Page 165 - Differential Diagnosis in Small Animal Cytology, The Skin and Subcutis
P. 165

er 9
                                                        Chapt
              152
                       Rhabdomyoma and rhabdomyosarcoma
  VetBooks.ir          Tumours of the skeletal muscle deriving from myofibroblasts or primitive mesenchymal cells
                       capable of differentiation into skeletal muscle cells.



                         Clinical features
                         •	  Very rare skin neoplasms in dogs and cats. The benign form is more rare than the
                             malignant counterpart.
                         •	  No age, breed or sex predilection reported. However, several cases of rhabdomyosar-
                             coma described in the literature have been observed in young dogs (< 2 years old).
                         •	  Rhabdomyoma has been primarily reported in the larynx and ear pinnae in dogs and
                             cats, respectively. Rhabdomyosarcoma may be observed in several locations in both
                             species. In cats, it may also develop at the site of previous injection or vaccination.
                         •	  Most tumours present  as firm,  poorly demarcated,  often multilobulated  masses,
                             which arise in the underlying muscle. Alopecia and ulceration are common.
                         •	  Rhabdomyoma is a slow-growing tumour.
                         •	  Rhabdomyosarcoma is characterized by a more aggressive behaviour and metastatic
                             potential.


                       Cytological features
                       •	  Variable cytological features, often non-specific.
                       •	  The cellularity is variable, from low to high.
                       •	  Background: clear and variably haemodiluted.
                       •	  Cell morphology greatly depends on the histological variant.
                       •	  They are often individualized, round to polygonal and with a low N:C ratio. Additional
                           populations of elongated cells and smaller cells with a high N:C ratio can also be seen (un-
                           differentiated rhabdomyoblasts).
                       •	  Nuclei are round, central to paracentral. They have granular chromatin. Prominent round
                           nucleoli are often visible in the malignant forms.
                       •	  Cytoplasm is abundant, basophilic, often granular, with poorly defined borders. Cytoplas-
                           mic cross-striation and paranuclear clear halo may be seen occasionally.
                       •	  Cellularity and cellular atypia are higher in malignant forms and may include marked an-
                           isocytosis/anisokaryosis, multinucleation and bizarre mitotic figures. Multinucleated cells
                           may have nuclei arranged in a linear fashion within the cytoplasm (strap cells).
                       Variants
                       Four different histological variants of rhabdomyosarcoma have been reported in the literature
                       and include botryoid, embryonal, alveolar and pleomorphic forms. The botryoid types mainly
                       affect the urinary bladder, whereas the other forms have been described originating from striated
                       muscle of the outer body surface.
                       •	  Embryonal rhabdomyosarcoma:
                           •	  This is the most common variant and has been reported in dogs and only rarely in cats.
                           •	  Head and neck are preferred anatomical locations.
                           •	  Cells may exhibit different stages of development from round to polygonal and often
                              show marked signs of atypia.
                           •	  A spindle-cell sub-variant has also been described in literature.
   160   161   162   163   164   165   166   167   168   169   170