Page 1057 - Equine Clinical Medicine, Surgery and Reproduction, 2nd Edition
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1032                                       CHAPTER 9



  VetBooks.ir  9.35                                       tumours in the horse, and must be differentiated
                                                          from the more common lymphoma, which can have
                                                          associated tumour cells in circulation.

                                                          Aetiology/pathophysiology
                                                          The underlying cause of lymphocytic leukaemia is
                                                          unknown.

                                                          Clinical presentation
                                                          Clinical signs tend to be vague and non-specific and
                                                          can include weight loss, poor appetite, weakness,
                                                          lethargy, oedema, colic, petechial haemorrhage,
                                                          fever and lymphadenopathy. ALL tends to occur in
                                                          younger horses.
           Fig. 9.35  Bone marrow aspirate from a horse
           with lymphocytic leukaemia. There is a monotypic   Differential diagnosis
           population of neoplastic lymphocytes present. Normal   The main differentials include other haematopoietic
           haematopoietic tissue is absent due to complete   tumours, particularly lymphoma, which can have
           effacement by neoplastic cells (Wright’s stain).  circulating tumour cells.

           developing haematopoietic cells. Further characteri-  Diagnosis
           sation of the cell type of origin can be difficult based   The diagnosis of leukaemia is based on observation
           on morphology alone in AML. Cytochemistry can   of atypical cells on blood smears and bone mar-
           be attempted, but results can be difficult to interpret.   row with ALL (Fig. 9.35) or increased numbers of
           The increased availability of cell lineage-specific   small lymphocytes with CLL. Cytopenia of other
           markers for individual species will result in a better   cell lines (erythrocytes, neutrophils, platelets) is
           ability to characterise these rare tumours in horses   variable, but is more likely with ALL. Bone mar-
           using immunohistochemical and flow-cytometric   row examination typically reveals hypercellularity
           techniques.                                    and increased proportion of blast cells (>20%) for
                                                          ALL. Flow cytometry can be used to determine
           Management/prognosis                           B-  or T-cell  origin,  although  markers  for  both
           The prognosis for AML is poor to grave in horses.   phenotypes can be present for a given tumour.
           The prognosis for MPNs and MDS are unknown,    Infiltration of other organs frequently occurs,
           as these are very poorly documented tumours in   including lymph nodes, liver, spleen, lungs, kid-
           this species. The uncommon occurrence of these   neys and GI tract.
           diseases has resulted in little study and therapeu-
           tic investigation. Chemotherapeutic options for  Management
           large animals tend to be very expensive and are   No treatment is effective for ALL and most horses
           unproven.                                      die or are euthanased soon after diagnosis. CLL is
                                                          a rare disease, and information on treatment is dif-
           LYMPHOPROLIFERATIVE DISEASE                    ficult to find.
           (LYMPHOCYTIC LEUKAEMIA)
                                                          Prognosis
           Definition/overview                            The prognosis for a horse with either ALL or
           Neoplastic proliferation of immature (acute lympho-  CLL is poor to grave. Most are euthanased or die
           cytic leukaemia, ALL) or mature (chronic lympho-  within days to weeks of diagnosis, with occasional
           cytic leukaemia, CLL) lymphocytes. These are rare   exceptions.
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