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MSc Biomedical Science Haematology (London UK)
BS Hons MLT (RMC)
 Presence of > 30% blasts in the bone marrow
at clinical presentation
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.
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
Marked cervical lymphadenopathy
in in a patient with Acute Lymphoblastic
Leukaemia
Purpura over the lower limbs in a
Patient with acute leukaemia
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
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
Acute Leukemia - Morphology
ACUTE LYMPHOBLASTIC LEUKEMIA
L1 - small cells with scant cytoplasm
Acute Lymphoblastic Leukaemia FAB Type ALL – L2
Large Heterogeneous population of blast cells; Nucleolated;
Low N: C ratio.
Acute Leukemia - Morphology
ACUTE LYMPHOBLASTIC LEUKEMIA
L2 - Large cells with variable cytoplasm, irregular
nuclear contours with clefting, and prominent one or
more nucleoli.
Acute Lymphoblastic Leukaemia FAB Type ALL – L3:
Lymphoblasts with strongly basophilic cytoplasm and showing
vacuolation. (B-ALL)
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.
Acid Phosphatase staining in ALL: Showing cytoplasmic positivity; Localized
staining in the Golgi zone. Reaction is typical of T- ALL
Periodic Acid Schiff (PAS) stain (Identifies glycogen, polysaccharides
and mucin)
in Acute Lymphoblastic Leukaemia
Block Positivity of Cytoplasm. Typical of B- ALL
 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
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+)
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.
ALL_Naseem. Acute Lymphoblastic leukemia presentation PPTpdf

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ALL_Naseem. Acute Lymphoblastic leukemia presentation PPTpdf

  • 1.
  • 2. MSc Biomedical Science Haematology (London UK) BS Hons MLT (RMC)
  • 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
  • 6. Marked cervical lymphadenopathy in in a patient with Acute Lymphoblastic Leukaemia
  • 7. Purpura over the lower limbs in a Patient with acute leukaemia
  • 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.