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A carcinoid is a rare neoplasm derived from neuroendocrine cells that may arise in the hepatobiliary system. This report described two cases of carcinoid of the gallbladder in dogs, with emphasis on the clinical, pathological and immunohistochemical aspects. Case 1 was a 10-year-old female Shih Tzu, with a history of prostration and occasional episodes of diarrhea and vomiting. Case 2 was a 10-year-old male Cocker Spaniel, with a history of diarrhea and abdominal pain. Abdominal ultrasonography suggested a neoplasm of the gallbladder in both cases. The dogs underwent cholecystectomy, and 10% formalin-fixed samples were sent for pathological examination. Histologically, a neoplastic proliferation of neuroendocrine cells was observed in the gallbladder submucosa of both cases. Immunohistochemical labeling for neuroendocrine antibodies, such as synaptophysin, neuron-specific enolase and chromogranin A, confirmed the diagnoses. Carcinoid of the gallbladder is a rare neoplasm in dogs, without specific clinical signs, but should be included in the differential diagnosis of lesions that affect this organ. [ABSTRACT FROM AUTHOR]

Neuroblastic tumors can originate from the central neuraxis, olfactory epithelium, adrenal medullary region or autonomous system. Ganglioneuroblastoma are a type of neuroblastic tumor, with very few case descriptions in animals. Diagnosis of facial nerve ganglioneuroblastoma was made in a feline leukemia virus-positive 11-month-old cat. The cat had hyporexia, left head tilt, depressed mental state, horizontal nystagmus, inability to retract the pinched left lip, anisocoria, ptosis, and absence of the menace reflex. Gross necropsy showed a mass at the left facial nerve root region. Histological examination of this mass showed neoplastic proliferation of neuroblasts arranged in a cohesive pattern and mature ganglion cells. Ganglion cells were positive for neurofilament, neuron-specific enolase, S100, and glial fibrillary acidic protein by immunohistochemistry, while neuroblasts were positive for vimentin, S100, neuron-specific enolase and feline leukemia virus. [ABSTRACT FROM AUTHOR]

Background: Aelurostrongylus abstrusus is a lungworm of cats with worldwide distribution. The adult forms of this parasite live in terminal bronchioles and alveoli, and can cause an asymptomatic disease or predominantly respiratory clinical signs, which can be occasionally cause of death. The aim of this study is to describe the epidemiological and pathological findings of infection by A. abstrusus through a necropsy retrospective study. Materials, Methods & Results: the necropsy records from the Department of Veterinary Pathology of the Universidade Federal do Rio Grande do Sul were recovered and cats diagnosed with lungworm by Aelurostrongylus abstrusus were selected since January 1998 until December 2015. General data, such as age, sex, breed, clinical signs, and macroscopic lesions, were analyzed and compiled. The histological slides were reviewed by optical microscopy and detailed the microscopic aspects. In this study, were identified 22 cats with varying degrees of lungworm by A. abstrusus, and in 45.5% of the cases, this was the cause of death. Most part of the cats were mixed breed (19/22), and there were no sex predisposition. The age of the cats ranged from four months to 11 years old, and the most frequent age group was three to six years, with nine cases reported. In 37.5% of the cases were reported respiratory clinical signs, such as dyspnea and nasal discharge, and in 62.5%, clinical signs were not specific. The gross findings of the lungs ranged from reddish, or yellowish or white areas, and presence of multiples small, firm, and whitish nodules, measuring more than two centimeters in diameter, with multifocal distribution in the lung surface. Histologically, there was varied amount of parasites in different stages in the alveolar spaces, associated with the inflammatory infiltrate composed of lymphocytes, plasma cells, macrophages, neutrophils and occasional multinucleated giant cells, and hypertrophy and hyperplasia of the pulmonary smooth muscle and the wall of the arteries. Discussion: Aelurostrongylus abstrusus is the principal parasite of lung of cats, with worldwide distribution. In this study, we observed that 40.9% of cases were reported as of 2012, and may be due to a larger propagation of definitive intermediate and paratenic hosts, climate changes and/or the increase of rearing cats, and the consequent increase of hospital routine. Agreeing with the others authors, there is no sex predilection, but differ in the age group, in to the present study, the most frequent age group was between "3 to 6 years" of age (52.9%). The gross findings observed were similar to those described by other authors. Histologically was observed varied amount of parasites, and the degree of inflammatory infiltrate were very similar, but with a slight difference in discrete infiltration (36.4%). Others researchers have identified predominantly severe inflammatory infiltrate (57.9%). Hypertrophy and hyperplasia of pulmonary smooth muscle and the wall of the arteries was moderate (50%), however, in previous studies were severe. The diagnosis of aelurostrongilosis through parasitological tests have proven the occurence this lung parasite in the study region, highlighting the importance of this study by adding epidemiological and pathological data on the disease. [ABSTRACT FROM AUTHOR]

