Polineuropatia motora em cão adulto / Motor polyneuropathy in an adult dog

Background: Nonambulatory flaccid tetraparesis can be the result of diseases of the peripheral nervous system and it is characterized by generalized lower motor neuron (LMN) signs, as weakness, tetraparesis/tetraplegia, decreased muscle tone and reflexes. The term polyneuropathy is used for dysfunction of multiple peripheral nerves. In Brazil, there are several etiologies for polyneuropathy in dogs, such as acute idiopathic polyradiculoneuritis, botulism and myasthenia gravis. Toxoplasma gondii is an uncommon cause of LMN diseases in dogs. The aim of this report was to describe a case of flaccid tetraplegia toxoplasmosis in an adult dog with a Toxoplasma gondii serology with a markedly elevated IgG titer of 1:4096. Case: A 4-year-old intact mongrel male dog, weighing 19.6 kg, was referred to the Veterinary Medical Teaching Hospital of the Universidade Estadual de Londrina (UEL) with a 5-day history of weakness that progressed to tetraparesis. Physical examination revealed no significant changes other than the dull and unkempt coat. Neurologic examination revealed severe tetraparesis that was worse in the pelvic limbs, with decreased muscle tone in all four limbs. Postural reactions and the interdigital reflex were absent in all four limbs, as was the patellar reflex, but pain perception was present. There were no clinical signs of dysfunction on examination of the cranial nerves. Laboratory tests were performed, and creatine kinase was elevated (819 U/L). Blood was drawn to look for antibodies to Toxoplasma gondii and Neospora caninum class IgG using the indirect immunofluorescence technique. The antibody titer for Toxoplasma gondii (IgG) was 1:4096. A chest radiograph was performed to look for megaesophagus, and a pulmonary pattern suggestive of mild diffuse pneumonia was observed. Treatment was performed with sulfamethoxazole and trimethoprim, and the dog's condition improved slightly. Discussion: Based on lower motor neuron findings, the neurologic lesion was localized in the nerve roots, peripheral nerves, neuromuscular junctions, or muscles. The most important diseases in the list of differential diagnoses were immune-mediated or infectious polyradiculoneuritis (toxoplasmosis, neosporosis), myasthenia gravis, toxic polyneuropathy (botulism, chronic organophosphate poisoning), and paraneoplastic polyneuropathy. Among these differential diagnoses, polyradiculoneuritis is one of the most common. It is an idiopathic inflammatory disease. Exposure to raccoon saliva (in the U.S.), vaccination, or infection have been proposed as precipitating causes, but the triggers of this disease remain unknown. Serology for neosporosis was negative, while IgG titers for toxoplasmosis were 1:4096. In a previous study, dogs with acute polyradiculoneuritis were more likely to have T. gondii IgG serum antibody titers than dogs without neurologic signs. Infection with the protozoa T. gondii and N. caninum can cause intense polyradiculoneuritis in dogs accompanied by myositis, especially in puppies. One treatment trial was based on the administration of sulfonamide-trimethoprim with pyrimethamine, whose efficacy in the treatment of toxoplasmosis in dogs has also been reported in the literature. Neurologic deficits improved slightly, and there is a possibility that certain signs may not disappear completely because of the permanent damage caused by inflammation of the nervous system, as observed in the present case. The case had the limitation that it was not possible to perform other laboratory tests to demonstrate histopathologically the presence of Toxoplasma gondii organisms in muscles or nerves. Recovery of normal function is less likely in protozoan polyradiculoneuritis than in noninfectious polyradiculoneuritis. Thus, in the present case, the main suspicion was polyradiculoneuritis secondary to toxoplasmosis. Although it is a rare condition, it is important to consider toxoplasmosis in dogs with LMN-type tetraparesis or tetraplegia.

