Page 1404 - Small Animal Internal Medicine, 6th Edition
P. 1404

1376   PART XIII   Hematology


            which the number of immature forms does not exceed the
            number  of  mature  neutrophils;  most  dogs  and cats  with    BOX 85.2
  VetBooks.ir  a regenerative left shift have leukocytosis. A degenera-  Causes of Neutrophilia in Cats and Dogs
            tive left shift occurs when the number of immature forms
            exceeds that of mature neutrophils; the number of the latter
            may be  normal, low, or high. Degenerative left  shifts are   Physiologic or Epinephrine-Induced Neutrophilia
                                                                  •  Fear (C)
            usually suggestive of an aggressive disease; toxic neutrophil   •  Excitement (?)
            changes (see earlier)  are common in  dogs and cats  with   •  Exercise (?)
            degenerative left shifts. Disorders commonly associated with   •  Seizures (D, C)
            degenerative left shifts  include pyothorax, septic peritoni-  •  Parturition (?)
            tis,  bacterial pneumonia, pyometra, prostatitis, and acute   Stress- or Corticosteroid-Induced Neutrophilia
            pyelonephritis. The term extreme neutrophilia refers to situ-
            ations in which the neutrophil count is above 50,000/µL   •  Pain (?)
                                                                  •  Anesthesia (?)
                   9
            (50 × 10 /L); it can be associated with a left shift or mature   •  Trauma (D, C)
            neutrophilia. Diseases typically associated with extreme   •  Neoplasia (D, C)
            leukocytosis include septic foci (e.g., pyometra), immune-  •  Hyperadrenocorticism (D)
            mediated diseases, hepatozoonosis, mycobacteriosis, and   •  Metabolic disorders (?)
            chronic myelogenous leukemia. A leukemoid reaction refers   •  Chronic disorders (D, C)
            to a marked neutrophilia with a severe left shift, which
            includes metamyelocytes and myelocytes. It indicates severe   Inflammation or Increased Tissue Demand
            inflammatory disease and may be difficult to distinguish   •  Infection (bacterial, viral, fungal, parasitic) (D, C)
            from chronic granulocytic (myelogenous) leukemia (see     •  Tissue trauma and/or necrosis (D, C)
            Chapter 80).                                          •  Immune-mediated disorders (D)
              Although a high percentage of cats and dogs with neutro-  •  Neoplasia (D, C)
            philia have underlying infectious disorders, neutrophilia is   •  Metabolic (uremia, diabetic ketoacidosis) (D, C)
                                                                  •  Burns (D, C)
            not synonymous with infection. Rather, neutrophilia in cats   •  Neutrophil function abnormalities (D)
            and dogs is commonly the result of inflammatory or neo-  •  Other (acute hemorrhage, hemolysis) (D, C)
            plastic processes. Several disorders resulting in neutrophilia
            are listed in Box 85.2.                              Note: Entries in boldface are common causes; entries in italics are
              Of note, neutrophilia commonly results from endogenous   relatively common causes; entries in regular typeface are
            epinephrine release (physiologic neutrophilia). This neutro-  uncommon causes.
            philia, which is associated with the release of neutrophils   C, Cat; D, dog; ?, poorly documented.
            from  the  MNP,  is transient  (lasting  20-30  minutes  after
            endogenous  release  of  catecholamines)  and  is  commonly
            associated with erythrocytosis and lymphocytosis, the latter   abdominal ultrasonography (e.g., peritonitis, pancreatic or
            primarily in cats.                                   hepatic abscess), and the collection of blood, urine, fluid,
              The endogenous release or exogenous administration of   or tissue samples for cytology and bacterial and fungal cul-
            corticosteroids results in stress- or corticosteroid-induced   tures. As noted, autologous or allogeneic neutrophils labeled
            neutrophilia, which are associated with decreased neu-  with radionuclides (e.g., technetium-99m or indium-111)
            trophil egress from the vasculature and increased bone   can  be  injected  intravenously  and  the  septic  focus  or  foci
            marrow release of neutrophils from the storage pool. Other   identified by gamma camera imaging, but this is rarely done;
            hematologic changes typical of a stress leukogram include   an inflammatory focus can also be detected by radiolabeled
            lymphopenia, eosinopenia, and monocytosis; the latter is   ciprofloxacin.
            uncommon in cats. These abnormalities are commonly seen   The treatment of dogs and cats with neutrophilia is aimed
            in sick dogs and cats. Dogs with hypoadrenocorticism and   at the primary cause. Empiric antibiotic therapy with a
            inflammatory/infectious diseases typically lack the neutro-  broad-spectrum bactericidal antibiotic (e.g., trimethoprim-
            philic response of normal dogs; that is, they are sick but do   sulfamethoxazole, enrofloxacin, cephalosporin, amoxicillin)
            not have a stress leukogram.                         is an acceptable approach if a cause for the neutrophilia
              Clinical signs in cats and dogs with neutrophilia are   cannot be identified after exhaustive clinical and clinico-
            usually secondary to the underlying disorder. Pyrexia may or   pathologic evaluation or as the first line of treatment in a
            may not be present. If the patient has persistent neutrophilia,   fairly asymptomatic dog or cat.
            the neutrophils display toxic changes (see  p. 1371), or a
            degenerative left shift is present, every effort should be made   EOSINOPENIA
            to identify a septic focus or an infectious agent promptly. The   Eosinopenia is defined as an absolute decrease in the number
            workup in these animals should include a thorough physical   of circulating eosinophils. It is commonly seen as part of the
            examination (e.g., abscess), thoracic and abdominal radi-  stress leukogram or with exogenous corticosteroid adminis-
            ography  (e.g.,  pneumonia,  pleural  or abdominal  effusion),   tration and is usually of little clinical relevance.
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