Page 1281 - Clinical Small Animal Internal Medicine
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132  Paraneoplastic Syndromes  1219

                 Anemia/Thrombocytopenia                          Thrombocytopenia is not a contraindication to bone
  VetBooks.ir  Etiology/Pathophysiology                           marrow sampling, as the associated hemorrhage typi-
                                                                  cally results in an autotransfusion into the marrow,
               Anemia and thrombocytopenia can be grouped together   thereby remaining clinically silent. Prolonged external
                                                                  pressure to the incision site within the skin may be nec-
               as hematologic paraneoplastic syndromes as they may   essary, however.
               occur  together  due  to a  common  pathophysiology.   Classically, pancytopenia will develop with a leukope-
               Immune‐mediated destruction due to mimicry of cell   nia followed by thrombocytopenia. Anemia will develop
               membrane‐associated receptors or other immune cross‐  last due to the longer half‐life of red blood cells in rela-
               reactions tends to be the most widely accepted etiology of   tion to platelets and white blood cells. This may not be
               secondary immune‐mediated hemolytic anemia (IMHA)   the case in clinical practice, as multiple factors affect the
               and thrombocytopenia. Symptoms of anemia and throm-  production and destruction of all bone marrow ele-
               bocytopenia are nonspecific to the cause and are covered   ments. It is not uncommon to encounter myelophthisis
               elsewhere.                                         in the face of thrombocytopenia alone, and any combina-
                                                                  tion of cytopenias should raise suspicion for bone
                                                                    marrow involvement.
               Diagnosis
                                                                   If the anemia is determined to be regenerative, bone
               When anemia is considered individually, it must first   marrow sampling is typically not necessary. Red blood
               be  determined to be regenerative or nonregenerative.   cell morphology may identify clues as to the source of the
               A  nonregenerative anemia may suggest bone marrow   anemia. A morphology review by an experienced pathol-
               involvement, especially in conjunction with other cyto-  ogist or lab technician should be obtained. Specifically,
               penias. Bone marrow disease must be differentiated   immune‐mediated disease may be  confirmed by the
               from an acute anemia in which a regenerative response   presence of a moderate to large amount of spherocytes.
               has not yet had time to develop. Typically, it will take an   Spherocytes are red blood cells that have undergone a
               average of 3–5 days to develop a moderate regenerative   loss of membrane due to removal of antigen–antibody
               response, depending on how suddenly the anemia devel-  complexes by the phagocytic portion of the immune sys-
               oped and the degree of anemia. Additionally, clinical   tem. This results in a loss of surface area with retention
               signs of anemia tend to be more severe the more acute   of volume. The consequence of this is the red blood cell
               the onset, as the body has time to adapt to a chronically   changing its morphology from a biconcave disc to a
               developing anemia.                                 sphere, resulting in the term “spherocyte.” Immune‐
                 A bone marrow biopsy and/or aspirate should be con-  mediated  hemolytic  anemia  may  also  be  diagnosed  by
               sidered in the face of a chronic, nonregenerative anemia.   identifying gross or microscopic autoagglutination. In
               The author prefers to begin with a bone marrow aspirate.   the absence of a significant number of spherocytes or
               If the aspirate is productive, a slide may be reviewed to   detectable autoagglutination, a Coombs test may be per-
               assess for cellularity. Bone marrow infiltration due to lym-  formed to identify an immune component to the anemia.
               phoma or myeloma tends to be highly cellular, and assum-  In the presence of visibly detectable autoagglutination, a
               ing bone marrow elements are observed in a   cellular   Coombs test is not necessary.
               sample, an aspirate may suffice. If the aspirate is nonpro-  A schistocyte is a red blood cell fragment that may
               ductive (i.e., a “dry” tap), a bone marrow biopsy may be   develop due to shearing forces. These fragments do not
               obtained. A biopsy may be necessary to obtain a diagnosis   have a central pallor and are irregular. Schistocytes may be
               of myelofibrosis or other chronically progressive bone   noted in IMHA, but they are most commonly recognized
               marrow disorders. With these chronic   conditions, bone   as a consequence of hemangiosarcoma. Red blood cells
               marrow elements are replaced by fibrosis and the aspirate   may be damaged as they travel through the smaller blood
               may be hemodilute or completely nonproductive.     vessels and fibrin strands of the tumor, and as such
                 As most animals present with a moderate to severe     schistocytes should prompt evaluation for an underlying
               anemia, these procedures are generally performed   vascular neoplasm. Anemia due to damage to red blood
               shortly after a component blood transfusion to improve   cells as they travel through the smaller capillary beds is
               the candidacy for anesthesia. It is important to remem-  often termed microangiopathic anemia. Microangiopathic
               ber that if a bone marrow aspirate or biopsy is deemed   anemia  may  be  seen  with  any  hypercoagulable  disease,
               necessary, it should be obtained before or within 12 hours   and should also alert the clinician to the potential for
               of beginning  steroid  therapy. Steroids, including  pred-  thrombosis. Fibrin strands and smaller blood clots may be
               nisone and dexamethasone, are directly cytotoxic to   noted with hyperadrenocorticism, pancreatitis and other
               lymphoma and myeloma cells. These are two of the more   nonneoplastic disorders, and these may all result in a
               common cancers that may infiltrate the bone marrow.   microangiopathic anemia.
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