Estabilização cirúrgica da coluna vertebral cervical em ovino / Cervical spinal cord surgical stabilization in a sheep

Background: Trauma is the main cause of spinal fractures and dislocations in humans and large animals. Clinical signspresent with acute onset and vary according to the location and severity of the spinal cord injury. The treatment of fractures in large animals depends on economic value, cost of procedures, prognosis, location and type of fracture. However,although spinal fractures in large animals are not uncommon, the literature about their clinical aspects and treatment isscanty. Therefore, the purpose of this report is to describe a surgical stabilization of atlantoaxial subluxation, fracture ofthe third cervical vertebra and C2-C3 subluxation.Case: An approximately 2-year-old Île-de-France sheep, weighing 101 kg, with a history of cervical trauma and nonambulatory tetraparesis was treated at the Veterinary Hospital of the Institution (UNIPAMPA). During physical examination, the animal presented good general physical condition and heart rate, respiratory rate and temperature was accordingto physiological parameters for the species. The animal remained in lateral decubitus, with minimal head and limb movements, and exhibited deep pain sensitivity. Clinical treatment with dexamethasone, limb physiotherapy and change inlateral decubitus position were employed, but failed to improve the animal’s condition. After five days of unresponsive toclinical treatment, the patient was referred to the neurology department, where it underwent neurological examination andradiographic examination of the cervical region was performed under general anesthesia. The radiographic examinationrevealed atlantoaxial subluxation, by displacement of the odontoid process into the vertebral canal, fracture of the thirdcervical vertebra and C2-C3 vertebral subluxation. The surgical planning aimed cervical vertebral instability repair usingatlantoaxial arthrodesis associated the stabilization of C1-C2 and C2-C3 vertebrae with Schanz pins and bone cement...

Estabilização cirúrgica da coluna vertebral cervical em ovino / Cervical spinal cord surgical stabilization in a sheep

Background: Trauma is the main cause of spinal fractures and dislocations in humans and large animals. Clinical signspresent with acute onset and vary according to the location and severity of the spinal cord injury. The treatment of fractures in large animals depends on economic value, cost of procedures, prognosis, location and type of fracture. However,although spinal fractures in large animals are not uncommon, the literature about their clinical aspects and treatment isscanty. Therefore, the purpose of this report is to describe a surgical stabilization of atlantoaxial subluxation, fracture ofthe third cervical vertebra and C2-C3 subluxation.Case: An approximately 2-year-old Île-de-France sheep, weighing 101 kg, with a history of cervical trauma and nonambulatory tetraparesis was treated at the Veterinary Hospital of the Institution (UNIPAMPA). During physical examination, the animal presented good general physical condition and heart rate, respiratory rate and temperature was accordingto physiological parameters for the species. The animal remained in lateral decubitus, with minimal head and limb movements, and exhibited deep pain sensitivity. Clinical treatment with dexamethasone, limb physiotherapy and change inlateral decubitus position were employed, but failed to improve the animals condition. After five days of unresponsive toclinical treatment, the patient was referred to the neurology department, where it underwent neurological examination andradiographic examination of the cervical region was performed under general anesthesia. The radiographic examinationrevealed atlantoaxial subluxation, by displacement of the odontoid process into the vertebral canal, fracture of the thirdcervical vertebra and C2-C3 vertebral subluxation. The surgical planning aimed cervical vertebral instability repair usingatlantoaxial arthrodesis associated the stabilization of C1-C2 and C2-C3 vertebrae with Schanz pins and bone cement...(AU)

Carcinoma com metástase em coluna vertebral em dois cães / Carcinoma with vertebral column metastasis in two dogs

