Polioencefalomalacia em ruminantes: aspectos etiológicos, clínicos e anatomopatológicos

Polioencefalomalacia é uma doença cosmopolita, multifatorial, que acomete bovinos,bubalinos, caprinos e ovinos. O termo polioencefalomalacia indica um diagnóstico morfológico deamolecimento por necrose (malacia) da substância cinzenta (pólio) do córtex cerebral. As causas de PEMsão variadas, no entanto possuem patogênese semelhante por promoverem alterações irreversíveis nometabolismo das células nervosas que invariavelmente evoluem para morte (necrose). As principaiscausas conhecidas são: deficiência de tiamina, intoxicação por enxofre, meningoencefalite porherpesvírus bovino tipo 5 (BoHV-5), intoxicação por sal associada a privação por água, intoxicação porchumbo, intoxicação por plantas que produzem tiaminases, amprólio e “Uva do Japão”.

Polioencephalomalacia is a cosmopolitan, multifactorial disease that affects cattle,buffaloes, goats and sheep. Polioencephalomalacia is a morphological diagnosis that means necrosis(malacia) in the cerebral cortex causing the softening of the gray matter (polio). Although the etiologicalagents are multiples, they have similar pathogenesis causing irreversible lesions in the metabolism ofnerve cells, leading to the cellular death. Among the main etiological agents are thiamine deficiency,sulfur intoxication, bovine herpesvirus type 5 (BHV-5) meningoencephalitis, salt intoxication associatedwith water deprivation, lead intoxication, intoxication by plants that produce thiaminases, amprolium andJapanese.

Angioglioma misdiagnosed as encephalomalacia on magnetic resonance imaging for over a decade.

We report a case of intractable seizures secondary to an angioglioma that was misdiagnosed as post-traumatic encephalomalacia for over a decade, with a discussion of the radiological findings and a review of the literature.

Bovine diseases causing neurological signs and death in Mexican feedlots.

The number of large feedlot operations, similar to that of USA and Canada, has notably increased in Mexico in the last three decades. Clinical and laboratory diagnoses of neurological diseases in feedlot cattle are crucial in Mexico and Central America because of the high incidence of bovine paralytic rabies (BPR). Because of its zoonotic potential, BPR must be promptly diagnosed and differentiated from other bovine neurological diseases such as thrombotic meningoencephalitis (TME), polioencephalomalacia (PEM) and botulism. More recently, BPR and botulism have been diagnosed with increasing frequency in Mexican feedlots. Neither BPR nor botulism has relevant gross lesions, thus post-mortem diagnosis without laboratory support is impossible. Herein, we describe five outbreaks of neurological diseases in Mexican feedlots in which BPR, botulism and PEM were diagnosed either independently or in combination. A diagram illustrating the most conspicuous pathologic findings and ancillary laboratory test required to confirm the diagnoses of these neurological diseases in feedlot cattle is proposed.

Focal symmetrical encephalomalacia in a goat.

Focal symmetrical encephalomalacia (FSE) is the most prominent lesion seen in the chronic form of enterotoxemia caused by Clostridium perfringens type D in sheep. However, this lesion has not been reported in goats. The current paper reports a case of FSE in a goat from the state of Paraíba in the Brazilian semiarid region. As reported by the farmer, 30, 4-48-month-old animals from a flock of 150 goats died after showing nervous signs, including blindness and recumbence, for periods varying between 1 and 14 days. The flock was grazing native pasture supplemented with wheat and corn bran. Additionally, lactating goats were supplemented with soybeans. A 4-month-old goat with nervous signs was examined clinically and then necropsied 3 days after the onset of clinical signs. Bilateral, focal, and symmetrical areas of brown discoloration were observed in the internal capsule and thalamus. Histologic lesions in these areas consisted of multifocal, bilateral malacia with a few neutrophils; endothelial cell swelling; perivascular edema; and hemorrhages. The etiology of these lesions was not determined. However, FSE is considered pathognomonic for C. perfringens type D enterotoxemia in sheep, and it is speculated that this microorganism was the etiologic agent in the present case. The flock had been vaccinated against type D enterotoxemia only once, approximately 3 months before the beginning of the outbreak. Insufficient immunity due to the incorrect vaccination protocol, low efficacy of the vaccine used, and a diet including large amounts of highly fermentable carbohydrates were suspected to be predisposing factors for this outbreak.

