Browsing by Author "Markovic-Lipkovski, Jasmina (6603725388)"
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Publication Childhood microscopic polyangiitis associated with MPO-ANCA(2006) ;Peco-Antic, Amira (7004525216) ;Bonaci-Nikolic, Branka (10839652200) ;Basta-Jovanovic, Gordana (6603093303) ;Kostic, Mirjana (56247970900) ;Markovic-Lipkovski, Jasmina (6603725388) ;Nikolic, Milos (56910382000)Spasojevic, Brankica (10839232100)We reviewed the clinical, histological and serological parameters of microscopic polyangiitis (MPA) associated with antineutrophil cytoplasmic antibodies (ANCA) specific to myeloperoxidase (MPO). Six girls and one boy aged 12.0±2.6 years (7-15 years) met the following inclusion criteria: (1) clinical manifestations of systemic small vessel involvement; (2) histological demonstration of pauci-immune necrotizing glomerulonephritis; and (3) serological findings of increased concentration of MPO-ANCA by ELISA test. The main clinical manifestations were: influenza-like symptoms (100%), hematuria/ proteinuria (100%), purpura (100%), pulmonary-renal syndrome (57%), acute renal failure (ARF) (29%), ischemic cerebral insults (29%), and necrotizing vasculitis of the skin (29%). All patients underwent renal biopsy examined by immunohistochemistry with expression of alpha-smooth muscle actin (alpha SMA) in glomerular and interstitial spaces. Patients were followed from 6 months to 5.5 years (35.4±23.2 months). None of the patients died. Two of seven children who had ARF progressed to end stage renal disease; one developed chronic renal failure, and four normalized renal function. ARF and central nervous system involvement at presentation were parameters of poor renal outcome. A high score of fibro-cellular glomerular crescents was associated with worse prognosis. Early treatment enables a favorable prognosis of MPO-ANCA-associated MPA in children. © IPNA 2005. - Some of the metrics are blocked by yourconsent settings
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 Expression of cadherin-8 in renal cell carcinoma and fetal kidney(2002) ;Blaschke, Sabine (57008885000) ;Mueller, Claudia A. (35475866600) ;Markovic-Lipkovski, Jasmina (6603725388) ;Puch, Sabine (6507685006) ;Miosge, Nicolai (7003976332) ;Becker, Volker (7102882305) ;Mueller, Gerhard A. (35467521800)Klein, Gerd (7403534358)Cadherins represent a family of calcium-dependent cell adhesion molecules with an important regulatory function for maintenance of tissue architecture. Alterations of cadherin expression have been demonstrated in the development and progression of different epithelial tumors. In renal cell carcinoma (RCC), the majority of tumors express N-cadherin and cadherin-6. Screening a series of 16 RCC cell lines for the expression of different novel type II cadherins by RT-PCR revealed a complex pattern of cadherin expression: cadherins 6 and 14 were expressed in most of the RCC cell lines, whereas cadherins 11, 12 and 13 could not be detected at all. Interestingly, cadherin-8, previously shown in mice to be restricted to the CNS and thymus during development, was detected by RT-PCR, immunofluorescence and in situ hybridization in 4 of 16 RCC cell lines as well as in paraffin sections of the corresponding human RCC biopsies. In normal renal tissue, however, cadherin-8 could be detected only during the early stages of kidney development. These results suggest that alterations of type II cadherin expression may play a role in RCC development. In particular, cadherin-8 may be involved in both kidney morphogenesis as well as tumorigenesis in some types of RCC. © 2002 Wiley-Liss, Inc. - Some of the metrics are blocked by yourconsent settings
Publication Expression of cadherin-8 in renal cell carcinoma and fetal kidney(2002) ;Blaschke, Sabine (57008885000) ;Mueller, Claudia A. (35475866600) ;Markovic-Lipkovski, Jasmina (6603725388) ;Puch, Sabine (6507685006) ;Miosge, Nicolai (7003976332) ;Becker, Volker (7102882305) ;Mueller, Gerhard A. (35467521800)Klein, Gerd (7403534358)Cadherins represent a family of calcium-dependent cell adhesion molecules with an important regulatory function for maintenance of tissue architecture. Alterations of cadherin expression have been demonstrated in the development and progression of different epithelial tumors. In renal cell carcinoma (RCC), the majority of tumors express N-cadherin and cadherin-6. Screening a series of 16 RCC cell lines for the expression of different novel type II cadherins by RT-PCR revealed a complex pattern of cadherin expression: cadherins 6 and 14 were expressed in most of the RCC cell