Leukemia: Difference between revisions

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'''For patient information click [[Leukemia (patient information)|here]]'''
'''For patient information click [[Leukemia (patient information)|here]]'''


{{CMG}}; {{AE}} {{SMP}}, {{USAMA}}, {{SSH}}
{{CMG}}; {{AE}} {{SMP}}, {{USAMA}}, {{SSH}}; {{GRR}} {{Nat}}


{{SK}} Leukaemia
{{SK}} Leukaemia
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{|  
{|  
! rowspan="3" align="center" style="background:#4479BA; color: #FFFFFF;" + |Disease
! rowspan="2" align="center" style="background:#4479BA; color: #FFFFFF;" + |Disease
! rowspan="3" align="center" style="background:#4479BA; color: #FFFFFF;" + |Etiology
! rowspan="2" align="center" style="background:#4479BA; color: #FFFFFF;" + |Etiology
! colspan="4" align="center" style="background:#4479BA; color: #FFFFFF;" + |Clinical Manifestation
! colspan="4" align="center" style="background:#4479BA; color: #FFFFFF;" + |Clinical Manifestation
! colspan="3" rowspan="2" align="center" style="background:#4479BA; color: #FFFFFF;" + |Laboratory Findings
! colspan="2" align="center" style="background:#4479BA; color: #FFFFFF;" + |Laboratory Findings
! rowspan="3" align="center" style="background:#4479BA; color: #FFFFFF;" + |Gold standard diagnosis
! rowspan="2" align="center" style="background:#4479BA; color: #FFFFFF;" + |Gold standard diagnosis
! rowspan="3" align="center" style="background:#4479BA; color: #FFFFFF;" + |Associated findings
! rowspan="2" align="center" style="background:#4479BA; color: #FFFFFF;" + |Associated findings
|-
|-
! rowspan="2" align="center" style="background:#4479BA; color: #FFFFFF;" + |Demography
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Demography
! rowspan="2" align="center" style="background:#4479BA; color: #FFFFFF;" + |History
! align="center" style="background:#4479BA; color: #FFFFFF;" + |History
! rowspan="2" align="center" style="background:#4479BA; color: #FFFFFF;" + |Symptoms
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Symptoms
! rowspan="2" |Signs
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Signs
|-
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Lab
! align="center" style="background:#4479BA; color: #FFFFFF;" + |CBC
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Histopathology
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Histopathology
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Other
|-
|-
! align="center" style="background:#DCDCDC;" + |[[Acute myelogenous leukemia]]<ref name="pmid30410824">{{cite journal |vauthors=Saif A, Kazmi SFA, Naseem R, Shah H, Butt MO |title=Acute Myeloid Leukemia: Is That All There Is? |journal=Cureus |volume=10 |issue=8 |pages=e3198 |date=August 2018 |pmid=30410824 |doi=10.7759/cureus.3198 |url=}}</ref><ref name="pmid23526416">{{cite journal |vauthors=Estey EH |title=Acute myeloid leukemia: 2013 update on risk-stratification and management |journal=Am. J. Hematol. |volume=88 |issue=4 |pages=318–27 |date=April 2013 |pmid=23526416 |doi=10.1002/ajh.23404 |url=}}</ref>
! align="center" style="background:#DCDCDC;" + |[[Acute myelogenous leukemia]]<ref name="pmid30410824">{{cite journal |vauthors=Saif A, Kazmi SFA, Naseem R, Shah H, Butt MO |title=Acute Myeloid Leukemia: Is That All There Is? |journal=Cureus |volume=10 |issue=8 |pages=e3198 |date=August 2018 |pmid=30410824 |doi=10.7759/cureus.3198 |url=}}</ref><ref name="pmid23526416">{{cite journal |vauthors=Estey EH |title=Acute myeloid leukemia: 2013 update on risk-stratification and management |journal=Am. J. Hematol. |volume=88 |issue=4 |pages=318–27 |date=April 2013 |pmid=23526416 |doi=10.1002/ajh.23404 |url=}}</ref>
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| align="left" style="background:#F5F5F5;" + |
* Clonal proliferation of malignant myeloid blast cells in the marrow  
* Clonal proliferation of malignant myeloid blast cells in the [[bone marrow]]
* Genetic abnormalities t(8;21), inv(16), and t(15;17)  
* Genetic abnormalities t(8;21), inv(16), and t(15;17)  
| align="left" style="background:#F5F5F5;" + |
| align="left" style="background:#F5F5F5;" + |
* The most common leukemia in adults
* The most common leukemia in adults
* Median age of 63 years old
* Median age of 63 years old
* More in [[Down syndrome]] or [[Bloom syndrome]]
| align="left" style="background:#F5F5F5;" + |
| align="left" style="background:#F5F5F5;" + |
* [[Smoking]], previous [[chemotherapy]] or [[radiation therapy]], [[myelodysplastic syndrome]], and exposure to the chemical [[benzene]]
* [[Smoking]], previous [[chemotherapy]] or [[radiation therapy]], [[myelodysplastic syndrome]], and exposure to the chemical [[benzene]]
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* Leukemic blasts  
* Leukemic blasts  
* Positive [[Auer rod|Auer rods]]
* Positive [[Auer rod|Auer rods]]
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| align="left" style="background:#F5F5F5;" + |
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* [[Flow cytometry]] > 20% blasts of [[myeloid]] lineage
* [[Flow cytometry]] > 20% blasts of [[myeloid]] lineage
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* Persistent or frequent [[infections]]
* Persistent or frequent [[infections]]
* Fatal within weeks or months if left untreated
* Fatal within weeks or months if left untreated
* [[Down syndrome]] or [[Bloom syndrome]]
|-
|-
! align="center" style="background:#DCDCDC;" + |[[Acute lymphoblastic leukemia]]<ref name="pmid30302234">{{cite journal |vauthors=Sawalha Y, Advani AS |title=Management of older adults with acute lymphoblastic leukemia: challenges & current approaches |journal=Int J Hematol Oncol |volume=7 |issue=1 |pages=IJH02 |date=March 2018 |pmid=30302234 |pmc=6176956 |doi=10.2217/ijh-2017-0023 |url=}}</ref><ref name="pmid23841506">{{cite journal |vauthors=Portell CA, Advani AS |title=Novel targeted therapies in acute lymphoblastic leukemia |journal=Leuk. Lymphoma |volume=55 |issue=4 |pages=737–48 |date=April 2014 |pmid=23841506 |doi=10.3109/10428194.2013.823493 |url=}}</ref>
! align="center" style="background:#DCDCDC;" + |[[Acute lymphoblastic leukemia]]<ref name="pmid30302234">{{cite journal |vauthors=Sawalha Y, Advani AS |title=Management of older adults with acute lymphoblastic leukemia: challenges & current approaches |journal=Int J Hematol Oncol |volume=7 |issue=1 |pages=IJH02 |date=March 2018 |pmid=30302234 |pmc=6176956 |doi=10.2217/ijh-2017-0023 |url=}}</ref><ref name="pmid23841506">{{cite journal |vauthors=Portell CA, Advani AS |title=Novel targeted therapies in acute lymphoblastic leukemia |journal=Leuk. Lymphoma |volume=55 |issue=4 |pages=737–48 |date=April 2014 |pmid=23841506 |doi=10.3109/10428194.2013.823493 |url=}}</ref>
