Page 171 - Differential Diagnosis in Small Animal Cytology, The Skin and Subcutis
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                       Feline progressive dendritic cell histiocytosis (FPH)
  VetBooks.ir          Histiocytic disease arising from interstitial dendritic cells.



                         Clinical features

                         •	  Disease of middle-aged to older cats (7–17 years).
                         •	  Presenting either as a solitary skin nodule or multiple papules, nodules or plaques.
                             Lesions measure up to 1.5 cm in diameter; they are firm, often alopecic, non-pruritic
                             and non-painful. They may wax and wane, but spontaneous regression does not
                             occur. Involvement of lymph nodes and internal organs can be observed.
                         •	  Preferred locations include the head, lower extremities and trunk.
                         •	  The initial clinical course is indolent and the neoplasm behaves like a low-grade dis-
                             ease. However, long-term prognosis is poor, as the disease is progressive.



                       Cytological features
                       •	  The cellularity is variable, from low to high.
                       •	  Background: clear to lightly basophilic, variably haemodiluted.
                       •	  Neoplastic cells are round to polygonal, rarely spindloid, with poorly defined cytoplasmic
                           borders. They exfoliate either individually or in poorly cohesive groups.
                       •	  Nuclei are oval to reniform, occasionally indented, paracentral to eccentric, with finely stippled to
                           reticular chromatin. A single, round and prominent nucleolus is occasionally visible.
                       •	  The cytoplasm is moderate to abundant and lightly basophilic. It may contain rare clear
                           vacuoles and, at times, it may appear wispy and paler at the outer edges.
                       •	  Anisocytosis and anisokaryosis are variable, generally moderate to marked. Binucleation,
                           multinucleation and rare mitotic figures can be found.
                       •	  Low numbers of small lymphocytes, mast cells and other inflammatory cells are not
                           uncommon.




                          Pearls and Pitfalls
                          Presumptive diagnosis can be attempted by assessment of the cytomorphology in con-
                          junction with the clinical presentation. Definitive confirmation of the dendritic lineage
                          requires immunophenotyping and this can be obtained specifically by demonstrating CD1
                          expression on cytological or histological preparations.
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