Search

Summary: The dentigerous cyst or temporal teratoma in horses is a well‐known congenital malformation that occurs in the temporal region and usually contains dental tissue. This case report describes two horses with a previously unreported variant of the dentigerous cyst associated with an exostosis arising from the temporal bone. The principal clinical sign was a draining tract opening at the margin of the right pinna in both horses. There was no evidence of an ectopic tooth on the radiographs or at ultrasonographic examination. Computed tomography combined with positive contrast sinography of the draining tract revealed bone formation arising from the supramastoid crest of the right temporal bone extending towards a cyst‐like structure but without direct connection in both cases. This bone formation was located at a site on the supramastoid crest, close to the external acoustic meatus, where ectopic teeth may also occur. Both cysts were removed surgically with a good long‐term outcome. [ABSTRACT FROM AUTHOR]

Background: Multiple diagnostic procedures, their results and interpretation in a case with severe lameness in fattening pigs are described. It is shown that selected diagnostic steps lead to identification of various risk factors for disease development in the affected herd. One focus of this case report is the prioritization of diagnostic steps to verify the impact of the different conditions, which finally led to the clinical disorder. Assessing a sufficient dietary phosphorus (P) supply and its impact on disease development proved most difficult. The diagnostic approach based on estimated calculation of phosphorus intake is presented in detail. Case presentation: On a farrow-to-finishing farm, lameness occurred in pigs with 30–70 kg body weight. Necropsy of three diseased pigs revealed claw lesions and alterations at the knee and elbow joints. Histologic findings were characteristic of osteochondrosis. All pigs were positively tested for Mycoplasma hyosynoviae in affected joints. P values in blood did not indicate a P deficiency, while bone ashing in one of three animals resulted in a level indicating an insufficient mineral supply. Analysis of diet composition revealed a low phosphorus content in two diets, which might have led to a marginal P supply in individuals with high average daily gains with respect to development of bone mass and connective tissue prior to presentation of affected animals. Finally, the impact of dietary factors for disease development could not be evidenced in all submitted animals in this case. Conclusions: Mycoplasma (M.) hyosynoviae was identified to be an important etiologic factor for disease. Other, non-infectious factors, such as osteochondrosis and claw lesions might have favored development of lameness. In addition, a relevant marginal P supply for pigs was found in a limited time period in a phase of intense growing, but the potential interaction with infection by M. hyosynoviae is unknown. The presented case of severe lameness in fattening pigs revealed that three different influences presumably act in pathogenesis. Focusing only on one factor and ignoring others might be misleading regarding subsequent decision-making for prevention and therapy. Finally, clinical symptoms disappeared after some changes in diet composition and anti-inflammatory treatment of individual animals. [ABSTRACT FROM AUTHOR]

The deterioration of ballast and the consequences of weak subsoil increase the need for track maintenance. These problems reduce the service life of tracks, and a higher maintenance budget is required. This paper introduces an innovative method for evaluating the condition of the ballast and the subsoil. Fractal analysis of the vertical track geometry enables infrastructure managers to determine the root cause of track irregularities by quantifying the wavelength characteristics of the common track geometry data. This methodology determines whether the ballast or the substructure condition is the cause of poor track quality. Fractal analysis has been carried out to date on the main network of the Austrian Federal Railways, which comprises some 4000 km of track, as well as within the network of Suisse Federal Railways (∼5000 km). Additionally, several lines in the United States (Amtrak), Belgium (InfraBel), and Denmark (BaneDanmark) have been evaluated. A detailed validation process has been carried out to investigate different characteristics and their correlation to the in situ behavior of the track. This research is now showing promising results after being cross-checked with historical data and compared to the implemented maintenance measures. On-site inspections have confirmed the evaluated component-specific condition. [ABSTRACT FROM AUTHOR]

Mitogen-activated protein kinase 6/extracellular signal-regulated kinase 3 (MAPK6/ERK3) is an atypical member of the MAPKs. An essential role has been suggested by the perinatal lethal phenotype of ERK3 knockout mice carrying a lacZ insertion in exon 2 due to pulmonary dysfunction and by defects in function, activation, and positive selection of T cells. To study the role of ERK3 in vivo, we generated mice carrying a conditional Erk3 allele with exon 3 flanked by loxP sites. Loss of ERK3 protein was validated after deletion of Erk3 in the female germ line using zona pellucida 3 (Zp3)-cre and a clear reduction of the protein kinase MK5 is detected, providing the first evidence for the existence of the ERK3/MK5 signaling complex in vivo. In contrast to the previously reported Erk3 knockout phenotype, these mice are viable and fertile and do not display pulmonary hypoplasia, acute respiratory failure, abnormal T-cell development, reduction of thymocyte numbers, or altered T-cell selection. Hence, ERK3 is dispensable for pulmonary and T-cell functions. The perinatal lethality and lung and T-cell defects of the previous ERK3 knockout mice are likely due to ERK3-unrelated effects of the inserted lacZ-neomycin resistance cassette. The knockout mouse of the closely related atypical MAPK ERK4/MAPK4 is also normal, suggesting redundant functions of both protein kinases. [ABSTRACT FROM AUTHOR]

