Sandbox: wdx causes: Difference between revisions

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! rowspan="6" style="background: #4479BA; color: #FFFFFF; text-align: center;" |Hematologic
! rowspan="6" style="background: #4479BA; color: #FFFFFF; text-align: center;" |Hematologic
|Hereditary neutrophilia
! align="center" style="background:#DCDCDC;" |Hereditary neutrophilia
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|Chronic idiopathic neutrophilia
! align="center" style="background:#DCDCDC;" |Chronic idiopathic neutrophilia
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|CML
! align="center" style="background:#DCDCDC;" |CML
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|Polycythemia Vera
! align="center" style="background:#DCDCDC;" |Polycythemia Vera
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|Hemolytic anemia
! align="center" style="background:#DCDCDC;" |Hemolytic anemia
!Marrow stimulation
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|Immature thrombocytopenia
! align="center" style="background:#DCDCDC;" |Immature thrombocytopenia
!Marrow stimulation
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! rowspan="6" style="background: #4479BA; color: #FFFFFF; text-align: center;" |Immunology/
! rowspan="6" style="background: #4479BA; color: #FFFFFF; text-align: center;" |Immunology/
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! style="background: #4479BA; color: #FFFFFF; text-align: center;" |Associated findings
! style="background: #4479BA; color: #FFFFFF; text-align: center;" |Associated findings
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|RA
! align="center" style="background:#DCDCDC;" |RA
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!JRA
! align="center" style="background:#DCDCDC;" |JRA
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!IBD
! align="center" style="background:#DCDCDC;" |IBD
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|Chronic hepatitis
! align="center" style="background:#DCDCDC;" |Chronic hepatitis
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|Acute Gout
! align="center" style="background:#DCDCDC;" |Acute Gout
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! rowspan="4" style="background: #4479BA; color: #FFFFFF; text-align: center;" |Metabolic
! rowspan="4" style="background: #4479BA; color: #FFFFFF; text-align: center;" |Metabolic
|Diabetic coma
! align="center" style="background:#DCDCDC;" |Diabetic coma
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|Acidosis
! align="center" style="background:#DCDCDC;" |Acidosis
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! align="center" style="background:#DCDCDC;" |Thyroid strom
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! align="center" style="background:#DCDCDC;" |Seizures
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Revision as of 17:20, 13 September 2018

Differentiating Leukocytosis from Other Diseases

  • There are no other mimickers of pancytopenia, as the diagnosis can be unequivocally established by laboratory testing (complete blood count).
Category Condition Etiology Mechanism Congenital Acquried Clinical manifestations Para−clinical findings Gold standard Associated findings
Demography History Symptoms Signs
Lab Findings
Appearance Fever Bleeding BP Splenomegaly Jaundice Other CBC PBS Bone marrow exam PT PTT UA
Physiologic Primary Secondary Plt HB WBC
Hematologic Hereditary neutrophilia
Chronic idiopathic neutrophilia
CML
Polycythemia Vera
Hemolytic anemia
Immature thrombocytopenia
Immunology/

Rheumatology

Condition Etiology Bone marrow infiltration Bone marrow failure Destruction/

sequestration/ redistribution

Congenital Acquried Demography History Appearance Fever Bleeding BP Splenomegaly Jaundice Other signs Plt HB WBC PBS Bone marrow exam PT PTT UA Gold standard Associated findings
RA
JRA
IBD
Chronic hepatitis
Acute Gout
Metabolic Diabetic coma
Acidosis
Thyroid strom
Seizures
Infections Condition Etiology Bone marrow infiltration Bone marrow failure Destruction/

sequestration/ redistribution

Congenital Acquried Demography History Appearance Fever Bleeding BP Splenomegaly Jaundice Other signs Plt HB WBC PBS Bone marrow exam PT PTT UA Gold standard Associated findings
Acute
Chronic
Medications Steriod
Lithium
Beta agonists
Cytokines
Other Post splenectomy
Down syndrome
Birth
Pregnancy
Category Condition Etiology Bone marrow infiltration Bone marrow failure Destruction/

sequestration/ redistribution

Congenital Acquried Demography History Appearance Fever Bleeding BP Splenomegaly Jaundice Other signs Plt HB WBC PBS Bone marrow exam PT PTT UA Gold standard Associated findings


  • Leukocytosis is defined as an elevated white blood cell (WBC) count greater than 11,000 per mm3 (11.0 × 109 per L).
  • The most common type of leukocytosis is neutrophilia.
    • Neutrophilia can be defined as an increase in the absolute number of mature neutrophils to greater than 7,000 per mm3 [7.0 × 109 per L].