Entries in Cases/Abstracts (68)

Saturday
Nov032018

An Incidental Finding

Adam Eggleston
University of Florida College of Veterinary Medicine

This case involves my own dog ‘Eimeria’.

She was my group’s second sophomore surgery canine which was performed in March of 2016. I was on anesthesia while two of my classmates who were in the role of surgeon and assistant performed the spay. After the routine spay, I decided to adopt the stray and named her Eimeria.

In December 2016 while getting ready for my Zoo medicine rotation, Eimeria began vomiting, urinating, defecating, and became laterally recumbent. I brought her into our ECC where she began to have hemorrhagic diarrhea. An AFAST was performed which showed a large, anechoic cystic structure in the right cranial abdomen with the right kidney not being visible. An ultrasound was performed indicating severe thickening of the gall bladder wall and a large fluid filled structure in the region of the right kidney, hydronephrosis was suspected.

One month later and I was able to watch a nephrectomy being performed on Eimeria. Her right kidney and a ureter with one of the best strangle knots I have ever seen, are currently sitting in a jar of formalin on my shelf. It turns out that Eimeria’s unknown anaphylactoid reaction was a blessing in disguise which allowed the incidental finding of severe hydronephrosis due to a ligated ureter.

Thursday
May242018

Case Report - Arteriovenous fistulas

Case Report "Catnip"

Victoria Demello

University of Georgia, College of Veterinary Medicine

 

ABSTRACT:

Arteriovenous fistulas (AV fistulas) have been reported in humans and animals. This condition is rare and can be either congenital or acquired. Acquired arteriovenous fistulas are often due to trauma including surgery. Congenital fistulas are due to vascular malformations. These fistulas are often reported in peripheral vasculature within veterinary medicine. We describe a case of suspected arteriovenous fistula versus suspected unclassified cardiomyopathy in a 5-month-old feline that quickly progressed to left- and right-sided congestive heart failure. Gross pathology and histopathology lesions revealed all chambers as dilated with interfiber edema. Extensive alveolar edema and frequent hemorrhage was noted in the lungs. Numerous hemosiderin macrophages within alveolar lumen were present.

 

CASE REPORT:

“Catnip”, 5-month old male intact DSH, presented to University of Georgia’s College of Veterinary Medicine’s (UGA CVM) Cardiology service for evaluation of a murmur diagnosed by the primary veterinarian. The cat was found when he was 9-weeks-old. He received his first round of kitten shots and was tested for FeLV and FIV. He was negative for both diseases. 3 weeks later, during the next vaccine appointment (12-week-old kitten), a right-sided grade IVV/VI systolic murmur was noted. The primary veterinarian recommended an echocardiogram. The cat did not have any clinical signs or symptoms reported at that time. The owner declined further diagnostic testing.

3 weeks later, at the next vaccine appointment, a grade V/VI right-sided systolic murmur was diagnosed by the primary veterinarian. An abdominal component to the cat’s breathing that was not present before was also noted. The owner reported the cat’s abdomen was becoming increasingly distended and the patient did not play as much as his littermate. The cat was bright, alert, and responsive at home, eating/drinking/urinating/defecating normally. Due to the increase in murmur severity and presence of clinical signs, a referral appointment to University of Georgia’s College of Veterinary Medicine’s Cardiology service was made.

On physical exam at the University of Georgia’s College of Veterinary Medicine’s Cardiology service, a grade IV/VI right systolic parasternal murmur was diagnosed. Temperature, and heart rate were within normal limits (99.3°F, 168 beats per minute). The jugular vein was distended and the respiration rate was increased with an abdominal component (72 breaths per minute). Increased inspiratory noise was also noted. Blood Pressure was 100mmHg (systolic). Packed cell volume/Total solids: 35%/5.6.

Thoracic radiographs (3-view) were performed and revealed severe generalized cardiomegaly with pulmonary arterial and venous distension and both left- and right-sided cardiac failure.

Echocardiogram findings showed right atrium dilation, right ventricle dilation. The tricuspid valve leaflets, right ventricular outflow tract including the pulmonic valve cusps and main pulmonary artery were within normal limits. The left atrium was severely dilated and was the left ventricle. The mitral valve leaflets, interventricular septum, left ventricular free wall were all normal as were the aortic valve cusps and ascending aorta. Abdominal effusion was present on echocardiogram. No cardiac masses or thrombi were present. Electrocardiogram showed sinus tachycardia.

The patient was suspected to have unclassified cardiomyopathy or a peripheral arteriovenous fistula. The patient was euthanized due to cardiomyopathy and secondary severe pulmonary edema.

Gross pathologic findings were dilation of all cardiac chambers with the most significant change within the right atrium. Wall thicknesses were measured (right atrium 1 mm; right ventricle 3 mm; left atrium 2mm; left ventricle 8mm). Pulmonary artery was enlarged with a circumference of 6mm. Circumference of the aorta was 5mm. Just medial to the left kidney, in the dorsal abdomen, was a large plexus of engorged vessels between the aorta and caudal vena cava. Measured as 4cm in length and 1.5cm in diameter. There was blood present in the trachea and the lungs were dark and diffusely and moderately congested.