Functional deficiencies of sulfite oxidase: Differential diagnoses in neonates presenting with intractable seizures and cystic encephalomalacia.

Sulfite oxidase is a mitochondrial enzyme encoded by the SUOX gene and essential for the detoxification of sulfite which results mainly from the catabolism of sulfur-containing amino acids. Decreased activity of this enzyme can either be due to mutations in the SUOX gene or secondary to defects in the synthesis of its cofactor, the molybdenum cofactor. Defects in the synthesis of the molybdenum cofactor are caused by mutations in one of the genes MOCS1, MOCS2, MOCS3 and GEPH and result in combined deficiencies of the enzymes sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase. Although present in many ethnic groups, isolated sulfite oxidase deficiency and molybdenum cofactor deficiency are rare inborn errors of metabolism, which makes awareness of key clinical and laboratory features of affected individuals crucial for early diagnosis. We report clinical, radiologic, biochemical and genetic data on a Brazilian and on a Turkish child with sulfite oxidase deficiency due to the isolated defect and impaired synthesis of the molybdenum cofactor, respectively. Both patients presented with early onset seizures and neurological deterioration. They showed no sulfite oxidase activity in fibroblasts and were homozygous for the mutations c.1136A>G in the SUOX gene and c.667insCGA in the MOCS1 gene, respectively. Widely available routine laboratory tests such as assessment of total homocysteine and uric acid are indicated in children with a clinical presentation resembling that of hypoxic ischemic encephalopathy and may help in obtaining a tentative diagnosis locally, which requires confirmation by specialized laboratories.

Polioencephalomalacia in ruminants in Brazil

Polioencephalomalacia (PEM) of ruminants is a complex disease. The term indicates a morphological diagnosis where severe cortical neuronal necrosis results in softening of cerebral grey matter. Initially though as a single disease caused by thiamine deficiency, it is currently believed that PEM is caused by different etiological agents through different pathogenic mechanisms or trough a single pathogenic mechanism triggered by different agents. In this paper the putative cases and pathogenesis of PEM in ruminants are critically reviewed and discussed. Also reviewed are the epidemiology, clinical signs, gross and histological findings and methods of diagnosis of cases of PEM described in ruminants in Brazil(AU)

Polioencephalomalacia in ruminants in Brazil

Polioencephalomalacia (PEM) of ruminants is a complex disease. The term indicates a morphological diagnosis where severe cortical neuronal necrosis results in softening of cerebral grey matter. Initially though as a single disease caused by thiamine deficiency, it is currently believed that PEM is caused by different etiological agents through different pathogenic mechanisms or trough a single pathogenic mechanism triggered by different agents. In this paper the putative cases and pathogenesis of PEM in ruminants are critically reviewed and discussed. Also reviewed are the epidemiology, clinical signs, gross and histological findings and methods of diagnosis of cases of PEM described in ruminants in Brazil

Early destructive lesions in the developing brain: clinical and electrographic correlates.

OBJECTIVE: Early brain insults can cause cavitary lesions including porencephaly (POR) and multicystic encephalopathy (MCE). The objective of this study was to investigate clinical and electrographic correlates associated to these types of destructive brain lesions. METHOD: Patients with POR and MCE were selected and submitted to clinical and Video-EEG monitoring. The following variables were analyzed: demographic data, type of lesion, presence of gliosis, perinatal complications, epilepsy, brain atrophy, and presence and frequency of epileptiform discharges. RESULTS: Twenty patients were included, 65% males, 35% females, ages ranging from 1 to 40 years, 14 with MCE and 6 with POR. Eighteen patients had hemiparesis, 19 had epilepsy (current or in the past), seven of them had refractory seizures, and 16 had epileptiform discharges. All patients with MCE had gliosis while only 2 with POR had it. CONCLUSIONS: No correlation was observed between type of lesion and clinical and electrographical outcome. However, a positive correlation was observed between frequency of discharges and presence of brain atrophy, and between MCE and gliosis.

