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LEUKEMOID &
LEUKOERYTASTIC
REACTION
Leukemoid reaction
• Secondary reversible marked increase of WBC count
>50000/cumm in response to a stimulus & immature
WBCs(blasts<5%) in peripheral blood resembling
leukaemia
• Seen in non leukemic conditions
Causes
Myeloid leukemoid reaction Lymphoid leukemoid reaction
Severe bacterial infection
e.g – Pneumonia, endocarditis,
Septicemia & cellullitis
Viral infections : IMN, chicken pox,
mumps, scarlet fever
Severe acute hemolysis Bacterial infections : TB, syphilis
Cancer metastatic to bone marrow
Others : eclampsia, burns, mercury
poisoning
Eosinophilic leukemoid reaction
Allergic states – asthma, urticaria
Parasitic diseases
Myeloid leukaemoid reaction
• Total WBC count increased (>50,000/cumm)
• Shift to left up to myelocyte
Differential diagnosis
Parameters Leukemoid
reaction
CML CNL
Age Any age Middle age Elderly
C/F As per
underlying cause
Splenomegaly + Hepatoslpenomegal
y
RBC Anaemia
minimal
Severe &
progressive
normal
TLC >50,000/cumm 50,000 -
morethan 1
lakh/cumm
> 25,000/cumm
LAP score Increased Decreased High
Cytogenetics nil BCR- ABL fusion BCR- ABL (-) &
CSF3R mutation(+)
Extra
medullary
myeloid
tumours
Absent Present Absent
Parameter Laekemoid reaction CML CNL
Peripheral smear Leukocytes of
mature forms, shift
to left , with
toxic granules
More immature
forms with basophilia
& eosinophilia.
Marked neutrophilia
with Pro myelo, meta
myelo & myelocytes
(<10%),
Band forms &
segmented forms
(>80%)
Bone marrow Hyper cellular
Myeloid hyperplasia,
orderly maturation
Markedly
Hypercellular with
Slight incraese in
blasts,
Pseudo gaucher cells
Hypercellular &
packed bone marrow
with increased
neutrophils,
myeloblast <5%
Leukemoid reaction
CML
CNL
Lymphoid leukemoid reaction
• Main differential is CLL/SLL
Parameters Lymphoid leukemoid
reaction
CLL
Age Any age > 60yrs
Onset Acute Insidious
Peripheral smear Reactive atypical lymphocytes Small lymphocytes,
Smudge cells
Clinical course Self limiting Progressive
Differentiation of leukaemoid reaction from
leukaemia
1. Clinical presentation
2. Presence of underlying condition
3. Morphology of blood smear
4. % of blasts in bone marrow
5. Correction of leukaemoid picture after treatment
of underlying disease
Leukoerythroblastic reaction
• Presence of immature neutrophil series & nucleated
red cells in peripheral blood
• WBC count – Normal/high
• Anaemia & high RDW
• Due to disturbance in bone marrow architecture
• This is known as myelophthisic anaemia
Mechanism
Two major mechanisms
- Altered marrow- blood barrier  due to marrow
infiltration
- Extra medullary haematopoiesis  as a
compensatory response to bone marrow stress
Causes
• Infectious diseases – miliary TB
• Cancers metastasize to bone marrow( m/c)– ca.lung, breast, prostate,
GIT, thyroid & kidney
• Haematological disorders - myelofibrosis,
thalassemia major after splenectomy,
haemolytic anaemia
lymphoma &
multiple myeloma
• Storage disorders (rare) - Gaucher’s disease
Niemann- pick disease
• RBC – Anisopoikilocytosis hypochomia
TEAR DROP cells, polychromasia
NRBCs
Retic Count (3-10%)
• WBC – Normal / Increased / Reduced
Shift to left
• Platelets - Normal / Reduced / Increased in
myelofibrosis abnormally large
• Bone marrow biopsy is necessary in all cases for definitive
diagnosis
Peripheral smear
References
• Robbins & Cotran pathologic basis of disease
• de Gruchy’s clinical haematology
• WHO tumours of haematolymphoid system

