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The analysis of cerebrospinal fluid has diagnostic, prognostic, and therapeutic value in neurological illnesses in horses. There are different methods for obtaining cerebrospinal fluid, with the collection between the C1 and C2 vertebrae being a more recent methodology, which allows the procedure to be performed in standing patients, without the limitations of general anesthesia and with a low contamination of the sample with blood, presenting itself as a practical alternative. This study evaluated the efficacy and safety of a local dural blockade in healthy horses submitted to cerebrospinal fluid collection by atlantoaxial puncture and the quality of the samples obtained by this procedure, which were submitted to physical, chemical, and cytological analyses. The animals were evaluated considering aspects such as pain, sensitivity, the presence of edema, temperature variations, and ultrasonographic alterations post-collection. Discrete local changes were observed after the puncture, and the procedure was considered safe and simple to perform. Lidocaine blockade could reduce the reaction elicited by the needle passing through the dura mater, and the samples obtained showed satisfactory quality and laboratory results consistent with the values compiled in the literature. Transient hyperthermia was observed in 70% (7/10) of the animals in the dural blockade group, and 80%(8/10) of the patients from the control group, totalizing 75% of all individuals evaluated. The rectal temperature alteration was observed 4 to 12 hours after the procedure and was entirely resolved without intervention by the 24-hour evaluation.

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The Mangalarga Marchador (MM) breed, which originated in Brazil, constitutes the largest number of horses in the country. The animals are versatile and used in several sports because of major investments made for the genetic improve-ment of the breed. In recent decades, advances in molecular techniques enabled the identification of genetic diseases in hor-ses. Conducting molecular tests and determining the occurrence of mutations are fundamental for the early identification and prevention of abnormalities. Among the known genetic diseases that occur in horses, the c.926G>A mutation in the GYS1gene that causes type 1 polysaccharide storage myopathy (PSSM1) stands out, because it has been identified in several breeds of horses. Although myopathy is common in MM horses, the occurrence of the c.926G>A mutation in the GYS1 gene has not yet been evaluated. The lack of knowledge about the possible presence of PSSM1 averts the adoption of control measures to prevent the spread of the disease in MM horses. Therefore, the aim of this study was to verify the occurrence of the muta-tion that causes PSSM1 in MM horses used in breeding programs. Blood DNA was extracted and the region of the GYS1gene containing the mutation was amplified and sequenced. No mutation in the GYS1 gene was found in the evaluated sam-ples. However, since clinical signs of myopathy are frequently observed in MM horses, further studies, including histological analysis, are necessary to establish the underlying causes. In addition, if there is a genetic pattern of occurrence, molecular studies should be considered.(AU)

A raça Mangalarga Marchador (MM), originária do Brasil, constitui a raça de maior número de equinos no país. Os animais são versáteis e utilizados em diversos esportes devido aos seus grandes investimentos em melhoramento genético. Nas últimas décadas, o avanço das técnicas moleculares permitiu a identificação de doenças genéticas em cavalos. A realização de testes moleculares e a determinação da ocorrência de mutações são fundamentais para a identificação precoce e prevenção de anormalidades. Dentre as doenças genéticas conhecidas em equinos, destaca-se a mutação c.926G>A no gene GYS1 causadora da miopatia por acúmulo de polissacarídeo tipo 1 (PSSM1), pois foi identificada em diversas raças equinas. Embora a miopatia seja comum em cavalos MM, a ocorrência da mutação c.926G>A no gene GYS1 ainda não foi avaliada. A falta de conhecimento sobre a possível presença de PSSM1 inviabiliza a adoção de medidas de controle para prevenir a disseminação da doença em equinos MM. Portanto, o objetivo deste estudo foi verificar a ocorrência da mutação causadora de PSSM1 em cavalos MM utilizados em programas de melhoramento. O DNA sanguíneo foi extraído e a região do gene GYS1contendo a mutação foi amplificada e sequenciada. Nenhuma mutação no gene GYS1 foi encontrada nas amostras avaliadas. No entanto, como sinais clínicos de miopatia são frequentemente observados em cavalos com MM, mais estudos, incluindo análises histológicas, são necessários para estabelecer as causas subjacentes. Além disso, se houver um padrão genético de ocorrência, estudos moleculares devem ser considerados.(AU)