Early destructive lesions in the developing brain: clinical and electrographic correlates

OBJECTIVE: Early brain insults can cause cavitary lesions including porencephaly (POR) and multicystic encephalopathy (MCE). The objective of this study was to investigate clinical and electrographic correlates associated to these types of destructive brain lesions. METHOD: Patients with POR and MCE were selected and submitted to clinical and Video-EEG monitoring. The following variables were analyzed: demographic data, type of lesion, presence of gliosis, perinatal complications, epilepsy, brain atrophy, and presence and frequency of epileptiform discharges. RESULTS: Twenty patients were included, 65 percent males, 35 percent females, ages ranging from 1 to 40 years, 14 with MCE and 6 with POR. Eighteen patients had hemiparesis, 19 had epilepsy (current or in the past), seven of them had refractory seizures, and 16 had epileptiform discharges. All patients with MCE had gliosis while only 2 with POR had it. CONCLUSIONS: No correlation was observed between type of lesion and clinical and electrographical outcome. However, a positive correlation was observed between frequency of discharges and presence of brain atrophy, and between MCE and gliosis.

OBJETIVO: Insultos cerebrais precoces podem causar lesões cavitárias incluindo porencefalias (POR) e encefalomalacias multicisticas (EMC). O objetivo deste estudo foi investigar correlatos clínicos e eletrográficos associados a estes dois tipos de lesões destrutivas. MÉTODO: Pacientes com POR e EMC foram selecionados e submetidos à avaliação neurológica e monitorização vídeo-eletrencefalográfica, analisando-se as seguintes variáveis: dados demográficos, tipo de lesão, presença de gliose, complicações perinatais, epilepsia, atrofia cerebral, presença e freqüência de descargas epilépticas. RESULTADO: Vinte pacientes foram incluídos, sendo 65 por cento do sexo masculino, 35 por cento do feminino, idades entre 1 e 40 anos, sendo 14 com EMC e 6 com POR. Dezoito pacientes tinham hemiparesia, 19 tinham ou tiveram epilepsia (7 deles refratários ao tratamento medicamentoso) e 16 deles tinham paroxismos epileptiformes. Todos com MCE tinham gliose associada, contra apenas 2 dos pacientes com POR. CONCLUSÃO: Não houve correlação entre tipo de lesão e evolução clínica e eletrográfica. Houve, entretando, correlação positiva entre freqüência de descargas epilépticas e presença de atrofia cerebral, e entre lesão do tipo EMC e presença de gliose.

Intoxicação por Ramaria flavo-brunnescens (Clavariaceae) em bovinos / Poisoning by Ramaria flavo-brunnescens (Clavariaceae) in cattle

Dois surtos de intoxicação pelo cogumelo Ramaria flavo-brunnescens são relatados em bovinos de duas fazendas localizadas nos municípios de Santa Maria e São Gabriel, no Rio Grande do Sul, no período de abril-maio de 2005. De um total de 180 bovinos de sobreano que tiveram acesso a bosques de eucaliptos, 19 adoeceram e 10 morreram. A evolução clínica foi de 8-15 dias e os sinais clínicos incluíam depressão, perda de peso, desidratação, salivação excessiva, afrouxamento e perda dos pêlos longos da cauda, alisamento da superfície dorsal da língua com ocasional ulceração, afrouxamento do estojo córneo dos chifres, fezes em forma de cíbalos e recobertas por película de muco, hipópion, hifema e opacidade da córnea. Dois novilhos tinham leucocitose devido a leve desvio regenerativo à esquerda. Os achados de necropsia confirmaram as observações clínicas e adicionalmente incluíam esofagite fibrinonecrótica, principalmente no terço distal do esôfago. Alterações histopatológicas na pele da cauda incluíam hiperqueratose ortoqueratótica, folículos pilosos com contornos irregulares, espessamento da camada de queratina tricolemal e formação ocasional de tampões de queratina; degeneração e necrose da bainha radicular externa também era observada. Nos cascos havia hemorragia, fibrina e infiltrado neutrofílico nas lâminas dérmicas, hiperplasia do topo das lâminas epidérmicas com queratinização irregular e retenção dos núcleos; várias lâminas epidérmicas estavam encurtadas e fundidas. Na mucosa da língua o epitélio de revestimento estava adelgaçado, com atrofia e perda das papilas filiformes, áreas multifocais de disqueratose e espongiose das células da camada basal. Em algumas porções havia perda do epitélio e a superfície da língua era formada por tecido de granulação e infiltrado inflamatório misto. A mucosa esofágica de seis novilhos apresentava vários graus de necrose epitelial e inflamação. A perda do epitélio de revestimento revelava uma área subjacente de tecido ... (AU)

