Browsing by Author "Milinković, Marija (56584187000)"
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Publication Early post-transplant lymphoproliferative disorder–Case of fatal lymphoma after kidney transplantation(2016) ;Laušević, Mirjana (12776161600) ;Markovic-Lipkovski, Jasmina (6603725388) ;Terzić, Tatjana (55916182400) ;Jovanović, Nataša (8561678300) ;Milinković, Marija (56584187000)Naumović, Radomir (55965061800)Introduction Post-transplant lymphoproliferative disorder (PTLD) is a common malignancy following organ transplantation. Risk for PTLD is associated with the use of anti-thymocyte globulin in the prevention and treatment of acute rejection following kidney transplantation. Case Outline We report a case of fatal PTLD presented with sudden onset of fever. A 33-year-old male patient with primary diagnosis of left kidney agenesia underwent kidney transplantation six years following hemodialysis treatment initiation. Deceased donor was a 66-year-old female whose cause of death was cerebrovascular accident. Immunosuppressive regimen consisted of basiliximab, corticosteroids, tacrolimus, and mycophenolate mofetil. Six months upon transplantation the patient was hospitalized due to fever of unknown origin. All microbiological samples were negative, but abdominal ultrasound revealed round solid mass in the right native kidney. Right nephrectomy was performed showing tumor 35 × 35 × 20 mm in size within the 70 × 40 × 35 mm kidney. Pathohistological analysis confirmed very rare monomorphic B-cell PTLD–B-cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and classical Hodgkin lymphoma. Conclusion We consider this case of PTLD following kidney transplantation particular because of the tumor mass in native kidney after basiliximab induction and rare pathohistology. In a transplanted patient with fever, PTLD must always be considered, irrespective of immunosuppressive regimen. © 2016. Srpski Arhiv za Celokupno Lekarstvo. All right reserved. - Some of the metrics are blocked by yourconsent settings
Publication High rate of native arteriovenous fistulas: How to reach this goal?(2015) ;Jemcov, Tamara (14010471900) ;Milinković, Marija (56584187000) ;Končar, Igor (19337386500) ;Kuzmanović, Ilija (6506347823) ;Jakovljević, Nenad (6602789702) ;Dragaš, Marko (25027673300) ;Ilić, Nikola (7006245465) ;Djorić, Predrag (6507877839) ;Dimić, Andreja (55405165000) ;Banzić, Igor (36518108700) ;Kravljača, Milica (55354580700) ;Nešić, Vidosava (6701399962)Davidović, Lazar (7006821504)The types of vascular accesses for hemodialysis (HD) include the native arteriovenous fistula (AVF), arteriovenous graft (AVG) and central venous catheter (CVC). Adequately matured native AVF is the best choice for HD patients and a high percentage of its presence is the goal of every nephrologist and vascular surgeon. This paper analyses the number and type of vascular accesses for HD performed over a 10-year period at the Clinical Center of Serbia, and presents the factors of importance for the creation of such a high number of successful native AVF (over 80%). Such a result is, inter alia, the consequence of the appointment of the Vascular Access Coordinator, whose task was to improve the quality of care of blood vessels in the predialysis period as well as of functional vascular accesses, and to promote the cooperation among different specialists within the field. Vascular access is the “lifeline” for HD patients. Thus, its successful planning, creation and monitoring of vascular access is a continuous process that requires the collaboration and cooperation of the patient, nephrologist, vascular surgeon, radiologist and medical personnel. © 2015, Serbia Medical Society. All rights reserved.
