Transcript Leukemia - Shanyar

LEUKAEMIA
DIAGNOSIS
Leukaemia is a disease resulting from the
neoplastic proliferation of haemopoietic
or lymphoid cells.
Leukaemias are broadly divided into:
(i) Acute leukaemias, which, if untreated, lead to
death in weeks or months.
(ii) chronic leukaemias, which, if untreated, lead
to death in months or years.
They are further divided into lymphoid, myeloid and
biphenotypic leukaemias, the latter showing both
lymphoid and myeloid differentiation.
Acute leukaemias are characterized by a defect in
maturation, leading to an imbalance between
proliferation and maturation; since cells of the leukaemic
clone continue to proliferate without maturing to end
cells.
Diagnosis of leukaemia.
The diagnosis of leukaemia and categorization
required the following parameters.
1- Morphology.
2-Cytochimestry
3-Immunophenotyping.
4-Cytogenetic.
5- Molecular study.
Acute Lymphoblastic Leukaemia
Background
Acute lymphoblastic leukemia (ALL) is the most common
malignancy diagnosed in children, representing nearly
one third of all pediatric cancers.
The annual incidence rate for acute lymphoblastic
leukemia is 30.9 cases per million population. The peak
incidence occurs in children aged 2-5 years.
Pathophysiology
In acute lymphoblastic leukemia, a lymphoid
progenitor cell becomes genetically altered
and subsequently undergoes dysregulated
proliferation, survival, and clonal expansion.
In most cases, the pathophysiology of transformed
lymphoid cells reflects the altered expression of
genes whose products contribute to the normal
development of B cells and T cells
Clinical feature.
Children with acute lymphoblastic leukemia (ALL) generally
Present with signs and symptoms that reflect bone marrow
infiltration and extramedullary disease.
Because leukemic blasts replace the bone marrow, patients
Present with signs of bone marrow failure, including anemia,
thrombocytopenia, and neutropenia.
Clinical manifestations include fatigue and pallor, petechiae and
bleeding, and fever.
In addition, leukemic spread may manifest as lymphadenopathy
And hepatosplenomegaly. Other signs and symptoms of leukemia
including weight loss, bone pain, and dyspnea.
The classification of ALL
FAB classification.
L1 ALL
L2 ALL
Cell size
Mainly small
Nuclear chromatin
Fairly homogeneous Heterogeneous
Nuclear shape
Mainly regular
Irregular; clefting
Nucleolus
Not visible
Usually visible
L3 ALL
Large, heterogeneous Large, homogeneous
Finely stippled,
Regular
Usually prominent
Amount of cytoplasm
Scanty Variable
abundant
Moderately abundant
Cytoplasmic basophilia
Slight to moderate
Variable
Strong
Cytoplasmic vacuolation
Variable
Variable
Often prominent
Clinical correlates of FAB categories of ALL
Many cases of L3 ALL represent a distinct entity that
requires specific management. However, the categorization
of a case as L1 or L2 ALL is of little importance.
The FAB L1 category includes more childhood
cases with a relatively good prognosis.
The incidence of ALL L1 falls with increasing age whereas
the incidence of ALL L2 does not vary much with age.
ALL L2 has generally been found to have a worse
prognosis, although the difference is not major.
WHO proposed classification of acute lymphoblastic leukemia
The recent WHO International panel on ALL recommends that
the FAB classification be abandoned, since the morphological
classification has no clinical or prognostic relevance.
1- Acute lymphoblastic leukemia/lymphoma Synonyms:
Former Fab L1/L2
i. Precursor B acute lymphoblastic leukemia/lymphoma.
Cytogenetic subtypes:
 t(12;21)(p12,q22) TEL/AML-1
 t(1;19)(q23;p13) PBX/E2A
 t(9;22)(q34;q11) ABL/BCR
 T(V,11)(V;q23) V/MLL
ii. Precursor T acute lymphoblastic leukemia/lymphoma
2- Burkett's leukemia/lymphoma Synonyms: Former FAB L3
3- Biphenotypic acute leukemia
Immunophenotyping
Characterization of the Immunophenotyping is referred to as
Immunophenotyping and is achieved by means of labeled
antibodies that recognize specific epitopes of cellular antigens.
In general, the most useful antibodies are monoclonal antibodies
(McAb) produced by hybridoma technology but, for some antigens,
polyclonal antibodies (PcAb) (antisera) are better.
The technique employed for Immunophenotyping may be
immunocytochemistry or, much more often, flow cytometry.
Immunophenotyping is essential for the diagnosis of B- or T-lineage
acute lymphoblastic leukaemia (ALL).
