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Comparaison des résultats des reconstructions par allogreffe ostéoarticulaire et par mégaprothèse après résection du genou
Authors: --- ---
Year: 2018 Publisher: Bruxelles: UCL. Faculté de médecine et de médecine dentaire,

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⁘ࡡ䌀ںtroduction: The literature review does not allow us to identify which technique, between the osteoarticular allografts and the megaprostheses, gives the best results for the knee reconstruction after resection of bone tumors. Therefore we reviewed the complications, the implant survival and the joint mobilities of both techniques to compare their results at the CUSL. Materials : We retrospectively reviewed the files of 26 patients who had megaprostheses reconstruction between 17/06/1987 and 20/01/2015.The average age was 24 years (range 9-58) and the average bone resection was 14,3cm (range 5-22). We reviewed the files of 11 patients who underwent an osteoarticular allograft reconstruction between 10/10/1994 and 14/01/2013. The average age was 14 years (range 9-27) and the average bone resection was 18cm (range 11-42).Results: For the megaprostheses, the average follow-up was 86 months (range 7-347) and the average survival time was 53 months (range 7-138). One patient died during the follow-up. The failures of the megaprostheses were due to : 5 aseptic loosening’s, 3 structural failures and 1 failure of the expandable mechanism. In the end, 2 patients had total femur prosthesis and 2 patients a allograft-prosthesis composites. The joint mobility was 99° for the flexion and -6 for the extension. For the allograft, the average follow-up was 44 months (range 11-219) and the average survival time was 28 months (range 3-86). Four patients died during the follow-up. The failures of the allografts were due to 3 deep infections associated with wound dehiscences, 2 nonunions, 2 local recurrences, 1 fracture and 1 fracture associated with nonunion. The joint mobility was 96° for the flexion and -22 for the extension. In the end, 2 patients underwent an amputation, 5 patients were converted to a megaprostheses and 1patient had total femur prosthesis. Conclusion: By comparing the results of both reconstructions, megaprostheses give better results than osteoarticular allografts in terms of implant survival, incidence of complications, reoperation and joint mobility. There were more local recurrences and deaths in the allograft group. In each option, complications are frequent and the risk of reoperation is high. The survival of the osteoarticular allografts and megaprostheses of our series were shorter compared with those reported in the literature but the complications were similar. Introduction: Dans la littérature, il n'est pas simple d'identifier quelle technique, entre les allogreffes ostéoarticulaires et les mégaprothèses, donne les meilleurs résultats pour la reconstruction du genou après résection de tumeurs osseuses. Nous avons donc revu les complications, les durées de vie et les mobilités articulaires des deux techniques afin de comparer leurs résultats au sein des Cliniques Universitaires Saint-Luc. Matériel : Nous avons revu rétrospectivement les dossiers de 26 patients ayant subi une reconstruction par mégaprothèse entre le 17/06/1987 et le 20/01/2015. L'âge moyen était de 24 ans (extrêmes 9-58) et la résection moyenne était de 14,3cm (extrêmes 5-22). Les dossiers de 11 patients ayant subi une reconstruction par allogreffe ostéoarticulaire entre le 10/10/994 et le 14/01/2013 ont été revus. L'âge moyen était de 14 ans (extrêmes 9- 27) et la résection moyenne de 18cm (extrêmes 11-42).Résultats : Le suivi moyen des mégaprothèses était de 86 mois (extrêmes 7-347) et la durée de vie moyenne était de 53 mois (extrêmes 7-138).Un patient est décédé. L'échec des mégaprothèses était dû à : 5 descellements aseptiques, 3 fractures d'implant et l défaillance du mécanisme d'allongement. Finalement, 2 patients ont eu une conversion en fémur totalement prothétique et 2 patients une reconstruction composite avec prothèse et allogreffe. La mobilité articulaire moyenne était de 99° pour la flexion et -6° pour l'extension. Le suivi moyen des patients avec une allogreffe ostéoarticulaire était de 44 mois (extrêmes 11-219) et la durée de vie moyenne était de 28 mois (extrêmes 3-86 mois). 4 patients sont décédés. L'échec des allogreffes était dû à : 3 infections profondes avec déhiscences de plaie, 2 pseudarthroses, 2 récidives locales, 1 fracture et 1 fracture associée à une pseudarthrose. La mobilité articulaire était de 96° pour la flexion et -22° pour l'extension. Finalement, 2 patients ont subi une amputation, 5 une conversion en mégaprothèse et 1 en fémur totalement prothétique. Conclusion : En comparant les résultats des deux techniques, les mégaprothèses donnent de meilleurs résultats que les allogreffes ostéoarticulaires en termes de durée de vie, d'incidence des complications, de ré intervention et de mobilité articulaire. Un nombre plus important de récidive et de décès ont été rencontrés dans le groupe allogreffe. Pour les deux techniques, les complications sont fréquentes et le risque de réintervention est élevé. En comparaison avec les résultats de la littérature, la durée de survie des allogreffes ostéoarticulaires et des mégaprothèses de notre série était inférieure à celle des articles revus, mais les complications étaient comparables.


