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This retrospective study evaluated canine patients with presumptively diagnosed meningoencephalomyelitis (ME) based on neurological clinical signs, cerebrospinal fluid (CSF) analysis, cross-sectional imaging, and infectious disease testing with a limited neurological-focused polymerase chain reaction (PCR) panel performed on blood and CSF. The first goal was to determine the proportion of dogs where the condition was caused by an infectious agent versus a probable immune-mediated etiology (i.e., meningoencephalomyelitis of unknown origin; MUO) in our geographic region. The secondary goals of this study were to examine and define associations between abnormal CSF test results and cross-sectional neuroimaging findings, in addition to defining the age and most common neurological clinical signs in each group of ME. A total of 168 dogs matched the inclusion criteria with magnetic resonance imaging (MRI) performed in 130 dogs and computed tomography (CT) performed in 38 dogs. Presumptive MUO was observed in 152/168 (90.5%) of dogs and infectious ME was identified in 16/168 (9.5%) of dogs (p < 0.0001). Canine distemper virus (CDV) was the most common cause of infectious ME in 10/16 dogs (62.5%). Of the total cases with a positive infectious disease result, 3/16 (18.7%) had normal CSF results and 13/16 (81.3%) had abnormal CSF results (p = 0.0078). MRI and CT abnormalities in the brain were detected in 74 and 39% of dogs with inflammatory CSF, respectively. MRI and CT abnormalities in the spinal cord were detected in 90 and 57% of dogs with inflammatory CSF results, respectively. Age was not significantly different between infectious ME and presumptive MUO groups (p = 0.15). Seizures were the most common clinical sign reported for both MUO (36.8% of cases) and infectious ME (31.2% of cases). In conclusion, presumptive MUO is significantly more common than infectious ME in this population of dogs. Furthermore, although normal CSF results were uncommon in dogs with infectious ME, this finding occurred in several patients (3/16), suggesting that infectious disease testing should be considered even in the face of normal CSF results. Finally, MRI was more sensitive than CT in the detection of abnormalities when dogs with ME had inflammatory CSF results but was not 100% sensitive, suggesting CSF analysis should be performed to rule out inflammation even when no abnormalities are detected on MRI or CT.

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Visna-maedi is a multisystemic and progressive inflammatory disease caused by a non-oncogenic retrovirus (Visna-maedi virus, VMV). An outbreak of visna-maedi occurred in Southern Brazil in sheep with clinical signs of blindness and stumbling gait. At post-mortem examination, all animals had similar lesions, including heavy non-collapsed lungs and multifocal yellow areas in the cerebral white matter, affecting mainly the periventricular region. These lesions corresponded histologically to lymphocytic interstitial pneumonia and histiocytic periventricular encephalitis surrounding areas of necrosis, in addition to significant demyelination in the brain. Serology was performed in all the sheep from the flock and 14% were seropositive for VMV. The presence of VMV was confirmed through PCR and partial sequencing of the 5'LTR. Sequencing demonstrated that the virus had 89.7 to 90.0% of nucleotide identity with VMV strains reported in the USA. This is the first description of clinical disease related to VMV in Brazil leading to economic losses. This study calls for the need to implement control measures to prevent the spread of small ruminant lentiviruses in Brazil.

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The lungworm Aelurostrongylus abstrusus is one of the main causes of respiratory diseases in cats worldwide. This report describes the unusual case of a kitten infected with A. abstrusus and presented to a veterinary clinic in Brazil with lethargy, dysphagia, non-ambulatory tetraplegia, and pelvic limbs bilateral myoclonus. The clinical picture of the kitten worsened with generalized flaccid tetraplegia and death a few days after hospitalization. At necropsy, hemorrhagic necrosis and subarachnoid hemorrhages were detected in several areas of the central nervous system. Nematode stages were found at post-mortem histological examinations in lungs, cerebellum, subarachnoid space of the brain and spinal cord. Microscopic and molecular (PCRs-coupled-sequencing protocols) examination showed the presence of A. abstrusus in histological samples. This study describes the first neurological aelurostrongylosis due to ectopic localization of adult worms in the central nervous system of a cat, causing acute hemorrhagic multifocal meningoencephalomyelitis. Further studies are necessary to elucidate whether unusual localizations and the migration of A. abstrusus are more frequent than expected.