This report describes the history, clinical examination and histopathology of a histiocytic sarcoma in a domestic ferret. Clinical signs were acute paraplegia and dysuria. Physical examination revealed a firm, smooth, touch-sensitive mass in and around the lumbar vertebral column. Neurologic examination was consistent with a lesion between spinal cord segments T3 and L3. Magnetic resonance images revealed bone lesions of L2 and L3 combined with compression of the spinal cord due to a homogenous, isointense mass that was diagnosed as a malignant round cell tumour and the ferret was euthanased. Histopathology confirmed the diagnosis of an infiltrative histiocytic sarcoma. [ABSTRACT FROM AUTHOR]

Clinical, gross, histopathologic, electron microscopic findings and enzymatic analysis of 4 captive, juvenile springboks (Antidorcas marsupialis) showing both polycystic kidneys and a storage disease are described. Springbok offspring (4 of 34; 12%) were affected by either one or both disorders in a German zoo within a period of 5 years (2008–2013). Macroscopic findings included bilaterally severely enlarged kidneys displaying numerous cysts in 4 animals and superior brachygnathism in 2 animals. Histopathologically, kidneys of 4 animals displayed cystic dilation of the renal tubules. In addition, abundant cytoplasmic vacuoles with a diameter ranging from 2 to 10 μm in neurons of the central and peripheral nervous system, hepatocytes, thyroid follicular epithelial cells, pancreatic islets of Langerhans and renal tubular cells were found in 2 springbok neonates indicative of an additional storage disease. Ultrastructurally, round electron-lucent vacuoles, up to 4 μm in diameter, were present in neurons. Enzymatic analysis of liver and kidney tissue of 1 affected springbok revealed a reduced activity of total hexosaminidase (Hex) with relatively increased HexA activity at the same level of total Hex, suggesting a hexosaminidase defect. Pedigree analysis suggested a monogenic autosomal recessive inheritance for both diseases. In summary, related springboks showed 2 different changes resembling both polycystic kidney and a GM2 gangliosidosis similar to the human Sandhoff disease. Whether the simultaneous occurrence of these 2 entities represents an incidental finding or has a genetic link needs to be investigated in future studies. [ABSTRACT FROM PUBLISHER]

The article presents an investigation of the lesions in 40 sheep, 2 goats and 16 cattle infected with Schmallenberg virus (SBV) validated by real-time quantitative reverse transcription polymerase chain reaction. All of the animals included in the research were aborted, stillborn or died during the perinatal period. It describes the macroscopic and histologic lesions and the most frequently observed malformations.

The article presents an investigation on the variable susceptibilities of oligodendrocytes in murine spinal cord associated in cuprizone-induced demyelination of the central nervous system (CNS). It analyzes the effect of copper chelator cuprizone in myelin protein alteration of the CNS of Swiss-Webster mice. It demonstrates the different susceptibility of brain and spinal cord in which lack of myelin loss has no significance difference with cuprizone-fed and control mice.

Background: Ocular involvement of syphilis still poses a clinical challenge due to the chameleonic behaviour of the disease. As the serodiagnosis has significant limitations, the direct detection of Treponema pallidum (TP) in the vitreous represents a desirable diagnostic tool. Methods: Real-time polymerase chain reaction (PCR) for the detection of TP was applied in diagnostic vitrectomies of two patients with acute chorioretinitis. Qualitative verification of TP by real-time PCR and melting point analysis according to a modified protocol was ruled out. Patients underwent complete ophthalmological examination with fundus photographs, fluorescein angiography, serological examination, antibiotic treatment and follow-up. Results: In two cases of acute chorioretinitis of unknown origin, real-time PCR of vitreous specimens of both patients provided evidence of TP and was 100% specific. Initial diagnosis of presumed viral retinitis was ruled out by PCR of vitreous specimen. Patients were treated with systemic antibiotics and showed prompt improvement in visual function and resolution of fundus lesions. Conclusions: With real-time PCR, detection of TP in the vitreous was possible and delivered a sensitive, quick and inexpensive answer to a disease rather difficult to assess. In cases of acute chorioretinitis, the use of PCR-based assays of vitreous specimens in the diagnostic evaluation of patients is advisable. Although syphilitic chorioretinitis is a rare disease, PCR should include search for TP, as diagnostic dilemmas prolong definitive treatment in a sight-threatening disease. [ABSTRACT FROM AUTHOR]

Copyright of Der Ophthalmologe is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Der Ophthalmologe is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The article presents a case study on mercury poisoning in a male German shepherd dog that experienced bloody diarrhea and vomiting. The laboratory examination of the dog shows moderate leucocytosis with initial symptomatic treatment that includes antibiotic and intravenous fluids. It suggests that heavy metal intoxication should be considered as possible cause of renal failure.