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1.
Acta sci. vet. (Impr.) ; 49(suppl.1): Pub.596-Jan 4, 2021. ilus
Artigo em Português | VETINDEX | ID: biblio-1458459

Resumo

Background: Renal dysplasia is a congenital disorder that occurs during differentiation of the renal parenchyma or as aconsequence of a functional and/or structural obstruction of the lower urinary tract. In wild animals, this pathology has beenreported in cynomolgus monkeys (Macaca fascicularis), golden hamsters (Mesocricetus auratus) and African elephants(Loxodanta africana). However, there are no reports of the disease in the giant anteater (Myrmecophaga tridactyla). Thus,this paper describes a case of renal dysplasia in a free-living giant anteater cub, which was sent to the wild animal clinicof the Federal University of Mato Grosso (UFMT) in Cuiabá, MT, Brazil.Case: The rescued animal had a good body condition score and clinical parameters within the normal range for the species.After a routine clinical evaluation, the anteater cub was subjected to radiography and ultrasound tests. Blood tests, serumtests for hepatic and renal profiles, urinalysis, urinary protein creatinine ratio, and chest X-rays did not reveal significantchanges. However, the abdominal ultrasound examination revealed a volumetric loss of about 1.17 cm in length in theleft kidney, and a renal length to aortic artery diameter ratio of approximately 2.8. This kidney showed irregular contours,loss of corticomedullary demarcation, with preserved echogenicity and cortical echotexture. The right kidney showedthe standard size of the species, with a length of approximately 3.08 cm. In view of the suspicion of renal dysplasia, acontrast-enhanced CT scan was performed in order to assess the dynamics of uptake and excretion of the contrast mediumin the affected kidney and in the ipsilateral collecting system. An examination of the tomographic images indicated thatthe volume of the left kidney was reduced, isodense in relation to the right kidney, with discrete and homogeneous uptakein all phases after administration of the contrast medium, no occurrence of nephrogram...


Assuntos
Animais , Nefropatias/veterinária , Xenarthra/anormalidades , Tomografia/veterinária , Ultrassonografia/veterinária
2.
Acta sci. vet. (Online) ; 49(suppl.1): Pub. 596, 19 jan. 2021. ilus
Artigo em Português | VETINDEX | ID: vti-762676

Resumo

Background: Renal dysplasia is a congenital disorder that occurs during differentiation of the renal parenchyma or as aconsequence of a functional and/or structural obstruction of the lower urinary tract. In wild animals, this pathology has beenreported in cynomolgus monkeys (Macaca fascicularis), golden hamsters (Mesocricetus auratus) and African elephants(Loxodanta africana). However, there are no reports of the disease in the giant anteater (Myrmecophaga tridactyla). Thus,this paper describes a case of renal dysplasia in a free-living giant anteater cub, which was sent to the wild animal clinicof the Federal University of Mato Grosso (UFMT) in Cuiabá, MT, Brazil.Case: The rescued animal had a good body condition score and clinical parameters within the normal range for the species.After a routine clinical evaluation, the anteater cub was subjected to radiography and ultrasound tests. Blood tests, serumtests for hepatic and renal profiles, urinalysis, urinary protein creatinine ratio, and chest X-rays did not reveal significantchanges. However, the abdominal ultrasound examination revealed a volumetric loss of about 1.17 cm in length in theleft kidney, and a renal length to aortic artery diameter ratio of approximately 2.8. This kidney showed irregular contours,loss of corticomedullary demarcation, with preserved echogenicity and cortical echotexture. The right kidney showedthe standard size of the species, with a length of approximately 3.08 cm. In view of the suspicion of renal dysplasia, acontrast-enhanced CT scan was performed in order to assess the dynamics of uptake and excretion of the contrast mediumin the affected kidney and in the ipsilateral collecting system. An examination of the tomographic images indicated thatthe volume of the left kidney was reduced, isodense in relation to the right kidney, with discrete and homogeneous uptakein all phases after administration of the contrast medium, no occurrence of nephrogram...(AU)


Assuntos
Animais , Xenarthra/anormalidades , Nefropatias/veterinária , Ultrassonografia/veterinária , Tomografia/veterinária
3.
Acta sci. vet. (Online) ; 48(suppl.1): Pub. 587, 22 dez. 2020. ilus
Artigo em Inglês | VETINDEX | ID: vti-31152

Resumo

Background: Deformities of the anterior thoracic wall are called pectus: pectus excavatum and pectus carinatum. Pectusexcavatum is characterised by dorsal deviation of the caudal region of the sternum while pectus carinatum consists ofprotrusion of the sternum and/or adjacent cartilage. Both defects may remain symptom-free, but respiratory and cardiacabnormalities have been reported. Another deformity observed in dogs is the swimming dog syndrome, which consists ofthe lateral opening of the thoracic and pelvic limbs, associated with the pedalling movement. These disorders are frequentlyreported in medical practice, are considered rare among canines. This report aims to describe a case of pectus excavatumassociated with the swimming dog syndrome (Case 1) and another case of pectus carinatum (Case 2).Cases: Case 1. An approximately 45-day-old male American Pitbull canine had difficulty standing. Physical examinationrevealed hyperextension of the thoracic and pelvic limb joints and flattening of the thorax. After radiographic examination, pectus excavatum and the swimming dog syndrome were confirmed. The conservative treatment with splinting andhydrotherapy was chosen. At the 3-month follow-up, slight improvement in the limbs and irregular and unsatisfactorygrowth of the thorax leading to episodes of dyspnoea were observed. Case 2. A female Pug, approximately 2 months old,had a thorax deformity. Physical examination revealed thorax protrusion, confirmed on radiography as pectus carinatum.Conservative therapy was provided using compressive bandage. One month later, the tutor reported improvement in thecondition and absence of respiratory changes.Discussion: Pectus deformities has low incidence, and cases to pectus carinatum, there is a sexual predisposition, that is,males are more predisposed, differing from Case 2, a female dog. In the cases of pectus excavatum, no genetic alterationwas directly related to its occurrence...(AU)


