Assessment of retinal atrophy in mixed breed dogs using spectral domain optical coherence tomography (SD-OCT) and electroretinography.

The aim of the study was to characterize retinal atrophy (RA) with progressive retinal atrophy symptoms in mixed breed dogs using ophthalmoscopy, spectral domain optical coherence tomography (SD-OCT) and electroretinography (ERG).The study was performed on 13 mixed breed dogs affected by retinal atrophy (11 males and 2 females that were 1.5-14 years old). Depending on the advancement of RA, SD-OCT examinations identified retinal abnormalities ranging from layer disorganisation to advanced atrophy. The most advanced RA occurred ventral to the optic disc. Total retinal thickness in both eyes (mean ± SD) was lower in dogs with RA compared to controls dorsally (77.7 ± 39.5 µm vs 173.5 ± 13.3 µm), ventrally (33.4 ± 29.9 µm vs 139.5 ± 10.8 µm), nasally (65.0 ± 34.5 µm vs 163.9 ± 11.0 µm) and temporally (61.8 ± 41.7 µm vs 171.9 ± 11.1 µm) to the optic disc. In dogs with locally normal architecture of inner retina, loss of definition of outer retinal layers occurred in many regions. Dark and light-adapted ERGs were reduced in 2 dogs with RA and were unrecordable in 11 dogs. Lesions evident in SD-OCT scans of mixed breed dogs affected with retinal atrophy initially appear ventrally to the optic disc and ventro-dorsally in advanced RA. In all mixed breed dogs with retinal atrophy, clinical signs and SD-OCT results correlate with ERG findings.

Ehlers-Danlos syndrome (cutaneous asthenia) in a Campbell's dwarf hamster (Phodopus campbelli).

A case of cutaneous asthenia in a Campbell's dwarf hamster is described. The animal was found to have hyperextensible skin, glaucoma and lens dislocation. Histopathological examination revealed an irregular, haphazard arrangement of collagen fibres in the dermis. The animal underwent surgical reduction of the skin folds which provided only temporary relief.

Un cas d'asthénie cutanée chez un hamster nain de Campbell est décrit. L'animal présente une peau hyperextensible, un glaucome et une luxation du cristallin. L'examen histopathologique révèle une disposition irrégulière et désordonnée des fibres de collagène dans le derme. L'animal a subi une réduction chirurgicale des plis cutanés qui n'a apporté qu'un soulagement temporaire.

Descreve­se um caso de astenia cutânea em um hamster anão de Campbell. O animal apresentou hiperextensibilidade cutânea, glaucoma e deslocamento de lentes. Ao exame histopatológico, observou­se um arranjo irregular e aleatório das fibras colágenas na derme. O animal foi submetido à redução cirúrgica das dobras cutâneas que resultou em alívio apenas temporário.

Se describe un caso de astenia cutánea en un hámster enano Campbell. Se examinó al animal obsevando piel hiperextensible, glaucoma y luxación del cristalino. El examen histopatológico reveló una orientación aleatoria e irregular de las fibras de colágeno en la dermis. Se utilizó una técnica de reducción quirúrgica de los pliegues de la piel que solo indujo una mejora temporal.

Prevalence of Encephalitozoon cuniculi Infection in Guinea Pigs (Cavia porcellus) in Poland with Different Clinical Disorders-A Pilot Study.

Encephalitozoonosis is a disease caused by E. cuniculi. It is diagnosed primarily in rabbits but is less frequently so in other animal species. E. cuniculi is classified among Microsporidia-fungi frequently found in the environment, that are resistant to numerous external factors. Apart from rabbits, rodents form the next group of animals most exposed to infection with these pathogens. The objective of the study was to analyze the prevalence of E. cuniculi infection in guinea pigs with different clinical disorders. The study included 67 animals with E. cuniculi infection confirmed via real-time PCR. The infected animals most frequently exhibited nervous and urinary system symptoms, as well as issues with vision organs, while several animals were also recorded as having problems with the respiratory system and thyroid gland dysfunction. The study shows that encephalitozoonosis constitutes a significant problem in rodents kept as domestic animals, which in turn may be a source of infection for humans.