First panel
B lymphoid CD19, CD22, CD79a, CD10
T lymphoid CD3, CD2, CD7
Second panel
If B lineage cm, k, l, CD20, CD24
If T lineage CD1a, SmCD3, CD4, CD5, CD8, anti-TCR
ab, anti-TCR gd
Cytogenetic study.
With techniques now available, 70–90% of cases of ALL
have a demonstrable cytogenetic abnormality.
In ALL, chromosomal abnormalities correlate
with other clinical and hematological factors
of prognostic importance but they also have
a considerable independent prognostic
significance.
B-lineage ALL
L1
L1
L1
L1
L1
high/ hyperdiploidy.
or L2/t(9;22)/BCR-ABL fusion
or L2/t(4;11)(q21;q23)
or L2/t(12;21)(p12;q22)/early precursor or common ALL
or L2/t(1;19)(q23;p13)/pre-B ALL
T-lineage ALL.
L1 or L2/t(10;14)(q24;q11)
Burkett's-lineage
L3/t(8;14)(q24;q32) or t(8;22)(q24;q11) or
t(2;8)(p12;q24).
Acute Myeloblastic Leukaemia
Distinguishing between AML and ALL
Correct assignment of patients to the categorize
AML and ALL is very important for prognosis
and choice of therapy.
The FAB group recommended the use of
MPO,SBB and non-specific esterase (NSE)
stains.
If Cytochemical reactions for myeloid cells are
negative, presumptive diagnosis of ALL must
be confirmed Immunophenotyping.
Background.
AML is the most common acute leukaemia affecting
adults, and its incidence increases with age.
Although AML is a relatively rare disease, accounting for
approximately 1.2% of cancer deaths in the United
States, its incidence is expected to increase as the
population ages.
Pathophysiology.
The malignant cell in AML is the myeloblast.
In normal haematopoiesis, the myeloblast is an immature precursor
of myeloid white blood cells; a normal myeloblast will gradually
mature into a mature white blood cell.
However, in AML, a single myeloblast accumulates genetic changes
which "freeze" the cell in its immature state and prevent
differentiation Such a mutation alone does not cause leukemia;
however, when such a "different combined with other maturation
which disrupt genes controlling proliferation, the result is the
uncontrolled growth of an immature clone of cells, leading to the
clinical entity of AML.
Clinical feature.
The symptoms of AML are caused by replacement of
normal bone marrow with leukemic cells, which causes a
drop in red blood cells, platelets, and normal white blood
cells.
These symptoms include fatigue, shortness of breath,
easy bruising and bleeding, and increased risk of
infection
The classification of AML
FAB classification.
M0 Undifferentiated acute myeloblastic leukemia.
M1 Acute myeloblastic leukemia with minimal maturation.
M2 Acute myeloblastic leukemia with maturation.
M3 Acute promyelocytic leukemia.
M4 Acute myelomonocytic leukemia.
M4 eosAcute myelomonocytic leukemia with eosinophilia.
Acute monocytic leukemia.
M6 Acute erythroid leukemia.
M7 Acute megakaryoblastic leukemia.
Criteria for the diagnosis of acute myeloid
leukaemia of M0
Blasts .30% of bone marrow nucleated cells
Blasts .30% of bone marrow non-erythroid cells <3%
of blasts positive for Sudan black B or for myeloperoxidase
by light microscopy.
Blasts demonstrated to be myeloblasts by immunological
markers or by ultrastructural cytochemistry.
AML M0 without differentiation
Criteria for the diagnosis of acute myeloid
leukaemia of M1.
Blasts 30% of bone marrow cells .Blasts .90% of bone marrow
non-erythroid cells .3% of blasts positive for peroxidase or
Sudan black B
Bone marrow maturing monocytic component (promonocytes to
monocytes) .10% of non-erythroid cells
Bone marrow maturing granulocytic component (promyelocytes to
polymorphonuclear leucocytes) .10% of non-erythroid cells
AMLM1 with minimal maturation.
Criteria for the diagnosis of acute myeloid
leukaemia of M2.
Blasts 30% of bone marrow cells. Blasts 30–89% of bone marrow
non-erythroid cells
Bone marrow maturing granulocytic component (promyelocytes to
polymorphonuclear leucocytes) >10% of non-erythroid cells
Bone marrow monocytic component (monoblasts to monocytes)
<20% of non-erythroid cells and other criteria for M4 not met
AML M2 shows Auer Rod and maturation
Acute hypergranular promyelocytic
Leukaemia M3 AML
In acute hypergranular promyelocytic
leukaemia the predominant cell is a highly
abnormal promyelocyte.
