Mastocytosis in the skin in dogs: A multicentric case series

Author:

Wyatt Eleanor K.1ORCID,Affolter Verena2,Borio Stefano3,Guillen Alexandra4,Verganti Sara56,Murphy Sue67,Ballarini Damiano8,Banovic Frane9,Schmidt Vanessa1,Tanis Jean‐Benoit110ORCID

Affiliation:

1. Department of Small Animal Clinical Sciences, Institute of Infection, Veterinary and Ecological Sciences University of Liverpool Liverpool UK

2. Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine University of California Davis California USA

3. Department of Veterinary Medicine and Epidemiology, School of Veterinary Medicine University of California Davis California USA

4. Department of Clinical Sciences and Services, Royal Veterinary College University of London Hatfield UK

5. Oncology Service Dick White Referrals Six Mile Bottom UK

6. Centre for Small Animal Studies Animal Health Trust Newmarket UK

7. College of Medicine & Veterinary Medicine, Royal (Dick) School of Veterinary Studies University of Edinburgh Roslin UK

8. Diagnostica Piccoli Animali Zugliano Italy

9. Department of Small Animal Medicine and Surgery, College of Veterinary Medicine University of Georgia Athens Georgia USA

10. Department of Molecular and Clinical Cancer Medicine, Institute of Systems, Molecular and Integrative Biology University of Liverpool Liverpool UK

Abstract

AbstractCanine cutaneous mastocytosis (CM) is rare in contrast to canine mast cell tumours. In humans, CM commonly affects children and is usually indolent with possible spontaneous resolution. Systemic mastocytosis (SM) with bone marrow involvement typically affects adults, can have a poor outcome, and often includes skin lesions. ‘Mastocytosis in the skin’ (MIS) is the preferred term of skin lesions, if bone marrow evaluations are not available, which is often the cases in dogs. In human SM and CM, KIT mutations are often detected. The veterinary literature suggests clinical resemblances between human and canine MIS, but data is limited, and KIT mutations are rarely assessed. This retrospective study describes clinicopathological findings, treatment and outcome of 11 dogs with suspected MIS. Dogs with multiple mast cell tumours were excluded. Histopathology reports (n = 5) or slides (n = 6) were reviewed. KIT mutation analysis including exons 8, 9, 11, 14 and 17 were analysed in eight dogs. Median age at diagnosis was 4 years (range, 1–12). Typical clinical signs included multifocal to generalised nodules and papules. Histologically, skin lesions were characterised by dermal infiltration of well‐differentiated mast cells. KIT mutations were detected in 3/8 dogs (exon 9: n = 2; exon 11: n = 1). One dog had mastocytaemia suggesting possible SM. Glucocorticoids were mostly successful with lesion improvement in all treated dogs (n = 8). This cohort highlights resemblances between human and canine MIS. Further studies are required to confirm these findings and establish diagnostic criteria for CM and MIS associated with SM in dogs.

Publisher

Wiley

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