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* History of drug exposure  
* History of drug exposure  
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* Generalized weakness  
* Generalized [[weakness]]
* [[Fatigue]]
* [[Fatigue]]
* [[Bleeding]]
* [[Bleeding]]
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* [[Hepatosplenomegaly]]
* [[Hepatosplenomegaly]]
* LAP
* [[Lymphadenopathy|LAP]]
* [[Dyspnea]]
* [[Dyspnea]]
* [[Pallor]]
* [[Pallor]]
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* [[Lymphoblast|Lymphoblasts]]  
* [[Lymphoblast|Lymphoblasts]]  
* Atypical cells
* Atypical cells
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* [[Bone marrow examination|Bone marrow biopsy]]
* [[Bone marrow examination|Bone marrow biopsy]]
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* All cells of the neutrophilic series, from [[Myeloblast|myeloblasts]] to mature [[Neutrophil|neutrophils]]
* All cells of the neutrophilic series, from [[Myeloblast|myeloblasts]] to mature [[Neutrophil|neutrophils]]
* [[Myelocyte]] bulge
* [[Myelocyte]] bulge
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* [[Bone marrow examination|Bone marrow biopsy]]
* [[Bone marrow examination|Bone marrow biopsy]]
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! align="center" style="background:#4479BA; color: #FFFFFF;" + |Demography
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Demography
! align="center" style="background:#4479BA; color: #FFFFFF;" + |History
! align="center" style="background:#4479BA; color: #FFFFFF;" + |History
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Constitutional symptoms
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Symptoms
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Other
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Signs
! align="center" style="background:#4479BA; color: #FFFFFF;" + |CBC
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Lab
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Histopathology
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Histopathology
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Other
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Gold standard diagnosis
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Gold standard diagnosis
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Associated findings
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Associated findings
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* Monoclonality of [[Light chain|kappa]] and [[Lambda (anatomy)|lambda]] producing [[B cell|B cells]]
* Monoclonality of [[Light chain|kappa]] and [[Lambda (anatomy)|lambda]] producing [[B cell|B cells]]
* Express [[CD19]], [[CD20]], [[CD23]], and [[CD5]] on the [[cell]] surface
* Express [[CD19]], [[CD20]], [[CD23]], and [[CD5]] on the [[cell]] surface
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* Positive direct antiglobulin (Coombs) test
* [[Hypogammaglobulinemia]]
* Elevated [[lactate dehydrogenase]] and [[beta-2 microglobulin]]
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* [[Flow cytometry]] of the [[Venous blood|peripheral blood]]
* [[Flow cytometry]] of the [[Venous blood|peripheral blood]]
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* [[Cytopenia]]
* [[Cytopenia]]
* [[Leukocytosis]] in 10 to 20 percent
* [[Leukocytosis]] in 10 to 20 percent
* [[Azotemia]]
* Abnormal [[liver function tests]]
* [[Hypergammaglobulinemia]]
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* [[Pancytopenia]] with [[monocytopenia]] and circulating tumor cells characteristic of HCL
* [[Pancytopenia]] with [[monocytopenia]] and circulating tumor cells characteristic of HCL
* Dry [[bone marrow]]
* Dry [[bone marrow]]
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* [[Azotemia]]
* Abnormal [[liver function tests]]
* [[Hypergammaglobulinemia]]
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* Analysis of [[Venous blood|peripheral blood]] + [[immunophenotyping]] by [[flow cytometry]]
* Analysis of [[Venous blood|peripheral blood]] + [[immunophenotyping]] by [[flow cytometry]]
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|-
|-
! align="center" style="background:#DCDCDC;" + |Large granular lymphocytic leukemia<ref name="pmid28128670">{{cite journal |vauthors=Matutes E |title=Large granular lymphocytic leukemia. Current diagnostic and therapeutic approaches and novel treatment options |journal=Expert Rev Hematol |volume=10 |issue=3 |pages=251–258 |date=March 2017 |pmid=28128670 |doi=10.1080/17474086.2017.1284585 |url=}}</ref><ref name="pmid28717070">{{cite journal |vauthors=Oshimi K |title=Clinical Features, Pathogenesis, and Treatment of Large Granular Lymphocyte Leukemias |journal=Intern. Med. |volume=56 |issue=14 |pages=1759–1769 |date=2017 |pmid=28717070 |pmc=5548667 |doi=10.2169/internalmedicine.56.8881 |url=}}</ref>​
! align="center" style="background:#DCDCDC;" + |Large granular lymphocytic leukemia<ref name="pmid28128670">{{cite journal |vauthors=Matutes E |title=Large granular lymphocytic leukemia. Current diagnostic and therapeutic approaches and novel treatment options |journal=Expert Rev Hematol |volume=10 |issue=3 |pages=251–258 |date=March 2017 |pmid=28128670 |doi=10.1080/17474086.2017.1284585 |url=}}</ref><ref name="pmid28717070">{{cite journal |vauthors=Oshimi K |title=Clinical Features, Pathogenesis, and Treatment of Large Granular Lymphocyte Leukemias |journal=Intern. Med. |volume=56 |issue=14 |pages=1759–1769 |date=2017 |pmid=28717070 |pmc=5548667 |doi=10.2169/internalmedicine.56.8881 |url=}}</ref>​
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* Clonal proliferation of cytotoxic T cells
* Clonal proliferation of [[Cytotoxic T cell|cytotoxic T cells]]
* Dysregulation of apoptosis through abnormalities in the Fas/Fas ligand pathway
* Dysregulation of [[apoptosis]] through abnormalities in the Fas/Fas ligand pathway
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* Rare
* Rare
* Median age 60 years
* Median age 60 years
* M = F
* M = F
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* Autoimmune diseases
* Autoimmune diseases
* Lymphoproliferative disorders