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Neurologic diseases are common in domestic cats, and infectious agents are suspected to be the primary cause in 30-45% of cases. Among infectious etiologies, those of bacterial origin are only sporadically characterized in the literature, with few of these reports correlating gross and histologic findings with confirmatory bacteriologic identification. Here, we describe bacterial meningitis and meningoencephalomyelitis associated with Pasteurella multocida in 3 domestic cats. Purulent exudate expanding the cerebral meninges was grossly evident in 2 of the cases. In all 3 cases, histologic changes included multifocal suppurative-to-necrosuppurative meningitis and/or meningoencephalomyelitis of variable severity. Intralesional colonies of gram-negative, short rod-shaped to coccobacillary bacteria were evident histologically in only 1 case. P. multocida was confirmed by routine bacteriologic culture in all cases. Based on our cases, we hypothesize that the upper respiratory system serves as the main portal of entry for P. multocida, leading to invasion of the central nervous system and possible systemic hematogenous dissemination. A case series of meningoencephalomyelitis associated with P. multocida infection in cats has not been reported previously, to our knowledge. We also review briefly other causes of meningoencephalomyelitis in cats.

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The objective of this study was to evaluate the pharmacokinetics of the standard cytarabine (Ara-C) protocol (50 mg/m2 subcutaneously every 12 hr for 2 days) used for dogs with neuroinflammatory disease and compare it to two more practical protocols (a single 200 mg/m2 subcutaneous dose and two 100 mg/m2 subcutaneous doses every 12 hr). Four client-owned dogs previously diagnosed with meningoencephalomyelitis of unknown origin were administered three distinct Ara-C protocols with a 21-day washout between each protocol. A complete blood count was performed seven days after each dosing protocol to assess for clinically relevant myelosuppression. No adverse events were observed. Plasma Ara-C concentrations were measured using a validated liquid chromatography coupled to tandem mass spectrometry assay. The mean maximal concentrations in this study were 4,230, 9,293, and 16,675 ng/ml for a single dose of 50, 100, and 200 mg/m2 , respectively. There was a linear relationship between dose and drug exposure. Drug exposure was similar regardless of the dosing protocol when the total dose was analyzed, with an area under the concentration versus time curve of 37,026, 38,465, and 32,510 ng × hr/ml for 50, 100, and 200 mg/m2 , respectively.

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Background: The Gurltia paralysans nematode was initially described in Chile and for many years it was believed that thedisease caused by this parasite was restricted to this country. However, in Argentina, Uruguay and more recently in Brazil,among other countries, cases of Gurltiosis have been described in both domestic and wild cats. This disease is chronic anddebilitating due to the progressive paralysis developed. This study aimed to describe the clinical, epidemiological and pathological aspects of G. paralysans infection in domestic cats of the Agreste region of the state of Pernambuco, Northeast Brazil.Case: Clinical, epidemiological and pathological aspects of G. paralysans infection in domestic cats in the rural area oftwo Agreste municipalities in the state of Pernambuco, Brazil, are described. Seven farms were visited, in which 11 maleand female affected felines were evaluated. Among these, euthanasia was performed in four cases, at the owners requestand due to the advanced stage of the disease. Clinical signs began with ataxia of the pelvic limbs and evolved to jumpingdifficulty, lateral falls, muscle atrophy, pelvic limb scarring, and paralysis at the most severe stage of the disease, whichdeveloped in a one-year period, approximately. According to the owners, the affected cats died between six months andone year after the initial clinical signs. At necropsy, there were segments of the spinal cord with extensive reddish areasin the dura, between T7 and S2, corresponding to varices. These were characterized by numerous congestive, dilatedand tortuous blood vessels observed in the dorsal plane, but more pronounced in the ventral plane of the meninges. Inthe bladder, multifocal areas of hemorrhage were observed. Histologically, vascular lesions in veins and venules of theleptomeninges were characterized by venous varices with thrombosis, fibrosis and intravascular parasites associated withmoderate...(AU)

