Small Animal Dermatology, 3rd edition

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chapter


24


Epitheliotropic


(Cutaneous) Lymphoma


DEFINITION/OVERVIEW


 Cutaneous T-cell lymphoma (CTCL), both epitheliotropic and nonepitheliotrophic,


is an uncommon cutaneous neoplasia affecting many species, including dogs and cats.


 Heterogeneous group of diseases with a prevalence of less than 1% of skin tumors in


dogs.


 The majority of CTCL cases are epitheliotropic (CEL) characterized by infiltration of


the epidermis and adnexal structures with malignant T cells.


ETIOLOGY/PATHOPHYSIOLOGY


 Cutaneous nonepitheliotrophic lymphoma (CnEL): caused by either B cells or T cells;


more often T cell in cats.


 Most often associated with CD3+lymphocytes.


 CnEL: large cell lymphoma characterized by infiltration of the dermis and subcutis


with heterogeneous groups of malignant cells; may be associated with FeLV in cats.


 Cutaneous epitheliotropic lymphoma, or “classic” MF (mycosis fungoides): most


common T cell lymphoma in dogs.


 Caused by epitheliotropic gamma delta T cells in 70% of cases (100% in pagetoid


form).


 Most often associated with CD4−/CD8+cytotoxic T cells: differs from disease of


human beings (predominantly CD4+/CD8−helper T cells).


 COX-2 is not expressed by neoplastic infiltrates in CEL; differs from disease in human


beings (significant expression of COX-2 by neoplastic lymphocytes).


 In one study, dogs with atopic dermatitis were at 12 times higher risk of developing


CEL than dogs without atopic dermatitis.


 Allergic skin disease producing chronic T cell activation and proliferation leading to


clonal expansion of neoplastic cells may be a cause; initial lesions often develop in
areas associated with atopic dermatitis.

 Peripheral lymphocytes with skin-homing receptors may be preferentially


sequestered in skin lesions.


 Spread of malignant cells to lymph nodes and organs occurs in the late tumor stage.


Blackwell’s Five-Minute Veterinary Consult Clinical Companion: Small Animal Dermatology, Third Edition.
Karen Helton Rhodes and Alexander H. Werner.
©2018 John Wiley & Sons, Inc. Published 2018 by John Wiley & Sons, Inc.


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