↓ leukopenias most often: neutropenia lymphopenia: less common – congenital id
DESCRIPTION
Leukocytes 4-10 000/mm 3 Differential count: neutrophils 60- 70%, eosinophils 2-4% basophils - up to 1% ly: 20 – 30%, mono 3-8%. ↓ Leukopenias most often: neutropenia lymphopenia: less common – congenital ID diseases, corticosteroid therapy - PowerPoint PPT PresentationTRANSCRIPT
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Leukocytes 4-10 000/mm3
Differential count:neutrophils 60- 70%, eosinophils 2-4%basophils - up to 1%ly: 20 – 30%, mono 3-8%
↓ Leukopenias
most often: neutropenia
lymphopenia: less common – congenital ID
diseases, corticosteroid therapy
↑ Proliferations : reactive – infections, other conditions
neoplastic
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NEOPLASTIC PROLIFERATIONS
OF WHITE CELLS A. myeloid
from the hematopoietic stem cells giving rise to cells of myeloid lineage thrombocytic, granulocytic, erythroid
Acute myelogenous (myeloid) leukaemias Myelodysplastic syndromes Chronic myeloproliferative neoplasms
B. lymphoid - tumors of lymphocytes, lymphomas and leukaemia Hodgkin lymphoma versus non-Hodgkin lymphomas; B- versus T- cell lymphomas precursor cells (B or T or NK) – lymphoblastic
versus mature cells – B or T (or NK)
C. histiocytoses – proliferative lesions of histiocytes
Langerhans histiocytosis
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Bone marrow(BM)
hypercellular
Dysplastic
Ineffective – bone marrow failure
Peripheral blood (PB)
Blood cells: few and pathological
(size, shape, function)
Myelodysplastic syndrome
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Myelodysplastic syndrome• clonal disorders of stem cells • defects of maturation in the BM - ineffective
hematopoiesis (progressive failure of BM function)
• cells in the PB : decreased numbers – pancytopenia + defective in function, pathological shapes
• BM: hypercellular,but dysplastic: pathological forms, architecture blasts may be increased(but less than 20%, threshold AML versus MDS)
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Myelodysplastic syndrome
Clinical symptoms and complications ???
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Myelodysplastic syndrome
Clinical symptoms and complications
• Anemia
• Thrombocytopenia - bleeding
• Leukopenia – infection
• (Splenomegaly +-)
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Myelodysplastic syndrome
purpura
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Myelodysplastic syndrome
• primary – de novo - old people – over 60
• secondary – therapy related – toxic exposure - worse prognosis
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Myelodysplastic syndromeSubcategories
• Refractory anemia –– unilineage dysplasia
• RA with ringed sideroblasts – the nucleus encircled by siderotic granules
• RA with multilineage dysplasia
• RA with excess blasts –more than 5%, less than 20%
• MDS unclassifiable
• MDS assoc. with isolated del. (5q) chromosome
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Sideroblastic anaemia (Perl´s stain)collars of iron granules around the nucleus
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(Chronic) myeloproliferative
neoplasms
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Chronic myeloproliferative diseases
Clonal disorders
Adults
1. Chronic myeloid leukemia
2. Polycythemia vera
3. Essential thrombocytemia
4. Chronic osteomyelofibrosis
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Chronic myeloproliferative diseases
Common principles: 1. Bone marrow: stem cell genetic abnormalities,
neoplastic proliferation of one or more (all) BM myeloid series (red, white, megakaryocytes)disorder of an individual series more pronounced in each of the categories
2. Peripheral blood: increased numbers of cells; relatively normal maturation
3. Splenomegaly, hepatomegalysequestration of excess blood cells, extramedullary hematopoiesis, leukaemic infiltration
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phases of the disease in time:
1. onset insidious
proliferative phase,
2. progression - spent phase -
osteomyelofibrosis
- blast phase
all can (do not have to) progress to AL; CML does it invariably)
Chronic myeloproliferative diseases
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Chronic myelogenous leukaemia (CML)
t(9; 22) – Philadelphia chromosome, bcr-abl gene pluripotent stem cell defect
abnormal fusion protein - increased tyrosine kinase activity
most striking : proliferation of G
increased cellularity
maturation retained (no hiatus leukaemicus)
hematopoiesis also extramedullary splenomegaly (hepatomegaly)
PB: leukocytosis – exceeds even 100 000/ mm3
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CML
PB: no hiatus leukaemicus; mature neutrophils, some metamyelocytes, and a myelocyte.
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Phases
1. chronic – aver. 3 ys
2. accelerated – gradual failure of response to treatment, increasing anemia and thrombocytopenia, basophilia
3. blast crisis –after accelerated phase or without the acceler. phase
Blast crisis = acute leukaemia - 70% myeloid, 30% lymphoblastic
Chronic myelogenous leukaemia (CML)
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Chronic myeloid leukaemia
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Chronic myeloid leukaemia
uric acid deposition
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Polycythaemia vera
• increased proliferation of all three series
• most striking: red cells
• hypercellular BM
• PB: HTC 60%, Hb over 180g/l
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Polycythaemia vera• increased RC mass - symptoms:
hypervolemia, blood stasis (mostly venous), cyanosis – stagnation and deoxygenation of blood
hypertension, thromboses, bleeding – abnormal blood flow, abnormalities of PLT
• granulopoiesis may be elevated
• plt elevated + functional abnormalities
• SPENT PHASE: myelofibrosis
(20%/10 ys)
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Polycythemia vera. Plethora.
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Polycythemia vera. Plethora.
