Aleksandra Pavlovic Markovic

Aleksandra Pavlovic Markovic


Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 May 2021 in Digestive Diseases
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AMAleksandra Pavlovic Markovic
Aleksandra Pavlovic Markovic
MLMilica Stojkovic Lalosevic
Milica Stojkovic Lalosevic
DMDragana Mijac
Dragana Mijac
TMTamara Milovanovic
Tamara Milovanovic
SDSanja Dragasevic
Sanja Dragasevic
MKMiodrag N. Krstic
Miodrag N. Krstic
Background: Jaundice is a common clinical finding in clinical practice of hepatologists and general practitioners. It occurs when serum bilirubin levels exceed 3 mg/dL. Summary: In this review, we summarize the pathophysiological mechanism of jaundice, clinical approach to the patient with jaundice, and laboratory and imaging techniques. Clinical presentation of jaundice manifests through yellow skin and sclera coloration. Evaluation of every patient includes detailed medical history and examination. In the laboratory, evaluation of enzymes of hepatic inflammation as well as cholestatic enzymes with serum bilirubin must be included. Additional laboratory analysis and imaging modalities are needed in order to differentiate jaundice etiology. Moreover, imaging is available and needed in further evaluation, and treatment is dependent on the underlying cause. Key Messages: In this review, we will outline the pathophysiological mechanism of jaundice, clinical approach to the patient with jaundice, and diagnostic and treatment approach to these patients.

28 March 2019 in Digestive Diseases
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Journal Article
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AMAleksandra Pavlovic Markovic
Aleksandra Pavlovic Markovic
SDSanja Dragasevic
Sanja Dragasevic
MKMiodrag Krstic
Miodrag Krstic
MLMilica Stojkovic Lalosevic
Milica Stojkovic Lalosevic
Tomica MilosavljevicTomica Milosavljevic
Tomica Milosavljevic
Background: The increasing incidence of duodenal neoplasm has underlined different methods of resection depending on the clinical presentation, endoscopic features and histopathology. In this comprehensive review, we systematically describe the current knowledge concerning the diagnosis and management of duodenal adenomas (DAs) and discuss data considering all possible therapeutic approaches. Summary: Among a variety of duodenal lesions, including neuroendocrine tumors and gastrointestinal stromal tumors, DAs present precancerous lesions of the duodenal papilla or non-ampullary region necessitating removal. DAs can occur sporadically (SDA) as rare lesions or relatively common in polyposis syndromes. The endoscopic resections of DA are associated with an increased degree of complexity due to distinctive anatomical properties of the duodenal wall, luminal diameter and the presence of ampulla with pancreatic and biliary drainage. The endoscopic techniques including cold snare polypectomy (CSP), endoscopic mucosal resection (EMR), and argon plasma coagulation ablation are suggested to be less invasive than surgical treatment, associated with shorter hospital stay and lower cost. According to the current clinical practice, surgery has been accepted as standard therapeutic approach in familial adenomatous polyposis patients with severe polyposis or DA not amenable to endoscopic resection. Key Messages: The strategy for endoscopic resection of DAs depends on the lesion size, morphology, location, and histopathology findings. Small adenomas are most frequently diagnosed and removed by standard CSP techniques, while large laterally spreading lesions and ampullary adenoma are referred for EMR or endoscopic papillectomy respectively. Screening colonoscopy is indicated in patients with SDA. Additional studies for new endoscopic strategies and techniques for curative therapy of DAs are needed to refine future management decisions. Complete resection of DA is considered curative, but nevertheless, long-term endoscopic follow-up is still required to detect and treat any recurrent arising lesions.

28 March 2024 in Medicina
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MLMilica Stojkovic Lalosevic
Milica Stojkovic Lalosevic
VCVesna Coric
Vesna Coric
TPTatjana Pekmezovic
Tatjana Pekmezovic
Tatjana SimicTatjana Simic
Tatjana Simic
AMAleksandra Pavlovic Markovic
Aleksandra Pavlovic Markovic
MPMarija Pljesa-Ercegovac
Marija Pljesa-Ercegovac
Background and Objectives: Despite improvements in screening programs, a large number of patients with colorectal cancer (CRC) are diagnosed in an advanced disease stage. Previous investigations imply that glutathione transferases (GSTs) might be associated with the development and progression of CRC. Moreover, the detoxification mechanism of oxaliplatin, which represents the first line of treatment for advanced CRC, is mediated via certain GSTs. The aim of this study was to evaluate the significance of certain GST genetic variants on CRC prognosis and the efficacy of oxaliplatin-based treatment. Materials and Methods: This prospective study included 523 patients diagnosed with CRC in the period between 2014 and 2016, at the Digestive Surgery Clinic, University Clinical Center of Serbia, Belgrade. Patients were followed for a median of 43.47 ± 17.01 months (minimum 1–63 months). Additionally, 109 patients with advanced disease, after surgical treatment, received FOLFOX6 treatment as a first-line therapy between 2014 and 2020. The Kaplan–Meier method was used to analyze cumulative survival, and the Cox proportional hazard regression model was used to study the effects of different GST genotypes on overall survival. Results: Individuals with the GSTM1-null genotype and the GSTP1 IleVal+ValVal (variant) genotype had significantly shorter survival when compared to referent genotypes (GSTM1-active and GSTP1 IleIle) (log-rank: p = 0.001). Moreover, individuals with the GSTM1-null genotype who received 5-FU-based treatment had statistically significantly shorter survival when compared to individuals with the GSTM1-active genotype (log-rank: p = 0.05). Conclusions: Both GSTM1-null and GSTP1 IleVal+ValVal (variant) genotypes are associated with significantly shorter survival in CRC patients. What is more, the GSTM1-null genotype is associated with shorter survival in patients receiving FOLOFOX6 treatment.