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Most genetic diseases affect purebred animals and are inherited as recessive genes. Cranioschisis refers to dysraphism, which occurs in the midline of the skull due to failure to close the cranial symphysis, which can lead to herniation of the meninges filled with cerebrospinal fluid (meningocele), where there is usually a projection of the meningeal tissue. Diagnosis is performed based on clinical examination, characteristic anatomopathological data, and complementary imaging tests. The surgical approach for correction of cranioschisis is the only described as a therapeutic solution and is indicated in cases in which the cranial synthesis defect does not allow for brain protrusion and there is only the occurrence of meningocele, in addition to the absence of severe signs of neurological alteration. This paper reports a case of the use of polymethylmethacrylate (PMMA) plaque to treat cranioschisis associated with meningocele in a Girolando heifer. The surgical opening of the frontonasal sacculation allowed draining a total liquid content of 488 mL, inspection, and suture of the envelope membrane. APMMA plaque, molded to the bone surface and anchored in the adjacent soft tissue, was used to cover the evidenced frontonasal bone opening. Despite the unfavorable prognosis of the disease, the cranioplasty surgery for the treatment of cranioschisis associated with meningocele using PMMA plaque obtained satisfactory results relative to the quality and maintenance of this animal's life, evaluated at 19 months postoperatively.(AU)

A maioria das doenças genéticas acometem animais de raça pura e herdados como genes recessivos.Acraniosquise refere-se à disrafia, que acontece na linha média do crânio pelo não fechamento da sínfise craniana, podendo levar a herniação das meninges repletas de líquido cefalorraquidiano (meningocele), onde geralmente existe projeção do tecido meningeal. O diagnóstico é realizado a partir do exame clínico, dados anatomopatológicos característicos e através da realização de exames complementares de imagem. Como solução terapêutica, a abordagem cirúrgica para correção das craniosquises é a única descrita, e é indicada em casos em que o defeito de síntese craniana não permita a protrusão encefálica e exista a ocorrência apenas da meningocele, além da inexistência de sinais graves de alteração neurológica. O artigo relata um caso de uso de placa de polimetilmetacrilato (PMMA) no tratamento de craniosquise associada à meningocele em uma bezerra Girolando. Instituiu-se a abertura cirúrgica da saculação fronto-nasal, permitindo a drenagem de conteúdo líquido total de 488 mL, inspeção e rafia de membrana envoltória. Para recobrimento da abertura óssea fronto-nasal evidenciada, utilizou-se uma placa de polimetilmetacrilato (PMMA), moldada à superfície óssea e ancorada em tecido mole adjacente. Concluiu-se que, apesar do prognóstico desfavorável da enfermidade, a cirurgia de cranioplastia para tratamento de craniosquise associada à meningocele, com a utilização de placa de PMMA, neste caso, obteve resultados satisfatórios em relação a qualidade e manutenção da vida deste animal, avaliando-se em 19 meses pós-operatório.(AU)

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The external ear extends from the pinna to the tympanic membrane, where it is supported and shaped by an arrangement of cartilages including the conchal, annular, scutiform, and external acoustic meatus. Environmental exposure can often lead to diseases of the external ear canal in animals. In horses, otitis primarily occurs due to infestation by ectoparasites, promoting local inflammation and infection. Chronic conditions can result in ear deformation, including auricular canal stenosis. While operative techniques for treating auricular stenosis are known, they are limited to companion animals, with few reports on horses. This study aimed to describe the modified lateral resection technique of the ear canal, which is commonly performed in small animals, for treating auricular canal stenosis in six horses. As a methodology, the intertragic notch was used as a reference for the incision due to species disparity. The ear canal cartilage was dissected, followed by resection of the lateral wall and the cartilaginous flap adhered to the skin. Excess skin was removed, and the ear canal was sutured to the skin with nylon thread. Our results indicated a significant improvement in the treatment of otitis in the treated horses, demonstrating a favorable evolution in the healing process and resolution of bacterial infections in all cases. In conclusion, the use of the modified lateral resection technique of the ear canal was successful in all six treated horses, providing access to clinical treatment of the canal without any occurrences of recurrence or postoperative complications