Refractive errors in mixed breed dogs of different ages.

The purpose of the study was to evaluate the occurrence and range of refractive errors in dogs of different ages. A total of 99 clinically healthy, mixed-breed mesocephalic dogs were included in the study and divided into three different age groups according to the current human/pet analogy chart: 40 adults (23 males, 17 females, 1-8 years old, 3-70 kg), 21 seniors (14 males, 7 females, 6-11 years old, 7-42 kg), and 38 geriatrics (22 males, 16 females, 8-13 years old, 5-45 kg). All the dogs underwent an ophthalmic examination, including Schirmer tear test, tonometry, biomicroscopy, and ophthalmoscopy. Neither eye drops nor pharmacological sedatives were administered before the autorefractometry. The refractive states were assessed bilaterally using a hand-held Retinomax 3 (Righton) autorefractor. The results underwent statistical analysis using Statistica v12 software (ANOVA and t-test). A P-value < 0.05 was considered as significant. Emmetropia, defined as a refractive state > -0.5 D and < +0.5 D, was found in 36% of the adult, 43% of the senior, and 38% of the geriatric patients. Anisometropia was found in 1% of the adult, 9.5% of the senior and 5.5% of the geriatric dogs when the refractive power of the two eyes differed ≥ 1.0 myopia ≤ -0.5 D and hyperopia ≥ +0.5 D were found in 23% and 41% of the adult eye globes as well as 24% and 33% in the senior dogs and 15% and 47% in the geriatric dogs, respectively. The maximal values of the myopia in the adult and geriatric dogs were -2.5 D and -2.75 D, respectively. The maximal values of the hyperopia in the adult and geriatric dogs were 1.75 D and 2.5 D, respectively. No statistically significant correlation was found between the groups. Ametropia is a common refractive state for dogs of different ages. The most frequent refractive state in ametropic mixed-bed dogs in all age groups is hyperopia.

The use of optical coherence tomography for skin evaluation in healthy rats.

BACKGROUND: Noninvasive diagnostic techniques allow for morphological and morphometric in vivo evaluation of the skin. Optical coherence tomography (OCT) is a method that allows visualization of dermal structures up to several 100 µm with a resolution of 3-7.5 µm. OBJECTIVES: The aim of the study was the morphological and morphometric assessment of rats' skin using SD-OCT. ANIMALS: Fifteen male Wistar rats, aged 3 and 8 months, weighing 350-450 g. MATERIALS AND METHODS: The skin of the plantar metatarsal area of the right pelvic limb was assessed. The measurements were performed using Spectral Domain Optical Coherence Tomography (SD-OCT) scans and histological images. RESULTS: Spectral Domain Optical Coherence Tomography could determine the boundary between the epidermis and the dermis. Apart from the stratum corneum (SC), it did not allow for the differentiation of the individual epidermal layers. In the SD-OCT and in the histological examination, the mean thicknesses of the layers (µm ± SD) were (respectively): SC 33.053 ± µm(SD 5.85, 29.675 ± 5.54; epidermis 88.2 ± 7.97, 65.126 ± 13.23; dermis 259.86 ± 18.29, 166.05 ± 31.88 µm. There was a correlation between the total epidermal SD-OCT and histological measurements (r = 0.43, p = 0.05). Bland-Altman plots revealed a bias of -19.18 (95% confidence interval) -39.21 to 0.84 µm) in the case of live epidermis (stratum granulosum, stratum spinous, stratum basale). CONCLUSIONS AND CLINICAL RELEVANCE: Spectral Domain Optical Coherence Tomography can be used to evaluate rat epidermis and dermis. The method enables the differentiation of the SC, as well as the epidermis and the dermis. SD-OCT and histological thickness dimensions of the epidermis and skin differ.