Background: Perinephric pseudocyst is defined as an accumulation of fluid in fibrous sacs surrounding one or both kidneys, and may be located in the subcapsular or extracapsular region. Histologically, it is characterized by the absence of an epithelial lining to the cyst wall and the term pseudocyst is used. This condition have been reported sporadically in cats, and is associated with chronic kidney disease, mainly in older animals. The diagnosis is based on imaging tests and the prognosis is related to the severity of renal dysfunction. The aim of this report is to describe an unusual presentation of perinephric pseudocyst in a very young female cat. Case: A mixed-breed 2-month-old female cat was evaluated for presenting abdominal distension and anatomical deformities of the limbs. Renomegaly on the left side was noted during abdominal palpation. On presentation, the serum creatinine was 134 µmol/L. Urinalysis showed mild proteinuria, presence of squamous and transitional cells, and rare bacteria. The urine specific gravity was 1.044 and urine protein to creatinine ratio was 0.23. Abdominal ultrasonography revealed a large anechoic subcapsular cyst on the left kidney, in adittion to dilatation of renal pelvis and calyces. The excretory urography showed left renomegaly, and the nephrogram and pyelogram were not clearly observed in this kidney, indicating unilateral deficiency in renal filtration. The cat was referred to unilateral left nephrectomy but died shortly before surgery. At necropsy, marked left kidney enlargment was observed (6.5 x 4.5 x 1.5 cm), with a cystic aspect, occupying almost the entire abdominal cavity. The cystic content was translucent and was compressing the renal parenchyma, resulting in hydronephrosis. The capsule forming the cyst wall was composed of connective tissue, characterizing the perinephric pseudocyst. Discussion: Reports show cases of perinephric pseudocyst affecting mostly older animals, above eight years old. In one retrospective study of 26 cases, 73% were male and the mean age was eleven years, ranging from four to 18 years old. Another study of 13 cases showed a mean age of 16 years. In this report, unexpectedly, the patient was too young compared to these other cases, but the clinical presentation was similiar. Being a young animal, in the absence of ureterolithiasis or history of trauma, it is suggested a congenital origin for the disease. Loss of renal function and azotemia may occur in about 90% of the cases by compression of the renal parenchyma by the pseudocyst or due to associated interstitial fibrosis. In this case, the serum creatinine concentration was above the reference value proposed for pediatric patients therefore, the cat may be considered azotemic. Beyond that, the excretory urography indicated no proper excretory function on the left kidney. It is proposed that the renal function was being compensated by the contralateral kidney. The clinical and imaging findings of this case are compatible with perinephric pseudocyst, which was confirmed by necropsy and histopathological examination. This condition is not commonly reported in cats of pediatric age, althought it must be considered as a differencial diagnosis to cats presenting abdominal distension and renomegaly, even young ones. Imaging tests were important in this case, not only to direct the diagnosis, but also contributing in evaluating the renal excretory function. [ABSTRACT FROM AUTHOR]

Hypercortisolism is a common endocrinopathy in dogs; however, in a few cases, bilateral functional adrenocortical adenomas cause spontaneous disease, and thrombotic events are considered uncommon complications. The aim of this report was to describe a case of bilateral adrenocortical adenoma in a dog with hyperadrenocorticism associated with distal aortic and iliac thrombosis, with emphasis on clinical and pathological aspects. A 15-year-old spayed female Dachshund with a previous clinical history of hyperadrenocorticism presented with acute bilateral hindlimb paraparesis. A vertebral thoracolumbar radiography was performed and did not present any evidence of intervertebral disk disease or vertebral abnormalities; however, abdominal ultrasound and vascular Doppler evaluation revealed bilateral adrenal enlargement in addition to an aortic and external iliac artery thrombus. The animal was euthanized. At necropsy, both adrenal glands were enlarged by well-demarcated neoplastic nodules in the parenchyma, and a thrombus caudal to the abdominal aorta bifurcation within the external iliac arteries that extended to the left external iliac artery was noted. Histological evaluation revealed a well-differentiated neoplastic proliferation of cortical epithelial cells, consistent with bilateral adenoma, and muscular necrosis in the pelvic limbs was also observed. Bilateral functional adrenocortical adenoma; although, very rare, should be considered as a cause of hypercortisolism, and aortic thrombosis in dogs should be considered as a possible consequence. [ABSTRACT FROM AUTHOR]