Background: Carcinomas are aggressive and invasive malignancies that originate from any type of epithelial cell and are responsible for many deaths in dogs. Carcinoma metastases occur primarily via the lymphatic route; however, they can occur by blood flow, thus reaching bone structures. In dogs, metastasis of mammary and squamous cell carcinomas to the skeletal system is poorly described. The aim of this study was to report two cases of dogs that developed metastases of carcinomas to the vertebral column. Cases: Case 1. A 10-year-old, male, mixed-breed dog with paralysis of the left pelvic limb, subcutaneous mass in the lumbar region, apathy, anorexia and progressive weight loss and with a previous history of amputation of the right pelvic limb resulting from squamous cell carcinoma (SCC) in the integument of the cranial face of the femorotibiopatellar joint. Due to the patient’s clinical condition and the negative prognosis associated with the neoplasia, euthanasia was performed. At necropsy, infiltrating the lumbar vertebrae from L5 to L7, a whitish and firm mass of approximately 15 x 8 cm was observed. Histologically, it comprised a malignant epithelial neoplastic development consisting of nests and cords interspersed with fibrovascular stroma, containing multiple keratine pearls. There was moderate to severe anisocytosis, severe anisokariosis, and about 4 mitosis figures for every 10 high power fields (400x). The histological features were consistent with an invasive SCC. Anti-cytokeratin and anti-p63 immunohistochemical (IHC) evaluations were performed, both with immunoreactivity in neoplastic cells. Case 2. An 8-year-old, female, Chihuahua with bilateral paralysis of the pelvic limbs, anorexia, and progressive weight loss, with a history of excision of solid mammary carcinoma. The clinical condition...

Carcinoma com metástase em coluna vertebral em dois cães / Carcinoma with vertebral column metastasis in two dogs

Background: Carcinomas are aggressive and invasive malignancies that originate from any type of epithelial cell and are responsible for many deaths in dogs. Carcinoma metastases occur primarily via the lymphatic route; however, they can occur by blood flow, thus reaching bone structures. In dogs, metastasis of mammary and squamous cell carcinomas to the skeletal system is poorly described. The aim of this study was to report two cases of dogs that developed metastases of carcinomas to the vertebral column. Cases: Case 1. A 10-year-old, male, mixed-breed dog with paralysis of the left pelvic limb, subcutaneous mass in the lumbar region, apathy, anorexia and progressive weight loss and with a previous history of amputation of the right pelvic limb resulting from squamous cell carcinoma (SCC) in the integument of the cranial face of the femorotibiopatellar joint. Due to the patients clinical condition and the negative prognosis associated with the neoplasia, euthanasia was performed. At necropsy, infiltrating the lumbar vertebrae from L5 to L7, a whitish and firm mass of approximately 15 x 8 cm was observed. Histologically, it comprised a malignant epithelial neoplastic development consisting of nests and cords interspersed with fibrovascular stroma, containing multiple keratine pearls. There was moderate to severe anisocytosis, severe anisokariosis, and about 4 mitosis figures for every 10 high power fields (400x). The histological features were consistent with an invasive SCC. Anti-cytokeratin and anti-p63 immunohistochemical (IHC) evaluations were performed, both with immunoreactivity in neoplastic cells. Case 2. An 8-year-old, female, Chihuahua with bilateral paralysis of the pelvic limbs, anorexia, and progressive weight loss, with a history of excision of solid mammary carcinoma. The clinical condition...(AU)

Cardiac fibroelastosis associated with thromboembolism and paresis in a cat: case report

A two-year-old, male, non-castrated cat was referred to the veterinary hospital with a three-month history of paresis of the pelvic limbs. Clinical examination revealed a discreet muffling of cardiac sounds and the presence of a degree III/VI holosystolic murmur. The animal was hospitalized and died of cardiorespiratory arrest. The heart had a thickened left ventricular endocardium characterized by the deposition of a fibrous white matter that was firmly adhered to the endocardium and also observed on the epicardium. Renal infarctions and thrombi in the atrium and bifurcation of the aorta were found. Microscopically, in the endocardium of the left ventricular chamber there was a diffuse and disorganized deposition of fibrous connective tissue filled with elastic fibers of varying thickness. In the left ventricular epicardium, the same lesion was observed, but with less extension. Clinical and anatomopathological findings were consistent with primary left ventricular endocardial and left ventricular epicardial fibroelastosis with secondary left ventricular congestive heart failure, thromboembolism and paresis.

