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1.
J Comp Pathol ; 157(4): 276-279, 2017 Nov.
Article in English | MEDLINE | ID: mdl-29169622

ABSTRACT

This case report describes congenital truncus arteriosus in a 1-month-old Eastern black rhinoceros (Diceros bicornis michaeli). From the first day of life the animal was underweight and from the 22nd day of life displayed respiratory signs that exacerbated with time leading eventually to collapse and death. Post-mortem examination revealed a single truncus arteriosus originating from the right ventricle leading to two separated pulmonary arteries and the aorta, with the ventricular septum showing a focal communicating defect. Based on the gross examination and current human classifications, the truncus arteriosus was classified as type III or A2. This is the first description of persistent truncus arteriosus in an Eastern black rhinoceros.


Subject(s)
Perissodactyla , Truncus Arteriosus, Persistent/veterinary , Animals
2.
Vet Comp Oncol ; 15(4): 1393-1402, 2017 Dec.
Article in English | MEDLINE | ID: mdl-27779366

ABSTRACT

Canine melanoma (CMM) more commonly affects the oral mucosa and the cutis. CMM shares several features with human melanomas (HMM), included resistance to a broad variety of antineoplastic chemotherapy agents. P-glycoprotein 1 (Pgp) expression is a well-recognized feature of multi-drug resistance and the purpose of this study was to investigate its expression in treatment naïve CMM. We also investigated Pgp association with tumour location and histological features. Histology records of CMM were retrieved, including patients from 2012-2014. Twenty-five cases of CMM were included in this study. Results revealed that Pgp is expressed in CMM and oral tumours were more likely to have a membranous Pgp expression (100%) than cutaneous tumours (66.6%) (P = 0.010). Cytoplasmic and nuclear Pgp expression could also be identified. Results of this study bring useful data that help in understanding one of the possible mechanisms responsible of intrinsic chemotherapy resistance in canine CMM.


Subject(s)
ATP Binding Cassette Transporter, Subfamily B, Member 1/metabolism , Dog Diseases/metabolism , Melanoma/veterinary , Mouth Neoplasms/veterinary , Skin Neoplasms/veterinary , Animals , Dog Diseases/pathology , Dogs , Female , Male , Melanoma/metabolism , Melanoma/pathology , Mouth Neoplasms/metabolism , Mouth Neoplasms/pathology , Skin Neoplasms/metabolism , Skin Neoplasms/pathology
3.
Vet J ; 201(2): 156-65, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24857252

ABSTRACT

Feline calicivirus (FCV) is a pathogen of felids and one of the most common causative agents of feline upper respiratory disease (URD). Reports of natural FCV pneumonia in the course of respiratory tract infections are sparse. Therefore, knowledge on the pathogenesis of FCV-induced lung lesions comes only from experimental studies. The aim of the present study was to assess the type and extent of pulmonary involvement in natural respiratory FCV infections of domestic cats and to identify the viral target cells in the lung. For this purpose, histology, immunohistochemistry and RNA-in situ hybridisation for FCV and relevant cell markers were performed on diagnostic post-mortem specimens collected after fatal URD, virulent systemic FCV or other conditions. All groups of cats exhibited similar acute pathological changes, dominated by multifocal desquamation of activated alveolar macrophages (AM) and occasional type II pneumocytes with fibrin exudation, consistent with diffuse alveolar damage (DAD). In fatal cases, this was generally seen without evidence of epithelial regeneration. In cats without clinical respiratory signs, type II pneumocyte hyperplasia was present alongside the other changes, consistent with the post-damage proliferative phase of DAD. FCV infected and replicated in AM and, to a lesser extent, type II pneumocytes. This study shows that lung involvement is an infrequent but important feature of FCV-induced URD. AM are the main viral target cell and pulmonary replication site, and their infection is associated with desquamation and activation, as well as death via apoptosis.


Subject(s)
Caliciviridae Infections/veterinary , Calicivirus, Feline/physiology , Cat Diseases/virology , Macrophages, Alveolar/virology , Respiratory Tract Infections/veterinary , Animals , Caliciviridae Infections/virology , Calicivirus, Feline/isolation & purification , Cats , Female , Immunohistochemistry/veterinary , In Situ Hybridization/veterinary , Male , Polymerase Chain Reaction/veterinary , RNA, Viral/analysis , Respiratory Tract Infections/virology , Virulence
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