ABSTRACT
A seven-year-old domestic shorthair cat, adopted 5 years previously with a corneal perforation of the left eye, was presented for investigation of a left orbital mass. Computed tomography revealed a metallic foreign body within a contrast-enhancing, heterogeneous orbital mass. Large cell lymphoma was diagnosed from a fine needle aspirate. The cat staged negatively and was treated with L-asparaginase, prednisolone and three fractions of radiation therapy. A rapid clinical remission was obtained and the cat remained in remission for 3 years after therapy. This is the first report of large cell lymphoma likely occurring secondary to a foreign body.
Subject(s)
Cat Diseases/etiology , Eye Foreign Bodies/veterinary , Forensic Ballistics , Lymphoma/veterinary , Orbital Neoplasms/veterinary , Animals , Biopsy, Fine-Needle/veterinary , Cat Diseases/diagnosis , Cats , Diagnosis, Differential , Eye Enucleation/veterinary , Eye Foreign Bodies/complications , Eye Foreign Bodies/surgery , Lymph Nodes/pathology , Lymphoma/diagnosis , Lymphoma/etiology , Male , Neoplasms, Radiation-Induced/diagnosis , Neoplasms, Radiation-Induced/veterinary , Orbital Neoplasms/diagnosis , Orbital Neoplasms/etiology , Sarcoma/diagnosis , Sarcoma/veterinary , Soft Tissue Neoplasms/diagnosis , Soft Tissue Neoplasms/veterinaryABSTRACT
An 8-year-old male dog was presented with a peri-urethral intrapelvic mass with the characteristics of a sarcoma on computed tomography and cytology evaluation. A two-step procedure leading to a permanent urinary diversion was performed. During the same procedure, the caudal pelvic urethra and mass were resected and an extrapelvic anastomosis of the pelvic portion of the urethra to its penile portion was performed after passage of the pelvic urethra through the inguinal canal. The procedure successfully produced a tension-free end-to-end urethral anastomosis and no complications were observed during the postoperative period. Histologically, the lesion was reported as a narrowly excised liposarcoma. A 4-week course of curative intent of radiotherapy was initiated 2 weeks after surgery. Eight months later, the dog was free of clinical signs.
ABSTRACT
Mucopolysaccharidosis (MPS) types I and VII are inborn errors of metabolism caused by mutation of enzymes involved in glycosaminoglycan catabolism, which leads to intralysosomal accumulation of glycosaminoglycans. In children, severe forms of MPS I and VII are characterized by somatic and neurologic manifestations, including a poorly understood hearing loss. The purpose of this study is to describe the age-related histopathologic changes of the ear in spontaneous canine models of MPS I and VII. Pathologic changes in the ear were assessed in MPS I and VII dogs ranging from 1.6 to 9.3 months of age. Paraffin-embedded sections of the whole ear and Epon-embedded semithin sections of the cochlea were examined. The following lesions were blindly scored in the middle and inner ear: inflammation, cells vacuolization, thickening of osseous and membranous structures, perivascular vacuolated macrophages infiltration, and bone resorption. All dogs had lysosomal storage within cells of tympanic membrane, ossicles, tympanic bone and mucosa, cochlear bone, spiral ligament, limbus, and stria vascularis. The MPS I dogs mainly had progressive cochlear lesions. The MPS VII dogs had severe and early middle ear lesions, including chronic otitis media and bone resorption. The MPS I dog only partially recapitulates the pathology seen in humans; specifically, the dog model lacks inflammatory middle ear disease. In contrast, the MPS VII dog has severe inflammatory middle ear disease similar to that reported in the human. In conclusion, the canine MPS VII model appears to be a good model to study MPS VII-related deafness.
Subject(s)
Dog Diseases/pathology , Ear Diseases/veterinary , Mucopolysaccharidosis I/veterinary , Mucopolysaccharidosis VII/veterinary , Animals , Dog Diseases/etiology , Dogs , Ear Diseases/etiology , Ear Diseases/pathology , Ear, Inner/pathology , Ear, Middle/pathology , Humans , Male , Mucopolysaccharidosis I/complications , Mucopolysaccharidosis I/pathology , Mucopolysaccharidosis VII/complications , Mucopolysaccharidosis VII/pathologyABSTRACT
A 5-month-old female Great Dane puppy was treated for hematochezia, tenesmus, and rectal prolapse by resection of a 10-cm-long segment of colon and rectum. Grossly, the colorectal segment had diffuse mucosal and submucosal thickening with multiple polypoid nodules. The histologic diagnosis was colorectal hamartomatous polyps with ganglioneuromatosis. Duplication of PTEN was detected by quantitative multiplex polymerase chain reaction testing. The presence of 2 hamartomatous colorectal lesions with PTEN mutation is similar to human Cowden syndrome.