A orelha externa se estende desde a pina até a membrana timpânica, onde sua sustentação e forma são garantidas pela disposição das cartilagens conchal, anular, escutiforme e meato acústico externo. Animais frequentemente apresentam doenças do canal auricular externo devido à exposição ambiental. Em equinos, a otite ocorre principalmente pela infestação de ectoparasitas favorecendo a inflamação e infecção local, que em condições crônicas, pode proporcionar deformações do ouvido, incluindo a estenose do canal auricular. Apesar de conhecidas, as técnicas operatórias indicadas na abordagem terapêutica de estenoses auriculares se limitam às espécies de animais de companhia, sendo escassos os relatos em equinos. Objetivou-se com esse trabalho descrever a técnica modificada de ressecção lateral do conduto auditivo, amplamente realizada em pequenos animais, no tratamento de estenose do canal auricular em seis equinos. Como metodologia, devido a disparidade entre espécies, utilizou-se a incisura intertrágica como referência para a incisão. Realizou-se a dissecção da cartilagem do canal auditivo, seguido pela ressecção da parede lateral e do retalho cartilaginoso aderido à pele. Foi removido o excesso de pele e suturado o canal auditivo à pele com fio de nylon. Os resultados obtidos indicaram melhora significativa na condução do tratamento de otite dos equinos tratados, demonstrando evolução favorável no processo de cicatrização e resolução das infecções bacterianas em todos os casos. Concluiu-se que a utilização da técnica de ressecção lateral do canal auditivo foi bem-sucedida nos seis animais tratados deste trabalho, promovendo o acesso para tratamento clínico do conduto, sem ocorrência de recidiva ou complicações pós-operatórias

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Hereditary myotonia (HM) is a genetic disorder that occurs due to mutations in the chloride channel and results in delayed relaxation of the skeletal muscles. HM has been described in 12 dog breeds, and in five of them, molecular studies of this disorder were performed and mutations in the CLCN1 gene were described. In this study, an affected American Bulldog with HM clinically characterized by muscle hypertrophy, myotonic discharges, and nondystrophic myotonia with a "warm-up" phenomenon was evaluated, and the candidate canine CLCN1 gene was sequenced. The molecular analysis revealed a frameshift mutation NM_001003124.2:c.436_437insCTCT that resulted in a frameshift and a premature stop codon NP_001003124.1:pTyr146SerfsTer49 . Two aberrant alternative CLCN1 transcripts were observed in an affected dog, the expected transcript with the 4 bp insertion, NM_001003124.2:r.436_437insctct, and an unexpected transcript containing parts of intron 6 in addition to the insertion in exon 4, NM_001003124.2:[r.436_437insctct;r.774_775ins79]. In conclusion, the frameshift mutation in the CLCN1 gene is associated with autosomal recessive HM in American Bulldog and this study constitutes the first description of the disease in this breed.

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Background: Osteosarcomas are common malignant bone tumors described in dogs, humans and cats. However, thereare rare reports in horses. The tumor etiology has not been fully elucidated. Clinical signs are associated to the tumorsize, location and growth characteristics. When located on the face, the most common findings are facial distortion, nasaldischarge and inspiratory dyspnea. The aim of this study was to report an osteoblastic osteosarcoma in a horse, located onthe right maxillary region with projections into the corresponding nostril.Case: A 6-year-old mixbreed saddle gelding, presenting bay coat was admitted to a University Hospital with a chronicsinusitis history. The animal was previously examined and treated by other veterinarians, who suspected of odontogenicmaxillary sinusitis, and therefore a repulsion of the fourth premolar from the right maxilla hemiarcade was performed.However, an improvement of the clinical signs was not observed and subsequently the gelding was referred to a VeterinaryHospital. During physical examination the patient presented dyspnea, tachypnea and tachycardia. An increase on the facesize was observed, together with a fetid and purulent nasal discharge. During oral cavity inspection, a diagonal wear wasdetected at the occlusal surface of the right hemiarcade; food accumulation was seen at the dental extraction site, and acommunication with the rostral maxillary sinus was evidenced, from where a purulent fetid discharge was draining. At theradiographic exam, well defined margins of a tumor were observed, with adjacent bone lysis and the presence of a centralnucleus showing a gross granular mineral radiopacity, distorting the frontal and nasal bones. During the endoscopic exam,a mass partially occluding the right nasal cavity close to the nasal opening was seen, which was blocking the progressionof the endoscopy. However, during the left cavity inspection, at the end of the nasal septum a mass...(AU)

