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               Melanoma

               Philip J. Bergman, DVM, PhD, DACVIM (Oncology)

               Katonah‐Bedford Veterinary Center, Bedford, Hills, NY, USA


                 Etiology/Pathophysiology/                          Signalment
               Epidemiology
                                                                  The most common oral malignancy in the dog is mela-
               Melanoma is a relatively common tumor of dogs, espe-  noma. Oral malignant melanoma is most commonly
               cially in those with significant levels of skin pigmenta-  diagnosed in Scottish terriers, golden retrievers, poo-
               tion. Melanomas in cats are relatively rare. The most   dles, and dachshunds. Oral melanoma is primarily a dis-
               common location for canine melanoma is the haired   ease of older dogs without gender predilection, but may
               skin, where they grossly appear to be small brown to   be seen in younger dogs. Additional oral tumor differen-
               black masses, but can also appear as large, flat, and/or   tials  include  squamous  cell  carcinoma,  fibrosarcoma,
               wrinkled masses. Primary melanomas also can occur in   epulides/odontogenic tumors, osteosarcoma, and oth-
               the oral cavity, nailbed, footpad, eye, gastrointestinal   ers. Melanomas in the oral cavities of dogs are found in
               tract, or mucocutaneous junction. Ocular melanomas of   the following locations in order of decreasing frequency:
               dogs and cats represent a distinct clinical syndrome and   gingiva, lips, tongue, and hard palate. Feline melanoma is
               will be discussed elsewhere. Metastatic sites for canine   relatively rare, but appears to be malignant in most cases.
               malignant melanoma (CMM) can be varied, including
               local draining lymph nodes, the lungs, liver, meninges,
               adrenals, etc.                                       Diagnosis/Pathology/Molecular
                 Melanoma arises from melanocytes, the cells which   Biology
               generate pigment through the melanosome by a number
               of melanosomal glycoproteins. In humans, cutaneous   Melanomas can be difficult to diagnose pathologically in
               melanoma can arise due to mutations induced by     some situations, especially anaplastic amelanotic mela-
               repeated, intense exposure to ultraviolet light (for exam-  nomas which can masquerade as soft tissue sarcomas.
               ple, frequent tanning or working outdoors). Melanoma is   Numerous investigators have attempted to increase the
               currently the most rapidly increasing incident human   precision of identification of melanomas predominantly
               cancer. Significant recent research into the etiology of   through immunohistochemical (IHC) means. This may
               human melanoma suggests multiple causes which are   be accomplished through the use of multiple IHC assays
               independent of the aforementioned UV‐associated    on suspected melanoma tissue or through the use of an
               mutagenesis. Since most breeds of dogs have a hair coat,   IHC cocktail of antibodies. The use of PNL2 and tyrosi-
               which affords them protection from sunlight, UV‐asso-  nase, beyond the typical use of Melan A and S100,
               ciated melanoma is a less likely primary causative agent   appears to hold particular promise.
               in the dog. However, pigment cells divide every time   The molecular characterization of canine and feline
               there is injury to the skin, or if there is constant   melanomas is not as well defined as it is in humans.
               trauma (for example, areas where dogs scratch or lick).   BRAF is a member of the MAPK signaling pathway,
               Nevertheless, risk factors for canine melanoma are not   which is commonly mutated in human cutaneous
               well established.                                    melanoma, but infrequently mutated in oral mucosal





               Clinical Small Animal Internal Medicine Volume II, First Edition. Edited by David S. Bruyette.
               © 2020 John Wiley & Sons, Inc. Published 2020 by John Wiley & Sons, Inc.
               Companion website: www.wiley.com/go/bruyette/clinical
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