Two oubreaks of poisoning by the mushroom Ramaria flavo-brunnescens are reported in cattle from two farms located in the municipalities of Santa Maria and São Gabriel, state of Rio Grande do Sul, during April-May 2005. Out of a total of 180 yearling calves that had access to a pasture with eucalyptus woods, 19 were affected and 10 died. The clinical courses were 8-15 days and clinical signs included depression, weight loss, dehydration, drooling, loosening and loss of the long hairs of the tip of the tail, smoothening of the dorsal surface of the tongue with occasional ulceration, loosening of the corneal encasement of horns, hard and ball-shaped feces covered with a film of mucous, hypopion, hyphema and corneal opacity. Two calves had leucocytosis due to mild regenerative left shift. Nine calves were necropsied. Necropsy findings confirmed the clinical observation and additionaly included fibrinonecrotic esophagitis, mainly in the distal third of the esophageal mucosa. Histopathological changes in the skin of the tail included orthokeratotic hyperkeratosis; hair folicles with irregular contours, thickening of the tricolemmal keratin layer with occasional formation of keratin plugs, and degeneration and necrosis of the outer root sheath. At the laminar region of the hooves, there was hyperplasia of the top of epidermal laminae with irregular keratinization and retention of nuclei; several epidermal laminae were shortened and fused. There was hemorrhage, fibrin and neutrophilic infiltrate in the dermal laminae. In the mucosa of the tongue there was thinning of the covering epithelium, atrophy and loss of filiform papillae, multifocal areas of dyskeratosis, and spongiosis of the basal cell layer. In some parts the epithelium was lost and the surface consisted of granulation tissue and mixed inflammatory cell infiltrate. The esophageal mucosae of six calves had varying degree of epithelial necrosis and inflammation. The loss of the covering epithelium revealed ... (AU)

Intoxicação por Ramaria flavo-brunnescens (Clavariaceae) em bovinos / Poisoning by Ramaria flavo-brunnescens (Clavariaceae) in cattle

Dois surtos de intoxicação pelo cogumelo Ramaria flavo-brunnescens são relatados em bovinos de duas fazendas localizadas nos municípios de Santa Maria e São Gabriel, no Rio Grande do Sul, no período de abril-maio de 2005. De um total de 180 bovinos de sobreano que tiveram acesso a bosques de eucaliptos, 19 adoeceram e 10 morreram. A evolução clínica foi de 8-15 dias e os sinais clínicos incluíam depressão, perda de peso, desidratação, salivação excessiva, afrouxamento e perda dos pêlos longos da cauda, alisamento da superfície dorsal da língua com ocasional ulceração, afrouxamento do estojo córneo dos chifres, fezes em forma de cíbalos e recobertas por película de muco, hipópion, hifema e opacidade da córnea. Dois novilhos tinham leucocitose devido a leve desvio regenerativo à esquerda. Os achados de necropsia confirmaram as observações clínicas e adicionalmente incluíam esofagite fibrinonecrótica, principalmente no terço distal do esôfago. Alterações histopatológicas na pele da cauda incluíam hiperqueratose ortoqueratótica, folículos pilosos com contornos irregulares, espessamento da camada de queratina tricolemal e formação ocasional de tampões de queratina; degeneração e necrose da bainha radicular externa também era observada. Nos cascos havia hemorragia, fibrina e infiltrado neutrofílico nas lâminas dérmicas, hiperplasia do topo das lâminas epidérmicas com queratinização irregular e retenção dos núcleos; várias lâminas epidérmicas estavam encurtadas e fundidas. Na mucosa da língua o epitélio de revestimento estava adelgaçado, com atrofia e perda das papilas filiformes, áreas multifocais de disqueratose e espongiose das células da camada basal. Em algumas porções havia perda do epitélio e a superfície da língua era formada por tecido de granulação e infiltrado inflamatório misto. A mucosa esofágica de seis novilhos apresentava vários graus de necrose epitelial e inflamação. A perda do epitélio de revestimento revelava uma área subjacente de tecido ...

