Browsing by Author "Menković, Nemanja (57113304600)"
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Publication Acute renal failure and hepatocellular damage as presenting symptoms of type ii aortic dissection(2016) ;Jovanović, Ivana (57223117334) ;Tešić, Milorad (36197477200) ;Antonijević, Nebojša (6602303948) ;Menković, Nemanja (57113304600) ;Paunović, Ivana (57197090935) ;Ristić, Arsen (7003835406) ;Vučićević, Vera (55550927000)Vujisić-Tešić, Bosiljka (6508177183)Introduction Pericardial effusion can be a consequence of a number of pathological conditions, and as such it can cause impaired left ventricular filling followed by decreased cardiac output and blood pressure. This kind of hemodynamic compromise and its consequences are extremely uncommon unless pericardial effusion causes tamponade. Case Outline We describe a very rare case of a 30-year old male patient, with an acute aortic dissection type II causing pericardial effusion without clinical nor echocardiographic signs of tamponade, while presenting with an acute renal and hepatic failure. After initial diagnostic uncertainties, and following final diagnosis of an acute aortic dissection, this patient underwent surgical aortic valve replacement with a satisfactory outcome. Conclusion It is important to underscore the significance of clinical situation of simultaneously existing acute renal and hepatic failures in the setting of a “non-tamponade” pericardial effusion, following a type II aortic dissection. Although most commonly aortic dissection presents itself with typical clinical symptoms or patient history data, it is not that unusual for it to be hidden in an entirely atypical clinical milieu as the one described in this case. © 2016. Srpski Arhiv za Celokupno Lekarstvo. All right reserved. - Some of the metrics are blocked by yourconsent settings
Publication Intramural haematoma and Penetrating aortic ulcer - outcome and treatment modalities: Report of four cases(2011) ;Končar, Igor (19337386500) ;Davidović, Lazar (7006821504) ;Čolić, Momčilo (7005003692) ;Dragaš, Marko (25027673300) ;Ilić, Nikola (7006245465) ;Menković, Nemanja (57113304600) ;Vučković, Maja (36790427100) ;Kalimanovska-Oštrić, Dimitra (6603414966) ;Cvetković, Slobodan (7006158672)Kostić, Dušan (7007037165)Introduction Intramural haematoma (IMH) and penetrating aortic ulcers (PAU) are the frequent cause of acute aortic syndrome that is disclosed with a rising frequency due to the development of new diagnostic methods. Different symptoms contribute to clinical misdiagnosis, while changeable locations and unpersuasive diameter can lead the radiologists to underestimate such changes. The outcome of PAU and IMH differs, and for the time being there are no data on prognostic factors. The diversity of symptoms and disease course is presented in four cases with different manifestations, treatment and outcome. Outline of Cases Two patients with IMH were treated conservatively due to the process extensiveness and its morphology. One patient had a complete restitution, while the other had progression of the disease. Other two patients with PAU were treated by surgery (stent graft implantation) according to the morphology and diameter of the aorta. Conclusion IMH and PAU should be suspected in patients with unclear clinical presentation (back and abdominal pains). Although outcome and complications of these diseases are well known, their incidence has not been fully studied. Endovascular treatment is less invasive and followed by a potentially lower rate of complications. However, usage of this method is justifiable only in patients with associated complications. - Some of the metrics are blocked by yourconsent settings
Publication Primary percutaneous coronary intervention in a patient with right internal mammary artery graft originating from arteria lusoria dextra(2013) ;Aleksandrić, Srdjan (35274271700) ;Stojković, Siniša (6603759580) ;Tomašević, Miloje (57196948758) ;Kostić, Jelena (57159483500) ;Banović, Marko (33467553500) ;Menković, Nemanja (57113304600)Ostojić, Miodrag (34572650500)Introduction Congenital anomalies of the aortic arch, although numerous and heterogeneous, occur in less than 1% of individuals at autopsies. Left aortic arch with an aberrant right subclavian artery, also called arteria lusoria dextra, is the most common anomaly of the aortic arch, occurring in 0.5-2.5% of individuals. Case Outline We report the case of a 48-year-old man suffering from acute inferoposterior-wall ST elevation myocardial infarction successfully treated by primary percutaneous coronary intervention. Ten years ago, the patient had undergone coronary artery bypass graft surgery with the implantation of two arterial grafts - left and right internal mammary arteries on both left anterior descending and right coronary artery. After several attempts to canulate truncus brachiocephalicus, angiogram revealed the left aortic arch with the aberrant right subclavian artery. To our knowledge, this is the first described case of primary percutaneous coronary intervention via the aberrant right subclavian artery and right internal mammary artery graft with stent implantation in the infarct related lesion of the distal segment of right coronary artery. Subsequent 64-multidetector computed tomography confirmed the angiographic findings. Conclusion Early recognition of congenital anomalies of the aortic arch and its great vessels, even before coronary artery bypass graft surgery, could be crucial for the urgent and successful treatment of patients with life-threatening conditions, such as ST segment elevation myocardial infarction.
