Page 1052 - Clinical Small Animal Internal Medicine
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990  Section 9  Infectious Disease

            alveolar‐interstitial patterns, pulmonary mass lesions,   involvement, radiographic lesions and clinical signs may
  VetBooks.ir  tracheobronchial lymphadenopathy, and/or single or   initially worsen with treatment. Initial worsening of radi­
                                                              ographic lesions does not appear to affect survival. Urine
            multiple  pulmonary  nodules  that  resemble  pulmonary
            neoplasia. Radiographs of affected bone typically show
                                                              Although a positive residual urine antigen titer at the
            osteolytic lesions, often accompanied by periosteal   antigen concentration declines with effective treatment.
              proliferation and soft tissue swelling.         time treatment is discontinued does not necessarily pre­
             A  diagnosis  of  blastomycosis is often  confirmed   dict that relapse will occur, a negative urine antigen test
            through cytologic examination of affected tissues, lung   is recommended before treatment is discontinued. Most
            washes or body fluids. The yeasts are 8–15 μm in  diameter,   dogs require at least 4–6 months of treatment, and some
            have a thick, refractile cell wall, and exhibit broad‐based   dogs may require treatment for more than one year,
            budding, although occasionally organisms are not visual­  especially those with osteoarticular infections or wide­
            ized. The organisms are usually accompanied by pyo­  spread dissemination. Treatment with amphotericin B
            granulomatous inflammation (Figure 109.2).        could be considered for dogs with severe disease with
             Other methods of diagnosis include histopathology   widespread dissemination, followed by azole therapy
            (e.g., of bone or tissue biopsies), fungal culture, antigen   after there has been a satisfactory clinical response to the
            testing, and molecular diagnosis with PCR‐based assays.   amphotericin B.
            Serologic tests for blastomycosis that detect antibody
            currently have poor sensitivity and specificity, and so the
            use of these tests is not recommended for routine diag­  Prognosis
            nosis. When performed on urine, assays for Blastomyces   Cure rates of 50–75% have been reported in dogs with
            cell wall galactomannan antigen (MiraVista Diagnostics,   blastomycosis; an additional 20–25% of dogs experience
            Indianapolis, IN) have high sensitivity (93.5%) and speci­  disease recurrence after treatment is discontinued,
            ficity (98%) for diagnosis of canine blastomycosis, but   which can occur as long as a year later. The most com­
            due  to  serologic  cross‐reactivity,  results  may  also  be   mon radiographic sequelae to pulmonary blastomycosis
              positive in dogs with other fungal infections, especially   are pulmonary bullae and persistent focal interstitial pat­
            histoplasmosis.                                   terns, presumably as a result of pulmonary fibrosis.
                                                              Involvement of the CNS, severe lung disease, and a high
            Therapy                                           band neutrophil count are negative prognostic factors.
            The most widely used specific therapy for blastomycosis
            in dogs is itraconazole or fluconazole. The duration of   Public Health Implications
            treatment should be based on serial monitoring of   Blastomyces dermatitidis causes disease in people. Direct
              clinical signs, radiographic lesions, and urine antigen   transmission between mammalian hosts does not occur,
            titers (i.e., every 4–8 weeks). For dogs with pulmonary   with the exception of inoculation of yeast via bite wound
                                                              or needle sticks. Laboratory personnel are at risk if
                                                                samples are cultured and should be warned that blasto­
                                                              mycosis is suspected prior to submission. Bodies of
                                                              deceased pets should be cremated rather than buried.
                                                              Dogs are sentinels for human exposure.



                                                                Histoplasmosis

                                                              Etiology/Pathophysiology
                                                              Histoplasma capsulatum is a dimorphic, soil‐borne
                                                                fungus. Microconidia produced by the fungus are inhaled
                                                              by mammalian hosts, and within the lungs transition to
                                                              the yeast phase, which replicates by budding within
                                                     10  m      alveolar macrophages. Some animals control the initial
                                                              infection but remain latently infected with small num­
            Figure 109.2  Cytology of a fine needle aspirate of a skin lesion   bers of yeasts. Subsequent immune suppression can lead
            from a dog showing a budding Blastomyces organism with
            associated pyogranulomatous inflammation. Source: Image   to reactivation years later. Replication of H. capsulatum
            courtesy of Dr Jed Overmann, University of Minnesota.  leads to a granulomatous inflammatory response, which
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