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Background: Osteosarcomas are common malignant bone tumors described in dogs, humans and cats. However, thereare rare reports in horses. The tumor etiology has not been fully elucidated. Clinical signs are associated to the tumorsize, location and growth characteristics. When located on the face, the most common findings are facial distortion, nasaldischarge and inspiratory dyspnea. The aim of this study was to report an osteoblastic osteosarcoma in a horse, located onthe right maxillary region with projections into the corresponding nostril.Case: A 6-year-old mixbreed saddle gelding, presenting bay coat was admitted to a University Hospital with a chronicsinusitis history. The animal was previously examined and treated by other veterinarians, who suspected of odontogenicmaxillary sinusitis, and therefore a repulsion of the fourth premolar from the right maxilla hemiarcade was performed.However, an improvement of the clinical signs was not observed and subsequently the gelding was referred to a VeterinaryHospital. During physical examination the patient presented dyspnea, tachypnea and tachycardia. An increase on the facesize was observed, together with a fetid and purulent nasal discharge. During oral cavity inspection, a diagonal wear wasdetected at the occlusal surface of the right hemiarcade; food accumulation was seen at the dental extraction site, and acommunication with the rostral maxillary sinus was evidenced, from where a purulent fetid discharge was draining. At theradiographic exam, well defined margins of a tumor were observed, with adjacent bone lysis and the presence of a centralnucleus showing a gross granular mineral radiopacity, distorting the frontal and nasal bones. During the endoscopic exam,a mass partially occluding the right nasal cavity close to the nasal opening was seen, which was blocking the progressionof the endoscopy. However, during the left cavity inspection, at the end of the nasal septum a mass...

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Tumors affecting Bartholins gland are considered rare in human medicine; there are few reports in the veterinary literature, with descriptions occurring only in cows. This article described the clinical and pathological findings associated with Bartholins gland adenoma in a goat. Clinically, a 7-year-old pregnant Saanen goat presented bilateral enlargement of the vulva that did not regress spontaneously after parturition. Grossly, these vulvar masses were multilobulated, contained cystic areas from which oozed a whitish fluid. Histopathology revealed an adenoma characterized by the proliferation of irregularly shaped neoplastic epithelial cells that formed tubular to glandular-like structures. These neoplastic cells demonstrated moderate anisokaryosis and evident nucleoli. The intratumoral proliferation index (PI) was estimated by immunoreactivity with the protein ki-67. Further, the glandular-like structures produced a Periodic Acid-Schiff positive secretion. A diagnosis of Bartholins gland adenoma was established due to the anatomic location of the neoplastic growths, the histopathological features, and the PI of the tumor.(AU)

Tumores que afetam a glândula de Bartholin são considerados raros em humanos e há poucos relatos na medicina veterinária, sendo descrito somente em vacas. Este artigo descreve os achados clínicos e patológicos associados ao adenoma na glândula de Bartholin em uma cabra. O animal da raça Saanen, com sete anos de idade e gestante apresentava aumento de volume bilateral na região da vulva, que não regrediu após o parto. Macroscopicamente, a massa era multilobulada, com presença de vários cistos preenchidos por uma secreção esbranquiçada. A histopatologia revelou um adenoma, caracterizado por proliferação de células epiteliais de formato irregular que formavam estruturas tubulares semelhantes à glândulas. Estas células neoplásicas apresentavam anisocariose moderada e nucléolos evidentes. O índice de proliferação celular intratumoral (PI) foi estimado por imunorreatividade à proteína ki-67. Além disso, a secreção produzida por essas estruturas do tipo glandular, foi positiva na coloração do Ácido Periódico-Schiff. O diagnóstico de adenoma da glândula de Bartholin foi estabelecido pela localização anatômica dos tumores neoplásicos, características histopatológicas e à PI do tumor.(AU)

