acute leukemia Flashcards
clinical symptoms
ymptoms due to: bone marrow failure tissue infiltration leukostasis other (DIC) usually short duration of symptoms. Constitutional symptoms fever and night sweats weight loss
labratory changes
Laboratory alterations WBC usually elevated blasts in peripheral blood normocytic anemia thrombocytopenia DIC
lab studies
Laboratory studies Morphology (smear, histology) Immunophenotyping Flow cytometry Cytogenetics Karyotyping FISH (fluorescence in situ hybridisation) Molecular genetics PCR, RT-PCR RFLP (restriction fragment length polymorphism) DNA microarray
all vs aml
ALL (lymphoblast) Blast size: small Cytoplasm: scant Chromatin: dense Nucleoli: indistinct Auer-rods: never present AML (myeloblast) large moderate fine, lacy prominent present in 50% flow cytometry: CD markers special stains (cytochemistry)
aml, all (b cells) and t cell all markers.
AML : CD13, CD33
ALL B-cell : CD10, CD19, CD22
T-cell : CD3, CD7
prog factors aml
AML:
– Good prognosis: t(8;21), t(15;17), inv(16)
– Poor prognosis: del(5q), complex cytogenetic alterations,
abnormal 3q
all prog factors
ALL:
– Good prognosis: hyperdiploidy, t(12;21)
– Poor prognosis: Philadelphia-chromosome, complex
karyotype, t(4;11), t(8;14
who and fab classifications
Current: WHO-classification
based on morphology, immunophenotype,
cytogenetic and molecular alteration It is
useful for planning treatment and predicting
prognosis
Previously used: FAB-classification (French
American British) – based on morphological and
cytochemical features only
all classification
WHO classification B-lymphoblastic leukemia/lymphoma – Recurrent genetic abnormalities – Not otherwise specified (NOS) T-lymphoblastic leukemia/lymphoma
FAB classification: previous system, being phased out
L1 – small, similar cells
L2 – large, different cells
L3 – large, different cells with vacuoles (not ALL, Burkitt)
Acute Myeloid Leukemia (AML)
classification- who
WHO-classification
AML with recurrent genetic abnormalities
AML with myelodysplasia-related changes
Therapy-related myeloid neoplasms
AML not otherwise categorized
Myeloid sarcoma
Myeloid proliferations related to Down syndrome
Acute Myeloid Leukemia (AML)
classification- fab
FAB-classification (of AML not otherwise categorized) M0: AML, minimally differentiated M1: AML, without maturation M2: AML, with granulocytic maturation Adult cases: 30 - 40%
M3: Acute promyelocytic leukemia (APL) t(15:17) is diagnostic: the retinoic acid receptor-alpha (RARA) gene is involved ATRA (all-trans retinoid acid) therapy: stimulates differentiation Granules contain procoagulants (thromboplastin-like) - massive DIC
M4: Acute myelomonocytic leukemia, M4eo: with eosinophilia
Gingival hyperplasia is frequent
M5: Acute monoblastic (M5a) or acute monocytic (M5b) leukemia
Often infiltrates into gingiva, skin and
CNS
M6: Acute erythroid leukemias
M7: Acute megakaryoblastic leukemia
treatment
Allogeneic Stem Cell Transplantation Combination chemotherapy first goal is complete remission further Rx to prevent relapse supportive medical care transfusions, antibiotics, proper isolation, hygiene, nutrition, supplements psycho-social support patient and family
treatment chemo
Treatment of most cases of acute myeloid leukemia (AML) is usually divided into 2 chemotherapy (chemo) phases:
Remission induction (often just called induction) Consolidation (post-remission therapy) Treatment usually needs to start as quickly as possible after the diagnosis because AML can progress very quickly. Sometimes another type of treatment needs to be started even before the chemo has had a chance to work.