Book
Syndromes myélodysplasiques : les agents hypométhylants comme alternative à l'allogreffe de cellules souches hématopoïétiques et chimiothérapie conventionnelles, est-ce possible ?
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Year: 2015 Publisher: Bruxelles: UCL. Faculté de pharmacie et des sciences biomédicales,

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Myelodysplastic syndromes are clonal hematopoietic stem-cell disorders characterized by chronic peripheral blood cytopenias and a hypercellular bone marrow. Hematopoietic stem cells transplantation is presently the only curative treatment for MDS, while other therapeutics like intensive chemotherapies and hypomethylating agents, only have the potential to improve the patient’s overall survival. The latter recently appeared for the treatment of MDS in Europe, and aroused great expectations on these therapies. Even they effectively bring new possibilities for patients; their improvement was not as great as expected. New questions are now raised up for their optimal use in MDS. This work aims to determine the position of hypomethylating agents towards other therapies and to suggest some lines of thought for new issues they raise. Les syndromes myélodysplasiques (SMD) englobent une série de troubles affectant les cellules souches hématopoïétiques. Les patients atteints de cette pathologie ont la particularité de présenter des cytopénies périphériques chroniques, tout en ayant une moelle osseuse riche en progéniteurs myéloïdes. Actuellement, la greffe de cellules souches hématopoïétiques est le seul traitement curatif pour les SMD, tandis que les autres options thérapeutique s, comme la chimiothérapie et les agents hypométhylants, ne laissent au mieux qu'un espoir de prolonger la survie du patient. Ces derniers sont récemment apparus sur le marché, et ont alors suscité de grandes attentes dans le traitement des SMD. Bien qu'apportant de nouvelles perspectives pour les patients, ils n 'ont malheureusement pas aussi bien répondu à ces attentes, et laissent par contre de nouvelles interrogations quant à leur usage optimal dans ce type de pathologie. Ce travail a pour but de positionner le rôle de ces nouvelles molécules par rapport aux traitements existants, et de proposer quelques pistes de réflexion quant aux interrogations que laissent les agents hypométhylants.


Book
Réparer les vivants
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ISBN: 9782070462360 2070462366 Year: 2015 Volume: 5942 Publisher: Paris : Gallimard,

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"" Le coeur de Simon migrait dans un autre endroit du pays, ses reins, son foie et ses poumons gagnaient d'autres provinces, ils filaient vers d'autres corps. " Réparer les vivants est le roman d'une transplantation cardiaque. Telle une chanson de geste, il tisse les présences et les espaces, les voix et les actes qui vont se relayer en vingt-quatre heures exactement. Roman de tension et de patience, d'accélérations paniques et de pauses méditatives, il trace une aventure métaphysique, à la fois collective et intime, où le coeur, au-delà de sa fonction organique, demeure le siège des affects et le symbole de l'amour. Ce roman a reçu dix prix littéraires parmi lesquels le prix du Roman des étudiants France Culture Télérarna2014,Ie Grand Prix RTL Lire 2014, le prix des lecteurs L'Express BFMTV 2014 et le prix Relay des Voyageurs 2014 avec Europe 1."-- back cover.

