The present case describes the diagnostic and therapeutic procedure of a dog with an intraocular osteosarcoma. According to the results of the diagnostic imaging studies, the tentative diagnosis of an intraocular neoplasm with perforation of the globe and orbital invasion of the tumour was made and an orbital exenteration was performed. The histopathological diagnosis of the extracted organ implied an intraocular, extraskeletal osteosarcoma. Seventy-seven days later the patient displayed an acute paraparesis. Clinical and diagnostic reevaluation using magnetic resonance imaging (MRI) was performed and the dog was euthanized at the owner's request. By means of MRI and necropsy, an additional axial osteosarcoma of the 6th lumbar vertebra and a malignant melanoma of the right tonsil were diagnosed.
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Clin Dermatol
July 2024
Department of Dermatology, University of Connecticut School of Medicine, Farmington, Connecticut, USA. Electronic address:
Metastatic tumors to the eye and eyelid are generally seen in patients with disseminated metastases in the setting of advanced disease. Occasionally, they can present as the first sign of occult malignancy. The choroid is the most common site of intraocular metastases secondary to its dense vascular supply.
View Article and Find Full Text PDFClin Dermatol
July 2024
Department of Dermatology, University of Connecticut School of Medicine, Farmington, Connecticut, USA; Department of Dermatology, University of Florida College of Medicine, Gainesville, Florida, USA. Electronic address:
Eur J Ophthalmol
September 2023
Universidad de Buenos Aires (UBA), Buenos Aires, Argentina.
Background: Osteosarcoma (OS) is the most common primary bone carcinoma. Adulthood most frequent intraocular malignant tumor is choroidal metastasis; however, these are rarely related to sarcomas. There are only two OS-related choroidal metastasis cases reported in the literature, both prior to 1970.
View Article and Find Full Text PDFJ Vet Med Sci
August 2020
Laboratory of Veterinary Pathology, Department of Veterinary Medicine, Nihon University, Fujisawa, Kanagawa 252-0813, Japan.
An 8-year-and-9-month-old male, lop-eared rabbit (Oryctolagus cuniculus) presented with gradual enlargement of the left eye to 4 × 4 × 4 cm and exophthalmos. The animal died 3 months later, and necropsy was performed. On gross pathology, the intraocular tissue was effaced and occluded by a hard, light-gray mass.
View Article and Find Full Text PDFMol Genet Genomic Med
December 2019
Medical Genetics Department, CHU Montpellier, Univ Montpellier, Montpellier, France.
Background: Retinoblastoma (Rb) is a rare intraocular malignant tumor in children with high overall survival. Predisposition to Rb is linked to RB1 germline mutations with high penetrance, but rare RB1 low-penetrance variants are also known. Rb survivors are at risk of second primary malignancies (SPMs), mostly osteosarcoma and soft-tissue sarcoma.
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