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1.
Bone Joint J ; 101-B(6): 739-744, 2019 Jun.
Article in English | MEDLINE | ID: mdl-31154835

ABSTRACT

AIMS: The aim of this study was to identify factors that determine outcomes of treatment for patients with chondroblastic osteosarcomas (COS) of the limbs and pelvis. PATIENTS AND METHODS: The authors carried out a retrospective review of prospectively collected data from 256 patients diagnosed between 1979 and 2015. Of the 256 patients diagnosed with COS of the pelvis and the limbs, 147 patients (57%) were male and 109 patients (43%) were female. The mean age at presentation was 20 years (0 to 90). RESULTS: In all, 82% of the patients had a poor response to chemotherapy, which was associated with the presence of a predominantly chondroblastic component (more than 50% of tumour volume). The incidence of local recurrence was 15%. Synchronous or metachronous metastasis was diagnosed in 60% of patients. Overall survival was 51% and 42% after five and ten years, respectively. Limb localization and wide surgical margins were associated with a lower risk of local recurrence after multivariable analysis, while the response to chemotherapy was not. Local recurrence, advanced patient age, pelvic tumours, and large volume negatively influenced survival. Resection of pulmonary metastases was associated with a survival benefit in the limited number of patients in whom this was undertaken. CONCLUSION: COS demonstrates a poor response to chemotherapy and a high incidence of metastases. Wide resection is associated with improved local control and overall survival, while excision of pulmonary metastases is associated with improved survival in selected patients. Cite this article: Bone Joint J 2019;101-B:739-744.


Subject(s)
Bone Neoplasms/surgery , Chondrosarcoma/surgery , Extremities/surgery , Osteosarcoma/surgery , Pelvic Neoplasms/surgery , Adolescent , Adult , Aged , Aged, 80 and over , Bone Neoplasms/pathology , Child , Child, Preschool , Chondrosarcoma/pathology , Combined Modality Therapy , Extremities/pathology , Female , Humans , Infant , Infant, Newborn , Male , Middle Aged , Neoplasm Recurrence, Local/pathology , Osteosarcoma/pathology , Pelvic Neoplasms/pathology , Retrospective Studies , Treatment Outcome
2.
Clin Radiol ; 74(7): 534-538, 2019 07.
Article in English | MEDLINE | ID: mdl-31000331

ABSTRACT

AIM: To evaluate if quantifying proton density fat fraction (PDFF) would be useful in separating lipoma, atypical lipomatous tumour (ALT) and liposarcoma in the extremities and trunk. In addition, differentiating ALT versus non-classical lipomas using magnetic resonance imaging (MRI)-based fatty acid composition (FAC) and three-dimensional (3D) texture analysis was tested. MATERIAL AND METHODS: This prospective study (undertaken between 2014-2017; comprising 20 women, 21 men) was approved by the Regional Ethical Review Board and informed consent was obtained from all participants. For PDFF and FAC 3D spoiled gradient multi-echo images were acquired. PDFF was analysed in 16 lipomas (25-76 years), 14 ALTs (42-78 years) and 11 myxoid liposarcomas (31-68 years). The difference of mean PDFF was tested with one-way analysis of variance. A support vector machine algorithm was used to find the separating mean PDFF values. RESULTS: Mean PDFF for lipomas was 90% (range 76-98%), for ALT 83% (range 62-91%), and for liposarcoma 4% (range 0-21%). The difference of mean PDFF for liposarcomas versus ALT and lipoma was significant (p=0.0001, for both), and for ALT versus lipoma (p=0.021). The optimal threshold for separating liposarcoma from ALT and lipoma was 41.5%, and for ALT and lipoma 85%. Texture analysis could not separate ALT and non-classical lipomas, while the difference for FAC unsaturation degree was significant (p=0.013). CONCLUSION: Measuring PDFF is a promising complement to standard MRI, to separate liposarcomas from ALT and lipomas. Lipomas that are not solely composed of fat cannot confidently be separated from ALT using PDFF, FAC, or texture analysis.