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Background: Post-anesthetic myopathy is the most common complication associated with general anesthesia in horses. Polysaccharide storage myopathy (PSSM) is characterized by an abnormal accumulation of glycogen and glycogen-related polysaccharides in the skeletal muscle, which is categorized in type 1 (PSSM1) and type 2 (PSSM2). The purpose of this study is to report the clinical, pathological and molecular findings in a Percheron mare with post-anesthetic myopathy associated with a PSSM1. Case: A 9-year-old Percheron mare was submitted to a caesarean section due to clinical dystocia during labor. Xylazine was employed during pre-anesthesia, followed by induction with ketamine and diazepam, while anesthetic maintenance was obtained with isoflurane. The mare showed good recovery, however 24 h later, sternal recumbency and hyperthermia (41° C) were observed. The mare was euthanized, and a necropsy was performed. Samples of multiple tissues were collected and routinely processed for histology. At necropsy, segments of skeletal muscles had bilateral pale areas. The kidneys had old and recent infarcts. The heart had whitish areas in the myocardium. The brain showed focally extensive reddish areas, with flattening of gyri. Histologically, skeletal muscle fibers had in the sarcoplasm multiple homogeneous globular clear eosinophilic formations, in addition to mild hyaline necrosis. In the heart and in the kidney, there were extensive areas of acute coagulative necrosis. The brain showed marked multifocal fibrinoid degeneration of vessels and hemorrhage. Refrigerated liver samples were submitted to DNA extraction to detect mutations in the GYS1 (type 1 PSSM) and RyR1 genes (malignant hyperthermia). A positive result for a homozygous dominant mutation in GYS1 (type 1 PSSM) was observed, while the mutation responsible for malignant hyperthermia was not identified.[...](AU)

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Background: Post-anesthetic myopathy is the most common complication associated with general anesthesia in horses. Polysaccharide storage myopathy (PSSM) is characterized by an abnormal accumulation of glycogen and glycogen-related polysaccharides in the skeletal muscle, which is categorized in type 1 (PSSM1) and type 2 (PSSM2). The purpose of this study is to report the clinical, pathological and molecular findings in a Percheron mare with post-anesthetic myopathy associated with a PSSM1. Case: A 9-year-old Percheron mare was submitted to a caesarean section due to clinical dystocia during labor. Xylazine was employed during pre-anesthesia, followed by induction with ketamine and diazepam, while anesthetic maintenance was obtained with isoflurane. The mare showed good recovery, however 24 h later, sternal recumbency and hyperthermia (41° C) were observed. The mare was euthanized, and a necropsy was performed. Samples of multiple tissues were collected and routinely processed for histology. At necropsy, segments of skeletal muscles had bilateral pale areas. The kidneys had old and recent infarcts. The heart had whitish areas in the myocardium. The brain showed focally extensive reddish areas, with flattening of gyri. Histologically, skeletal muscle fibers had in the sarcoplasm multiple homogeneous globular clear eosinophilic formations, in addition to mild hyaline necrosis. In the heart and in the kidney, there were extensive areas of acute coagulative necrosis. The brain showed marked multifocal fibrinoid degeneration of vessels and hemorrhage. Refrigerated liver samples were submitted to DNA extraction to detect mutations in the GYS1 (type 1 PSSM) and RyR1 genes (malignant hyperthermia). A positive result for a homozygous dominant mutation in GYS1 (type 1 PSSM) was observed, while the mutation responsible for malignant hyperthermia was not identified.[...]

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ABSTRACT: Tumors affecting Bartholin's gland are considered rare in human medicine; there are few reports in the veterinary literature, with descriptions occurring only in cows. This article described the clinical and pathological findings associated with Bartholin's gland adenoma in a goat. Clinically, a 7-year-old pregnant Saanen goat presented bilateral enlargement of the vulva that did not regress spontaneously after parturition. Grossly, these vulvar masses were multilobulated, contained cystic areas from which oozed a whitish fluid. Histopathology revealed an adenoma characterized by the proliferation of irregularly shaped neoplastic epithelial cells that formed tubular to glandular-like structures. These neoplastic cells demonstrated moderate anisokaryosis and evident nucleoli. The intratumoral proliferation index (PI) was estimated by immunoreactivity with the protein ki-67. Further, the glandular-like structures produced a Periodic Acid-Schiff positive secretion. A diagnosis of Bartholin's gland adenoma was established due to the anatomic location of the neoplastic growths, the histopathological features, and the PI of the tumor.

