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155  Mast Cell Neoplasia  1365

                 Adjuvant therapy with vinblastine/lomustine or     Feline Mast Cell Tumors
  VetBooks.ir  Palladia for high‐grade MCT is recommended even if   Epidemiology
               the mass has been completely excised. Most adjuvant
               treatment protocols strive for 3–6 months of therapy,
               depending on tumor response and the patient’s toler-  Feline MCTs represent the second most common skin
               ance. In the adjuvant setting, chemotherapy results in   tumor in the cat. A genetic correlation has been linked to
               median overall survival times of 11–16 months.     young Siamese cats. In addition, cats may develop both a
                                                                  visceral form of MCT that primarily originates in the
                                                                  spleen and a primary intestinal form.
               Prognosis
               Multiple factors have prognostic value for canine   Signalment
               MCTs. A subset of tumors have a more aggressive    Cutaneous forms of feline MCTs are most commonly
               behavior based on their anatomic location. MCTs    found in cats 10 years of age, with no reported gender
               of  the inguinal region (groin, perivulvar, scrotal,   predilection. Siamese less than 4 years of age are reported
                 perianal) have historically been regarded as having   to be predisposed to the less common histiocytic form of
               greater  metastatic potential. Newer information has   cutaneous MCT. Visceral (both spleen and intestinal
               revealed  that survival is dependent on histologic   involvement) forms more commonly occur in older cats.
               grade. However, dogs with MCTs in these locations,
               specifically preputial and scrotal, have a decreased   History and Clinical Signs
               disease‐free interval as both local recurrence and the
               development of subsequent MCTs are common. The     The majority of cutaneous lesions occur on the head and
               biologic behavior of tumors in these areas is still   neck but can occur throughout the body. The most com-
               debated so it is reasonable to use caution and proceed   mon presentation is a red, raised dermal lesion. As in the
               with routine MCT staging and more routine follow‐up   canine form, MCTs can appear with many other cutane-
               regardless of grade.                               ous manifestations including ulcerations, plaques, etc.
                 Mucocutaneous MCT (muzzle, vulva, sclera, etc.) and   (Figure 155.6).
               oral locations (tongue, palate) have a greater metastatic   Both abdominal forms of MCT result in a systemically ill
               potential regardless of grade and should be aggressively   patient. Vomiting, lethargy, and weight loss are most com-
               staged at the time of cytologic diagnosis.         monly noted. Splenomegaly can be severe on abdominal
                 Mast cell tumors are the third most common tumor of   palpation while an intestinal mass is not always detected.
               the canine nailbed and have a more aggressive behavior
               compared to a traditional cutaneous MCT. Finally, pri-  Diagnosis
               mary visceral mastocytosis should be considered a highly
               aggressive  neoplasm  which  is  a  terminal  condition  for   Cytology is an appropriate diagnostic tool for both cuta-
               most dogs.                                         neous and visceral lesions. Because of the incidence of
                 As previously stated, histopathologic grading offers
               the most accurate prognosis. The majority of grade I
               (Patnaik) or low‐grade (Kiupel) tumors are cured with
               complete excision. Less than 10% of grade I MCTs are
               reported to metastasize, with a median survival time of
               greater than two years. Alternatively, over 80% of grade
               III MCTs will metastasize and the median survival for
               high‐grade MCT is less than four months.
                 Various proliferation markers may be used for addi-
               tional prognostic information. Dogs with a Ki‐67 index
               of <1.8 had a median survival time that was not reached
               within the time frame of the study and suggested a cura-
               tive outcome. Those with a Ki‐67 >1.8 had a median sur-
               vival  time  of  9.7 months. While  increases  in  both
               AgNORs and PCNA repeatedly support more aggressive
               tumors, they appear to only be prognostically valuable in
               conjunction  with tumor  grade.  When evaluated  inde-  Figure 155.6  A clinically aggressive feline MCT. Note the change
               pendently of grade, both indices are ineffective in deter-  in coloration and ulceration throughout the lesion as well as the
               mining prognosis.                                  bruising at the base of the mass.
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