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Osteoporosis is one of the most common disorders of bone metabolism, this being a condition that causes pain, frequently causing fractures, as a result of the reduction of bone mass and density. The purpose of this study is the establishment and testing of an experimental protocol to induce osteoporosis in laboratory rats by ovariectomy, at 9 months old. It is desirable that osteoporosis is successfully induced so that various biomaterials for treating pathologic bone healing can be further tested. For this study, 20 Sprague-Dawley rats were split into 2 groups of 10 individuals, which were then operated, while 10 were left as control. Clinical examination was performed each week, but mainly 4 months after surgery, biochemistry and osteodensitometry were determined by CT - scanning to compare the differences between the ovariectomized group and the control group. The rats were humanly euthanasied at 20 weeks post ovariectomy and histological analyses were performed. Biochemistry revealed that progesterone level was decreased by ~50%, calcium values were decreased, alkaline phosphatase was increased and the Ca:P ratio was also altered. Nevertheless, the analysis of bone density (BMD) revealed a decrease in the ovariectomized group compared with the control group and the histological analysis confirmed the induction of osteoporosis pathology. In conclusion, osteoporosis by means of estrogenic deficit, was successfully induced in 9-month-old Sprague-Dawley rats.

Canine leishmaniasis (CanL) is a zoonotic disease considered endemic in the Mediterranean region. Romania is traditionally regarded as a non-endemic country. Considering the zoonotic character of the disease, this study aims to increase the knowledge on diagnostic aspects of CanL. A 2-year-old, mix breed male dog, recently returned from Italy had a history of progressive weight loss and skin lesions. The clinical examination was followed by hematology and serum biochemistry, fine-needle aspiration of lymph nodes, impression smears, VetExpert® rapid test Leishmania Ab, and PCR. The clinical examination revealed muscle atrophy, non-pruritic crusting dermatitis, ulcers, and lymphadenopathy. Hematology showed severe anemia. The serum biochemistry revealed hyperproteinaemia, hypoalbuminemia, hyperglobulinemia. Cytological exams evidenced the intracellular amastigotes in macrophages, confirmed by rapid test and PCR. In Romania, under the light of the new case reports, leishmaniasis should be reconsidered from both veterinary and public health perspective.

Lymphomas occur by clonal expansion of lymphoid cells and have distinctive morphological and immunophenotypic features. Determination of canine lymphoma immunophenotype is useful for accurate prognosis and further therapy. In the suggested study, we performed an immunohistochemical evaluation of some cases with canine lymphoma diagnosed in the Department of Pathology (Faculty of Veterinary Medicine, Cluj-Napoca, Romania), in order to characterize them. The investigation included 39 dogs diagnosed with different anatomical forms of lymphoma, following necropsy analysis or assessment of biopsies. The diagnosis of lymphoma was confirmed by necropsy and histopathology (Hematoxylin-eosin stain) examinations. The collected specimens were analyzed by immunohistochemistry technique (automatic method) using the following antibodies: CD3, CD20, CD21 and CD79a. The analyzed neoplasms were characterized as follows: about 64.10% of cases were diagnosed as B-cell lymphomas, 33.34% of cases as T-cell lymphomas, whereas 2.56% of cases were null cell type lymphomas (neither B nor T). Most of multicentric (80%), mediastinal (60%) and primary central nervous system lymphomas (100%) had B immunophenotype, while the majority of cutaneous (80%) and digestive (100%) lymphomas had T immunophenotype. Immunohistochemical description of canine lymphomas can deliver some major details concerning their behavior and malignancy. Additionally, vital prognosis and efficacy of some therapeutic protocols are relying on the immunohistochemical features of canine lymphoma.