* [[Lymphoproliferative disorders|Lymphoproliferative]] disorders
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* Generalized weakness  
* Generalized [[weakness]]
* [[Fatigue]]
* [[Fatigue]]
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* Mostly asymptomatic  
* Mostly asymptomatic  
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* Modest lymphocytosis
* Modest [[lymphocytosis]]
* Neutropenia
* [[Neutropenia]]
* Anemia
* [[Anemia]]
* Thrombocytopenia
* [[Thrombocytopenia]]
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* Large lymphocytes with a condensed round or oval nucleus, abundant pale basophilic cytoplasm, and small azurophilic granules
* Large [[Lymphocyte|lymphocytes]] with a condensed round or oval nucleus, abundant pale basophilic cytoplasm, and small azurophilic granules
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* Multiple serological abnormalities including rheumatoid factor, antinuclear antibody, antiplatelet antibodies, antineutrophil antibodies, positive direct Coombs test, hyper- or hypogammaglobulinemia, monoclonal gammopathies, and elevated β2-microglobulin
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* Biopsy and flow cytometry + T-cell receptor gene rearrangement studies
* Biopsy and flow cytometry + T-cell receptor gene rearrangement studies
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* Recurrent bacterial infection
* Recurrent bacterial infection
|-
|-
! align="center" style="background:#DCDCDC;" + |[[Chronic neutrophilic leukemia]]<ref name="pmid29512199">{{cite journal |vauthors=Elliott MA, Tefferi A |title=Chronic neutrophilic leukemia: 2018 update on diagnosis, molecular genetics and management |journal=Am. J. Hematol. |volume=93 |issue=4 |pages=578–587 |date=August 2018 |pmid=29512199 |doi=10.1002/ajh.24983 |url=}}</ref>
! align="center" style="background:#DCDCDC;" + |[[Chronic neutrophilic leukemia]]<ref name="pmid29512199">{{cite journal |vauthors=Elliott MA, Tefferi A |title=Chronic neutrophilic leukemia: 2018 update on diagnosis, molecular genetics and management |journal=Am. J. Hematol. |volume=93 |issue=4 |pages=578–587 |date=August 2018 |pmid=29512199 |doi=10.1002/ajh.24983 |url=}}</ref>
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* Mature granulocytic proliferation in the blood and marrow
* Mature granulocytic proliferation in the blood and [[bone marrow]]
* Point mutations in the CSF3R gene
* Point mutations in the [[CSF3R]] gene
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* Very rare
* Very rare
* M = F
* M = F
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* Multiple myeloma
* [[Multiple myeloma]]
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* Generalized weakness  
* Generalized [[weakness]]
* [[Fatigue]]
* [[Fatigue]]
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* [[Hepatosplenomegaly]]
* [[Hepatosplenomegaly]]
* Pruritus
* [[Pruritus]]
* Gout
* [[Gout]]
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* Peripheral blood neutrophilia (> 25 x 10<sup>9</sup>/L) with myeloid precursors (promyelocytes, myelocytes, metamyelocytes)
* Peripheral blood [[neutrophilia]] (> 25 x 10<sup>9</sup>/L) with myeloid precursors (promyelocytes, myelocytes, metamyelocytes)
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* Elevated [[leukocyte alkaline phosphatase]]
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* Toxic granulation in the [[Neutrophil|neutrophils]]
* Toxic granulation in the [[Neutrophil|neutrophils]]
* Nuclear hypersegmentation
* Nuclear hypersegmentation
* Increased myeloid:erythroid ratio > 20:1
* Increased myeloid:erythroid ratio > 20:1
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* Elevated [[leukocyte alkaline phosphatase]]
* [[World Health Organization|WHO]] diagnostic criteria include leukocytosis of ≥ 25 x 109/L  
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* WHO diagnostic criteria include leukocytosis of ≥ 25 x 109/L  
* More than 80% neutrophils,  
* More than 80% neutrophils,  
* Less than 10% circulating neutrophil precursors with blasts  
* Less than 10% circulating neutrophil precursors with blasts  
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* Poor prognosis
* Poor prognosis
* Absence of the Philadelphia chromosome or a BCR/ABL fusion gene
* Absence of the Philadelphia chromosome or a BCR/ABL fusion gene
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! align="center" style="background:#4479BA; color: #FFFFFF;" + |Demography
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Demography
! align="center" style="background:#4479BA; color: #FFFFFF;" + |History
! align="center" style="background:#4479BA; color: #FFFFFF;" + |History
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Constitutional symptoms
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Symptoms
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Other
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Signs
! align="center" style="background:#4479BA; color: #FFFFFF;" + |CBC
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Lab
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Histopathology
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Histopathology
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Other
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Gold standard diagnosis
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Gold standard diagnosis
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Associated findings
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Associated findings
|-
|-
! align="center" style="background:#DCDCDC;" + |[[Chronic eosinophilic leukemia]]
! align="center" style="background:#DCDCDC;" + |[[Chronic eosinophilic leukemia]]
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* There is no known cause for chronic eosinophilic leukemia.
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* It hasn't been linked to a specific chromosome or genetic abnormality.
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* Unknown
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* Unknown
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* Constitutional
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* [[Rash]]
* [[Rhinitis]]
* [[Gastritis]]
* [[Thromboembolism]]<nowiki/>related
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* [[Hypertension]]
* [[Eczema]], [[mucosal]][[ulcers]], [[erythema]]
* [[Angioedema]]
 