Cardiac fibroelastosis associated with thromboembolism and paresis in a cat: case report

A two-year-old, male, non-castrated cat was referred to the veterinary hospital with a three-month history of paresis of the pelvic limbs. Clinical examination revealed a discreet muffling of cardiac sounds and the presence of a degree III/VI holosystolic murmur. The animal was hospitalized and died of cardiorespiratory arrest. The heart had a thickened left ventricular endocardium characterized by the deposition of a fibrous white matter that was firmly adhered to the endocardium and also observed on the epicardium. Renal infarctions and thrombi in the atrium and bifurcation of the aorta were found. Microscopically, in the endocardium of the left ventricular chamber there was a diffuse and disorganized deposition of fibrous connective tissue filled with elastic fibers of varying thickness. In the left ventricular epicardium, the same lesion was observed, but with less extension. Clinical and anatomopathological findings were consistent with primary left ventricular endocardial and left ventricular epicardial fibroelastosis with secondary left ventricular congestive heart failure, thromboembolism and paresis.(AU)

Neoplasia do plexo braquial com infiltração medular / Brachial plexus neoplasia with spinal cord infiltration: report case

Tumores originados no sistema nervoso periférico não são comuns na clínica veterinária e seu diagnóstico é difícil. Por ser uma patologia de curso lento e insidioso muitos profissionais demoram a suspeitar dos tumores de plexo braquial, retardando muito o diagnóstico e tratamento. Os sinais clínicos observados são claudicação, dor à palpação axilar,monoparesia e, em casos mais graves, com infiltração neoplásica na medula espinhal, o paciente pode apresentar tetraparesia. Foi atendida uma cadela fox paulistinha com 10 anos de idade apresentando tetraparesia não ambulatória. O exame clínico foi sugestivo de uma lesão de medula espinhal (C6-T2), suspeitando-se de doença do disco intervertebral ou neoplasia medular. A mielografia foi realizada e mostrou compressão caudal a C6. O animal foi então submetido àhemilaminectomia para descompressão, sendo observada infiltração neoplásica das raízes nervosas na medula espinhal impossível de ser resseccionada. O paciente foi eutanasiado. O plexo braquial, os nervos espinhais e a medula foram colhidos e enviados para examehistopatológico, confirmando-se o diagnóstico de tumor maligno de bainhade nervo periférico (TMNP). O presente relato mostrou um caso cujo curso clínico da doença foi atípico, dificultando o diagnóstico. Conclui-se que sempre se deve considerar a possibilidade de neoplasias de plexo braquial em pacientes com histórico de claudicação crônica de membros torácicos não responsiva a repouso e anti-inflamatórios.

Primary tumour of peripheral nerves are not common in veterinary practice and its diagnosis is difficult. Being a condition of slow and insidious course many professionals are slow to suspect the brachial plexus tumors, delaying diagnosis and treatment. The clinical signs observed in this disease are lameness, pain axillary palpation, monoparesis and in severe cases with neoplastic infiltration in the spinalcord, the patient may experience tertraparesia. A female dog Fox Paulistinha with 10-year-old was met with tetraparesia not ambulatory. Clinical examination was suggestive of a spinal cord injury (C6-T2),suspected presence of disc herniation and spinal cord cancer. The myelography was performed and showed compressive C6 flow. The animal was then subjected to a decompression Hemilaminectomy being observed neoplastic infiltration of the nerve roots in the spinal cord impossible to beresected. The patient was euthanized, the brachial plexus, the spinal nerves and the affected spinal cord were collected and sent for histopathological examination, confirming the diagnosis of malignantperipheral nerve sheath tumor (MPNST) in the brachial plexus. This report shows a brachial plexus tumors case whose clinical course of the disease was atypical making diagnosis difficult. The conclusion is that youshould always consider the brachial plexus tumors in patients with a history of chronic lameness forelimbs unresponsive to rest and anti-inflammatory.

