Page 1056 - Equine Clinical Medicine, Surgery and Reproduction, 2nd Edition
P. 1056

H aemolymphatic system                                   1031



  VetBooks.ir  of PCV. Initially, PCV should be monitored every  Clinical presentation
                                                         Horses are typically presented with vague signs of
          few days. The goal should be to maintain a PCV of
          <0.50 l/l (50%). Secondary polycythaemia caused
                                                         argy, inappetence, weight loss and weakness. More
          by hypoxia should not be treated by aggressive   disease that may include poor performance, leth-
          phlebotomy because the increased PCV is a com-  specific signs indicating haematological involvement
          pensatory mechanism. If the PCV is not markedly   may include pale mucous membranes and petechial
          elevated (<0.60 l/l [<60%]), removal of smaller vol-  or ecchymotic haemorrhages.  Intermittent fever
          umes of blood is indicated. The primary cause of   may be present when opportunistic infections occur
          hypoxia must be addressed. In humans and small   due to neutropenia.
          animals, hydroxyurea has been used to induce
          reversible bone marrow suppression; however, its  Differential diagnosis
          use has not been reported in horses.           If the presence of circulating atypical cells is con-
                                                         firmed, the primary differential diagnoses are myelo-
          Prognosis                                      proliferative and lymphoproliferative disorders.
          The prognosis for relative polycythaemia is good
          if appropriate fluid therapy is administered and the  Diagnosis
          cause of dehydration can be addressed. Cases of sec-  Diagnosis of AML is based on the observation of
          ondary polycythaemia carry a more guarded prog-  atypical cells on blood smears or in bone marrow
          nosis, especially those due to neoplasia.      (Fig. 9.34), while MPNs can be recognised based on
                                                         inappropriate accumulation of mature cells. MDS
          MYELOPROLIFERATIVE DISEASE                     usually results in one or more peripheral blood cyto-
          (MYELOID LEUKAEMIA)                            penias, with accompanying dysplastic features in


          Definition/overview
          Tumours of developing non-lymphocytic haema-    9.34
          topoietic cells including those derived from eryth-
          rocytes, granulocytic cells, monocytic cells and
          platelets are classified into acute myeloid leukaemia
          (AML), myeloproliferative neoplasms (MPNs) and
          myelodysplastic syndrome (MDS). These diseases
          are often collectively referred to as leukaemias and
          are rare in horses.

          Aetiology/pathophysiology
          Neoplastic transformation of any cell line may occur,
          but the underlying cause is usually unknown in
          horses. Unregulated proliferation of a cell line at a
          certain stage of development results in the increased
          autonomous production of these cells in bone mar-
          row, which can then infiltrate other tissues and be
          found in circulating blood. The tumour replaces nor-
          mal haematopoietic cells, resulting in cytopenias in   Fig. 9.34  Blood smear from a horse with acute
          other cell lines due to lack of production. Neoplastic   myeloid leukaemia. A monotypic population of
          cells are often observed in circulation, as they are   large round cells with round-to-indented nuclei
          released from bone marrow. Other tissues affected   and multiple prominent nucleoli is pictured
          may include the spleen, liver and lymph nodes.  (Wright’s stain). (Photo courtesy RM Jacobs)
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