13
Q

What is tyrosine kinase inhibitor in CML?

A

It targets BCR-ABL gene and inhibits the activity of tyrosine kinase
- First generation: imatinib
Well-tolerated and 87% of patients achieve complete haematological response
- Second generation: dasatinib, nilotinib
If patient is intolerant or unresponsive to first line

PCR for BRC-ABL is used for monitoring response to therapy
It is NOT a cure.

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14
Q

Failure of marrow failure

A
  • Iron/B12/folate deficiency
  • Marrow infiltration by lymphoma or non-haematological malignancy
  • Aplastic anaemia – viral, toxic, autoimmune
  • Chronic inflammatory disease – anaemia
  • Lack of simulating factors due to liver/renal disease  EPO, TPO
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15
Q

What are some causes of splenomegaly

A

Causes of splenomegaly (CHICAGO)

  • Cancer
  • Haematological (sickle cell anaemia, leukemia, lymphoma)
  • Infection/inflammation (Hep, HIV, TB, malaria)
  • Congestion (portal hypertension)
  • Autoimmune (Rheumatoid arthritis, SLE)
  • Glycogen storage disorders
  • Other
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