* [[Ataxia]]
* [[Anemia]]
* [[Lymphadenopathy]]
* [[Hepatosplenomegaly]]
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*[[Leukocytosis]] with left shift
*[[Eosinophilia]]
*[[Basophilia]]
*[[Monocytosis]]
*[[Anemia]]
*[[Thrombocytopenia]]
*↑ [[B12]] levels
*↑ [[LDH]]
 
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* Hypercelluar with ↑ [[eosinophilic]]<nowiki/> precursors, ↑ [[eosinophils]], and atypical [[mononuclear cells]]
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*[[Heart failure]] [[Lung fibrosis]]
*[[Encephalopathy]]
*Erythema annulare centrifugam
|-
|-
! align="center" style="background:#DCDCDC;" + |[[Chronic monocytic leukemia electrocardiogram|Chronic monocytic leukemia]]
! align="center" style="background:#DCDCDC;" + |[[Chronic monocytic leukemia electrocardiogram|Chronic monocytic leukemia]]
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|-
|-
! align="center" style="background:#DCDCDC;" + |[[Prolymphocytic leukemia]] (PLL)
! align="center" style="background:#DCDCDC;" + |[[Prolymphocytic leukemia]] (PLL)
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! align="center" style="background:#DCDCDC;" + |[[T-cell large granular lymphocyte leukemia|T-cell large granular lymphocytic leukemia]] (TLGL)
! align="center" style="background:#DCDCDC;" + |[[T-cell large granular lymphocyte leukemia|T-cell large granular lymphocytic leukemia]] (TLGL)
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! align="center" style="background:#4479BA; color: #FFFFFF;" + |Demography
! align="center" style="background:#4479BA; color: #FFFFFF;" + |History
! align="center" style="background:#4479BA; color: #FFFFFF;" + |History
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Constitutional symptoms
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Symptoms
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Other
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Signs
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! align="center" style="background:#4479BA; color: #FFFFFF;" + |Lab
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Histopathology
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! align="center" style="background:#4479BA; color: #FFFFFF;" + |Gold standard diagnosis
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! align="center" style="background:#4479BA; color: #FFFFFF;" + |Associated findings
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! align="center" style="background:#DCDCDC;" + |[[Aggressive NK-cell leukemia]] (ANKL)
! align="center" style="background:#DCDCDC;" + |[[Aggressive NK-cell leukemia]] (ANKL)
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! align="center" style="background:#DCDCDC;" + |[[Adult T-cell leukemia|Adult T-cell leukemia/lymphoma]] (ATLL)
! align="center" style="background:#DCDCDC;" + |[[Adult T-cell leukemia|Adult T-cell leukemia/lymphoma]] (ATLL)<ref name="wiki1">Human T-lymphotropic virus. Wikipedia (2015) https://en.wikipedia.org/wiki/Human_T-lymphotropic_virus#Transmission Accessed on November, 3 2015</ref><ref name="pmid18042693">{{cite journal |vauthors=Matutes E |title=Adult T-cell leukaemia/lymphoma |journal=J. Clin. Pathol. |volume=60 |issue=12 |pages=1373–7 |year=2007 |pmid=18042693 |pmc=2095573 |doi=10.1136/jcp.2007.052456 |url=}}</ref><ref name="wiki">Adult T-cell leukemia/lymphoma. Wikipedia (2015) https://en.wikipedia.org/wiki/Adult_T-cell_leukemia/lymphoma Accessed on November, 3 2015</ref><ref name="pmid20425378">{{cite journal| author=Mahieux R, Gessain A| title=Adult T-cell leukemia/lymphoma and HTLV-1. | journal=Curr Hematol Malig Rep | year= 2007 | volume= 2 | issue= 4 | pages= 257-64 | pmid=20425378 | doi=10.1007/s11899-007-0035-x | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20425378  }}</ref><ref name="wiki2">Adult T-cell leukemia/lymphoma. Wikipedia (2015) https://en.wikipedia.org/wiki/Adult_T-cell_leukemia/lymphoma Accessed on November, 3 2015</ref><ref name="pmid180426932">{{cite journal| author=Matutes E| title=Adult T-cell leukaemia/lymphoma. | journal=J Clin Pathol | year= 2007 | volume= 60 | issue= 12 | pages= 1373-7 | pmid=18042693 | doi=10.1136/jcp.2007.052456 | pmc=PMC2095573 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18042693  }}</ref>
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* Adult T-cell leukemia is caused by an infection with [[HTLV]].
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* Common [[genetic mutation]]s involved in the development of adult T-cell leukemia can be found [[Adult T-cell leukemia pathophysiology|here]].
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* The incidence of adult T-cell leukemia increases with age, and the median age at diagnosis is 57 years.
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* Males are more commonly affected with adult T-cell leukemia than females.
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* The male to female ratio is approximately 1.4 to 1.
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:* [[Abdominal pain]]
:* [[Constipation]]
:* [[Nausea]] and [[vomiting]]
:* [[Fatigue]]
:* Generalized [[weakness]]
:* [[Cough]]
:* Recurrent [[infection]]s
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:* [[Fever]]
:* [[Weight loss]]
:* Recurrent [[bleeding]]
:* [[Anorexia]]