17 December 2007 in Journal of Medical Case Reports
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MSMirjana Sumarac-Dumanovic
Mirjana Sumarac-Dumanovic
DMDragan Micic
Dragan Micic
MKMiodrag Krstic
Miodrag Krstic
MGMaja Georgiev
Maja Georgiev
ADAleksandar Diklic
Aleksandar Diklic
AMAleksandra Pavlovic Markovic
Aleksandra Pavlovic Markovic
Insulinoma is a rare pancreatic endocrine tumour and is typically sporadic and solitary. Over 90% of all insulinomas are benign. Cystic insulinomas are also rare. It is not difficult to determine the site of such neoplasm, as cystic insulinomas are usually 4–10 cm in diameter. We present the case of a patient with a histologically confirmed cystic insulinoma diagnosed after approximately 10 years of hypoglycaemia symptoms. This case is unique because of the small size (2.2 cm) of the tumour. Endoscopic ultrasound (EUS) was useful for localizing this tumour.

23 April 2024 in Diagnostics
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JNJelena Martinov Nestorov
Jelena Martinov Nestorov
ASAleksandra Sokic-Milutinovic
Aleksandra Sokic-Milutinovic
AMAleksandra Pavlovic Markovic
Aleksandra Pavlovic Markovic
MKMiodrag Krstic
Miodrag Krstic
A retrospective study in patients who underwent video capsule endoscopy (VCE) between 2006 and 2016 was conducted in the Clinic for gastroenterology and Hepatology, University Clinical Center of Serbia. A total of 245 patients underwent VCE. In 198 patients the indication was obscure gastrointestinal bleeding (OGIB), with 92 patients having overt and the other 106 occult bleeding. The remaining 47 patients underwent VCE due to suspected small bowel (SB) disease (i.e., Von Hippel–Lindau syndrome, familial adenomatous polyposis, Peutz Jeghers syndrome, Crohn’s disease, prolonged diarrhea, abdominal pain, congenital lymphangiectasia, protein-losing enteropathy, tumors, refractory celiac disease, etc.). VCE identified a source of bleeding in 38.9% of patients (in the obscure overt group in 48.9% of patients, and in the obscure occult group in 30.2% of patients). The most common findings were angiodysplasias, tumors, Meckel’s diverticulum and Crohn’s disease. In the smaller group of patients with an indication other than OGIB, 38.3% of patients had positive VCE findings. The most common indication is OGIB, and the best candidates are patients with overt bleeding; patients with IBD should be evaluated in this setting.

26 December 2025 in Journal of Gastrointestinal and Liver Diseases
Verified
Journal Article
Open access
IPIvana Pantic
Ivana Pantic
Ioannis PapanikolaouIoannis Papanikolaou
Ioannis Papanikolaou
Sofija LugonjaSofija Lugonja
Sofija Lugonja
MLMilica Stojkovic Lalosevic
Milica Stojkovic Lalosevic
AMAleksandra Pavlovic Markovic
Aleksandra Pavlovic Markovic
TMTamara Milovanovic
Tamara Milovanovic
Background and Aims: Despite the reduction of the gender gap in medicine, uneven gender distribution has remained in several medical fields, including gastroenterology. We aimed to evaluate differences in clinical and academic training between male and female gastroenterologists. Methods: We distributed a web-based survey to physicians who have completed their training and are currently working in the field of gastroenterology in five Balkan countries: Serbia, Republic of North Macedonia, Montenegro, Greece and Romania. Results: The questionnaire was sent to 1220 physicians. A total of 229 questionnaires were filled out and 214 were included in the analysis. The overall response rate was 18.8%. Almost half of respondents were women (n=97, 45.3%). The proportion of male physicians having children was higher compared to females, which was of statistical significance (88.0% vs. 64.9%, p<0.05). Women have in general reported beginning endoscopic training as well as mastering endoscopic procedures later in clinical training, when compared to males. On average, males reported higher median time in performing endoscopies per week, as well as higher grades in self-assessment scales in colonoscopy performance. Conclusions: Gender inequity exists during the gastroenterology clinical training. Women are especially vulnerable during the training period because training years coincide with the expected childbearing age and are therefore less likely to have children compared to their male colleagues.