Contexte - Les techniques de diagnostic non invasives permettent une évaluation morphologique et morphométrique in vivo de la peau. La tomographie par cohérence optique (OCT) est une méthode qui permet de visualiser les structures dermiques jusqu'à plusieurs centaines de micromètres avec une résolution de 3 à 7,5 µm. Objectifs - Le but de l'étude était l'évaluation morphologique et morphométrique de la peau des rats par SD-OCT. Animaux - Quinze rats Wistar mâles, âgés de 3 et 8 mois, pesant 350-450 g. Matériels et méthodes - La peau de la zone métatarsienne plantaire du membre pelvien droit a été évaluée. Les mesures ont été réalisées à l'aide de scaners SD-OCT (Spectral Domain Optical Coherence Tomography) et d'images histologiques Résultats - Le SD-OCT a pu déterminer la frontière entre l'épiderme et le derme. En dehors de la couche cornée (SC), il n'a pas permis la différenciation des couches épidermiques individuelles. Au SD-OCT et à l'examen histologique, les épaisseurs moyennes des couches (µm ± SD) étaient (respectivement) : SC 33,053 ± µm (SD 5,85, 29,675 ± 5,54 ; épiderme 88,2 ± 7,97, 65,126 ± 13,23 ; derme 259,86 ± 18,29, 166,05 ± 31,88 µm). Il y avait une corrélation entre le SD-OCT épidermique total et les mesures histologiques (r = 0,43, P = 0,05) Les tracés de Bland-Altman ont révélé un biais de -19,18 (intervalle de confiance à 95 %) -39,21 à 0,84 µm) dans le cas d'épiderme vivant (stratum granulosum, stratum spinous, stratum basale). Conclusions et pertinence clinique - Le SD-OCT peut être utilisé pour évaluer l'épiderme et le derme de rat. La méthode permet de différencier le SC, ainsi que l'épiderme et le derme. Le SD-OCT et les dimensions d'épaisseur histologiques de l'épiderme et de la peau diffèrent.

Introducción - las técnicas de diagnóstico no invasivas permiten la evaluación morfológica y morfométrica in vivo de la piel. La tomografía de coherencia óptica (OCT) es un método que permite la visualización de estructuras dérmicas de hasta varios cientos de micrómetros con una resolución de 3 a 7,5 µm. Objetivos - El objetivo del estudio fue la evaluación morfológica y morfométrica de la piel de ratas mediante SD-OCT. Animales - Quince ratas Wistar macho, de 3 y 8 meses de edad, con un peso de 350 a 450 g. Materiales y métodos - Se evaluó la piel de la zona metatarsiana plantar del miembro pélvico derecho. Las mediciones se realizaron utilizando escaneos SD-OCT (Tomografía de Coherencia Óptica de Dominio Espectral) e imágenes histológicas. Resultados - SD-OCT pudo determinar el límite entre la epidermis y la dermis. Aparte del estrato córneo (SC), no permitía la diferenciación de las capas epidérmicas individuales. En la SD-OCT y en el examen histológico, los espesores medios de las capas (µm ± SD) fueron (respectivamente): SC 33.053 ± µm (SD 5.85, 29.675 ± 5.54; epidermis 88.2 ± 7.97, 65.126 ± 13.23; dermis 259.86 ± 18,29, 166,05 ± 31,88 µm. Hubo una correlación entre el SD-OCT epidérmico total y las mediciones histológicas (r = 0,43, P = 0,05). Las gráficas de Bland-Altman revelaron un sesgo de -19,18 (intervalo de confianza del 95 %) -39,21 a 0,84 µm) en el caso de epidermis viva (estrato granuloso, estrato espinoso, estrato basal). Conclusiones y relevancia clínica- SD-OCT se puede utilizar para evaluar la epidermis y la dermis de rata. El método permite diferenciar el SC, así como la epidermis y la dermis. Las dimensiones de grosor de la epidermis y la piel difieren entre SD-OCT y la histología.