lines, whereas cadherins 11, 12 and 13 could not be detected at all. Interestingly, cadherin-8, previously shown in mice to be restricted to the CNS and thymus during development, was detected by RT-PCR, immunofluorescence and in situ hybridization in 4 of 16 RCC cell lines as well as in paraffin sections of the corresponding human RCC biopsies. In normal renal tissue, however, cadherin-8 could be detected only during the early stages of kidney development. These results suggest that alterations of type II cadherin expression may play a role in RCC development. In particular, cadherin-8 may be involved in both kidney morphogenesis as well as tumorigenesis in some types of RCC. © 2002 Wiley-Liss, Inc. - Some of the metrics are blocked by yourconsent settings
Publication Human α-defensins HNPs-1, -2, and -3 in renal cell carcinoma: Influences on tumor cell proliferation(2002) ;Müller, Claudia A. (35475866600) ;Markovic-Lipkovski, Jasmina (6603725388) ;Klatt, Tatjana (6603115299) ;Gamper, Jutta (57194483352) ;Schwarz, Gerold (7201633896) ;Beck, Hermann (7202345872) ;Deeg, Martin (7004751454) ;Kalbacher, Hubert (26643483100) ;Widmann, Susanne (6507491562) ;Wessels, Johannes T. (7102231847) ;Becker, Volker (7102882305) ;Müller, Gerhard A. (35467521800)Flad, Thomas (6602514381)The α-defensins human neutrophil peptides (HNPs)-1, -2, and -3 have been described as cytotoxic peptides with restricted expression in neutrophils and in some lymphocytes. In this study we report that HNPs-1, -2, and -3 are also expressed in renal cell carcinomas (RCCs). Several RCC lines were found to express mRNA as well as the specific peptides of HNP-1, -2, and -3 demonstrated by reverse transcriptase-polymerase chain reaction, mass spectrometric, and flow cytometric analyses. At physiological concentrations HNPs-1, -2, and -3 stimulated cell proliferation of selected RCC lines in vitro but at high concentrations were cytotoxic for all RCC lines tested. As in RCC lines, α-defensins were also detected in vivo in malignant epithelial cells of 31 RCC tissues in addition to their expected presence in neutrophils. In most RCC cases randomly, patchy immunostaining of α-defensins on epithelial cells surrounding neutrophils was seen, but in six tumors of higher grade malignancy all tumor cells were diffusely stained. Cellular necrosis observed in RCC tissues in association with extensive patches of HNP-1, -2, and -3, seemed to be related to high concentrations of α-defensins. The in vitro and in vivo findings suggest that α-defensins are frequent peptide constituents of malignant epithelial cells in RCC with a possible direct influence on tumor proliferation. - Some of the metrics are blocked by yourconsent settings
Publication Primary non-hodgkin lymphoma of urinary bladder with nine years later renal involvement and absence of systemic lymphoma: A case report(2008) ;Terzic, Tatjana (55916182400) ;Radojevic, Sanja (56581990900) ;Cemerikic-Martinovic, Vesna (6602432953) ;Stevanovic, Radmila (36875127400) ;Citlucanin, Sanja (24478374400) ;Mitrovic, Dragan (7004955837) ;Stojimirovic, Biljana (7004273397)Markovic-Lipkovski, Jasmina (6603725388)Aims: Primary bladder non-Hodgkin lymphoma (PBNHL) is very rare, especially as extranodal B-small lymphocytic lymphoma (B-SLL). Also, late isolated renal manifestation of PBNHL is extremely unusual. We report a very rare type of extranodal B-SLL of bladder wall with extremely unusual late isolated renal involvement, clinically manifested by nephrotic syndrome and incipient renal failure. A case report: A 56-year-old woman was presented with a solitary tumor of bladder wall, with history of dysuria and night sweating. A transvaginal needle biopsy of the tumor was performed, and diagnosis of primary extranodal B-SLL was made in the absence of bone marrow, lymph node, or blood involvement. She was treated with chemotherapy until the achievement of complete remission. Nine years later, she developed nephrotic syndrome. The renal biopsy revealed parenchymal lymphoma's involvement associated with glomerular lesion. Immunohistochemical analysis confirmed the same imunophenotype of lymphoma cells like in bladder wall nine years ago. Restaging procedure showed no evidence of disease elsewhere. Conclusion: To our knowledge, it is the first case of association of very rare primary bladder B-SLL with late isolated renal involvement. © 2007 Humana Press Inc. - Some of the metrics are blocked by yourconsent settings