Allografts in orthopaedic practice
Authors: ---
ISBN: 0683023004 Year: 1992 Publisher: Baltimore (Md.) : Williams & Wilkins,

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Bone biology and healing
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ISBN: 128193383X 9786611933838 9812791299 9789812791290 9812382801 9789812382801 Year: 2003 Publisher: River Edge, NJ : World Scientific,

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This book describes succinctly the factors which affect the incorporation of massive and morsellised allografts after transplantation. Unless special precautions are taken, massive allografts when implanted can undergo stress fatigue, due to the limited incorporation at the graft-host interface. Immunological and cell signalling growth factors can be shown to greatly influence the behaviour of the graft. The bone-biological processes are illustrated in terms of demineralised bone, which can initiate bone induction due to the protection and availability of the original bone-morphogenic protein.

Cardiac reconstructions with allograft tissues
Author:
ISBN: 1280263563 9786610263561 0387265155 0387949623 1441928596 Year: 2005 Publisher: New York, NY : Springer,

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Cryopreserved allograft tissues are now standard materials for the reconstructive cardiac surgeon. Since publication of the first edition ("Cardiac Reconstructions with Allograft Valves") in 1989, the field has progressed dramatically with increased clinical use of cardiovascular allograft tissues, with the development of new surgical techniques, and with advances in the understanding of the fundamentals of valve transplantation biology and cryopreservation. As a result, over two-thirds of the present volume represents new material. Fifty-six authors bring their expertise to thirteen comprehensive, lavishly illustrated sections which discuss the principles of the use of homograft valves, major clinical series of homograft valves for both left and right ventricular outflow tracts, cryopreserved allograft tissue for cardiac reconstruction, cell biology of heart valve leaflets, cryobiology of heart valve preservation, morphological, biochemical, and explant pathology studies of allograft heart valves, allograft valve banking, as well as detailed explanation of surgical techniques for valve and root methods for left and right ventricular outflow tract reconstructions, the Ross operation and variants, and complex reconstructions. A final section presents potential future directions for the field. Over 400 illustrations, created expressly for this book, depict the surgical techniques from the perspective of the surgeon standing at the operating table. All surgeons performing pediatric and/or adult valve replacements and reconstructive cardiac surgeries will benefit from the described methods. Cardiothoracic residents and cardiologists will also find the text useful. It will provide the surgeon with an enhanced understanding of the biological and material properties of allografts and increased familiarity with the range of surgical techniques applicable for the use of these valves, particularly in the successful management of challenging cardiac reconstructions.>.


Dissertation
Mechanistic and functional interrelationships between vegf-induced angiogenesis, cell mediated immunity and allograft erejection
Authors: ---
ISBN: 909018466X Year: 2004


Book
Cells and Materials for Disease Modeling and Regenerative Medicine
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Year: 2021 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

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Materials science and engineering are strongly developing tools with increasing impact in the biotechnological and biomedical areas. Interestingly, research in molecular and cellular biology is often at the core of the design and development of materials-based approaches, providing biological rationale. Focused on research relying on biology–materials interaction, IJMS launched a Special Issue named “Cells and Materials for Disease Modeling and Regenerative Medicine”. The aim of the Special Issue was to generate a compilation of in vitro and in vivo strategies based on cell–material interactions. This book compiles the papers published in that Special Issue and includes a selection of six original scientific experimental articles and six comprehensive reviews. We are convinced that this collection of articles shows representative examples of the state of the art in the field, unveiling the relevance of materials research in generating new regenerative medicine and disease modeling approaches.


Book
Cells and Materials for Disease Modeling and Regenerative Medicine
Authors: ---
Year: 2021 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

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Materials science and engineering are strongly developing tools with increasing impact in the biotechnological and biomedical areas. Interestingly, research in molecular and cellular biology is often at the core of the design and development of materials-based approaches, providing biological rationale. Focused on research relying on biology–materials interaction, IJMS launched a Special Issue named “Cells and Materials for Disease Modeling and Regenerative Medicine”. The aim of the Special Issue was to generate a compilation of in vitro and in vivo strategies based on cell–material interactions. This book compiles the papers published in that Special Issue and includes a selection of six original scientific experimental articles and six comprehensive reviews. We are convinced that this collection of articles shows representative examples of the state of the art in the field, unveiling the relevance of materials research in generating new regenerative medicine and disease modeling approaches.