Contexto - Técnicas diagnósticas não invasivas permitem a avaliação morfológica e morfométrica in vivo da pele. A tomografia de coerência óptica (OCT) é um método que possibilita a visualização de estruturas dérmicas de até centenas de micrômetros com uma resolução de 3-7,5 µm. Objetivos - O objetivo do estudo foi a avaliação morfométrica e morfológica da pele de ratos utilizando SD-OCT. Animais - Quinze ratos Wistar machos, de três a oito meses de idade, pesando de 350 a 450 g. Materiais e métodos - A pele da região metatársica plantar do membro pélvico direito foi avaliada. As mensurações foram realizadas utilizando o SD-OCT (Spectral Domain Optical Coherence Tomography) e imagens histológicas. Resultados - A SD-OCT foi capaz de determinar o limite entre derme e epiderme. A exceção do estrato córneo (SC), não foi possível a diferenciação das camadas da epiderme individualmente. Na SD-OCT e na avaliação histológica, as espessuras médias das camadas fora, (µm ± DP), respectivamente: SC 33,053 ± 5,85; 29,675 ± 5,54; epiderme 88,2 ± 7,97; 65,126 ± 13,23; derme 259,86 ± 18,29; 166,05 ± 31,88 µm. Houve correlação entre SD-OCT e avaliação histológica nas mensurações da epiderme total (r = 0,43, P = 0,05). Os gráficos de Bland-Altman revelaram um viés de -19,8% (95% de intervalo de confiança) - 39,21 a 0,84 µm) no caso da epiderme viva (estrato espinhoso, estrato granuloso e estrato basal). Conclusões e relevância clínica - SD-OCT pode ser utilizada para avaliar a derme e a epiderme de ratos. Este método permite a diferenciação do SC, bem como da derme e epiderme. Pode haver discrepância na espessura da epiderme e da pele na SD-OCT e análise histológica.

Proteomic Analysis of Tear Film in Canine Diabetic Patients with And Without Retinopathy.

Introduction: Diabetic retinopathy (DR) is the leading cause of blindness in human and animal patients. Early detection and treatment of the disease are important and can be facilitated by proteomic approaches providing biomarkers. Material and Methods: Tear films were collected on Schirmer strips from 32 canine patients (12 diabetic dogs without changes in the retina, 8 diabetic dogs with signs of DR, and 12 control dogs). Two-dimensional electrophoresis was used to separate tear film proteins prior to their identification with matrix-assisted laser desorption/ionisation-tandem time-of-flight mass spectrometry and interrogation of protein function databases to find matches. Results: Five significantly differentially expressed proteins were identified; of those, one was downregulated (2'-5'-oligoadenylate synthase 3) and four were upregulated in the tear film of two diabetic groups (Ras-related protein RAB-13; aldo-keto-reductase family 1 member C3; 28S ribosomal protein S31, mitochondrial; and 60S ribosomal protein L5). The differentially expressed proteins identified in the tear film were involved in signalling pathways associated with impaired protein clearance, persistent inflammation and oxidative stress. Conclusion: The results of our study confirm that the pathological process in the retina in the course of diabetes mellitus causes changes in the tear film proteome.

Morphometrical analysis of the canine choroid in relation to age and sex using spectral domain optical coherence tomography.

This study determined the choroidal thickness of senior (SN, n = 24) and middle-aged (MA, n = 17) healthy, mixed-breed mesocephalic dogs, both males (M) and females (F), using spectral domain optical coherence tomography (SD-OCT). The dogs were divided into two groups for examination: MA dogs (4-7 years old; 6 M, 11 F) and SN dogs (8-13 years old; 12 M, 12 F). Choroidal thickness of the dogs was investigated using SD-OCT radial and linear scans. The software of the device allowed determination of the exact measurement location on the choroid. Measurements of the choroid were taken manually using the SD-OCT calliper function at distances of 5,000-6,000 µm (dorsal and ventral) and 4,000-7,000 µm (nasal and temporal) from the optic disc. Mean (µm ± SD) (MA, SN) dorsal (188 ± 28, 184 ± 33), ventral (116 ± 23, 111 ± 16), temporal (152 ± 31, 151 ± 26), and nasal (135 ± 27, 132 ± 18) choroidal thicknesses demonstrated significant differences (P < 0.02-0.001) between all areas within each group. The choroid was thickest in the dorsal region and thinnest in the ventral region. There were no significant differences based on age. Mean (µm ± SD) (M, F) dorsal (181 ± 32, 190 ± 30), ventral (117 ± 16, 11 ± 21), temporal (150 ± 26, 153 ± 30), and nasal (128 ± 20, 138 ± 23) choroidal thicknesses demonstrated significant differences (P < 0.05) between dorsal and nasal regions. The choroidal thickness in dogs depends on the area assessed independently of their age and sex.