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Leukemoid and lekoerythroblastic reaction

  • 2. Leukemoid reaction • Secondary reversible marked increase of WBC count >50000/cumm in response to a stimulus & immature WBCs(blasts<5%) in peripheral blood resembling leukaemia • Seen in non leukemic conditions
  • 3. Causes Myeloid leukemoid reaction Lymphoid leukemoid reaction Severe bacterial infection e.g – Pneumonia, endocarditis, Septicemia & cellullitis Viral infections : IMN, chicken pox, mumps, scarlet fever Severe acute hemolysis Bacterial infections : TB, syphilis Cancer metastatic to bone marrow Others : eclampsia, burns, mercury poisoning Eosinophilic leukemoid reaction Allergic states – asthma, urticaria Parasitic diseases
  • 4. Myeloid leukaemoid reaction • Total WBC count increased (>50,000/cumm) • Shift to left up to myelocyte
  • 5. Differential diagnosis Parameters Leukemoid reaction CML CNL Age Any age Middle age Elderly C/F As per underlying cause Splenomegaly + Hepatoslpenomegal y RBC Anaemia minimal Severe & progressive normal TLC >50,000/cumm 50,000 - morethan 1 lakh/cumm > 25,000/cumm LAP score Increased Decreased High Cytogenetics nil BCR- ABL fusion BCR- ABL (-) & CSF3R mutation(+) Extra medullary myeloid tumours Absent Present Absent
  • 6. Parameter Laekemoid reaction CML CNL Peripheral smear Leukocytes of mature forms, shift to left , with toxic granules More immature forms with basophilia & eosinophilia. Marked neutrophilia with Pro myelo, meta myelo & myelocytes (<10%), Band forms & segmented forms (>80%) Bone marrow Hyper cellular Myeloid hyperplasia, orderly maturation Markedly Hypercellular with Slight incraese in blasts, Pseudo gaucher cells Hypercellular & packed bone marrow with increased neutrophils, myeloblast <5%
  • 8. CML
  • 9. CNL
  • 10. Lymphoid leukemoid reaction • Main differential is CLL/SLL Parameters Lymphoid leukemoid reaction CLL Age Any age > 60yrs Onset Acute Insidious Peripheral smear Reactive atypical lymphocytes Small lymphocytes, Smudge cells Clinical course Self limiting Progressive
  • 11.
  • 12. Differentiation of leukaemoid reaction from leukaemia 1. Clinical presentation 2. Presence of underlying condition 3. Morphology of blood smear 4. % of blasts in bone marrow 5. Correction of leukaemoid picture after treatment of underlying disease
  • 13. Leukoerythroblastic reaction • Presence of immature neutrophil series & nucleated red cells in peripheral blood • WBC count – Normal/high • Anaemia & high RDW • Due to disturbance in bone marrow architecture • This is known as myelophthisic anaemia
  • 14. Mechanism Two major mechanisms - Altered marrow- blood barrier  due to marrow infiltration - Extra medullary haematopoiesis  as a compensatory response to bone marrow stress
  • 15. Causes • Infectious diseases – miliary TB • Cancers metastasize to bone marrow( m/c)– ca.lung, breast, prostate, GIT, thyroid & kidney • Haematological disorders - myelofibrosis, thalassemia major after splenectomy, haemolytic anaemia lymphoma & multiple myeloma • Storage disorders (rare) - Gaucher’s disease Niemann- pick disease
  • 16. • RBC – Anisopoikilocytosis hypochomia TEAR DROP cells, polychromasia NRBCs Retic Count (3-10%) • WBC – Normal / Increased / Reduced Shift to left • Platelets - Normal / Reduced / Increased in myelofibrosis abnormally large • Bone marrow biopsy is necessary in all cases for definitive diagnosis
  • 18. References • Robbins & Cotran pathologic basis of disease • de Gruchy’s clinical haematology • WHO tumours of haematolymphoid system