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Basics

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BASICS

Overview!!navigator!!

  • Term used to describe concurrent decrease in circulating erythrocytes, leukocytes, and thrombocytes
  • Rare in horses
  • Usually associated with disrupted hematopoiesis due to either a failure of stem cells to undergo differentiation (aplastic anemia) or destruction of the bone marrow microenvironment by neoplastic, fibrous, or inflammatory diseases (myelophthisis)

Signalment!!navigator!!

N/A

Signs!!navigator!!

  • Clinical signs reflect inadequate numbers of functional cells in blood or tissues and are usually nonspecific—weight loss, lethargy, poor performance, and intermittent pyrexia
  • Onset is often insidious
  • Hemorrhage due to thrombocytopenia—petechiation, epistaxis, mucosal bleeding, blood in feces, or prolonged bleeding from wounds
  • Mucous membrane pallor, tachycardia, and systolic heart murmur with marked anemia
  • Secondary infections due to leukopenia

Causes and Risk Factors!!navigator!!

  • Aplastic anemia may be congenital or acquired and can result from intrinsic stem cell failure or disruption of stem cell interactions in the bone marrow. It is often idiopathic, but is rarely associated with administration of drugs (e.g. phenylbutazone, chloramphenicol, estrogens, trimethoprim, or pyrimethamine) or secondary to infectious disease (e.g. EIA virus or Anaplasma phagocytophilum)
  • Myelophthisis has been associated with myelofibrosis, myelodysplasia, myeloproliferative disorders, or lymphoproliferative disorders

Diagnosis

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DIAGNOSIS

Differential Diagnosis!!navigator!!

  • See Causes and Risk Factors
  • Hemorrhage from vasculitis or thrombocytopenia unassociated with bone marrow dysfunction
  • Lethargy, pallor, petechiae, and edema may occur in piroplasmosis (Babesia caballi or Theileria equi infection)
  • Familial megakaryocytic and myeloid hypoplasia in Standardbred horses
  • Concurrent immune-mediated anemia and thrombocytopenia

CBC/Biochemistry/Urinalysis!!navigator!!

  • Anemia, thrombocytopenia, and leukopenia
  • Leukopenia—primarily due to a neutropenia without a left shift
  • Lymphocyte count may be normal
  • Anemia occurs after other derangements due to longer lifespan of erythrocytes (140 days) compared with thrombocytes (5 days) and neutrophils (12 h)
  • Examination of blood smears for A. phagocytophilum morulae in neutrophils, erythrocyte parasites (B. caballi, T. equi), absence of platelets, or abnormal leukocytes in leukemia

Other Laboratory Tests!!navigator!!

  • Serology—B. caballi, T. equi, or A. phagocytophilum
  • Coggins test—EIA
  • Coombs test

Imaging!!navigator!!

  • Radiography of the skeleton and thorax—multiple myeloma
  • Abdominal and thoracic ultrasonography—lymphoproliferative disorders

Other Diagnostic Procedures!!navigator!!

  • Bone marrow aspiration/biopsy
  • Obtain from the sternum or proximal rib (adults) and sternum, rib, or tuber coxae (foals)
  • Biopsies best for confirmation of bone marrow hypoplasia and myelofibrosis
  • Normal myeloid to erythroid ratio is 0.5–1.5: <0.5 suggests a regenerative erythrocyte response or myeloid hypoplasia
  • Urine protein electrophoresis for detection of Bence Jones proteins in multiple myeloma
  • Serum protein electrophoresis—monoclonal gammopathy suggests lymphoproliferative neoplasia
  • Immunophenotypic techniques for classification of leukemia

Pathologic Findings!!navigator!!

  • Variable, dependent on the cause of pancytopenia
  • Leukoproliferative disorders—neoplastic cells in bone marrow samples
  • Myelofibrosis—replacement of bone marrow with fibrous tissue
  • Aplastic anemia—hypocellularity and fat infiltration of bone marrow

Treatment

TREATMENT

  • Remove suspected causative medications
  • Supportive care; avoid trauma, rest

Medications

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MEDICATIONS

Drug(s) of Choice!!navigator!!

  • Immunosuppressive treatment (e.g. corticosteroids) if immune-mediated disease is present
  • Antimicrobial therapy if secondary infections occur
  • Blood or platelet-rich plasma transfusions provide only temporary improvement
  • Androgens may stimulate erythropoiesis in remaining hematopoietic tissue
  • No treatment for EIA exists
  • Treatment for A. phagocytophilum (oxytetracycline) or piroplasmosis (imidocarb dipropionate)

Contraindications/Possible Interactions!!navigator!!

  • Immune status may be compromised by corticosteroid treatment
  • Imidocarb is potentially fatal in donkeys

Follow-up

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FOLLOW-UP

Patient Monitoring!!navigator!!

  • Monitor for pyrexia, lethargy, pallor, hemorrhage
  • Regular hematologic monitoring

Prevention/Avoidance!!navigator!!

N/A

Possible Complications!!navigator!!

Hemorrhage, secondary infections.

Expected Course and Prognosis!!navigator!!

  • Anaplastic anemia; unpredictable prognosis
  • Myeloproliferative and lymphoproliferative disorders; hopeless prognosis

Miscellaneous

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MISCELLANEOUS

Associated Conditions!!navigator!!

N/A

Age-Related Factors!!navigator!!

N/A

Zoonotic Potential!!navigator!!

N/A

Pregnancy/Fertility/Breeding!!navigator!!

N/A

Abbreviations!!navigator!!

EIA = equine infectious anemia

Suggested Reading

Sellon DC, Wise LN. Disorders of the hematopoietic system. In: Reed SM, Bayly WM, Sellon DC, eds. Equine Internal Medicine, 3e. St. Louis, MO: WB Saunders, 2010:730776.

Author(s)

Author: Kristopher Hughes

Consulting Editors: David Hodgson, Harold C. McKenzie, and Jennifer L. Hodgson