:* [[Night sweat]]s
:* [[Bone pain]]
:* [[Hypercalcemia]]
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! align="center" style="background:#DCDCDC;" + |[[Sezary syndrome]]
! align="center" style="background:#DCDCDC;" + |[[Sezary syndrome]]<ref name="pmid21883142">{{cite journal |vauthors=Wong HK, Mishra A, Hake T, Porcu P |title=Evolving insights in the pathogenesis and therapy of cutaneous T-cell lymphoma (mycosis fungoides and Sezary syndrome) |journal=Br. J. Haematol. |volume=155 |issue=2 |pages=150–66 |date=October 2011 |pmid=21883142 |pmc=4309373 |doi=10.1111/j.1365-2141.2011.08852.x |url=}}</ref><ref name="pmid27121473">{{cite journal |vauthors=Woollard WJ, Pullabhatla V, Lorenc A, Patel VM, Butler RM, Bayega A, Begum N, Bakr F, Dedhia K, Fisher J, Aguilar-Duran S, Flanagan C, Ghasemi AA, Hoffmann RM, Castillo-Mosquera N, Nuttall EA, Paul A, Roberts CA, Solomonidis EG, Tarrant R, Yoxall A, Beyers CZ, Ferreira S, Tosi I, Simpson MA, de Rinaldis E, Mitchell TJ, Whittaker SJ |title=Candidate driver genes involved in genome maintenance and DNA repair in Sézary syndrome |journal=Blood |volume=127 |issue=26 |pages=3387–97 |date=June 2016 |pmid=27121473 |doi=10.1182/blood-2016-02-699843 |url=}}</ref><ref name="pmid266071833">{{cite journal |vauthors=Wilcox RA |title=Cutaneous T-cell lymphoma: 2016 update on diagnosis, risk-stratification, and management |journal=Am. J. Hematol. |volume=91 |issue=1 |pages=151–65 |date=January 2016 |pmid=26607183 |pmc=4715621 |doi=10.1002/ajh.24233 |url=}}</ref><ref name="pmid25386354">{{cite journal |vauthors=Horesh N, Horowitz NA |title=Does gender matter in non-hodgkin lymphoma? Differences in epidemiology, clinical behavior, and therapy |journal=Rambam Maimonides Med J |volume=5 |issue=4 |pages=e0038 |date=October 2014 |pmid=25386354 |pmc=4222427 |doi=10.5041/RMMJ.10172 |url=}}</ref><ref name="pmid24421750">{{cite journal |vauthors=Al Hothali GI |title=Review of the treatment of mycosis fungoides and Sézary syndrome: A stage-based approach |journal=Int J Health Sci (Qassim) |volume=7 |issue=2 |pages=220–39 |date=June 2013 |pmid=24421750 |pmc=3883611 |doi= |url=}}</ref><ref name="pmid266071835">{{cite journal |vauthors=Wilcox RA |title=Cutaneous T-cell lymphoma: 2016 update on diagnosis, risk-stratification, and management |journal=Am. J. Hematol. |volume=91 |issue=1 |pages=151–65 |date=January 2016 |pmid=26607183 |pmc=4715621 |doi=10.1002/ajh.24233 |url=}}</ref><ref name="pmid231971992">{{cite journal |vauthors=Yamashita T, Abbade LP, Marques ME, Marques SA |title=Mycosis fungoides and Sézary syndrome: clinical, histopathological and immunohistochemical review and update |journal=An Bras Dermatol |volume=87 |issue=6 |pages=817–28; quiz 829–30 |date=2012 |pmid=23197199 |pmc=3699909 |doi= |url=}}</ref><ref name="pmid23074497">{{cite journal |vauthors= |title=Extracorporeal photophoresis: an evidence-based analysis |journal=Ont Health Technol Assess Ser |volume=6 |issue=6 |pages=1–82 |date=2006 |pmid=23074497 |pmc=3379535 |doi= |url=}}</ref>
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* The cause of Sezary syndrome has not been identified.
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* Sezary syndrome might have one or more of the [[chromosomal]] [[abnormalities]], such as the loss or gain of [[Genetics|genetic]].
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* The prevalence of Sezary syndrome is exact unknown.
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*The median age at diagnosis of [[Sézary syndrome]] is 60 years of age.
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*Sezary syndrome is more commonly observed among [[Old age|elderly]] [[Patient|patients]].
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*[[Male|Males]] are more commonly affected with Sezary syndrome than [[Female|females]](2:1).
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*The majority of sezary syndrome [[Patient|patients]] present with developing [[lymphadenopathy]] and [[erythroderma]] for weeks to months.
*Early clinical features of Sezary syndrome include:
:*Mimic [[psoriasis]]
:*[[Chronic (medical)|Chronic]] [[eczema]]
:*[[Atopic dermatitis (patient information)|Atopic dermatitis]]
:*[[Leprosy]]
:*Lichenoid [[pityriasis]]
*In Sezary syndrome single or multiple [[Lesion|lesions]] (thin [[erythematous]] [[Plaque|plaques]] or flat patch) is a typical [[skin]] involvement  in the [[gluteal]] region or [[Thigh|thighs]]. <ref name="Olsen2015">{{cite journal|last1=Olsen|first1=Elise A.|title=Evaluation, Diagnosis, and Staging of Cutaneous Lymphoma|journal=Dermatologic Clinics|volume=33|issue=4|year=2015|pages=643–654|issn=07338635|doi=10.1016/j.det.2015.06.001}}</ref>
*[[Patient|Patients]] with Sezary syndrome  often have a history of several years of [[Eczema|eczematous]] or [[dermatitis]] [[skin]] [[Lesion|lesions]] before the [[diagnosis]] is finally established.
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* Widespread [[erythema]]
** In Sezary syndrome widespread [[erythema]] can be finely scaly, indurated, or even resemble livido [[reticularis]]
* Indurated
* Resemble livido [[reticularis]]
* [[Erythema]](Not seen in some [[Patient|patients]])
* The severity of [[erythema]] [[body surface area]] (BSA) involved may wax and wane(>80% of BSA)
 