Subject(s)
Lipoma/diagnostic imaging , Liposarcoma/diagnostic imaging , Magnetic Resonance Imaging/methods , Soft Tissue Neoplasms/diagnostic imaging , Adult , Aged , Diagnosis, Differential , Female , Humans , Male , Middle Aged , Prospective Studies , Protons
3.
Int J Immunopathol Pharmacol ; 18(1): 121-32, 2005.
Article in English | MEDLINE | ID: mdl-15698517

ABSTRACT

The aim of the present study was to investigate the impact of a successful anti-myxosporean medication on the innate immune system of fish intensively cultured in the Mediterranean basin. For this purpose, juvenile and adult gilthead seabream (S. aurata L.) naturally infected with Polysporoplasma sparis in the kidney were used in a small-scale field trial. The infected fish were treated orally with the combination of salinomycin and amprolium, two drugs well known for their anti-coccidial effect in other animals. Drug efficacy and safety was evaluated in terms of changes observed in histopathology, mortality and P. sparis intensity and prevalence rate. Phagocytic functions of head-kidney leucocytes were also investigated at the end as well as one month post the medication. Salinomycin with amprolium exhibited a significant reduction in intensity and prevalence rate in both juvenile and adult fish, and no histopathological evidence for toxic side effects was observed. In addition, the successful treatment was closely correlated with a complete restoration of the diminished phagocytic ability and capacity as well as NO, and lysozyme secretion in a time dependent manner. This data suggests that salilomycin with amprolium can be an alternative treatment for myxosporean infections in tropical fish, possibly exhibiting their action through the enhancement of host innate functions.


Subject(s)
Amprolium/therapeutic use , Anti-Bacterial Agents/therapeutic use , Ciliophora , Coccidiostats/therapeutic use , Fish Diseases/drug therapy , Perciformes/microbiology , Phagocytosis/physiology , Protozoan Infections/drug therapy , Pyrans/therapeutic use , Animals , Cell Adhesion , Diet , Fish Diseases/immunology , Fish Diseases/microbiology , Kidney/microbiology , Leukocytes/immunology , Muramidase/physiology , Nitric Oxide/physiology , Perciformes/immunology , Protozoan Infections/immunology
4.
Int J Immunopathol Pharmacol ; 17(3): 343-52, 2004.
Article in English | MEDLINE | ID: mdl-15461868

ABSTRACT

The need for a vaccine against Leishmania spp., a major cause of worldwide morbidity and mortality, is urgent. We tested the efficacy of an experimental vaccination in murine models of cutaneous leishmaniasis, using dendritic cells (DCs) pulsed with synthetic or native parasite antigens. DCs pulsed with peptide 154-169aa of gp63 or soluble promastigote lysate (SPL) triggered antigen-specific immune responses and efficiently reduced lesion formation and parasite load of genetically susceptible BALB/c mice infected with Leishmania major. This effect was accompanied by a modulation of the cellular immune response towards a Th1 profile. Vaccination of genetically resistant CBA mice with DCs pulsed with peptide 154-169aa or SPL did not affect the course of the disease, whereas pulsing with the epitope 467-482aa of gp63 resulted in disease exacerbation, accompanied by a switch to a Th2 profile. In view of our continuously growing knowledge about the immunobiology of DCs, these findings suggest that vaccination with DCs pulsed with defined peptides could be a strategy against infectious diseases. Peptide selection is a prerequisite as they can differentially regulate the type of immune response in susceptible or resistant hosts.


Subject(s)
Dendritic Cells/drug effects , Dendritic Cells/immunology , Leishmaniasis, Cutaneous/prevention & control , Metalloendopeptidases/immunology , Metalloendopeptidases/therapeutic use , Peptides/therapeutic use , Protozoan Vaccines/therapeutic use , Animals , Antigens, Protozoan/immunology , Body Burden , Bone Marrow Cells/drug effects , Bone Marrow Cells/immunology , Cytokines/biosynthesis , Immunity, Cellular , Immunoglobulin G/biosynthesis , Immunoglobulin G/genetics , Leishmaniasis, Cutaneous/immunology , Leishmaniasis, Cutaneous/parasitology , Mice , Mice, Inbred BALB C , Mice, Inbred CBA , Th1 Cells/immunology , Vaccination
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