RESUMO: Tumores que afetam a glândula de Bartholin são considerados raros em humanos e há poucos relatos na medicina veterinária, sendo descrito somente em vacas. Este artigo descreve os achados clínicos e patológicos associados ao adenoma na glândula de Bartholin em uma cabra. O animal da raça Saanen, com sete anos de idade e gestante apresentava aumento de volume bilateral na região da vulva, que não regrediu após o parto. Macroscopicamente, a massa era multilobulada, com presença de vários cistos preenchidos por uma secreção esbranquiçada. A histopatologia revelou um adenoma, caracterizado por proliferação de células epiteliais de formato irregular que formavam estruturas tubulares semelhantes à glândulas. Estas células neoplásicas apresentavam anisocariose moderada e nucléolos evidentes. O índice de proliferação celular intratumoral (PI) foi estimado por imunorreatividade à proteína ki-67. Além disso, a secreção produzida por essas estruturas do tipo glandular, foi positiva na coloração do Ácido Periódico-Schiff. O diagnóstico de adenoma da glândula de Bartholin foi estabelecido pela localização anatômica dos tumores neoplásicos, características histopatológicas e à PI do tumor.

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A paralisia periódica hipercalêmica (HYPP) é uma das principais enfermidades genéticas de caráter dominante que acometem cavalos da raça Quarto de milha (QM). A HYPP é causada por uma mutação pontual no gene SCN4A e, apesar de estar presente nos cavalos QM no Brasil, dados sobre a prevalência da HYPP são escassos. O objetivo deste trabalho foi verificar a prevalência da mutação responsável pela HYPP em cavalos QM, utilizados nas modalidades esportivas de rédeas (n=160), apartação (n=160), tambor e baliza (n=160), corrida (n=160) e conformação (n=101). Foram utilizados DNA sanguíneo dos 741 equinos; o teste genético para enfermidade foi padronizado e as amostras sequenciadas para identificação da mutação no gene alvo. A prevalência de HYPP na população amostrada foi de 4,2%, sendo que somente na linhagem de conformação foram identificados animais positivos (30,7%). Medidas de controle mais efetivas devem ser adotadas para diminuir a prevalência da HYPP.

Hyperkalemic Periodic Paralysis (HYPP) is one of the major dominant genetic diseases which affect Quarter horses (QH). The HYPP is caused by a point mutation in the SCN4A gene and despite the presence of HYPP in Brazilian QH, limited data on the disease prevalence are available. The aim of this study was to investigate the HYPP mutation in QH belonging to reining (n=160), cutting (n=160), barrel racing (n=160), racing (n=160) and halter (n=101) competitive disciplines. Blood DNA from 741 horses were used. Genetic tests were standardized and samples were sequenced to identify the mutation on the target gene. The prevalence of HYPP on the sampled population was 4.2% and the positive animals (30.7%) were only identified in the halter lineage. More effective actions on HYPP control should be done to reduce the disease prevalence. .

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A paralisia periódica hipercalêmica (HYPP) é uma das principais enfermidades genéticas de caráter dominante que acometem cavalos da raça Quarto de milha (QM). A HYPP é causada por uma mutação pontual no gene SCN4A e, apesar de estar presente nos cavalos QM no Brasil, dados sobre a prevalência da HYPP são escassos. O objetivo deste trabalho foi verificar a prevalência da mutação responsável pela HYPP em cavalos QM, utilizados nas modalidades esportivas de rédeas (n=160), apartação (n=160), tambor e baliza (n=160), corrida (n=160) e conformação (n=101). Foram utilizados DNA sanguíneo dos 741 equinos; o teste genético para enfermidade foi padronizado e as amostras sequenciadas para identificação da mutação no gene alvo. A prevalência de HYPP na população amostrada foi de 4,2%, sendo que somente na linhagem de conformação foram identificados animais positivos (30,7%). Medidas de controle mais efetivas devem ser adotadas para diminuir a prevalência da HYPP.(AU)

Hyperkalemic Periodic Paralysis (HYPP) is one of the major dominant genetic diseases which affect Quarter horses (QH). The HYPP is caused by a point mutation in the SCN4A gene and despite the presence of HYPP in Brazilian QH, limited data on the disease prevalence are available. The aim of this study was to investigate the HYPP mutation in QH belonging to reining (n=160), cutting (n=160), barrel racing (n=160), racing (n=160) and halter (n=101) competitive disciplines. Blood DNA from 741 horses were used. Genetic tests were standardized and samples were sequenced to identify the mutation on the target gene. The prevalence of HYPP on the sampled population was 4.2% and the positive animals (30.7%) were only identified in the halter lineage. More effective actions on HYPP control should be done to reduce the disease prevalence. .(AU)

