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  3. Prognostic clinical and histopathological features of canine cutaneous epitheliotropic T-cell lymphoma.
 

Prognostic clinical and histopathological features of canine cutaneous epitheliotropic T-cell lymphoma.

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Date of Publication
March 2023
Publication Type
Article
Division/Institute

Institut für Tierpath...

Contributor
Dettwiler, Martina Andrea
Institut für Tierpathologie (ITPA)
Mauldin, Elizabeth A
Jastrebski, Sara
Gillette, Deborah
Stefanovski, Darko
Durham, Amy C
Subject(s)

600 - Technology::630...

Series
Veterinary pathology
ISSN or ISBN (if monograph)
1544-2217
Publisher
Sage
Language
English
Publisher DOI
10.1177/03009858221140818
PubMed ID
36541607
Uncontrolled Keywords

T-cell canine cutaneo...

Description
Canine cutaneous epitheliotropic T-cell lymphoma is a neoplasm with heterogeneous clinical and histopathological presentations. Survival times and responses to therapy are variable, and indicators to predict outcomes are lacking. Clinical and histopathological parameters from 176 archival cases from the University of Pennsylvania and University of Bern (2012-2018) were investigated for associations with clinical outcomes. Histopathological evaluation used digitized whole slide images and QuPath software. Cases included 107 female and 69 male dogs from 48 breeds, with a mean age of 10.4 years. Most common clinical signs were erythema (n = 131), crusting (n = 108), and scaling (n = 102). Affected sites were haired skin (n = 159), lip (n = 74), nasal planum (n = 49), and paw pads (n = 48). The median survival time (MST) was 95 days (1-850). Dogs had 4.26-fold and 2.82-fold longer MST when treated with chemotherapy and prednisone, respectively, than when receiving supportive care. Haired skin involvement (hazard ratio [HR]: 2.039, 95% confidence interval [CI]: 1.180-3.523), erosions/ulcers (HR: 1.871, 95% CI: 1.373-2.548), nodules (HR: 1.496, 95% CI: 1.056-2.118), and crusting (HR: 1.454, 95% CI: 1.061-1.994) were clinical parameters predicting poor outcomes, whereas complete posttherapeutic clinical remission (HR: 0.469, 95% CI: 0.324-0.680) and a stable disease (HR: 0.323, 95% CI: 0.229-0.456) were associated with longer survival. Histopathological features associated with the increased risk of death were extensive infiltration of the panniculus (HR: 2.865, 95% CI: 1.565-4.809), mitotic count ≥7/high-power field (HR: 3.027, 95% CI: 2.065-4.439), cell diameter ≥10.0 µm (HR: 2.078, 95% CI: 1.281-3.372), and nuclear diameter ≥8.3 µm (HR: 3.787, 95% CI: 1.647-8.707).
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/116483
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