Assuntos
Animais , Masculino , Cães , Pectus Carinatum/patologia , Pectus Carinatum/veterinária , Tórax em Funil/patologia , Tórax em Funil/veterinária , Parede Torácica/anormalidades , Dispneia/veterinária , Radiografia Torácica/veterinária
4.
Acta sci. vet. (Impr.) ; 48(suppl.1): Pub.587-4 jan. 2020. ilus
Artigo em Inglês | VETINDEX | ID: biblio-1458414

Resumo

Background: Deformities of the anterior thoracic wall are called pectus: pectus excavatum and pectus carinatum. Pectusexcavatum is characterised by dorsal deviation of the caudal region of the sternum while pectus carinatum consists ofprotrusion of the sternum and/or adjacent cartilage. Both defects may remain symptom-free, but respiratory and cardiacabnormalities have been reported. Another deformity observed in dogs is the swimming dog syndrome, which consists ofthe lateral opening of the thoracic and pelvic limbs, associated with the pedalling movement. These disorders are frequentlyreported in medical practice, are considered rare among canines. This report aims to describe a case of pectus excavatumassociated with the swimming dog syndrome (Case 1) and another case of pectus carinatum (Case 2).Cases: Case 1. An approximately 45-day-old male American Pitbull canine had difficulty standing. Physical examinationrevealed hyperextension of the thoracic and pelvic limb joints and flattening of the thorax. After radiographic examination, pectus excavatum and the swimming dog syndrome were confirmed. The conservative treatment with splinting andhydrotherapy was chosen. At the 3-month follow-up, slight improvement in the limbs and irregular and unsatisfactorygrowth of the thorax leading to episodes of dyspnoea were observed. Case 2. A female Pug, approximately 2 months old,had a thorax deformity. Physical examination revealed thorax protrusion, confirmed on radiography as pectus carinatum.Conservative therapy was provided using compressive bandage. One month later, the tutor reported improvement in thecondition and absence of respiratory changes.Discussion: Pectus deformities has low incidence, and cases to pectus carinatum, there is a sexual predisposition, that is,males are more predisposed, differing from Case 2, a female dog. In the cases of pectus excavatum, no genetic alterationwas directly related to its occurrence...


Assuntos
Masculino , Animais , Cães , Parede Torácica/anormalidades , Pectus Carinatum/patologia , Pectus Carinatum/veterinária , Tórax em Funil/patologia , Tórax em Funil/veterinária , Dispneia/veterinária , Radiografia Torácica/veterinária
5.
Ci. Rural ; 50(8): e20190589, July 3, 2020. ilus
Artigo em Inglês | VETINDEX | ID: vti-28342

Resumo

Congenital anomalies are hereditary or acquired, and their location and intensity are determining factors for the survival of animals. Some cases are rare, often unidentified, poorly reported and of unknown etiology. This paper reports a congenital malformation in a French bulldog, demonstrating the importance of accurate diagnosis for surgical decisions. The use of new technologies such as computed tomography and rapid prototyping enables the analysis of morphofunctional changes, resulting in excellent results for clinical cases in which it is difficult to identify and scale the anatomical deformities. Through this feature, it is possible to accurately recreate anatomical structures of interest, enabling greater assertiveness in deciding the treatment to be established, whether surgical or not. Castration of animals that survive this condition due to hereditary etiology is recommended.(AU)


Anomalias congênitas possuem caráter hereditário ou adquirido, sendo que sua localização e intensidade são fatores determinantes para a sobrevivência do animal. Algumas são raras, muitas vezes não identificadas, pouco relatadas e com etiologia desconhecida. O presente trabalho registra um caso de malformação congênita em um bulldog francês, demonstrando a importância do diagnóstico preciso para a decisão cirúrgica. A utilização de novas tecnologias como tomografia computadorizada e prototipagem rápida possibilitam a análise de alterações morfofuncionais, tendo ótimo resultado para casos clínicos em que há dificuldade em identificar e dimensionar deformidades anatômicas. Através desse recurso é possível recriar com precisão estruturas anatômicas de interesse, possibilitando maior assertiva na decisão do tratamento a ser estabelecido, sendo ele cirúrgico ou não. É recomendada a castração dos animais que sobreviveram a essa condição, devido a etiologia hereditária.(AU)


Assuntos
Animais , Cães , Impressão Tridimensional , Anormalidades Congênitas/veterinária , Doenças do Cão , Tomografia Computadorizada por Raios X/veterinária
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