Chronic lymphocytic leukemia differential diagnosis: Difference between revisions

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==Differenting Chronic lymphocytic leukemia from other Diseases==
==Differenting Chronic lymphocytic leukemia from other Diseases==
===Differentials based on Biomarkers===
* Chronic lymphocytic leukemia must be differentiated from other diseases that cause [[weight loss]],  [[night sweats]], [[hepatosplenomegaly]], and palpable [[lymph node]]s, such as [[hairy cell leukaemia]], prolymphocytic leukaemia, [[follicular lymphoma]], and [[mantle cell lymphoma]].
* Based on the expression of cell surface markers, the table below differentiates chronic lymphocytic leukemia from other diseases that cause similar clinical presentations:
<br>
{| style="border: 0px; font-size: 90%; margin: 3px; width: 1000px"
| valign="top" |
|+
! style="background: #4479BA; width: 600px;" | {{fontcolor|#FFF|'''Differential Diagnosis'''}}
! style="background: #4479BA; width: 300px;" | {{fontcolor|#FFF|'''Surface Immunoglobulin'''}}
! style="background: #4479BA; width: 300px;" | {{fontcolor|#FFF|'''CD5'''}}
! style="background: #4479BA; width: 400px;" | {{fontcolor|#FFF|'''CD22/FMC7'''}}
! style="background: #4479BA; width: 300px;" | {{fontcolor|#FFF|'''CD23'''}}
! style="background: #4479BA; width: 300px;" | {{fontcolor|#FFF|'''CD79b'''}}
! style="background: #4479BA; width: 300px;" | {{fontcolor|#FFF|'''CD103'''}}
|-
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" |
'''Chronic lymphocytic leukemia'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Weakly positive'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Positive'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Negative'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Positive'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Negative'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Positive/Negative'''
|-
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" |
'''[[Prolymphocytic leukemia]]'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Strongly positive'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Negative'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Positive'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Negative'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Positive'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Negative'''
|-
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" |
'''[[Hairy cell leukemia]]'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Strongly positive'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Negative'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Positive'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Negative'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Positive/Negative'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Positive'''
|-
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" |
'''[[Mantle cell lymphoma]]'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Positive'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Positive'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Strongly positive'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Negative'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Strongly positive'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Negative'''
|-
| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" |
'''[[Follicular lymphoma]]'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Strongly positive'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Negative'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Positive'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Negative'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Strongly positive'''
| style="padding: 5px 5px; background: #F5F5F5;" align="center" |
'''Negative'''
|}
<br>
* Chronic lymphocytic leukemia must also be differentiated from other causes of fever, hepatosplenomegaly, and lymph node swelling such as:
:* [[Splenic marginal zone lymphoma]]
:* Nodal marginal zone [[lymphoma]]
:* [[Lymphoplasmacytic lymphoma]]
:* [[Sézary syndrome]]
:* Smoldering [[adult T cell leukemia]]
===Other Differentials===
The following table differentiates chronic lymphocytic leukemia from other leukemias that may present with similar clinical features such as [[fever]], [[fatigue]], [[weight loss]], recurrent [[infections]] and elevated [[leukocyte counts]]. The following are the differentials:
{| class="wikitable"
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Characteristic
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Causes
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Laboratory abnormalities
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Physical examination
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Therapy
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Other associations
|-
|[[Acute myeloid leukemia|'''Acute myeloid leukemia''']]
|
* [[Chromosomal]] instability
* Sporadic [[mutations]]
* Prior exposure to [[benzene]]
* Prior exposure to alkylating agents
