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Monocytosis and Monocytopenia

Monocytosis

It is a condition in which absolute monocyte count is more than 800/cmm in adults.

 

Causes

  • Myeloid neoplasms
    • MDS (25% patients have monocytosis)
    • Acute monocytic leukemia.
    • Acute myelomonocytic leukemia.
    • Chronic myelomonocytic leukemia.
    • Juvenile myelomonocytic leukemia.
    • CML (m BCR-positive type)
    • Polycythemia vera.
    • Lymphoid neoplasms- NHL, HD, myeloma, macroglobulinemia, T cell lymphoma
  • Inflammatory and immune disorders.
    • RA
    • SLE
    • Temporal arteritis
    • Kawasaki disease
    • Myositis
    • Polyarthritis nodosa
    • Sarcoidosis
    • Inflammatory bowel disease
    • Immune thrombocytopenia
  • Infections
    • Mycobacterial infections
    • Subacute bacterial endocarditis
    • Brucellosis
    • Dengue hemorrhagic fever
    • Resolution phase of acute bacterial infections
    • Syphilis
    • CMV infection
    • Influenza
    • Varicella zoster virus
    • Rickettsia.
    • Protozoal infections (Ex: Leishmaniosis)
    • Chronic fungal infections
  • GI disorders.
    • Alcoholic liver disease
    • Inflammatory bowel disease.
    • Sprue
  • Miscellaneous
    • Parturition
    • Glucocorticoid administration
    • Depression
    • Chronic stress
    • Thermal injury
    • Marathon running
    • Chronic neutropenia.
    • Drug induced neutropenia.
    • WiskotAdlrich syndrome
    • Immune hemolytic anemia.
    • Sickle cell anemia
    • Post splenectomy state
    • Recovery from myelosuppression
    • Non hematopoietic malignancies
    • Exogenous cytokine administration: G-CSF, IL10.
    • Myocardial infarction/ Cardiac bypass surgery
    • Lipid storage disorders

 

Monocytopenia

Causes:

  • Aplastic anemia
  • Myelodysplastic syndrome
  • Hairy cell leukemia
  • Glucocorticoid therapy 
  • Monocytopenia- Mycobacterium Avium Complex syndrome- Autosomal dominant/ sporadic mutation of GATA, Bone marrow is hypocellular with reticulin fibrosis, multilineage dysplasia is seen, Cytogenetics: del 7 and trisomy 8. Treatment- HSCT
  • Drugs: Chemotherapy, interferon alpha
  • Radiation therapy
  • Overwhelming sepsis
  • Stress

 

Clinical manifestations:

  • Increased risk of infection with mycobacteria, listeria, brucella, trypanosomes and other granuloma producing organisms

 

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