Histopathology of the heart revealed modest interfiber edema in all but was most severe in the right atrium and right ventricle. Extensive alveolar edema and frequent hemorrhage was noted in the lungs. Numerous hemosiderin macrophages within alveolar lumen were present.

 

DISCUSSION

AV fistulas are abnormal connections between an artery and vein. This abnormal connection causes abnormal blood flow throughout the body creating murmus. AV fistulas are most common secondary to penetrating trauma injuries in both veterinary and human medical literature. There have only been a handful of reported AV fistulas in veterinary literature with a majority occurring due to trauma (secondary to gun shots, animal bites, etc).

One case (Bolton et al) illustrated a congenital AV fistula in a 3 month old feline presented for acute dyspnea. This fistula was identified due to the abnormal murmur heard during a routine physical exam. On presentation, the feline had cyanotic oral mucous membranes and a gallop rhythm on cardiac auscultation. Further diagnostics (thoracic radiographs, ECG, CBC and serum chemistry) revealed an enlarged heart. Angiography was performed, as well, which showed a plexus of blood vessels between the aorta and caudal vena cava. This paper was published in 1976 before echocardiography was readily available. Angiography was able to illustrate a clear picture of the AV fistula. This fistula was able to be surgically ligated prior to permanent cardiac musculature changes. This cat survived but ultimately lived a shortened life span. Due to the complications and prognosis of untreated AV fistulas, prompt identification, diagnosis, and intervention is key.

In the case of Catnip, his AV fistula was discovered too late. He presented to the UGA Cardiology service with fulminant congestive heart failure characterized by severe dilation of all 4 cardiac chambers. Catnip was euthanized due to his poor prognosis.

Catnip was approximately 12 weeks old when his murmur was fist ausculted. Murmurs are created due to the abnormal turbulent blood flow within the heart or vessels. Murmurs in young animals (animals less than 6 months old) are not an uncommon finding. These murmurs are referred to as physiologic murmurs. These murmurs are characterized by an absence of structural cardiac disease. Students are often taught that grade 1/6 to 2/6 in young animals (less than 6 months of age) without any clinical signs are most often physiologic or “innocent” murmurs. Murmurs that meet this criteria often disappear with time. However, murmurs grade 3/6 and higher should always undergo cardiologic evaluation including echocardiogram. These murmurs are pathologic (arising from structural cardiac disease) in nature regardless of the age of the animal.

It is important to understand the grading of murmurs and the difference between physiologic and pathologic murmurs because of cases like this. A veterinarian’s physical exam is the most important way to detect a problem early. Moving forward, a detailed understanding of cardiac murmurs, and education of owners with animals that have murmurs is essential to early detection of AV fistulas.

References:

1. “Arteriovenous Fistula of the Aorta and Caudal Vena Cava Causing congestive heart failure in a cat”. Bolton, Gary, Edwards, N. Joel, Hoffer, R.E.. Journal of the American Veterinary Medical Association. July/August 1976

2. “Peripheral Acquired Arterivenous Fistula: A report of 4 cases and literature review”. Bouayad, H., Feeney, D.A., Lipowitz, AJ, Levine, S.H., Hayden, D.W.. Journal of the American Animal Hospital Association. June 1986.

3. “Arteriovenous fistulas: Pathophysiology, Diagnosis, and Treatment”. The Small Animal Compendium. May 1989

Saturday
Apr212018

Students in Research

Student research is important to the field of veterinary medicine; is provides students will the skills and experience to pursue careers in research medicine, help make advances in the profession and medicine, and practice their critical thinking skills. Kerry from the University of Minnesota shares her own abstract on the research she was involved in.


The efficacy of sorafenib in a mouse model of radiation-induced dermatitis

University of Minnesota, College of Veterinary Medicine

by Kerry Goldin


Radiation therapy (RT) is prescribed in approximately 50% of cancer patients in North America. Radiation-induced dermatitis (RID) is a common side effect of RT, affecting up to 95% of patients. The effects of RID range from mild to severe and can lead to pain, disfigurement and may impede completion of the treatment regimen. While the pathophysiology of RID is partially known, a complete understanding is lacking and there are no clear effective therapeutic strategies. The objectives of this study were to: 1) characterize the microscopic features of RID in a hairless mouse model and 2) determine the effect of sorafenib, a tyrosine kinase inhibitor, on the clinical and microscopic progression of RID.  To define the dose-response effect in SKH1-hr1 mice following RT, a dose escalation (15 Gy, 20Gy, 25Gy, 30Gy) study was performed. To characterize the microscopic pathology of RID in SKH-hr1 mice and examine the efficacy of sorafenib, 2 groups (sorafenib+vehicle and vehicle only, n=5 / group) were irradiated. To evaluate the sequential effects of RT +/- treatment, biopsies were collected at 4 time points (2hr, 10d, 12d, 18d post RT). Mice were sacrificed at 24 days post RT. Tissues were collected for light microscopic and IHC analysis (VEGFR2, CD31, and TGF beta-1). Histopathologic evaluation revealed progressive epithelial thickening, and loss of sebaceous and follicular structures. The SKH1-hr1 mice appear to be an adequate model for RID. A single administration of topical sorafenib administered 24 hours prior to RT did not mitigate acute clinical RID but resulted in reduced VEGFR2 expression, reduced TGF beta-1 expression, and diminished epidermal hyperplasia with no effect on CD31 expression. 

