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1446  Section 12  Skin and Ear Diseases

            every 48 hours. Regression of the lesions may take 2–8   Clinical Signs
  VetBooks.ir  weeks. If remission has not been achieved after four   The clinical signs are characterized by firm, hair‐covered
            weeks of daily immunosuppressive doses of glucocorti-
                                                              to partially alopecic, erythematous papules, nodules, or
            coids, the case may require combination therapy with
            other immunosuppressive drugs such as azathioprine or   plaques. Lesions develop more commonly on the head
                                                              and distal extremities, and less commonly on the pinnae,
            ciclosporin. Topical and intralesional corticosteroids   eyes, trunk, and abdomen. Lesions involving the tongue
            have been effective in some cases, and may be the treat-  and prepuce have been seen in individual dogs. In most
            ment of choice when systemic immunosuppressive ther-  cases, the lesions are multiple and are not associated
            apy is contraindicated. In addition to immunosuppressive   with pain or pruritus. Occasionally, draining tracts and
            treatment, vitamin E and potassium iodide have been   ulceration can be observed, especially on lesions local-
            recommended, but their efficacy is unknown.
                                                              ized to the feet (Figure 164.5).
                                                                Lymphadenopathy was present in 31% of the cases in a
            Prognosis                                         review including 29 dogs. Systemic signs associated with
                                                              this syndrome have not been reported. The condition
            The prognosis is usually good, with most cases showing   may resolve spontaneously or take a waxing and waning
            a good response to treatment. Some cases may require   course.
            prolonged immunosuppressive therapy.

                                                              Diagnosis
              Sterile Granuloma/Pyogranuloma
            Syndrome                                          Clinical differential diagnoses include bacterial and fun-
                                                              gal infections, foreign bodies, SNP, cutaneous eosino-
                                                              philic granulomas, and cutaneous neoplasms. Diagnosis
            Sterile granuloma/pyogranuloma syndrome (SGPS) is an   of SGPS is based on its clinical appearance, histopatho-
            uncommon disease presenting clinically with cutaneous   logic findings, and failure to document the presence of
            papules,  nodules  or  plaques  of  unknown  origin.  The   microorganisms. Wedge biopsies should be performed
            lesions may be solitary or multiple, and localized or   to  collect  samples  that  include  the  epidermis,  dermis,
            generalized.
                                                              and subcutaneous tissue. The samples should be col-
                                                              lected aseptically if they are being submitted for cultures.
            Pathogenesis                                      Histopathologically, SGPS is characterized by multifocal,
                                                              nodular to diffuse pyogranulomatous/granulomatous
            Sterile granuloma/pyogranuloma syndrome is an idio-  dermal infiltrates. Special stains on biopsy samples are
            pathic canine skin disorder. The pathogenesis is   negative. Aerobic and anaerobic bacterial cultures and
            unknown, but the inflammatory nature of the infiltrate,   fungal culture from fresh tissue samples are also nega-
            failure to demonstrate infectious agents, and the good to   tive. Some organisms are difficult to culture or identify
            excellent response to immunomodulating drugs support   with routine methods, and molecular studies such as
            it being an immune‐mediated disorder. However, it has
            been hypothesized that SGPS may be related to an
            immune  response  against  persistent  endogenous  or
            exogenous antigens,  such as  Leishmania spp.  or
            Mycobacterium spp. organisms or incomplete clearing of
            associated antigens, causing a granulomatous/pyogranu-
            lomatous inflammatory reaction. The presence of
            Leishmania spp. DNA has been documented in cases of
            SGPS in Spain and Italy. The finding of antigenic frag-
            ments or organisms may become possible as we advance
            our diagnostic techniques.


            Signalment
            Sterile granuloma/pyogranuloma syndrome can affect
            dogs of any age and gender, but in a retrospective study
            24/29 cases were male. It is seen more frequently in the   Figure 164.5  Partially alopecic, erythematous and ulcerated
                                                              nodule present in the interdigital space of digits 4 and 5 in a
            Great Dane, boxer, golden retriever, collie, dachshund,   dog with sterile granulomatous pyogranulomatous syndrome.
            English bulldog, and Weimaraner.                  Source: Courtesy of Dr Wendy Lorch.
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