In the majority of cases, blasts are fewer than
30% of bone marrow nucleated cells. The
distinctive cytological features are sufficient to permit a
diagnosis and
In some cases there are giant granules or
multiple Auer rods, which are often present
in sheaves or ‘faggots’. Most cases have a minority of cells
that are agranular.
M3 AML has been found to be very sensitive
to the differentiating capacity of all-transretinoic acid (ATRA). Following such therapy
an increasing proportion of cells beyond the
promyelocyte stage are apparent.
AML M3 leukaemic promyelocytes
AML M3
Criteria for the diagnosis of acute myeloid
leukaemia of M4.
Blasts .30% of bone marrow cells
Blasts .30% of bone marrow non-erythroid cells
Bone marrow granulocytic component 20% of non-erythroid cells
Significant monocytic component as shown by one of the following:
Bone marrow monocytic component 20% of non-erythroid cells and
peripheral blood monocytic.
Bone marrow resembling M2 but peripheral blood monocytic
component .5000/cumm.
AML M4 myeloblast and leukaemic monocyte
Criteria for the diagnosis of acute myeloid
leukaemia of M5
Blasts .30% of bone marrow cells
Blasts .30% of bone marrow non-erythroid cells
Bone marrow monocytic component .80% of non-erythroid
cells
Acute monoblastic leukaemia (M5a)
Monoblasts .80% of bone marrow monocytic component
Acute monocytic leukaemia (M5b)
Monoblasts <80% bone marrow monocytic component
AML M5 monoblasts
Criteria for the diagnosis of acute myeloid
leukaemia of M6
Erythroblasts .50% of bone marrow
nucleated cells
Blasts 30% of bone marrow non-erythroid
cells
AML M6 erythroblasts
Criteria for the diagnosis of acute myeloid
leukaemia of M7
Blasts 30% of bone marrow nucleated cells.
Blasts demonstrated to be megakaryoblasts by
immunological markers, ultrastructural examination
or ultrastructural cytochemistry
AML M7 megakaryoblast
AML M7 many megakaryocytes
The WHO classification of AML.
Therapy-related AML and MDS. Alkylating agent-related Topoisomerase
II-inhibitor-related Other types
AML with recurrent cytogenetic abnormalities*
AML with t(8;21)(q22;q22)
AML with abnormal bone marrow eosinophils with
inv(16)(p13q22) or t(16;16)(p13;q22)
Acute promyelocytic leukemia with
t(15;17)(q22;q12)
AML with 11q23 (MLL) abnormalities.
AML with multilineage dysplasia following MDS.
AML not otherwise categorized. This group is nearly similar to FAB
group, but blast cells are 20% in stead of 30%
CHRONIC MYELOID
LEUKAEMIAS
The World Health Organization (WHO)
classification assigns some chronic myeloid
leukaemias to a myeloproliferative category and
others, in which there are also dysplastic
features, to a myeloproliferative/myelodysplastic
category
Classification of the chronic myeloid leukaemias,
based on the WHO classification.
Myeloproliferative disorders
Chronic myelogenous leukaemia Chronic neutrophilic
leukaemia
Chronic eosinophilic leukaemia
Basophilic leukaemia
Mast cell leukaemia
Myelodysplastic/myeloproliferative disorders
Chronic myelomonocytic leukaemia
Chronic myelomonocytic leukaemia with eosinophilia
Myelodysplastic/myeloproliferative disorder associated with
t(5;12)(q33;p13)*
Atypical chronic myeloid leukaemia
Juvenile myelomonocytic leukaemia
Chronic granulocytic leukaemia
Chronic granulocytic leukaemia (CGL) is a disease
entity with specific haematological, cytogenetic
and molecular genetic features.
Alternative designations are chronic myelogenous
leukaemia, chronic myeloid leukaemia and chronic
myelocytic leukaemia.
CGL is a disease of
bi- or triphasic with a chronic and an acute
phase and, sometimes, an intervening
accelerated phase
The chronic phase of chronic granulocytic
leukaemia
Clinical and haematological features.
CGL is predominantly a disease of adults. The usual clinical
presentation is with splenomegaly, hepatomegaly, symptoms
of anaemia, and systemic symptoms such as sweating and
weight loss.
Occasionally this is an incidental diagnosis when a blood
count is performed for another reason.
The peripheral blood usually shows anemia
and leucocytosis with a very characteristic
differential count.
The two predominant cell types are the myelocyte
and the mature neutrophil .
Almost all patients have an absolute
basophilia and more than 90% have
eosinophilia.