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O carcinoma de células escamosas (CCE) é um tumor maligno das células epidérmicas, dos queratinócitos. É uma neoplasia de crescimento lento, localmente invasiva e ocasionalmente metastática. Está diretamente associado com a exposição prolongada à luz ultravioleta, em áreas glabras ou onde há falta de pigmento da epiderme. Os tumores podem apresentar aspecto produtivo ou erosivo e são diagnosticados histologicamente. A escolha do tratamento depende da extensão tumoral, localização e função esperada doanimal. A cisplatina é o agente anticancerígeno mais eficaz no tratamento de tumores sólidos, no entanto a sua utilização em tratamentos sistêmicos tem sido limitada, devido à toxicidade. A administração intratumoral permite maximizar a concentração do fármaco, minimizando efeitos de exposição aos demais tecidos. Relata-se o caso de um ovino, da raça Santa Inês, que apresentava massa tumoral em região próximo à borda coronária do dígito lateral do membro pélvico esquerdo. O diagnóstico de CCE foi determinado por exame clínico e avaliação histopatológica, sendo o animal submetido à tratamento com o uso de cisplatina (Fauldcispla®, Libbs)intralesional, em veículo aquoso, na dose de 0,97 mg/cm3 de tumor, em planos paralelos, a cada duas semanas, totalizando-se quatro aplicações. A terapia antineoplásica proporcionou resultados satisfatórios neste caso, ocorrendo à regressão completa da massa tumoral, sem presença de recidivas ou manifestação de efeitos adversos(AU)

The squamous cell carcinoma (SCC) is a malignant tumor of epidermal cells, the keratinocytes. It is a slow growing cancer, locally invasive and occasionally metastatic. Is directly associated with prolonged exposure to ultraviolet light, in glabrous areas or at sites lacking skin pigment. The tumors can have productive or erosive appearance and is diagnosed histologically. Treatment depends on the tumor extent, location and expected the animal function. Cisplatin is the most effective anticancer agent in the treatment of solid tumors,however its systemic use has been limited due to toxicity. The intratumoral administration allows for maximum concentration of the drug while minimizing effects of exposure to other tissues. We herein a SCC tumor in a sheep, Santa Ines breed, near the coronary border of the lateral digit of the left pelvic limb. The diagnosis of SCCwas determined by clinical examination followed by histopathological evaluation of the mass. The animal was treated with intralesional cisplatin (Fauldcispla®, Libbs) in an aqueous vehicle at a dose of 0.97 mg / cm3 of tumor, injected in parallel planes, every two weeks, and four applications. The antineoplastic therapy was satisfactory as shown by the complete regression of the tumor mass, lack of adverse effects and no recurrence(AU)

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O carcinoma de células escamosas (CCE) é um tumor maligno das células epidérmicas, dos queratinócitos. É uma neoplasia de crescimento lento, localmente invasiva e ocasionalmente metastática. Está diretamente associado com a exposição prolongada à luz ultravioleta, em áreas glabras ou onde há falta de pigmento da epiderme. Os tumores podem apresentar aspecto produtivo ou erosivo e são diagnosticados histologicamente. A escolha do tratamento depende da extensão tumoral, localização e função esperada doanimal. A cisplatina é o agente anticancerígeno mais eficaz no tratamento de tumores sólidos, no entanto a sua utilização em tratamentos sistêmicos tem sido limitada, devido à toxicidade. A administração intratumoral permite maximizar a concentração do fármaco, minimizando efeitos de exposição aos demais tecidos. Relata-se o caso de um ovino, da raça Santa Inês, que apresentava massa tumoral em região próximo à borda coronária do dígito lateral do membro pélvico esquerdo. O diagnóstico de CCE foi determinado por exame clínico e avaliação histopatológica, sendo o animal submetido à tratamento com o uso de cisplatina (Fauldcispla®, Libbs)intralesional, em veículo aquoso, na dose de 0,97 mg/cm3 de tumor, em planos paralelos, a cada duas semanas, totalizando-se quatro aplicações. A terapia antineoplásica proporcionou resultados satisfatórios neste caso, ocorrendo à regressão completa da massa tumoral, sem presença de recidivas ou manifestação de efeitos adversos