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Background: The Gurltia paralysans nematode was initially described in Chile and for many years it was believed that thedisease caused by this parasite was restricted to this country. However, in Argentina, Uruguay and more recently in Brazil,among other countries, cases of Gurltiosis have been described in both domestic and wild cats. This disease is chronic anddebilitating due to the progressive paralysis developed. This study aimed to describe the clinical, epidemiological and pathological aspects of G. paralysans infection in domestic cats of the Agreste region of the state of Pernambuco, Northeast Brazil.Case: Clinical, epidemiological and pathological aspects of G. paralysans infection in domestic cats in the rural area oftwo Agreste municipalities in the state of Pernambuco, Brazil, are described. Seven farms were visited, in which 11 maleand female affected felines were evaluated. Among these, euthanasia was performed in four cases, at the owners’ requestand due to the advanced stage of the disease. Clinical signs began with ataxia of the pelvic limbs and evolved to jumpingdifficulty, lateral falls, muscle atrophy, pelvic limb scarring, and paralysis at the most severe stage of the disease, whichdeveloped in a one-year period, approximately. According to the owners, the affected cats died between six months andone year after the initial clinical signs. At necropsy, there were segments of the spinal cord with extensive reddish areasin the dura, between T7 and S2, corresponding to varices. These were characterized by numerous congestive, dilatedand tortuous blood vessels observed in the dorsal plane, but more pronounced in the ventral plane of the meninges. Inthe bladder, multifocal areas of hemorrhage were observed. Histologically, vascular lesions in veins and venules of theleptomeninges were characterized by venous varices with thrombosis, fibrosis and intravascular parasites associated withmoderate...

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Proventricular dilatation disease (PDD) is a lethal and important disease of captive psittacine birds, and affects a wide range of species, including endangered ones, and lacks an effective treatment. This report describes PDD in three blue-and-gold macaws (Ara ararauna) in southern Brazil. All three macaws originated from the same aviary and presented similar clinical signs including anorexia, apathy, emaciation and prostration. At necropsy, one of the macaws presented an enlarged proventriculus. Histologically, lymphoplasmacytic infiltrates was observed in the ganglia and nerves of the esophagus, crop, proventriculus, ventriculus, heart, adrenal glands, and adrenal medulla of all three cases. Two macaws had meningoencephalomyelitis and one had myocarditis. Immunohistochemistry identified PaBV antigen in the brain, proventricular, ventricular ganglia, and epicardial ganglia, and cardiomyocytes of all three macaws.(AU)

A doença da dilatação proventricular (PDD) e uma importante e fatal doença de psitacídeos de cativeiro, que afeta uma grande variedade de espécies e não tem um tratamento efetivo até o momento. Este relato descreve PDD em três araras canindé (Ara ararauna) no sul do Brasil. Todas as três araras eram provenientes do mesmo criatório e apresentaram sinais clínicos semelhantes incluindo anorexia, apatia, emaciação e prostração. Na necropsia, uma das araras apresentou proventrículo dilatado. No exame histopatológico, infiltrados linfoplasmacitários foram observados em gânglios e nervos do esôfago, inglúvio, proventrículo, moela, coração, glândulas adrenais e rins de todos os casos. Adicionalmente, meningoencefalomielite foi observada em duas araras e miocardite em uma. A imuno-histoquímica identificou antígenos de PaBV no encéfalo, coração, proventrículo e moela de todos os casos.(AU)

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Proventricular dilatation disease (PDD) is a lethal and important disease of captive psittacine birds, and affects a wide range of species, including endangered ones, and lacks an effective treatment. This report describes PDD in three blue-and-gold macaws (Ara ararauna) in southern Brazil. All three macaws originated from the same aviary and presented similar clinical signs including anorexia, apathy, emaciation and prostration. At necropsy, one of the macaws presented an enlarged proventriculus. Histologically, lymphoplasmacytic infiltrates was observed in the ganglia and nerves of the esophagus, crop, proventriculus, ventriculus, heart, adrenal glands, and adrenal medulla of all three cases. Two macaws had meningoencephalomyelitis and one had myocarditis. Immunohistochemistry identified PaBV antigen in the brain, proventricular, ventricular ganglia, and epicardial ganglia, and cardiomyocytes of all three macaws.(AU)

A doença da dilatação proventricular (PDD) e uma importante e fatal doença de psitacídeos de cativeiro, que afeta uma grande variedade de espécies e não tem um tratamento efetivo até o momento. Este relato descreve PDD em três araras canindé (Ara ararauna) no sul do Brasil. Todas as três araras eram provenientes do mesmo criatório e apresentaram sinais clínicos semelhantes incluindo anorexia, apatia, emaciação e prostração. Na necropsia, uma das araras apresentou proventrículo dilatado. No exame histopatológico, infiltrados linfoplasmacitários foram observados em gânglios e nervos do esôfago, inglúvio, proventrículo, moela, coração, glândulas adrenais e rins de todos os casos. Adicionalmente, meningoencefalomielite foi observada em duas araras e miocardite em uma. A imuno-histoquímica identificou antígenos de PaBV no encéfalo, coração, proventrículo e moela de todos os casos.(AU)

