Leukaemia Flashcards

1
Q

what translocations are seen in Acute lymphocytic leukaemia?

A

10: 14
12: 21

4: 11
9: 22

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2
Q

what are the S&S of ALL?

A

childhood disease

Marrow failure symptoms

  • Pallor, SOB, lethargy
  • petechiae, purpuric rash
  • fever

Infiltrative symptoms

  • lymphadenopathy
  • hepatosplenomegaly
  • parotid enlargement
  • bone pain
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3
Q

what investigations are done in ALL and what is seen?

A

FBC

  • anaemia, neutropenia, thrombocytopenia
  • leukocytosis

peripheral blood smear
- leukaemic lymphoblasts

BM aspiration and biopsy

  • Hypercellularity
  • > 20% lymphoblasts

U&E’s

  • increased calcium due to bone infiltration
  • Increased K+ due to leukaemic cell lysis

Cytogenetics

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4
Q

define AML

A

expression of myeloid blasts in the bone marrow, peripheral blood or extramedullary tissues. Bone marrow blasts >20% is diagnostic

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5
Q

what are the chromosomal abnormalities in AML?

A

15:17
8:21
deletions at 5 or 7

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6
Q

what are the clinical features of AML?

A

disease of older age (AMLderly)

Marrow failure

  • anaemia symptoms
  • thrombocytopenic symptoms

Infiltrative

  • lymphadenopathy
  • hepatosplenomegaly
  • Gum swelling
  • Bone pain
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7
Q

What investigations are done in AML and what do they show?

A

FBC

  • anaemia, neutropenia, thrombocytopenia, large RBCs
  • leukocytosis

Blood film
- bilobed nuclei, hypergranulated blasts and AUER rods

Bone marrow aspiration and biopsy
- blast >20%, auer rods

U&E’s
- increased calcium, potassium and urea

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8
Q

what distinctive feature is present in the myeloid blast cells of AML?

A

Auer rods (Dan auerbach has AML)

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9
Q

what is chronic lymphocytic leukaemia?

A

indolent lymphoproliferative disorder in which monoclonal B lymphocytes are predominantly found in peripheral blood

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10
Q

what are the S&S of CLL?

A
anaemia 
lymphadenopathy 
hepatosplenomegaly 
recurrent infection 
B-symptoms 
petechiae
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11
Q

what are B-symptoms?

A

fever, chills, night sweats, weight loss and fatigue

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12
Q

what investigations are done in CLL and what would they show?

A

WBC count with differential
- lymphocytosis

Blood film
- smudge cells, spherocytes and polychromasia

FBC
- reduced Hb and platelets is not overly common but is poor prognostic indicator

Flow cytometry for CD5, CD19, CD20

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13
Q

how is CLL staged?

A
0 = lymphocytosis alone 
1 = lymphocytosis + lymphadenopathy 
2 = lymphocytosis + hepato/splenomegaly 
3 = lymphocytosis + anaemia 
4= lymphocytosis + thrombocytopenia

(ALHAT)

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14
Q

what is CML?

A

malignant clonal disorder of the haematopoietic stem cell that results in marked myeloid hyperplasia of bone marrow

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15
Q

what is the cytogenetic change in CML?

A

phildelphia chromosome

9:22 leading to BCR/ABL gene on Ch22

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16
Q

what are the S&S of CML?

A

mostly asymptomatic

B- symptoms

Features of gout due to increased purine breakdown

Hepatosplenomegaly and bruising

17
Q

What would investigations show in CML?

A

FBC

  • Increased WCC
  • Anaemia
  • Variable platelets

Peripheral blood smear

  • all WBC’s mature or maturing myeloids
  • elevated basophils and eosinophils
  • Absolute basophil >20% = accelerated phase of disease

Bone marrow biopsy
- hypercellular with granulocyte hyperplasia

cytogenetics
- phildelphia chromosome