Two oubreaks of poisoning by the mushroom Ramaria flavo-brunnescens are reported in cattle from two farms located in the municipalities of Santa Maria and São Gabriel, state of Rio Grande do Sul, during April-May 2005. Out of a total of 180 yearling calves that had access to a pasture with eucalyptus woods, 19 were affected and 10 died. The clinical courses were 8-15 days and clinical signs included depression, weight loss, dehydration, drooling, loosening and loss of the long hairs of the tip of the tail, smoothening of the dorsal surface of the tongue with occasional ulceration, loosening of the corneal encasement of horns, hard and ball-shaped feces covered with a film of mucous, hypopion, hyphema and corneal opacity. Two calves had leucocytosis due to mild regenerative left shift. Nine calves were necropsied. Necropsy findings confirmed the clinical observation and additionaly included fibrinonecrotic esophagitis, mainly in the distal third of the esophageal mucosa. Histopathological changes in the skin of the tail included orthokeratotic hyperkeratosis; hair folicles with irregular contours, thickening of the tricolemmal keratin layer with occasional formation of keratin plugs, and degeneration and necrosis of the outer root sheath. At the laminar region of the hooves, there was hyperplasia of the top of epidermal laminae with irregular keratinization and retention of nuclei; several epidermal laminae were shortened and fused. There was hemorrhage, fibrin and neutrophilic infiltrate in the dermal laminae. In the mucosa of the tongue there was thinning of the covering epithelium, atrophy and loss of filiform papillae, multifocal areas of dyskeratosis, and spongiosis of the basal cell layer. In some parts the epithelium was lost and the surface consisted of granulation tissue and mixed inflammatory cell infiltrate. The esophageal mucosae of six calves had varying degree of epithelial necrosis and inflammation. The loss of the covering epithelium revealed ...

Lesiones isquémico-anóxicas del encefalo en fetos y recién nacidos fallecidos: estudio anatomopatológico / Ischemic-anoxic lesions in still births and dead newborns: anatomopathologic study

Se realiza un estudio anatopatológico de las lesiones isquémico-anóxicas en fetos y recién nacidos fallecidos. Se indica que las lesiones encontradas fueron de 2 tipos. Se describen las características estructurales y de localización, su relación con la hemorragia cerebral y la madurez estructural de los fetos y recién nacidos (AU)

Lesiones isquémico-anóxicas del encefalo en fetos y recién nacidos fallecidos: estudio anatomopatológico / Ischemic-anoxic lesions in still births and dead newborns: anatomopathologic study

Se realiza un estudio anatopatológico de las lesiones isquémico-anóxicas en fetos y recién nacidos fallecidos. Se indica que las lesiones encontradas fueron de 2 tipos. Se describen las características estructurales y de localización, su relación con la hemorragia cerebral y la madurez estructural de los fetos y recién nacidos

Avian encephalomalacia in Barbados, West Indies: a description of spontaneous field cases with feed analyses.

The clinical, necropsy and histopathological findings in four natural outbreaks of encephalomalacia are reported. Feed analyses implicated low levels of vitamin E as the probable cause of the condition. Treatment with vitamin E has proved to be very effective. The instability of vitamin E in animal feed ingredients during long periods of shipment into the Caribbean may be important in the pathogenesis of the disease.

Avian encephalomalacia in Barbados, West Indies: a description of spontaneous field cases with feed analyses

The clinical, necropsy and histopathological findings in four natural outbreaks of encephalomalcia are reported. Feed analyses implicated low levels of vitamin E as the probable cause of the condition. Treatment with vitamin E has proved to be very effective. The instability of vitamin E in animal feed ingredients during long priods of shipment to the Caribbean may be important in the pathogenesis of the disease. (AU)