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Meningoencefalite granulomatosa (MEG) é uma condição inflamatória do sistema nervoso central (SNC) de causa idiopática e ocorrência esporádica. A lesão pode ser disseminada, focal ou ocular e foi descrita primeiramente por Braund, Vandevelde e Walker em 1978. Afeta principalmente cães de raças toy como poodles e terriers, mas, também, pode ser vista em cães maiores. É principalmente uma doença de cães jovens a meia idade (de 1 a 8 anos), mas pode ocorrer em qualquer idade (BRAUND, 1985; ETTINGER et al, 2004; MUÑANA et al, 1998;). Alguns estudos não identificaram tais predileções (THOMAS, 1998). Foi atendido em uma clinica veterinária situada em Santa Maria (RS) um canino, fêmea, cor preta, raça Labrador Retriever, seis anos de idade e pesando 35 kg. O animal chegou à clínica com o relato de que havia convulsionado várias vezes até chegar ao consultório.(AU)

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Meningoencefalite granulomatosa (MEG) é uma condição inflamatória do sistema nervoso central (SNC) de causa idiopática e ocorrência esporádica. A lesão pode ser disseminada, focal ou ocular e foi descrita primeiramente por Braund, Vandevelde e Walker em 1978. Afeta principalmente cães de raças toy como poodles e terriers, mas, também, pode ser vista em cães maiores. É principalmente uma doença de cães jovens a meia idade (de 1 a 8 anos), mas pode ocorrer em qualquer idade (BRAUND, 1985; ETTINGER et al, 2004; MUÑANA et al, 1998;). Alguns estudos não identificaram tais predileções (THOMAS, 1998). Foi atendido em uma clinica veterinária situada em Santa Maria (RS) um canino, fêmea, cor preta, raça Labrador Retriever, seis anos de idade e pesando 35 kg. O animal chegou à clínica com o relato de que havia convulsionado várias vezes até chegar ao consultório.

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Varicella-zoster virus (VZV) meningoencephalomyelitis is a rare but severe neurological complication of VZV reactivation in immunocompromised patients. We report the case of an HIV-infected individual who developed an acute and severe meningoencephalomyelitis accompanied by a disseminated cutaneous eruption due to VZV. The presence of VZV DNA in cerebrospinal fluid was confirmed by polymerase chain reaction (PCR) technique. The patient started undergoing an intravenous acyclovir therapy with a mild recovery of neurological manifestations. Varicella-zoster virus should be included as a cause of acute meningoencephalomyelitis in patients with AIDS. Early diagnosis followed by specific therapy should modify the rapid and fulminant course for this kind of patients.

A meningoencefalomielite pelo vírus varicela-zoster (VVZ) é uma complicação neurológica rara mas grave da reativação do VVZ em pacientes imunocomprometidos. Nós relatamos o caso de um indivíduo infectado por HIV que desenvolveu uma meningoencefalomielite aguda e grave acompanhada por uma erupção cutânea por causa do VVZ. A presença do DNA do VVZ no líquor foi confirmada pela técnica de reação em cadeia da polimerase (PCR). O paciente iniciou uma terapia intravenosa com aciclovir com uma leve recuperação das manifestações neurológicas. O vírus varicela-zoster deve ser incluído como uma causa de meningoencefalomielite nos pacientes com AIDS. O diagnóstico precoce seguido por terapia específica pode modificar o curso rápido e fulminante deste tipo de pacientes.

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A meningoencefalomielite granulomatosa (MEG) ocorre em cães de todas as raças, em qualquer idade e já foi descrita em vários países. Sua etiologia não é definida, mas sugere-se que uma reação de hipersensibilidade retardada esteja envolvida. Nas lesões há ocorrência de profuso infiltrado de células B e T, além de macrófagos. No presente estudo verificou-se, com técnicas de imunoistoquímica, a distribuição e a morfologia de astrócitos imunorreativos à proteína glial fibrilar ácida no encéfalo de cães acometidos por MEG e também as proporções de células imumorreativas a IgG, IgMe CD3. Foram utilizados seis cães, três machos e três fêmeas, com idade entre dois e seis anos. Observou-se acentuada astrocitose principalmente ao redor das lesões, com aumento da área do corpo celular e da área nuclear em 302,6(porcento) e 88,9(porcento), respectivamente. Os processos citoplasmáticos dos astrócitos tornaram-se mais evidentes, aparecendo, às vezas, como fragmentos no neurópilo. Do total de células inflamatórias infiltrads, 37,9(porcento) era, IgG positivas, 23,5(porcento) IgM positivas e 12(porcento) CD3 positivas. Conclui-se que na MEG ocorre uma expressiva astrocitose associada com a presença de alta proporção de células imunes (AU)

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