The platelet count is most often normal or
somewhat elevated but is low in about 5%
of cases.
BM film of a patient with CGL showing neutrophil leucocytosis with left shift.
The bone marrow is intensely hypercellular
with marked granulocytic hyperplasia and
with the myeloid/erythroid (M:E) ratio
being greater than 10:1.
There is hyperplasia of neutrophil,
eosinophil and basophil lineages.
Bone marrow shows myeloid hyperplasia.
CGL in accelerated phase and blast
Transformation
After a variable period in chronic phase, usually
several years, CGL undergoes further evolution.
There may be an abrupt transformation to an
Acute leukaemia, designated blast transformation,
or there may be an intervening phase of
accelerated disease.
The WHO group have suggested the following
criteria for accelerated phase:
(i) Myeloblasts constitute 10–19% of peripheral blood
white cells or bone marrow nucleated cells.
(ii) peripheral blood basophiles are 20% or more of
nucleated cells.
(iii) there is persistent thrombocytopenia or persistent
thrombocytosis that does not respond to treatment.
(iv) there is an increasing white cell count and increasing
spleen size that does not respond to treatment.
(v) cytogenetic evolution .
(vi) there is marked granulocyte dysplasia or prominent
proliferation of small dysplastic megakaryocytes in
large clusters or sheets.
Blast transformation phase.
Transformation may be myeloid or lymphoid.
It is important to make the distinction since
there lymphoblastic transformation. Lymphoid
blast crisis is more likely to emerge suddenly
without a preceding accelerated phase
Cytogenetic and molecular genetic features
CGL was the first malignant disease for which a
consistent association with an acquired nonrandom cytogenetic abnormality was recognized.
In 1960 Nowell and Hungerford reported its
Association with an abnormal chromosome designated the
Philadelphia (Ph) chromosome after the city of its
discovery.
Karyotype of a patient with CGL showing t(9;22)
Chronic lymphocytic leukaemia
Chronic lymphocytic leukaemia (CLL) is a chronic
B-lineage lymphoproliferative disorder defined by
characteristic morphology and immunophenotype.
Small lymphocytic lymphoma is an equivalent lymphoma
without circulating neoplastic cells
CLL is the most common leukaemia in western
Europe and North America with an incidence in
different surveys varying between 1 and more
than 10/100 000/year.
The incidence is lower in Chinese, Japanese and
South American Indians.
It is typically a disease of the elderly with a
higher incidence in males
Clinical feature.
In the later stages, CLL is characterized
by lymphadenopathy, hepatomegaly,
splenomegaly and eventually by impairment
of bone marrow function.
In the early stages of the disease there are
no symptoms or abnormal physical findings
and the diagnosis is made incidentally
Various arbitrary levels of absolute lymphocyte
count have been suggested for the diagnosis of
CLL (for example greater than 10 000/cumm).
But the demonstration of a monoclonal population
of B lymphocytes with a characteristic
immunophenotype permits diagnosis at an earlier
stage when the lymphocyte count is less elevated.
A scoring system for the immunophenotypic
diagnosis of chronic lymphocytic leukaemia (CLL)
Score 1 for each of the following:
• Weak expression of SmIg
• Expression of CD5
• Expression of CD23
• No expression of FMC7
• No expression of CD22
A score of ≥4 points is confirmatory of CLL
Peripheral blood chronic lymphocytic leukaemia showing
two mature lymphocytes and one smear cell
Peripheral blood findings
In the early stages of the disease the Peripheral
blood abnormality is confined to the lymphocytes.
Later in the disease course there is a normocytic,
normochromic anaemia and thrombocytopenia.
Neutropenia is uncommon unless cytotoxic therapy
has been administered
Bone marrow findings.
The bone marrow aspirate is hypercellular
as a consequence of infiltration by
lymphocytes with similar features to those
in the peripheral blood.
Lymphocytes percentage in the bone
marrow is 40% of all nucleated marrow cells total.
Rai staging system for chronic lymphocytic
leukaemia
0 Peripheral blood and bone marrow lymphocytosis only.
I Intermediate Lymphocytosis and lymphadenopathy.
II Intermediate Lymphocytosis plus hepatomegaly,
splenomegaly or both.
III Lymphocytosis and anaemia (haemoglobin
concentration less than 11 g/dl).
IV Lymphocytosis and thrombocytopenia (platelet count
less than 100 000/cmm)
CLL Transformation.
Chronic lymphocytic leukaemia may undergo
two types of transformation.
1-Prolymphocytoid transformation.
2-large cell transformation, referred to as
Richter’s syndrome.
CLL with transformation to PLL