Monday
Dec182017

Students in Research

Analyzing the health of two wild horse populations residing in diverse biomes in Arizona

Sydney St. Clair, College of Veterinary Medicine, Midwestern University

 

Wild horses have been the focus of several heated public debates for years, yet there is little quantitative data to draw from to support or contradict any intervention involving them. Published scientific research is in large part limited to studies of reproductive behavior and contraception studies, with rare papers addressing environmental impact and only a single study evaluating health of individual animals, a parasite evaluation on a herd of wild horses in Nova Scotia. In this study, we will use noninvasive methods to build health profiles on two populations of wild horses found in different environments within Arizona, which will expand the knowledge of them both as a herd and as individuals. Fecal samples will be collected to analyze different aspects of the health status of the wild horses, such as parasites, volatile fatty acids, pH, cortisol, sand content, microbiome DNA, and genomic DNA. Body condition score of the horses will also be noted for comparison over time. This unique resource provides an untapped opportunity to make a significant contribution to improve the management of the wild horses of Arizona for the benefit of the horses, humans and the environment. Additionally, a precedent may be set for health studies of wild horses in other states and countries. The ability to make our data set available to other researchers, biologists, environmental scientists, agriculturalists, veterinarians and policy makers will contribute significantly to this effort.

Thursday
Nov022017

Veterinary Students in Research

Viral-mediated oncolysis of cancer cells isolated from canine tumors

Kirsha B Fredrickson and Amy L MacNeill
Department of Microbiology, Immunology and Pathology, Colorado State University

The three classic arms of cancer therapy are surgical resection, chemotherapeutics, and radiation. As these fields have progressed we have greatly improved cancer survival rates in both companion animals and humans. However, with the complexities of neoplastic disease and their ability to further mutate due to genomic instability, these classic approaches are not always successful and often have undesirable adverse effects. Oncolytic virotherapy has the potential to be highly effective with minimal adverse effects due to targeted lysis of neoplastic cells. Studies were performed to evaluate the oncolytic effects of recombinant myxoma virus (MYXV) on canine osteosarcoma and soft tissue sarcoma primary cell cultures. The tumor samples were obtained following surgical excision. Once cultured, cells were evaluated for vimentin using
immunocytochemistry and for alkaline phosphatase activity using nitroblue tetrazolium chloride/5-bromo- 4-chloro- 3- indolyl phosphate toluidine solution. The cancer cell-lines were then inoculated with recombinant myxoma virus expressing a red fluorescent protein and collected after 48-hours. Cytopathic effects were assessed at 24-hour and 48- hour time points via fluorescent microscopy. Ability of the virus to replicate within the cancer cells was confirmed via Western immunoblot detection of late MYXV protein production. The findings of this study suggest that canine osteosarcoma and soft tissue sarcoma primary cell cultures are lacking antiviral mechanisms and susceptible to MYXV infection leading to oncolysis. Viral-mediated oncolysis of cancer cells isolated from canine tumorsKirsha B Fredrickson and Amy L MacNeillDepartment of Microbiology, Immunology and Pathology, Colorado State UniversityThe three classic arms of cancer therapy are surgical resection, chemotherapeutics, andradiation. As these fields have progressed we have greatly improved cancer survival ratesin both companion animals and humans. However, with the complexities of neoplasticdisease and their ability to further mutate due to genomic instability, these classicapproaches are not always successful and often have undesirable adverse effects.Oncolytic virotherapy has the potential to be highly effective with minimal adverseeffects due to targeted lysis of neoplastic cells. Studies were performed to evaluate theoncolytic effects of recombinant myxoma virus (MYXV) on canine osteosarcoma and soft tissue sarcoma primary cell cultures. The tumor samples were obtained followingsurgical excision. Once cultured, cells were evaluated for vimentin usingimmunocytochemistry and for alkaline phosphatase activity using nitroblue tetrazoliumchloride/5-bromo- 4-chloro- 3- indolyl phosphate toluidine solution. The cancer cell-lineswere then inoculated with recombinant myxoma virus expressing a red fluorescentprotein and collected after 48-hours. Cytopathic effects were assessed at 24-hour and 48-hour time points via fluorescent microscopy. Ability of the virus to replicate within thecancer cells was confirmed via Western immunoblot detection of late MYXV proteinproduction. The findings of this study suggest that canine osteosarcoma and soft tissuesarcoma primary cell cultures are lacking antiviral mechanisms and susceptible toMYXV infection leading to oncolysis.
Page 1 ... 4 5 6 7 8 ... 14 Next 5 Entries »