Neoplasia do plexo braquial com infiltração medular / Brachial plexus neoplasia with spinal cord infiltration: report case

Tumores originados no sistema nervoso periférico não são comuns na clínica veterinária e seu diagnóstico é difícil. Por ser uma patologia de curso lento e insidioso muitos profissionais demoram a suspeitar dos tumores de plexo braquial, retardando muito o diagnóstico e tratamento. Os sinais clínicos observados são claudicação, dor à palpação axilar,monoparesia e, em casos mais graves, com infiltração neoplásica na medula espinhal, o paciente pode apresentar tetraparesia. Foi atendida uma cadela fox paulistinha com 10 anos de idade apresentando tetraparesia não ambulatória. O exame clínico foi sugestivo de uma lesão de medula espinhal (C6-T2), suspeitando-se de doença do disco intervertebral ou neoplasia medular. A mielografia foi realizada e mostrou compressão caudal a C6. O animal foi então submetido àhemilaminectomia para descompressão, sendo observada infiltração neoplásica das raízes nervosas na medula espinhal impossível de ser resseccionada. O paciente foi eutanasiado. O plexo braquial, os nervos espinhais e a medula foram colhidos e enviados para examehistopatológico, confirmando-se o diagnóstico de tumor maligno de bainhade nervo periférico (TMNP). O presente relato mostrou um caso cujo curso clínico da doença foi atípico, dificultando o diagnóstico. Conclui-se que sempre se deve considerar a possibilidade de neoplasias de plexo braquial em pacientes com histórico de claudicação crônica de membros torácicos não responsiva a repouso e anti-inflamatórios.(AU)

Primary tumour of peripheral nerves are not common in veterinary practice and its diagnosis is difficult. Being a condition of slow and insidious course many professionals are slow to suspect the brachial plexus tumors, delaying diagnosis and treatment. The clinical signs observed in this disease are lameness, pain axillary palpation, monoparesis and in severe cases with neoplastic infiltration in the spinalcord, the patient may experience tertraparesia. A female dog Fox Paulistinha with 10-year-old was met with tetraparesia not ambulatory. Clinical examination was suggestive of a spinal cord injury (C6-T2),suspected presence of disc herniation and spinal cord cancer. The myelography was performed and showed compressive C6 flow. The animal was then subjected to a decompression Hemilaminectomy being observed neoplastic infiltration of the nerve roots in the spinal cord impossible to beresected. The patient was euthanized, the brachial plexus, the spinal nerves and the affected spinal cord were collected and sent for histopathological examination, confirming the diagnosis of malignantperipheral nerve sheath tumor (MPNST) in the brachial plexus. This report shows a brachial plexus tumors case whose clinical course of the disease was atypical making diagnosis difficult. The conclusion is that youshould always consider the brachial plexus tumors in patients with a history of chronic lameness forelimbs unresponsive to rest and anti-inflammatory.(AU)

Prototheca zopfii genotype 2 disseminated infection in a dog with neurological signs

ABSTRACT: Prototheca zopfii is an alga that can cause disease in animals and humans. Here, we reported a case of systemic protothecosis in a 2-year-old female Boxer. The animal exhibited tetraparesis and vertical nystagmus. It died two weeks after the onset of clinical signs and was necropsied. At gross examination, whitish areas were identified in the heart. Oval or round structures were observed by microscopic examination, some of which formed morula-like structures compatible with algae in the heart, skeletal muscle, and brain. Growth of Prototheca sp. was observed in the heart after culture at 37°C on Sabouraud agar medium with chloramphenicol. Immunohistochemical analysis of the heart and brain using an anti-Prototheca zopfii polyclonal antibody yielded positive results. Genotyping of the cultured agent from brain and heart samples was performed by restriction fragment length polymorphism of a specific 18S rDNA fragment. P. zopfii genotype 2 was reported to be the cause of disseminated protothecosis in this dog with manifestation in the brain, heart, and skeletal muscle.