Aggressive squamous cell carcinoma of the cranium of a dog.

BACKGROUND: The authors report a case of keratinized squamous cell carcinoma (SCC) in a 14-year-old dog with extensive cranial bone invasion. To our knowledge, this is the first description of such a case of cranial keratinized SCC with aggressive generalized osteolysis described in a dog. CASE PRESENTATION: The 14-year-old dog was referred for radiological examination with suspicion of head trauma with clinical signs of head deformation, exophthalmos and nasal discharge. The skull radiographs showed a large osteolytic defect of the frontal bone and parietal bone in the region of the external sagittal crest. Findings from the skull CT scan included generalized osteolysis in the region of parietal bone, frontal bones, maxilla on the right side and the nasal bone including the dorsal nasal concha. In the area of bone loss, new soft tissue formation with multifocal foci of mineralization was visible. The ultrasound examination revealed hypoechogenic changes with hyperechoic foci consistent with mineralization and poor vascularization. The brain and ocular structures were without visible changes. Fine needle aspiration cytology (FNAC) was performed, and squamous cell carcinoma was suspected. After 3 months, the re-presented to the clinic. The dog became progressively listless, his appetite was decreased, and he became acutely blind. Follow-up skull CT scan revealed significant osteolysis, which affected a significant aspect of the cranium. All bone defects had been replaced by new 3.5 cm-thick soft tissue formations with multifocal small 1-2 mm areas of mineralization. There was no evidence of metastasis. Histological examination confirmed the suspicion of squamous cell carcinoma. CONCLUSIONS: This paper is the first report of cranial SCC in a dog causing extensive bone osteolysis. The lesions in this dog originated from the frontal and parietal bones including frontal sinuses. There are variants of tumors that arise from squamous epithelium or resemble SCC in the skull. These examples include adenosquamous carcinoma and proliferating trichilemmal tumours. In addition, there is possible malignant transformation caused by papilloma viruses. In the veterinary literature, there is only one similar description of adenosquamous carcinoma in a cat with similar clinical manifestations. It is justified to suspect a process of neoplastic epithelial origin in all cases of aggressive and extensive skull bone lysis. This issue should be subject to further investigation.

Assessment of corneal and conjunctival metaplasia by impression cytology during the treatment of canine keratoconjunctivitis sicca.

The purpose of this study was to assess the condition of cells in the conjunctiva and corneal epithelium prior to and during cyclosporine- or tacrolimusbased treatment of keratoconjunctivitis sicca (KCS). The study was performed on 40 dogs with KCS. The dogs were divided into two groups of 20 animals each. In Group I, 0.75% cyclosporine eye drops were administered three times a day, while in Group II 0.02% tacrolimus eye drops were administered twice daily. Additionally, each group was subdivided into three subgroups based on the results of the Schirmer I tear test (STT I). Evaluation of cellular metaplasia in the cornea and the palpebral and bulbar conjunctiva based on the Nelson-Adams scale was performed by impression cytology using Millipore round filters (Millipore VSWP 01300 DA) of 25 µm pore diameter applied to the studied area. Ophthalmological and cytological examinations were performed prior to the treatment as well as after one and two months of therapy. In both groups, a decrease in Nelson-Adams values was observed, corresponding to the increasing STT values [Rxy Spearman statistically significant correlation coefficient values between -0.75 (P < 0.001) and -0.45 (P < 0.01)]. The absence of goblet cells was observed in all dogs, regardless of the KCS stage. Goblet cells reappeared following both tacrolimus- and cyclosporine-based treatment in impression cytology specimens classified as 0 in the Nelson-Adams scale. The extent of corneal and conjunctival metaplasia in the course of tacrolimus- and cyclosporine-based treatment of KCS decreases with increasing STT values.