* Prior exposure to [[Topoisomerase II|topoisomerase II inhibitors]]
* [[Germline]] ''[[RUNX1]]'' [[mutation]]
|
* [[Anemia]]
* [[Thrombocytopenia]]
* [[Neutropenia]]
* Elevated [[LDH]]
* Elevated [[uric acid]]
* Elevated [[phosphorus]]
* Elevated [[potassium]]
* Low [[calcium]]
* Greater than 20% [[myeloblasts]] on [[bone marrow]] aspirate.
|
* [[Pyrexia]]
* Evidence of [[infection]]
* [[Pallor]]
* [[Mucosal]] [[bleeding]] (less common than in [[acute promyelocytic leukemia]])
* [[Bruising]] (less common than in [[acute promyelocytic leukemia]])
|
* [[Cytarabine]]
* [[Anthracycline]]
* [[Enasidenib]]
* [[Liposomal]] [[daunorubicin]] plus [[cytarabine]]
* [[Gemtuzumab ozogamicin|Gemtuzumab ozogamycin]]
* [[Midostaurin]]
* [[Enasidenib]]
* Ivosidenib
* [[Stem cell transplant]]
|
* Variable [[prognosis]] based on [[cytogenetic]] and molecular profile
* Five new [[Food and Drug Administration|FDA]]-approved therapies became available in 2017-2018
|-
|[[Acute promyelocytic leukemia|'''Acute promyelocytic leukemia''']]
|
* Prior exposure to alkylating agents
* Prior exposure to [[topoisomerase II]] inhibitors
* [[Chromosomal translocation|Translocation]] between [[Chromosome 15 (human)|chromosomes 15]] and [[Chromosome 17 (human)|17]]
* Creation of PML-RAR''alpha'' [[gene]] product
* Differentiation block in [[myeloid cells]]
|
* Low [[white blood cell]] count (typically)
* [[Anemia]]
* [[Neutropenia]]
* [[Thrombocytopenia]]
* Low [[fibrinogen]]
* Elevated prothrombin time (PT)
* Elevated partial thromboplastin time (PTT)
|
* [[Mucosal bleeding]]
* [[Petechiae]]
* [[Ecchymoses]]
* Evidence of [[infection]]
* [[Pallor]]
* [[Thrombosis]]
|
* [[All-trans retinoic acid|All-''trans'' retinoic acid]] (ATRA)
* Arsenic trioxide
* [[Cytarabine]]
* [[Anthracycline]]
|
* Presence of [[Auer rods]] in promyelocytes
* High risk for early death from [[hemorrhagic]] complications
|-
|[[Acute lymphoblastic leukemia|'''Acute lymphoblastic leukemia''']]
|
* [[Chromosomal]] instability
* Sporadic [[mutations]]
|
* [[Anemia]]
* [[Thrombocytopenia]]
* [[Neutropenia]]
* Elevated [[LDH]]
* Elevated [[uric acid]]
* Elevated [[phosphorus]]
* Elevated [[potassium]]
* Low [[calcium]]
* Greater than 20% [[lymphoblasts]] on [[bone marrow]] aspirate
|
* [[Neurological|Neurologic]] deficits
* [[Pallor]]
* [[Lymphadenopathy]]
|
* HyperCVAD ([[cyclophosphamide]], [[vincristine]], [[doxorubicin]], [[dexamethasone]])<ref name="pmid28665419">{{cite journal| author=Terwilliger T, Abdul-Hay M| title=Acute lymphoblastic leukemia: a comprehensive review and 2017 update. | journal=Blood Cancer J | year= 2017 | volume= 7 | issue= 6 | pages= e577 | pmid=28665419 | doi=10.1038/bcj.2017.53 | pmc=5520400 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28665419  }} </ref>
* R-HyperCVAD (inclusion of [[rituximab]])
* Peg-asparaginase
* [[Intrathecal]] [[methotrexate]]
* [[Intrathecal]] [[cytarabine]]
* [[Blinatumomab]] (bispecific [[T cell]] engager)
* [[Inotuzumab ozogamicin|Inotuzumab]] ozogamycin (anti-CD22 antibody)
* [[Tisagenlecleucel]] (chimeric antigen receptor T (CAR-T) cell therapy)
* [[Stem cell transplant]]
|
* Sanctuary sites include the [[central nervous system]] ([[CNS]]) and [[testes]]
|-
|[[Chronic myelogenous leukemia|'''Chronic myeloid leukemia''']]
|
* [[Translocation]] between [[Chromosome 9 (human)|chromosomes 9]] and [[Chromosome 22|22]]
* Creation of [[Bcr-abl|BCR-Abl]] [[gene]] product
|
* Elevated [[white blood cell]] count
* Presence of [[white blood cell]] precursors at various stages of maturation
* Presence of excess metamyelocytes, [[basophils]], [[eosinophils]], and [[band cells]]
|
* [[Splenomegaly]]
* [[Abdominal tenderness]]
* [[Pallor]]
* Evidence of [[infection]]
|
* [[Imatinib]]
* [[Nilotinib]]
* [[Dasatinib]]
* [[Bosutinib]]
* [[Ponatinib]]
* [[Omacetaxine]]
|
* High response rate to [[tyrosine kinase inhibitors]]
* Risk for development of T315I [[kinase]] domain [[mutation]]
* Typically does not require [[stem cell transplant]]
* Three phases include chronic, accelerated, and blast phase
|-
|-
|[[Chronic lymphocytic leukemia|'''Chronic lymphocytic leukemia''']]
|
* Chromosomal instability
* Sporadic [[mutations]]
* [[Infections]]
|
* Elevated absolute [[lymphocyte]] count (in all stages)
* Presence of >5000 clonal [[B cells]] per microliter in peripheral blood
* Anemia (in Rai stage III)
* [[Thrombocytopenia]] (in Rai stage IV)
|
* [[Lymph node enlargement]] in Rai stage I
* [[Splenomegaly]] in Rai stage II
* [[Hepatomegaly]] in Rai stage II
* [[Pallor]]
* [[Bleeding]]
|
* Fludarabine
* Cyclophosphamide
* Rituximab
* Obinutuzumab
* Ofatumumab
* Ibrutinib
* Venetoclax
|
* Associated with [[autoimmune hemolytic anemia]], which occurs in 10-25% of patients with CLL
* Associated with [[immune thrombocytopenia purpura]]
* Associated with [[pure red cell aplasia]]
* Treatment with corticosteroids or anti-leukemic therapy will correct the autoimmune complications of CLL
|}


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==References==

Revision as of 16:32, 12 February 2019

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