ABSTRACT
A 3-yr-old male captive bobcat (Lynx rufus) presented with chronic ataxia and right-sided head tilt. Magnetic resonance imaging (MRI) revealed cerebellar crowding and compression consistent with Chiari-like malformation. The clinical signs did not improve after surgical occipital craniectomy, and 2 mo postoperatively a second MRI showed hydromyelia and continued cerebellar compression. The bobcat was euthanized, and necropsy showed chronic focal cerebellar herniation and chronic multifocal atlanto-occipital joint osteophyte proliferation. Histology confirmed the presence of a thick fibrous membrane along the caudal aspect of the cerebellar vermis, suggestive of postoperative adhesions, and axonal degeneration of the cervical spinal cord, even in sections without a central canal lesion. These lesions appear to have been complications associated with surgical correction of the Chiari-like malformation.
Subject(s)
Arnold-Chiari Malformation/veterinary , Cerebellar Diseases/veterinary , Decompression, Surgical/veterinary , Lynx , Syringomyelia/veterinary , Animals , Arnold-Chiari Malformation/surgery , Cerebellar Diseases/pathology , Cerebellar Diseases/surgery , Male , Syringomyelia/pathologyABSTRACT
A 22-yr-old, captive-born, presumed female Hoffmann's two-toed sloth (Choloepus hoffmanni) presented in respiratory distress with severe dehydration and symptoms of hypotension. During treatment, dysphagia was noted and oral examination revealed enlarged palatine tonsils and mucosal plaques. Bloodwork showed a decreased sodium:potassium ratio, a low baseline cortisol, a decreased adrenocorticotropin response test, and a blunted aldosterone stimulation test. All values were compared to a healthy male Hoffmann's two-toed sloth at the same facility. Despite aggressive medical management and treatment for hypoadrenocorticism, the sloth was found deceased. Necropsy revealed abdominal effusion, multifocal plaques throughout the upper gastrointestinal tract, and testes. Histopathology showed marked adrenal cortical atrophy and intranuclear mucosal inclusions in the gastrointestinal tract; advanced molecular techniques did not uncover any viral etiologies. This is the first reported case of hypoadrenocorticism in a sloth.
Subject(s)
Addison Disease/veterinary , Sloths , Addison Disease/diagnosis , Addison Disease/pathology , Animals , Desoxycorticosterone/administration & dosage , Desoxycorticosterone/analogs & derivatives , Desoxycorticosterone/therapeutic use , Fatal Outcome , MaleABSTRACT
A 9.5-year-old, male castrated Walker Hound was presented for evaluation of progressive weakness, anorexia, and weight loss. Imaging revealed multiple abdominal and thoracic masses and ascites; fine-needle aspirates of mesenteric and splenic masses confirmed malignancy, most likely histiocytic sarcoma. Laboratory analyses revealed increased ionized calcium and parathyroid hormone-related peptide (PTH-rP) concentrations, and concurrent low-normal parathyroid hormone concentration, consistent with humoral hypercalcemia of malignancy. Necropsy was performed after euthanasia. The dog had disseminated histiocytic sarcoma, including sarcomatosis, as well as bilateral thyroid carcinoma. PTH-rP immunostaining was positive in the thyroid carcinoma but negative in the histiocytic neoplasm. These results suggest that thyroid carcinoma-associated hypercalcemia can be caused by tumor secretion of PTH-rP.
Subject(s)
Carcinoma/veterinary , Dog Diseases/metabolism , Histiocytic Sarcoma/veterinary , Hypercalcemia/metabolism , Parathyroid Hormone-Related Protein/metabolism , Thyroid Neoplasms/veterinary , Animals , Blood Cell Count/veterinary , Carcinoma/metabolism , Carcinoma/pathology , Dog Diseases/pathology , Dogs , Gene Expression Regulation, Neoplastic , Histiocytic Sarcoma/metabolism , Histiocytic Sarcoma/pathology , Hypercalcemia/genetics , Male , Parathyroid Hormone-Related Protein/genetics , Thyroid Neoplasms/metabolism , Thyroid Neoplasms/pathologyABSTRACT
A 16-year-old female umbrella cockatoo (Cacatua alba) was presented for a fluctuant, right-sided cervical mass that extended from the caudolateral edge of the right mandible to the coelomic inlet. Results of initial diagnostic tests were consistent with a cystic mass containing hemorrhage. Surgical exploration and removal of the mass was done, but because the hyoid apparatus was incorporated in the base of the cyst, complete surgical excision was not possible. Histopathologic results were consistent with a branchial cyst with carcinoma. Five months after surgery, the cockatoo exhibited intermittent periorbital swelling and epistaxis, and cytologic results of a fluid aspirate from the right infraorbital sinus were consistent with carcinoma. Results of magnetic resonance imaging revealed extensive abnormal T2 and short-tau inversion-recovery hyperintense tissue associated with the right side of the head and neck, infiltrating between muscle planes and extending into the right retro-orbital tissue and nasal cavity. At 7 months after surgery, the bird was severely dyspneic and was euthanatized. To our knowledge, this is the first report describing the diagnosis, management, and histologic characteristics associated with a branchial cyst with carcinoma in an animal.