* Patches and [[Plaque|plaques]] to [[erythroderma]]
* [[Keratosis pilaris]]
* [[Alopecia]] ([[hair loss]])
* [[Ectropion]]
* [[Keratoderma]]
* [[Hypertrophy (medical)|Hypertrophic]] [[Nail (anatomy)|nails]]
* Erosions
* [[Lichenification]]
* [[Trouble]] regulating [[Body Temperature|body temperature]]
* [[Abnormal|Abnormalities]] of [[fingernails]] and [[toenails]]
 
* [[Lymphadenopathy]]
* [[Viscera|Viscer]]
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! align="center" style="background:#DCDCDC;" + |[[Myelodysplastic syndrome]]
! align="center" style="background:#DCDCDC;" + |[[Myelodysplastic syndrome]]
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*Constitutional symptoms
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*[[Bleeding]]
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*[[Pallor]]
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*[[Petechiae]]
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*[[Organomegaly]]
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* [[Pancytopenia]]
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*Hypercellular/ normocellular [[bone marrow]] with [[Dysplastic change|dysplastic]] changes
*Macro-ovalocytes
*Basophilic stippling
*[[Howell-Jolly body]]
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*[[Leukemia]] transformation
*Acquired pseudo-Pelger-Huët anomaly
*Infection
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! align="center" style="background:#DCDCDC;" + |[[Myeloproliferative disorders]]
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! align="center" style="background:#DCDCDC;" + |[[Leukemoid reaction]]
! align="center" style="background:#DCDCDC;" + |[[Leukemoid reaction]]
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==References==
==References==
{{Reflist|2}}
{{Reflist|2}}
[[Category:Medicine]]
[[Category:Medicine]]
[[Category:Hematology]]
[[Category:Hematology]]
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[[Category:Oncology]]
[[Category:Oncology]]
[[Category:Up-To-Date]]
[[Category:Up-To-Date]]
[[Category:Primary care]]
[[Category:Differential diagnosis]]
[[Category:Differential diagnosis]]