Keywords

Research & information: general --- Leigh syndrome --- mitochondrial disorder --- iPSC --- NSC --- neuron --- disease modeling --- mtDNA --- high hydrostatic pressure --- devitalization --- decellularization --- allografts --- regenerative medicine --- bone and cartilage regeneration --- dentogenesis --- amelogenesis --- dentinogenesis --- cementogenesis --- drug release materials --- scaffolds --- odontogenic cells --- stem cells --- whole-tooth regeneration --- psoriasis --- cyclic adenosine monophosphate --- cholera toxin --- isoproterenol --- tissue engineering --- extracellular matrix --- collagen --- elastin --- bladder --- compliance --- microarchitecture --- biomimicry --- blood cancer --- bone marrow --- niche --- microenvironment --- 3D models --- tumor-on-a-chip --- leukemia --- myeloma --- biomaterials --- cytokines --- growth factors --- cardiac tissue regeneration --- adipose tissue --- fibrosis --- in vitro models --- in vivo models --- dental pulp stem cells --- osteogenesis --- rheumatoid arthritis --- mesenchymal stromal cells --- co-culture --- 3D cell culture --- explants --- joint-on-a-chip --- piezoelectric --- electroactive --- patterning --- cell differentiation --- bone tissue engineering --- Leigh syndrome --- mitochondrial disorder --- iPSC --- NSC --- neuron --- disease modeling --- mtDNA --- high hydrostatic pressure --- devitalization --- decellularization --- allografts --- regenerative medicine --- bone and cartilage regeneration --- dentogenesis --- amelogenesis --- dentinogenesis --- cementogenesis --- drug release materials --- scaffolds --- odontogenic cells --- stem cells --- whole-tooth regeneration --- psoriasis --- cyclic adenosine monophosphate --- cholera toxin --- isoproterenol --- tissue engineering --- extracellular matrix --- collagen --- elastin --- bladder --- compliance --- microarchitecture --- biomimicry --- blood cancer --- bone marrow --- niche --- microenvironment --- 3D models --- tumor-on-a-chip --- leukemia --- myeloma --- biomaterials --- cytokines --- growth factors --- cardiac tissue regeneration --- adipose tissue --- fibrosis --- in vitro models --- in vivo models --- dental pulp stem cells --- osteogenesis --- rheumatoid arthritis --- mesenchymal stromal cells --- co-culture --- 3D cell culture --- explants --- joint-on-a-chip --- piezoelectric --- electroactive --- patterning --- cell differentiation --- bone tissue engineering


Multi
On allograft rejection in human liver transplantation : An immunohistologic study
Author:
ISBN: 9090025081 Year: 1988 Publisher: Groningen

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Keywords

Liver Transplantation. --- Graft Rejection. --- Cyclosporins --- Transplantation, Homologous. --- Transplantation Immunology. --- Immunology, Transplantation --- Transplantation --- Organ Transplantation --- Tissue Transplantation --- Cell Transplantation --- Allogeneic Transplantation --- Allografting --- Homografting --- Homologous Transplantation --- Transplantation, Allogeneic --- Allografts --- Rejection, Transplant --- Transplantation Rejection --- Transplant Rejection --- Graft Rejections --- Rejection, Graft --- Rejection, Transplantation --- Rejections, Graft --- Rejections, Transplant --- Rejections, Transplantation --- Transplant Rejections --- Transplantation Rejections --- Delayed Graft Function --- Grafting, Liver --- Hepatic Transplantation --- Transplantation, Hepatic --- Transplantation, Liver --- Graftings, Liver --- Hepatic Transplantations --- Liver Grafting --- Liver Graftings --- Liver Transplantations --- Transplantations, Hepatic --- Transplantations, Liver --- Liver --- administration & dosage. --- transplantation --- Theses --- GRAFT REJECTION, drug effects --- CYCLOSPORINS --- Transplantation immunology --- administration and dosage --- homologous --- GRAFT REJECTION, drug effects. --- Transplantation immunology. --- transplantation. --- administration and dosage. --- homologous. --- Graft rejection, drug effects. --- Administration and dosage. --- Transplantation. --- Homologous. --- Allogeneic Grafting --- Grafting, Allogeneic --- Allogeneic Cells --- Liver Transplant --- Liver Transplants --- Transplant, Liver --- Liver Transplantation --- Graft Rejection --- Transplantation, Homologous --- Transplantation Immunology --- administration & dosage

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