Publication Primary non-hodgkin lymphoma of urinary bladder with nine years later renal involvement and absence of systemic lymphoma: A case report(2008) ;Terzic, Tatjana (55916182400) ;Radojevic, Sanja (56581990900) ;Cemerikic-Martinovic, Vesna (6602432953) ;Stevanovic, Radmila (36875127400) ;Citlucanin, Sanja (24478374400) ;Mitrovic, Dragan (7004955837) ;Stojimirovic, Biljana (7004273397)Markovic-Lipkovski, Jasmina (6603725388)Aims: Primary bladder non-Hodgkin lymphoma (PBNHL) is very rare, especially as extranodal B-small lymphocytic lymphoma (B-SLL). Also, late isolated renal manifestation of PBNHL is extremely unusual. We report a very rare type of extranodal B-SLL of bladder wall with extremely unusual late isolated renal involvement, clinically manifested by nephrotic syndrome and incipient renal failure. A case report: A 56-year-old woman was presented with a solitary tumor of bladder wall, with history of dysuria and night sweating. A transvaginal needle biopsy of the tumor was performed, and diagnosis of primary extranodal B-SLL was made in the absence of bone marrow, lymph node, or blood involvement. She was treated with chemotherapy until the achievement of complete remission. Nine years later, she developed nephrotic syndrome. The renal biopsy revealed parenchymal lymphoma's involvement associated with glomerular lesion. Immunohistochemical analysis confirmed the same imunophenotype of lymphoma cells like in bladder wall nine years ago. Restaging procedure showed no evidence of disease elsewhere. Conclusion: To our knowledge, it is the first case of association of very rare primary bladder B-SLL with late isolated renal involvement. © 2007 Humana Press Inc. - Some of the metrics are blocked by yourconsent settings
Publication The red wine polyphenol resveratrol induced relaxation of the isolated renal artery of diabetic rats: The role of potassium channels(2019) ;Gojkovic-Bukarica, Ljiljana (6602830901) ;Markovic-Lipkovski, Jasmina (6603725388) ;Heinle, Helmut (7003342814) ;Cirovic, Sanja (36027425000) ;Rajkovic, Jovana (57194111917) ;Djokic, Vladimir (57194103231) ;Zivanovic, Vladimir (6602108920) ;Bukarica, Ana (57204673993)Novakovic, Radmila (36947545500)The effect of resveratrol on vasculature of diabetic animal is not defined. This study was aimed at evaluating how alloxan-induced diabetes alters the relaxation of the isolated rat renal artery (RA) to resveratrol and determining whether prolong hyperglycemia modifies the expression of potassium (K) channels in the wall of RA. Diabetes reduced the sensitivity to resveratrol in RA. According to K channel blocker affinity, it seems that different subtype of K channels were involved in the resveratrol-induced relaxation of RA of normal rats and only voltage-sensitive Kv1 channels took part in the resveratrol effect on the RA of diabetic rats. Endothelial dysfunction developed during diabetes led to down-regulation of the expression of almost all tested K channels, while up-regulation of Kv1.3 channel expression was only noticeable. Having in mind that Kv1.3 channels have a prominent role in insulin signalling, these results suggest renovascular protective effect of resveratrol in diabetes. © 2018 Elsevier Ltd - Some of the metrics are blocked by yourconsent settings
Publication The red wine polyphenol resveratrol induced relaxation of the isolated renal artery of diabetic rats: The role of potassium channels(2019) ;Gojkovic-Bukarica, Ljiljana (6602830901) ;Markovic-Lipkovski, Jasmina (6603725388) ;Heinle, Helmut (7003342814) ;Cirovic, Sanja (36027425000) ;Rajkovic, Jovana (57194111917) ;Djokic, Vladimir (57194103231) ;Zivanovic, Vladimir (6602108920) ;Bukarica, Ana (57204673993)Novakovic, Radmila (36947545500)The effect of resveratrol on vasculature of diabetic animal is not defined. This study was aimed at evaluating how alloxan-induced diabetes alters the relaxation of the isolated rat renal artery (RA) to resveratrol and determining whether prolong hyperglycemia modifies the expression of potassium (K) channels in the wall of RA. Diabetes reduced the sensitivity to resveratrol in RA. According to K channel blocker affinity, it seems that different subtype of K channels were involved in the resveratrol-induced relaxation of RA of normal rats and only voltage-sensitive Kv1 channels took part in the resveratrol effect on the RA of diabetic rats. Endothelial dysfunction developed during diabetes led to down-regulation of the expression of almost all tested K channels, while up-regulation of Kv1.3 channel expression was only noticeable. Having in mind that Kv1.3 channels have a prominent role in insulin signalling, these results suggest renovascular protective effect of resveratrol in diabetes. © 2018 Elsevier Ltd
