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Leukemia
—
Leukemia is a disease characterized by the progressive
overproduction of WBC which usually appear in the
circulating blood in an immature form.
—
It accounts 8% of all human cancers & is common
malignancy in children & young adults.
—
Proliferation takes place in the bone marrow and in
certain forms, the lymphoid tissues
Etiology –
—
Genetic Factors :
- Seen where there is a presence of congenital
disorders such as Down’s, Bloom’s, Kleinfelters
and Wiskott Aldrich Syndromes
—
Environmental
a) Ionising
Hiroshima and
Factors :
radiation (increased incidence in
Nagasaki)
b) Chemical Carcinogens
Benzene & Formaldehyde)
c) Drugs
(Alkylating agents –
—
Infection-EBV, HTLV-1
Pathogenesis –
—
Arises following malignant transformation of a single
clone of cells belonging to myeloid or lymphoid series
—
Acute leukemia :
- Defect in maturation beyond the myeloblast
level in AML and lymphoblast in ALL
—
Cells proliferate in the bone marrow and spread to
other tissues
—
Philapdelphia Chromosome –
- Thought to be a partial deletion of the long arm
of chromosome 22
- Now recognized to be the translocation of
chromosomal material from chromosome 22 to
chromosome 9
Classification:
—
Acute lymphocytic (lymphoblastic) leukemia
(ALL)
—
Chronic lymphocytic leukemia (CLL)
Both involve immature lymphocytes and their
progenitors in the bone marrow, the spleen, lymph
nodes, CNS, and other tissue
—
Acute myelogenous (myeloblastic) leukemia
(AML)
—
Chronic myelogenous leukemia (CML)
Both involve the pluri-potent myeloid stem cells in
bone marrow and interfere with the maturation of all
blood cells
CLASSIFICATION OF ACUTE LEUKAEMIAS
Acute Vs chronic leukemia
Acute Leukemia
—
It is characterized by neoplastic proliferation of large
number of abnormal immature leukocytes in the
marrow that infiltrate the lymph nodes,liver,spleen &
eventually all body systems.
—
In addition to this, production of other blood cells
inhibited.
are
—
Clinical manifestations are divided into 2 groups
- Due to bone marrow failure
- Due to Organ infiltration
Bone Marrow Failure :
a. Anemia ( pallor, lethargy, dyspnoea )
b. Bleeding manifestations ( Petechiae, bleeding gums )
Infections
c.
d. Fever
Organ Infiltration :
Pain and tenderness { bone infarcts by leukemic
cells }
Lymphadenopathy and enlargement of tonsils
Splenomegaly
Hepatomegaly
Gum Hypertrophy
Chloroma {Localised tumour forming mass
occuring in the skin or orbit due to local
infiltration of the tissues}
Meningeal involvement
a.
b.
c.
d.
e.
f.
g.
Lab Findings :
a. Blood findings
Bone marrow examination :
- Cellularity : The bone marrow is hypercellular
but sometimes a blood tap or dry tap occurs
- Leukemic Cells : Tightly packed with blast cells
- Erythropoiesis : Reduced
- Megakaryocytes : Reduced or absent
Chronic Leukemia
—
In contrast to acute leukemia, chronic leukemia
develops so insidiously that the disease
months or even several years.
may be for
—
Occurs more in males of middle age.
—
Two types :
a. Chronic Myeloid leukemia
b. Chronic Lymphocytic Leukemia
Clinical features:
Fever, chills, night sweatsand other f lu-like
symptoms
Weakness and fatigue
Neurological symptoms (headaches)
Enlarged liver and spleen
Frequent infection
Bone pain
Joint pain
Dizziness
Nausea
Swollen tonsils
Diarrhea
Paleness
Malaise
—
—
—
—
—
—
—
—
—
—
—
—
—
—Unintentional weight loss
Chronic Myeloid Leukemia :
—
Comprises about 20% of leukemia
incidence in 3-4th decades of life
and has its peak
—
Both sexes equally affected
Laboratory Findings :
a. Blood Picture :
Bone Marrow Examination :
a. Cellularity : Hypercellularity with total or partial
replacement of fat spaces
b. Myeloid Cells : Predominate in the bone marrow
Erythropoiesis : Normoblastic but presence
reduction
of
c.
d. Megakaryocytes : Smaller in size
Cytogenetics show the presence of philadelphia
chromosome
Chronic Lymphocytic Leukemia :
—
Constitutes about 25% of all leukemias
—
Disease of the elderly with male predeliction
Oral manifestation:
—
Occurinbothacuteandchronic
monocytic
—
Commoninmonocyticleukemia
forms-myeloid,lymphoid,
—
Manifestationsareseenmorecommonlyintheacutestageof
thedisease
—
Theoral manifestations are lesscommonin children becoz of
moreprevalence of AML in that agegroup.
Oral manifestation:
—
Gingival hyperplasia with bleeding.
—
Gingival tissue becomes swollen & edematous due
leukemic cell infiltration.
—
Ecchymosis and hematoma formation in the oral
cavity.
—
Multiple larger irregular ulcers develop in the oral
mucosa.
—
Oral infections
to
—
Rapid loosening of teeth due to necrosis of the PDL.
Laboratory investigation:
—
WBC total count may be either normal or abnormally
or extremely high.
low
—
DC of WBC may reveal that one type of leukocyte
overwhelmingly predominant.
