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We characterized the immunohistochemical expression profiles of dysgerminomas from a 16-y-old maned wolf and 13 domestic dogs using the following biomarkers: Sal-like protein 4 (SALL4), octamer-binding transcription factor 3/4 (OCT3/4), placental alkaline phosphatase (PLAP), c-kit, and vimentin. The maned wolf had nonspecific and long-standing clinical signs of lethargy, anorexia, and weight loss, and was euthanized because of poor prognosis. At autopsy, the left ovary was effaced by a 12 × 8 × 6 cm mass, comprised of anaplastic cells with a mitotic count of 20 mitoses in 10 high power fields. Dysgerminomas from 7 of 13 domestic dogs had nuclear expression of SALL4. Dysgerminomas from the maned wolf and 2 domestic dogs had both nuclear and cytoplasmic expression of SALL4. Cytoplasmic expression of PLAP and OCT3/4 was present in dysgerminomas from the maned wolf and 3 (PLAP) or 4 (OCT3/4) domestic dogs. All dysgerminomas expressed vimentin. Membranous c-kit expression was rare in the dysgerminoma from the maned wolf, and variable in dysgerminomas from 4 domestic dogs. A dysgerminoma from a domestic dog had cytoplasmic expression of c-kit. SALL4 is a useful marker to confirm germ cell origin of dysgerminoma in canids.

A 12-year-old female mixed-breed dog presented with lameness, pain, and an enlarged, non-ulcerated, nodular mass in the region proximal to the tarsal joint of the right pelvic limb. Surgical excision was performed, revealing a 6.5 cm mass adherent to the deep flexor tendon and adjacent tissues. The cut section had cysts filled with blackened clotted material, which exuded reddish serous fluid. Microscopically, the cysts were filled with red blood cells and were either denuded or covered by synoviocytes. In addition, the mass was characterized by marked fibrovascular connective tissue associated with siderophages and multinucleated giant cells. These findings were consistent with those of pigmented villonodular tenosynovitis, a rare condition affecting several animal species and humans. RESUMO: Uma cadela de 12 anos, sem raça definida, apresentou claudicação, algia e aumento de volume não ulcerado, de aspecto nodular, na região proximal à articulação do tarso do membro pélvico direito. A excisão cirúrgica foi optada e revelou uma massa de 6,5 cm de diâmetro, aderida ao tendão flexor profundo e aos tecidos adjacentes. Ao corte, exsudava líquido seroso avermelhado e cistos preenchidos por material coagulado enegrecido foram observados. Microscopicamente, a massa apresentava formações císticas frequentemente preenchidas por hemácias, que encontravam-se ora revestidas por sinoviócitos, ora desnudas. Havia ainda acentuada quantidade de tecido fibrovascular associado a siderófagos e células gigantes multinucleadas. Esses achados foram consistentes com tenossinovite vilonodular pigmentada, uma rara condição que afeta diversas espécies de animais e humanos.

portuguesMalformacoes congenitas sao alteracoes funcionais e estruturais dos sistemas, tecidos ou orgaos que podem ocorrer na fase embrionaria ou fetal. Malformacoes na medula espinhal, como hipoplasia segmentar da medula espinhal (HSME) e siringomielia, possuem raras descricoes em bovinos. Uma bezerra Girolando, proveniente do Municipio de Valenca, RJ, foi atendida no Hospital Veterinario da Universidade Federal Rural do Rio de Janeiro (UFRRJ), com quadro de incoordenacao motora. A avaliacao clinica, na coluna vertebral, a linha dorsal da regiao toracica havia uma area com depressao de 5 cm. Ao exame neurologico foi observado propriocepcao reduzida, extensao de membros pelvicos com aumento da atividade nociceptiva e reducao de reflexo anal. Ao exame radiografico, o corpo vertebral T11 apresentou forma trapezoidal em cunha com hemivertebra ventral, provavel agenesia ou hipoplasia dos processos espinhosos T11-T12 e fusao dos processos espinhosos T9-T10. A mielografia indicou compressao medular extradural provocada pelas malformacoes vertebrais. A necropsia nao foram observados os processos espinhosos T11-T12, o canal medular apresentou estenose cranial (T11-T13) e, na medula espinhal toracica (T8-T11) foram observados poros de 1-3 mm na substância branca. A microscopia, os segmentos T9-T11 apresentaram dilatacoes cisticas na substância branca e os segmentos T8-T9, formacoes de areas cisticas de tamanhos variados; nos segmentos T11-T13 denotou-se moderada reducao da substância cinzenta ao redor do canal central da medula. O presente trabalho tem o objetivo de apresentar os achados clinicos e patologicos desta bezerra Girolando com HSME e siringomielia, que devem ser diferenciadas de outras sindromes da medula espinhal. As malformacoes congenitas possuem importância economica e sua etiologia e diagnostico sao fundamentais para a conducao de programas de controle de doencas e selecao de progenitores EnglishCongenital malformations are functional and structural changes in organ systems, tissues, or organs that may develop during the embryonic or fetal phase. Spinal cord malformations, such as segmental hypoplasia of the spinal cord (SHSC) and syringomyelia, are rare in bovines. A Girolando calf from Valenca, Rio de Janeiro, was admitted to the Veterinary Hospital of Universidade Federal Rural do Rio de Janeiro because of motor incoordination. Clinical evaluation revealed a 5-cm depression area in the spine at the dorsal line of the thoracic region. Neurological examination revealed reduced proprioception, pelvic limb extension with increased nociceptive activity, and reduced anal reflex. In radiographic examination, the body of the T11 vertebra had a trapezoidal wedge shape with ventral hemivertebra, probable agenesis or hypoplasia of the T11-T12 spinous processes, and fusion of the T9-T10 spinous processes. Myelography revealed extradural spinal compression caused by vertebral malformations. Necropsy showed no spinous processes (T11-T12), cranial stenosis in the medullary canal (T11-T13), and 1-3-mm pores in the white matter of the thoracic spinal cord (T8-T11). Microscopy revealed cystic dilatations in the white matter (T9-T11), cystic areas of varying sizes (T8-T9), and moderate reduction in the gray matter around the central canal of the medulla (T11-T13). Here, we reported the clinical and pathological findings of SHSC and syringomyelia in a Girolando calf. The features should be differentiated from other spinal cord syndromes. Congenital malformations are of economic importance, and their etiology and diagnosis are fundamental to disease control and progenitor-selection programs