RESUMO: A prototecose é uma infecção causada por algas, causadora de doenças em animais e seres humanos. O presente trabalho tem por objetivo relatar um caso de prototecose sistêmica em um canino fêmea, da raça Boxer de dois anos de idade. O animal apresentava tetraparesia e nistagmo vertical. O animal morreu duas semanas após o início dos sinais clínicos e foi realizado o exame de necropsia. Os achados macroscópicos se caracterizavam principalmente por áreas esbranquiçadas no miocárdio. Na histologia observou-se estruturas ovais ou redondas, algumas apresentando estruturas como mórulas compatíveis com Prototheca no coração, músculo esquelético e encéfalo. No cultivo do miocárdio em meio Agar Sabouraud com Chloramphenicol a 37oC foi observado o crescimento de Prototheca sp. No teste imuno-histoquímico do coração, cérebro e cerebelo com anticorpo policlonal anti-P. zopffi, foi observada marcação positiva. Teste de PCR a partir da cultura do agente usando uma sequência de 18S rDNA foi realizado para a tipificação do genótipo. P. zopfii genótipo 2 foi encontrado como causa de prototecose disseminada no encéfalo, coração e músculo esquelético nesse cão.

Prototheca zopfii genotype 2 disseminated infection in a dog with neurological signs

ABSTRACT: Prototheca zopfii is an alga that can cause disease in animals and humans. Here, we reported a case of systemic protothecosis in a 2-year-old female Boxer. The animal exhibited tetraparesis and vertical nystagmus. It died two weeks after the onset of clinical signs and was necropsied. At gross examination, whitish areas were identified in the heart. Oval or round structures were observed by microscopic examination, some of which formed morula-like structures compatible with algae in the heart, skeletal muscle, and brain. Growth of Prototheca sp. was observed in the heart after culture at 37°C on Sabouraud agar medium with chloramphenicol. Immunohistochemical analysis of the heart and brain using an anti-Prototheca zopfii polyclonal antibody yielded positive results. Genotyping of the cultured agent from brain and heart samples was performed by restriction fragment length polymorphism of a specific 18S rDNA fragment. P. zopfii genotype 2 was reported to be the cause of disseminated protothecosis in this dog with manifestation in the brain, heart, and skeletal muscle.(AU)

RESUMO: A prototecose é uma infecção causada por algas, causadora de doenças em animais e seres humanos. O presente trabalho tem por objetivo relatar um caso de prototecose sistêmica em um canino fêmea, da raça Boxer de dois anos de idade. O animal apresentava tetraparesia e nistagmo vertical. O animal morreu duas semanas após o início dos sinais clínicos e foi realizado o exame de necropsia. Os achados macroscópicos se caracterizavam principalmente por áreas esbranquiçadas no miocárdio. Na histologia observou-se estruturas ovais ou redondas, algumas apresentando estruturas como mórulas compatíveis com Prototheca no coração, músculo esquelético e encéfalo. No cultivo do miocárdio em meio Agar Sabouraud com Chloramphenicol a 37oC foi observado o crescimento de Prototheca sp. No teste imuno-histoquímico do coração, cérebro e cerebelo com anticorpo policlonal anti-P. zopffi, foi observada marcação positiva. Teste de PCR a partir da cultura do agente usando uma sequência de 18S rDNA foi realizado para a tipificação do genótipo. P. zopfii genótipo 2 foi encontrado como causa de prototecose disseminada no encéfalo, coração e músculo esquelético nesse cão.(AU)