—
The platelet count & Hb levels are usually low.
is
Bone marrow aspiration:
—
Bone marrow aspiration reveals an increase in the no.
bone marrow cells with an increase in the leukocyte
series.
of
Treatment :
—
Antileukemic chemotherapy & radiotherapy.
—
Repeated blood transfusions.
—
Maintenance treatments

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Leukemia .pptx. ........,..................

  • 1. Leukemia — Leukemia is a disease characterized by the progressive overproduction of WBC which usually appear in the circulating blood in an immature form. — It accounts 8% of all human cancers & is common malignancy in children & young adults. — Proliferation takes place in the bone marrow and in certain forms, the lymphoid tissues
  • 2. Etiology – — Genetic Factors : - Seen where there is a presence of congenital disorders such as Down’s, Bloom’s, Kleinfelters and Wiskott Aldrich Syndromes — Environmental a) Ionising Hiroshima and Factors : radiation (increased incidence in Nagasaki) b) Chemical Carcinogens Benzene & Formaldehyde) c) Drugs (Alkylating agents – — Infection-EBV, HTLV-1
  • 3. Pathogenesis – — Arises following malignant transformation of a single clone of cells belonging to myeloid or lymphoid series — Acute leukemia : - Defect in maturation beyond the myeloblast level in AML and lymphoblast in ALL — Cells proliferate in the bone marrow and spread to other tissues
  • 4. — Philapdelphia Chromosome – - Thought to be a partial deletion of the long arm of chromosome 22 - Now recognized to be the translocation of chromosomal material from chromosome 22 to chromosome 9
  • 5.
  • 6. Classification: — Acute lymphocytic (lymphoblastic) leukemia (ALL) — Chronic lymphocytic leukemia (CLL) Both involve immature lymphocytes and their progenitors in the bone marrow, the spleen, lymph nodes, CNS, and other tissue — Acute myelogenous (myeloblastic) leukemia (AML) — Chronic myelogenous leukemia (CML) Both involve the pluri-potent myeloid stem cells in bone marrow and interfere with the maturation of all blood cells
  • 8. Acute Vs chronic leukemia
  • 9. Acute Leukemia — It is characterized by neoplastic proliferation of large number of abnormal immature leukocytes in the marrow that infiltrate the lymph nodes,liver,spleen & eventually all body systems. — In addition to this, production of other blood cells inhibited. are — Clinical manifestations are divided into 2 groups - Due to bone marrow failure - Due to Organ infiltration
  • 10. Bone Marrow Failure : a. Anemia ( pallor, lethargy, dyspnoea ) b. Bleeding manifestations ( Petechiae, bleeding gums ) Infections c. d. Fever
  • 11. Organ Infiltration : Pain and tenderness { bone infarcts by leukemic cells } Lymphadenopathy and enlargement of tonsils Splenomegaly Hepatomegaly Gum Hypertrophy Chloroma {Localised tumour forming mass occuring in the skin or orbit due to local infiltration of the tissues} Meningeal involvement a. b. c. d. e. f. g.
  • 12. Lab Findings : a. Blood findings
  • 13. Bone marrow examination : - Cellularity : The bone marrow is hypercellular but sometimes a blood tap or dry tap occurs - Leukemic Cells : Tightly packed with blast cells - Erythropoiesis : Reduced - Megakaryocytes : Reduced or absent
  • 14. Chronic Leukemia — In contrast to acute leukemia, chronic leukemia develops so insidiously that the disease months or even several years. may be for — Occurs more in males of middle age. — Two types : a. Chronic Myeloid leukemia b. Chronic Lymphocytic Leukemia
  • 15. Clinical features: Fever, chills, night sweatsand other f lu-like symptoms Weakness and fatigue Neurological symptoms (headaches) Enlarged liver and spleen Frequent infection Bone pain Joint pain Dizziness Nausea Swollen tonsils Diarrhea Paleness Malaise — — — — — — — — — — — — — —Unintentional weight loss
  • 16. Chronic Myeloid Leukemia : — Comprises about 20% of leukemia incidence in 3-4th decades of life and has its peak — Both sexes equally affected
  • 17. Laboratory Findings : a. Blood Picture :
  • 18. Bone Marrow Examination : a. Cellularity : Hypercellularity with total or partial replacement of fat spaces b. Myeloid Cells : Predominate in the bone marrow Erythropoiesis : Normoblastic but presence reduction of c. d. Megakaryocytes : Smaller in size Cytogenetics show the presence of philadelphia chromosome
  • 19. Chronic Lymphocytic Leukemia : — Constitutes about 25% of all leukemias — Disease of the elderly with male predeliction
  • 21. Oral manifestation: — Gingival hyperplasia with bleeding. — Gingival tissue becomes swollen & edematous due leukemic cell infiltration. — Ecchymosis and hematoma formation in the oral cavity. — Multiple larger irregular ulcers develop in the oral mucosa. — Oral infections to — Rapid loosening of teeth due to necrosis of the PDL.
  • 22. Laboratory investigation: — WBC total count may be either normal or abnormally or extremely high. low — DC of WBC may reveal that one type of leukocyte overwhelmingly predominant. — The platelet count & Hb levels are usually low. is Bone marrow aspiration: — Bone marrow aspiration reveals an increase in the no. bone marrow cells with an increase in the leukocyte series. of
  • 23. Treatment : — Antileukemic chemotherapy & radiotherapy. — Repeated blood transfusions. — Maintenance treatments