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Polycythemia veradistension of retinal vessels
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Gouty tophi
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Polycythemia vera, spent phase, advanced marrow myelofibrosis. Massive splenomegaly (3020 gm; normal: 150 to 200 gm)largely owing to extramedullary hematopoiesis
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Essential thrombocythaemia• the least common CMPD• PLT exceed 600 000 /mm3• BM: increased cellularity,
megakaryocytes: abnormal,
often large• PB: PLT: often large• Symptoms: • thrombosis and hemorrhage – abnormalities of quantity
and quality of PLT• rel. indolent
Giant platelets
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Essential thrombocythaemia
haemorrhages
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Essential thrombocythaemia
thrombosis, gangrene
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Chronic idiopathic myelofibrosis • abnormal neoplastic megakaryocytes release
fibrogenic factors – PDGF and TGFastimulate fibroblasts to proliferation
• early: BM hypercellular, minimal fibrosis• progression: BM hypocellular, fibrotic;
osteosclerosis• obliteration of BM space: extramedullary
hematopoiesis - spleen; later: liver• PB: leukoerythroblastic=erytroid and
granulocytic precursors• 20% - progression to AML
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Primary myelofibrosis (peripheral blood smear). Two nucleated erythroid precursors and several teardrop-shaped red cells(dacryocytes). Immature myeloid cells present in other fields. An identical picture - in other diseases producing marrow distortion and fibrosis.
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Leukaemia
• Acute – myeloid; lymphoblastic - B, T
• Chronic – myeloid, lymphocytic – B, T
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Acute leukaemia (AL)Common: acute courseuntreated: death in weeks, monthsProblems – symptoms result from:A. failure of normal hematopoiesis –
anemia, neutropenia, thrombocytopeniaB. infiltration of organs by neoplastic cells
• 1. Myeloid (adults)• 2. Lymphoblastic (young; B or T)
further subdivision:genetics, morphology, immunophenotype
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Acute myeloid leukaemia• Categories:• AML with recurrent gen. abnormalities –balanced
translocations, often complete remission, favourable prognosis (fusion gene - chimeric protein); – t(15;17) – AML M3 – promyelocytic – treatment
with transretinoic acid;– t(8; 21) or inversion of chromosome 16
• AML therapy related • AML with multilineage dysplasia• AML – NOS- minim.differentiated• Without maturation• With maturation
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• FAB classification = French – American – British
• M0 – without maturation – myeloblastic• M1 – without maturation• M2 – with maturation• M3 – promyelocytic – now categorised rather
according to the genetics – t(15; 17)• M4 – myelomonocytic• M5 – a – monoblastic, b- monocytic• M6 – erythroid• M7 – megakaryoblastic
Acute myeloid leukaemia
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Acute myeloblastic leukaemia: Staphylococcus aureus lesions
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Acute myeloblastic leukaemiamixed infectionStreptococci, Candidaprevious chemotherapyand neutropenia
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AML, M5leukaemic infiltrationof the gumsexpansion andthickeningpartial coverings of the teeth
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Myeloid sarcoma
Tumour mass of immature myeloid cells
Extramedullary (bone)
Association - before or concurrently:
1. AML (or as a relapse)
2. Chronic myelogenous leukaemia
other myeloproliferative disorders
3. MDS
Extramedullary myeloid tumour, granulocytic sarcoma, chloroma
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Myeloid sarcomaLocalization
1. Bones – subperiosteal
(skull, paranasal sinuses, sternum, ribs, vertebrae, pelvis)
2. Lymph nodes
3. Skin
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Myeloid sarcoma - poorly differentiated
…a high index of suspicion...Stains: CHAE, MPO, lysozyme; CD15,
CD68, CD117, CD43 (CD43 only!)
Differential diagnosis1. Lymphoblastoma2. Burkitt lymphoma3. Large cell lymphoma4. Small round cell tumours
(neurobl., Ewing/PNET, medullobl.)
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Myeloid sarcoma
Prognosis
If + MPD, MDS = as a blast transformation
If + AML – as this AML
If isolated: curative radiotherapy
prolonged survival
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Precursor (lymphoblastic)B-cell neoplasmsB-acute lymphoblastic leukaemia/
lymphoblastic lymphoma
• 1. Leukaemia (more common): involves the bone marrow and PB
• 2. occasionally solid primary nodal or extranodal mass /B-lymphopblastic lymphoma/ without PB and BM involevement
- leukaemization possible. biologic unity of B-ALL and B-LBL, division arbitrary
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Precursor (lymphoblastic)B-cell neoplasms
• Small to medium sized cells
• scant cytoplasm, dispersed chromatin, and inconspicuous nucleoli
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Acute lymphoblastic leukemia/lymphoma. Lymphoblasts: condensed nuclear chromatin, small nucleoli, and scant agranular cytoplasm
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Lymphoblastic leukaemia• More common B• B-ALL – children, but also adults; relatively
frequent, good prognosis• Children: 95% complete remission, 80%
cured /adults worse/
Lymphoblastoma (LBL)• More common: T• B-LBL – rare
T-LBL- rapidly growing mass in mediastinum, adolescent male
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Acute B-cell lymphoblastic leukaemia• B-ALL – children, but also adults; relatively frequent • B-LBL - much less common - skin, bone, soft tissues,
LN
• Symptoms: BM failure• Enlarged LN, liver, spleen• Antigenic profile:TdT, CD10 (CALLA) various degree
of differentiation, B-antigens (CD79a, CD20)• Genetic abnormalities– prognostically important
– Good: hyperdiploidy; t (12, 21)– Poor: t(9, 22), hypodiploidy
• In general: a good prognosis leukaemia• Children: 95% complete remission, 80% cured /adults
worse/
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Precursor T cell neoplasms
• T-ALL– less common than B-ALL
• T-ALL, T-LBL - adolescent male
• clinically: similarities with B-ALL;
• all acute leukemias share some clinical similarities
• But difference: AML adults, ALL: children
• T-LBL - rapidly growing mass in mediastinum