Malignant catarrhal fever (MCF) is an infectious, pansystemic and highly fatal disease with wide geographic distribution. The species that are clinically prone to it include cattle, deer and bison. In Brazil, the disease in ruminants and deer is associated with the contact with sheep, especially during labor, when the fetal remains that are eliminated contain the ovine herpesvirus 2 (OvHV-2). The outbreak took place in a conservationist property in the city of Casimiro de Abreu/RJ, which hosted 23 Sambar deer, and, of these, 19 died, showing neurological signs. The deer lived in a location together with 15 male and female meat sheep. A female specimen of the Sambar deer (Rusa unicolor), aged approximately three years, which had presented with neurological clinical signs was referred to necropsy in the Setor de Anatomia Patológica at Universidade Federal Rural do Rio de Janeiro (SAP/UFRRJ). During necropsy, cerebrospinal fluid was sampled for analysis; fragments of several organs were fixated in 10% buffered formalin and processed for histopathological analysis. Fragments of occipital lobe, cerebellum and bulb were collected to perform the polymerase chain reaction (PCR). The diagnosis of this outbreak was based on epidemiological, clinical and pathological findings, and on the amplification of the OvHV-2 DNA through PCR. The histological changes were the base to confirm the MCF case and were characterized by degeneration of vascular endothelial cells, fibrinoid vasculitis, hyperplasia and necrosis of lymphoid organs. However, PCR was an important tool to confirm the diagnosis. MCF as an important disease with nervous symptomatology in deer.

Background: Emphysematous rumenitis is a condition characterized by gas filled bubbles or cysts in the ruminal mucosa. Although a similar pathology is reported from swine and humans, the incidence of this disease in cattle seems to be scarce. The etiology of emphysematous rumenitis is uncertain once many factors can be involved in its pathogeny, a single cause is difficult to ascertain. This lesion usually fails to display specific clinical signs; however, some degree of malabsorption and weight loss is expected. We described a case of emphysematous granulomatous submucosal rumenitis in a 2.5-yearold feedlot Nellore steer that presented reduction on daily weight gain.Case: Rumen fragments of a 2.5-year-old Nellore steer were submitted for histopathological evaluation at the Sector of Pathological Anatomy (SAP) of the Rural Federal University of Rio de Janeiro, Brazil. The specimens were part of an experimental trial to evaluate the effect of phosphorus (P) supplementation on nutrient intake, performance and P balance in fifty feedlot Nellore steers. Following a short adaptation period, in which behavioral observations were made twice daily to assess possible adverse factors, all steers were fed with balanced diet for one hundred and sixteen days. The steers were then slaughtered in order to evaluate macroscopic changes in the gastrointestinal system. Rumen and abomasum of each steer was emptied, washed with tap water and grossly examined. One steer presented ruminal lesion, while the other forty-nine did not show any ruminal injury. Throughout the experiment the affected steer showed reduction of daily weight gain; but during clinical examination no additional clinical sign was seen. At gross inspection, a reduction in the amount of muscular and adipose tissue was seen. Multiple coalescent bullous elevated structures measuring three to ten mm diameter were covering about 40% of the ruminal surface. The affected ruminal mucosa showed irregular and atrophic papillae. Rumen samples were processed routinely and stained with Hematoxylin and Eosin, Period Acid Schiff (PAS), Grocott’s Methenamine Silver (GMS), Ziehl-Neelsen (ZN), Brown-Hopps (Gram), Giemsa and Toluidine Blue (TB) stains. Additionally formalin-fixed, paraffin wax-embedded sections were stained with a primary polyclonal rabbit antibody for Escherichia coli. Histologically the submucosa was largely replaced by cyst-like enlarged lymphatic vessels filled with gaseous content and the ruminal submucosa was infiltrated by macrophages, multinucleated giant cells, eosinophils, lymphocytes and plasma cells. Special stains were negative for granules within the mast cells, fungi, acid-fast bacilli, bacteria and protozoa. E. coli was immuno-labeled only at the ruminal epithelial surface.Discussion: This paper provided a description of a rare and possible underdiagnosed condition in cattle to highlight the necessity of recognizing ruminal changes during slaughterhouse inspection. The spontaneous and extensive emphysematous rumenitis described in this paper showed histological similarities with the analogous condition documented in the small and large intestine, mesentery and mesenteric lymph node of swine. The etiology and pathogenesis of emphysematous submucosal rumenitis remain unknown. We believe that the lesion described was the reason for the decrease of weight gain of the steer; therefore it should be considered as a differential diagnosis for conditions that affect weight gain and performance of cattle.Keywords: cattle, veterinary pathology, feedlot, emphysema, rumen.