Latest revision as of 22:30, 29 July 2020

Leukemia Microchapters

Home

Patient Information

Overview

Classification

AML
CML
ALL
CLL

Differentiating Leukemia from other Diseases

Epidemiology and Demographics

Prognosis

For patient information click here

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Seyedmahdi Pahlavani, M.D. [2], Usama Talib, BSc, MD [3], Sadaf Sharfaei M.D.[4]; Grammar Reviewer: Natalie Harpenau, B.S.[5]

Synonyms and keywords: Leukaemia

Overview

Leukemia (Greek leukos, “white”; haima, “blood”) can be defined as a group of hematopoietic stem cell malignancies due to genetic abnormalities that may lead to clonal proliferation of these cells. These group of diseases are classified based on the type of hematopoietic stem cell involved and the duration of the disease. The leukemias are the most common malignancies among children younger than 15 years. Among them, Acute Lymphoblastic Leukemia (ALL) is the most common leukemia and accounts for 77% of childhood leukemia. However, Chronic Lymphocytic Leukemia (CLL) is the most common form of leukemia in adults, and it accounts for 30% of all leukemias in the United States. The increased rate of proliferation and decreased rate of apoptosis in this progeny of cells may compromise normal bone marrow function and ultimately result in marrow failure. Clinical manifestations, diagnosis, laboratory findings, and therapy are different according to the type of malignancy.

Classification

Leukemia may be classified as follows:

 
 
 
 
 
 
 
 
Leukemia
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Lymphoid progeny
 
 
 
 
 
 
 
Myeloid progeny
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Acute lymphoblastic leukemia (ALL)
 
 
 
Chronic lymphocytic leukemia (CLL)
 
Acute Myeloid Leukemia (AML)
 
 
 
Chronic myeloid leukemia (CML)




Differentiating Leukemia from other Diseases

Leukemia must be differentiated from various diseases that cause weight loss, night sweats, hepatosplenomegaly, and palpable lymph nodes, such as hairy cell leukemia, prolymphocytic leukemia, follicular lymphoma, and mantle cell lymphoma. Based on the expression of cell surface markers, the table below differentiates different types of leukemia from other diseases that cause similar clinical presentations:[1]

Disease Etiology Clinical Manifestation Laboratory Findings Gold standard diagnosis Associated findings
Demography History Symptoms Signs Lab Histopathology
Acute myelogenous leukemia[2][3]
  • Clonal proliferation of malignant myeloid blast cells in the bone marrow
  • Genetic abnormalities t(8;21), inv(16), and t(15;17)
  • The most common leukemia in adults
  • Median age of 63 years old
Acute lymphoblastic leukemia[4][5]
  • Arrest of lymphoblasts
  • Chromosomal translocations: t(9;22) , t(12;21), t(5;14), t(1;19)
  • The most common cancer in children
  • Peak 2-5 years of age
  • Boys > girls
  • History of cancer
  • History of drug exposure
  • CNS involvement
Chronic myelogenous leukemia[6][7]
  • Median age 50 years old
Disease Etiology Demography History Symptoms Signs Lab Histopathology Gold standard diagnosis Associated findings
Chronic lymphocytic leukemia[8]
  • The most common leukemia in adults in western countries
  • M > F
  • Median age 70 years old
Hairy cell leukemia[9][10]
  • Accumulation of small mature B cell lymphoid cells with abundant cytoplasm and "hairy" projections
  • BRAF mutation
  • Uncommon
  • Median age 50 to 55 years old
  • M >> F
  • More common in Caucasians than Blacks
Large granular lymphocytic leukemia[11][12]
  • Rare
  • Median age 60 years
  • M = F
  • Mostly asymptomatic
  • Large lymphocytes with a condensed round or oval nucleus, abundant pale basophilic cytoplasm, and small azurophilic granules
  • Biopsy and flow cytometry + T-cell receptor gene rearrangement studies
  • Recurrent bacterial infection
Chronic neutrophilic leukemia[13]
  • Mature granulocytic proliferation in the blood and bone marrow
  • Point mutations in the CSF3R gene
  • Very rare
  • M = F
  • Toxic granulation in the neutrophils
  • Nuclear hypersegmentation
  • Increased myeloid:erythroid ratio > 20:1
  • WHO diagnostic criteria include leukocytosis of ≥ 25 x 109/L
  • More than 80% neutrophils,
  • Less than 10% circulating neutrophil precursors with blasts
  • Poor prognosis
  • Absence of the Philadelphia chromosome or a BCR/ABL fusion gene
Disease Etiology Demography History Symptoms Signs Lab Histopathology Gold standard diagnosis Associated findings
Chronic eosinophilic leukemia
  • There is no known cause for chronic eosinophilic leukemia.
  • It hasn't been linked to a specific chromosome or genetic abnormality.
  • Unknown
  • Unknown
Chronic monocytic leukemia
Prolymphocytic leukemia (PLL)
T-cell large granular lymphocytic leukemia (TLGL)
Disease Etiology Demography History Symptoms Signs Lab Histopathology Gold standard diagnosis Associated findings
Aggressive NK-cell leukemia (ANKL)
Adult T-cell leukemia/lymphoma (ATLL)[14][15][16][17][18][19]
  • Adult T-cell leukemia is caused by an infection with HTLV.
  • Common genetic mutations involved in the development of adult T-cell leukemia can be found here.
  • The incidence of adult T-cell leukemia increases with age, and the median age at diagnosis is 57 years.
  • Males are more commonly affected with adult T-cell leukemia than females.
  • The male to female ratio is approximately 1.4 to 1.
Sezary syndrome[20][21][22][23][24][25][26][27]
  • The cause of Sezary syndrome has not been identified.
  • Sezary syndrome might have one or more of the chromosomal abnormalities, such as the loss or gain of genetic.
  • The prevalence of Sezary syndrome is exact unknown.
  • The median age at diagnosis of Sézary syndrome is 60 years of age.
  • Sezary syndrome is more commonly observed among elderly patients.
  • Males are more commonly affected with Sezary syndrome than females(2:1).
Myelodysplastic syndrome Biopsy
  • Leukemia transformation
  • Acquired pseudo-Pelger-Huët anomaly
  • Infection
Myeloproliferative disorders
Leukemoid reaction

