3. Presence of > 30% blasts in the bone marrow
at clinical presentation
4. Acute Lymphoblastic Leukaemia is
the common form of leukaemia in
children
Its incidence is highest at 3 – 7 years,
falling off by 10 years.
There is a lower frequency of ALL
after 10 years of age with a secondary
rise after the age of 40.
5. CLINICAL FEATURES OF
ACUTE LYMPHOBLASTIC
LEUKAEMIA
Clinical features are secondary to the following:
1. Bone Marrow Failure leading to:
- Anaemia (pallor; lethargy; dyspnoea)
- Neutropenia (fever; malaise; features of mouth ,
throat, skin, respiratory, perianal or other infections)
- Thrombocytopenia (spontaneous bruises; purpura;
bleeding gums and menorrhagia)
2. Organ infiltration – tender bones, lymphadenopathy,
moderate splenomegaly, hepatomegaly
If CNS involvement then headache, nausea,
vomiting blurring of vision and diplopia
Testicular infiltration
8. FAB Classification of Acute Lymphoblastic leukaemia
ALL – L1: Small monomorphic blasts with high N:C ratio
ALL – L2: Large. hetrogenous,nucleolated , low N:C ratio
ALL - L3: Burkitt type , basophilic and vacuolated
cytoplasm. (B-ALL)
The L1 blast show uniform, small uniform, small blast
cells with scanty cytoplasm.
The L2 type comprise mixed population of small and
large blasts with more prominent nucleoli and cytoplasm.
The L3 blasts are large with prominent nucleoli.
strongly basophilic cytoplasm and cytoplasmic vacuoles.
FRENCH AMERICAN AND BRITISH (FAB)
CLASSIFICATION OF ACUTE LYMPHOBLASTIC
LEUKAAEMIAS
9. Acute Lymphoblastic Leukaemia:
FAB Type ALL – L1
Lymphoblasts show monomorphic
appearance, very high N:C ratio;
Nucleoliare indistinct; Chromatin is
course and there is condensation
of chromatin along nuclear membrane
P. Film analysis
10. Acute Leukemia - Morphology
ACUTE LYMPHOBLASTIC LEUKEMIA
L1 - small cells with scant cytoplasm
11. Acute Lymphoblastic Leukaemia FAB Type ALL – L2
Large Heterogeneous population of blast cells; Nucleolated;
Low N: C ratio.
12. Acute Leukemia - Morphology
ACUTE LYMPHOBLASTIC LEUKEMIA
L2 - Large cells with variable cytoplasm, irregular
nuclear contours with clefting, and prominent one or
more nucleoli.
13. Acute Lymphoblastic Leukaemia FAB Type ALL – L3:
Lymphoblasts with strongly basophilic cytoplasm and showing
vacuolation. (B-ALL)
14. Acute Leukemia - Morphology
ACUTE LYMPHOBLASTIC LEUKEMIA
L3 - Medium to large cells
with moderately
abundant intensely
basophilic cytoplasm
and prominent
cytoplasmic vacuolation,
regular nuclear contours,
prominent nucleoli.
15. Acid Phosphatase staining in ALL: Showing cytoplasmic positivity; Localized
staining in the Golgi zone. Reaction is typical of T- ALL
16. Periodic Acid Schiff (PAS) stain (Identifies glycogen, polysaccharides
and mucin)
in Acute Lymphoblastic Leukaemia
Block Positivity of Cytoplasm. Typical of B- ALL
17. WBC normal, upto 200*109/l or ( 4.00-11.0 x
10 9/L)
P film morphology
Bone marrow hypercellular >30% leukemic blasts
X-rays lytic bone lesions & mediastinal mass
Immunophenotyping CD2,CD3,CD7 positive in T-
ALL
Cd 79a, CD19,CD22,CD10 positive in B-LL
Cytogenetic analysis
Biochemical tests uric acid , serum LDH hyper
calcemia
Lumbar puncture CSF pressure & Leukaemic cells
18.
19.
20. Determinant Favourable Unfavourable
Age 3-7 yrs <1, >10 yrs
Sex Female Male
Race White Black
WBC Count <10 X 10 9/l >50 X10 9/l
Time of Remission <4weeks >4 weeks
Organomegaly Absent Massive
Mediastinal mass Absent Present
CNS Leukaemia Absent Present
FAB Morphology L1 L2,L3
Immunophenotype Early Pre B cell T-cell,B-cell
Cytogenetics Hyperdiploidy Pseudodiploidy
t(9;22)
t(8;14)
t(4;11)
t(14q+)
21. TREATMENT OF ACUTE LEUKAEMIAS
General Supportive Treatment:
Blood products support to treat anaemia and
thrombocytopenia.
Antibiotic coverage to treat infections.
Insertion of central venous catheter (Hickman) via a
skin tunnel from the chest into the superior vena cava to
give access for giving chemotherapy , blood products,
antibiotics, intravenous feeding, etc.
Prevention of vomiting.