The squamous cell carcinoma (SCC) is a malignant tumor of epidermal cells, the keratinocytes. It is a slow growing cancer, locally invasive and occasionally metastatic. Is directly associated with prolonged exposure to ultraviolet light, in glabrous areas or at sites lacking skin pigment. The tumors can have productive or erosive appearance and is diagnosed histologically. Treatment depends on the tumor extent, location and expected the animal function. Cisplatin is the most effective anticancer agent in the treatment of solid tumors,however its systemic use has been limited due to toxicity. The intratumoral administration allows for maximum concentration of the drug while minimizing effects of exposure to other tissues. We herein a SCC tumor in a sheep, Santa Ines breed, near the coronary border of the lateral digit of the left pelvic limb. The diagnosis of SCCwas determined by clinical examination followed by histopathological evaluation of the mass. The animal was treated with intralesional cisplatin (Fauldcispla®, Libbs) in an aqueous vehicle at a dose of 0.97 mg / cm3 of tumor, injected in parallel planes, every two weeks, and four applications. The antineoplastic therapy was satisfactory as shown by the complete regression of the tumor mass, lack of adverse effects and no recurrence

Assuntos

RESUMO

A hipersensibilidade a picada de insetos é a dermatite alérgica mais comum em equinos, sendo uma importante causa de prurido. O objetivo deste trabalho foi relatar um caso da enfermidade, onde são descritos os sinais clínicos, diagnóstico o tratamento instituído, os resultados obtidos, bem como o manejo dos equinos portadores da doença.

Insect bite hypersensivity is the most common allergic skin disease of the horse and commonly pruritic cause. This case report aimed to described clinical sings, diagnosis, treatment and difficulty clinical management with this horses.

Assuntos

RESUMO

Dentre os animais domésticos, a espécie bovina é a que mais apresenta problemas com distocias, causando um grande prejuízo econômico para o produtor. As distocias podem ocorrer por várias causas, e variar de um ligeiro atraso no desencadeamento normal do parto ou até mesmo a incapacidade de parir, necessitando quase que sempre da intervenção de um Médico Veterinário, e pode ser corrigida apenas com manobras obstétricas, em casos mais graves cesariana ou quando o produto estiver morto a fetotomia. Este trabalho tem como objetivo, mostrar a importância da intervenção do Médico Veterinário nos casos de distocia em vacas e as possibilidades disponíveis para terminar um parto.

Among domestic animals, the bovine species is presented more problems with dystocia, causing great economic loss to the producer. The dystocia can occur for various reasons, and vary from a slight delay in triggering normal labor or even the inability to give birth, almost always requiring the intervention of a veterinarian, and can be corrected only with obstetric maneuvers, in most cases serious caesarean or when the product is dead fetotomia. This paper aims to show the importance of the intervention of the veterinarian in cases of dystocia in cows and the possibilities available to complete a delivery.

Assuntos

RESUMO

Dentre os animais domésticos, a espécie bovina é a que mais apresenta problemas com distocias, causando um grande prejuízo econômico para o produtor. As distocias podem ocorrer por várias causas, e variar de um ligeiro atraso no desencadeamento normal do parto ou até mesmo a incapacidade de parir, necessitando quase que sempre da intervenção de um Médico Veterinário, e pode ser corrigida apenas com manobras obstétricas, em casos mais graves cesariana ou quando o produto estiver morto a fetotomia. Este trabalho tem como objetivo, mostrar a importância da intervenção do Médico Veterinário nos casos de distocia em vacas e as possibilidades disponíveis para terminar um parto. (AU)

Among domestic animals, the bovine species is presented more problems with dystocia, causing great economic loss to the producer. The dystocia can occur for various reasons, and vary from a slight delay in triggering normal labor or even the inability to give birth, almost always requiring the intervention of a veterinarian, and can be corrected only with obstetric maneuvers, in most cases serious caesarean or when the product is dead fetotomia. This paper aims to show the importance of the intervention of the veterinarian in cases of dystocia in cows and the possibilities available to complete a delivery. (AU)

Assuntos

RESUMO

A hipersensibilidade a picada de insetos é a dermatite alérgica mais comum em equinos, sendo uma importante causa de prurido. O objetivo deste trabalho foi relatar um caso da enfermidade, onde são descritos os sinais clínicos, diagnóstico o tratamento instituído, os resultados obtidos, bem como o manejo dos equinos portadores da doença. (AU)

Insect bite hypersensivity is the most common allergic skin disease of the horse and commonly pruritic cause. This case report aimed to described clinical sings, diagnosis, treatment and difficulty clinical management with this horses. (AU)

Assuntos