Epidemiology and Demographics

Prevalence

  • In the United States, the age-adjusted prevalence of leukemia is 75.3 per 100,000 in 2011.[29]

Incidence

  • The delay-adjusted incidence of leukemia in 2011 was estimated as 15.48 per 100,000 individuals in the United States.
  • In 2011, the age-adjusted incidence of leukemia was 13.66 per 100,000 individuals in the United States.

Age

  • The overall age-adjusted incidence of leukemia in the United States between 2007 and 2011 was 13 per 100,000 occurrences. The age-adjusted incidence of leukemia by age category is:
    • Under 65 years: 6.5 per 100,000
    • 65 and over: 57.9 per 100,000
  • Shown below is a table depicting the overall age-adjusted incidence of leukemia per 100,000 individuals by age in the United States between 2007 and 2011 for the different types of leukemia.
Acute lymphoblastic leukemia Chronic lymphocytic leukemia Acute myeloid leukemia Chronic myeloid leukemia
All ages 1.7 4.4 3.8 1.7
<65 1.7 1.4 1.8 0.9
≥65 1.6 25.2 17.5 6.8

Gender

  • In the United States, the age-adjusted prevalence of leukemia by gender in 2011 was:
    • In males: 92.7 per 100,000
    • In females: 60.7 per 100,000
  • In the United States, the delay-adjusted incidence of leukemia by gender in 2011 was:
    • In males: 19.93 per 100,000 persons
    • In females: 11.89 per 100,000 persons
  • In the United States, the age-adjusted incidence of leukemia by gender on 2011 was:
    • In males: 17.58 per 100,000 persons
    • In females: 10.49 per 100,000 persons
  • Shown below is an image depicting the delay-adjusted incidence and observed incidence of leukemia by gender and race in the United States between 1975 and 2011. These graphs were gathered from SEER: The Surveillance, Epidemiology, and End Results Program of the National Cancer Institute.
These graphs are adapted from SEER: The Surveillance, Epidemiology, and End Results Program of the National Cancer Institute. - Delay-adjusted incidence and observed incidence of leukemia by gender and race in the United States between 1975 and 2011

Race

  • Shown below is a table depicting the age-adjusted prevalence of leukemia by race in 2011 in the United States.
All Races White Black Asian/Pacific Islander Hispanic
Age-adjusted prevalence 75.3 per 100,000 83.5 per 100,000 45.9 per 100,000 41.2 per 100,000 57.1 per 100,000
  • Shown below is an image depicting the incidence of leukemia by race in the United States between 1975 and 2011.

Incidence of leukemia by race in the United States between 1975 and 2011

API: Asian/Pacific Islander; AI/AN: American Indian/ Alaska Native

Prognosis

5-Year Survival

  • Between 2004 and 2010, the 5-year relative survival of patients with leukemia was 60.3%.
  • When stratified by age, the 5-year relative survival of patients with leukemia was 68.5% (44.1% for patients <65 and ≥ 65 years of age respectively).
  • Shown below is a table depicting the 5-year relative survival of patients by the type of leukemia in the United States between 2004 and 2010.
Acute lymphoblastic leukemia Chronic lymphocytic leukemia Acute myeloid leukemia Chronic myeloid leukemia
5-year survival 70% 83.5% 25.4% 59.9%

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