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Background: The swimmer puppy syndrome, characterized by an abnormal puppy development, is rare in cats, and commonly observed between the 2nd and 3rd week of life. The puppy affected by the syndrome has difficulty with ambulation, abduction and paresis of the hindlimbs and, occasionally, the forelimbs. The recommended treatment consists of using bandages around the affected limbs and physiotherapy while remaining on non-slip floors and soft surfaces. This paper reports the occurrence of the swimmer puppy syndrome in an entire litter of cats, emphasizing the discussion about the types of treatments for the disease. Case: Three 11 day-old kittens of non-defined breed (NDB) were referred to the Veterinary Hospital with locomotion disability. The mother of the kittens was found on the street. Upon clinical examination, the only observed abnormality was that the kittens remained in constant sterna recumbency while the hindlimbs were extended and displaced laterally. After examination, it was decided to accompany the animals until the third week of life for re-evaluations. At 25 days old, the kittens showed less severe sternal recumbency. However, the hindlimbs remained in constant abduction and displaced laterally and caudally while producing rotational movements similar to swimming when trying to move around. The chest and pelvic radiographs detected normal bone density, and joint...(AU)

Deficiência de cobre em suínos: caracterização clínico-patológica / Copper deficiency in swine: clinical-pathologic characterization

São relatados dois casos de deficiência de cobre em suínos (A e B), fêmeas, sem raça definida, de três meses de idade, provenientes de propriedade rural em Planaltina, GO. Os animais apresentavam incoordenação, paresia de membros pélvicos, com progressão para os membros torácicos e andar com flexão da articulação metacarpo-falangeana. Na propriedade de origem dos animais, outros dois suínos apresentavam atrofia da musculatura da coxa e posição sentada quando parados. O rebanho recebia dieta não-balanceada constituída por milho, soro de leite e sobras de lavoura. Na necropsia, não foram observadas alterações significativas, mas histologicamente havia vacuolização periaxonal multifocal no tronco encefálico e na medula espinhal, quantidade discreta de esferoides axonais e macrófagos no interior dos vacúolos. A coloração com azul rápido de luxol (ARL) para mielina demonstrou que as áreas de vacuolização caracterizavam focos de desmielinização. Amostras de fígado dos dois suínos apresentaram níveis de cobre muito abaixo do normal, de 13,1 partes por milhão (ppm) (suíno A) e 5,7ppm (suíno B). Este trabalho descreve dois casos de desmielinização medular e de tronco encefálico devido à deficiência de cobre em suínos jovens.(AU)

Two cases of copper deficiency are described in three-month-old female crossbred piglets from a swine herd in Planaltina, GO. The animals presented incoordination, hindlimbs paresis progressing to the forelimbs, and gait with flexion of the metacarpofalangeal articulation. On the farm of origin of the animals, other two piglets presented atrophy of thigh muscle and sitting position when in station. The herd was fed with unbalanced diet consisting of corn, whey and leftover crop. On necropsy no significant changes were observed, but histologically there was multifocal periaxonal vacuolization in the brainstem and in spinal cord, discrete amount of axonal spheroids and macrophages in the vacuoles. The luxol fast blue (LFB) stain for myelin showed that the vacuolated sites represent demyelinated areas. Liver sample of the two piglets had very low copper levels, 13.1 parts per million (ppm) in swine A and 5.7 (ppm) in swine B. This paper describes two cases of spinal cord and brainstem demyelination due to copper deficiency in piglets.(AU)

Síndrome do filhote nadador em gato: relato de caso / Swimmer puppy syndrome in cat: case report / Síndrome del cachorro nadador en gato: relato de caso

A síndrome do filhote nadador, também conhecida como síndrome do filhote tartaruga ou splay leg, representa um raro transtorno caracterizado pela hipoplasia miofibrilar, que afeta o desenvolvimento motor, tanto de animais de produção quanto de companhia. O presente artigo relata o caso de um filhote de gato, SRD, de 25 dias, com abdução dos quatro membros e diagnóstico clínico de síndrome do gato nadador. Foi realizado tratamento clínico com uso de bandagens, fisioterapia e termoterapia, sendo verificada recuperação completa em seis dias após o início do tratamento. A identificação precoce da desordem associado à terapia intensiva foram responsáveis pela evolução favorável deste caso, o que permite evidenciar a eficácia do tratamento clínico na resolução da síndrome do gato nadador.(AU)

Swimming cub syndrome also known as the flat turtle syndrome or splay leg, represents a rare disorder characterized by myofibrillar hypoplasia, which aftects the motor development of both production and companion animais. This article reports the case of a zs-olo-cav mongrel kitten, with abduction of the four limbs and clinical diagnosis of swimmer cat syndrome. Clinical treatment with bandages, physiotherapy and thermotherapy was performed, and complete recovery was verified six days after the start of treatment. The early identification of the disorder associated with intensive care was responsible for the favorable evolution of this case, which allows to evidence the eftectiveness of clinical treatment in the resolution of swimmer cat syndrome.(AU)

El síndrome del cría nadador, también conocido como síndrome del cachorro plano, del cachorro tortuga o splay leg, representa un raro trastorno caracterizado por la hipoplasia miofibrilar, que afecta ai desarrollo motor, tanto de animales de producción y de compaõía. El presente artículo relata el caso de un gato, SRD, de 25 días, con abducción de los cuatro miembros y el diagnóstico clínico del síndrome del gato nadador. Se realizó un tratamiento clínico con el uso de vendajes, fisioterapia y termoterapia, y se verificó una recuperación completa seis días después del inicio del tratamiento. La identificación precoz del desorden asociado a la terapia intensiva fue responsable de la evolución favorable de este caso, que permite evidenciar la eficacia del tratamiento clínico en la resolución del síndrome dei gato nadador.(AU)

Síndrome do filhote nadador em gato: relato de caso / Swimmer puppy syndrome in cat: case report / Síndrome del cachorro nadador en gato: relato de caso

A síndrome do filhote nadador, também conhecida como síndrome do filhote tartaruga ou splay leg, representa um raro transtorno caracterizado pela hipoplasia miofibrilar, que afeta o desenvolvimento motor, tanto de animais de produção quanto de companhia. O presente artigo relata o caso de um filhote de gato, SRD, de 25 dias, com abdução dos quatro membros e diagnóstico clínico de síndrome do gato nadador. Foi realizado tratamento clínico com uso de bandagens, fisioterapia e termoterapia, sendo verificada recuperação completa em seis dias após o início do tratamento. A identificação precoce da desordem associado à terapia intensiva foram responsáveis pela evolução favorável deste caso, o que permite evidenciar a eficácia do tratamento clínico na resolução da síndrome do gato nadador.

Swimming cub syndrome also known as the flat turtle syndrome or splay leg, represents a rare disorder characterized by myofibrillar hypoplasia, which aftects the motor development of both production and companion animais. This article reports the case of a zs-olo-cav mongrel kitten, with abduction of the four limbs and clinical diagnosis of swimmer cat syndrome. Clinical treatment with bandages, physiotherapy and thermotherapy was performed, and complete recovery was verified six days after the start of treatment. The early identification of the disorder associated with intensive care was responsible for the favorable evolution of this case, which allows to evidence the eftectiveness of clinical treatment in the resolution of swimmer cat syndrome.

El síndrome del cría nadador, también conocido como síndrome del cachorro plano, del cachorro tortuga o splay leg, representa un raro trastorno caracterizado por la hipoplasia miofibrilar, que afecta ai desarrollo motor, tanto de animales de producción y de compaõía. El presente artículo relata el caso de un gato, SRD, de 25 días, con abducción de los cuatro miembros y el diagnóstico clínico del síndrome del gato nadador. Se realizó un tratamiento clínico con el uso de vendajes, fisioterapia y termoterapia, y se verificó una recuperación completa seis días después del inicio del tratamiento. La identificación precoz del desorden asociado a la terapia intensiva fue responsable de la evolución favorable de este caso, que permite evidenciar la eficacia del tratamiento clínico en la resolución del síndrome dei gato nadador.