Marko Barešić

Dr. Marko Barešić

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Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

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

Representative Publications

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19 December 2022 in Biomedicines
Verified
Journal Article
Open access
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Mislav RadićMislav Radić
Mislav Radić
SNSrđan Novak
Srđan Novak
MBMarko Barešić
Marko Barešić
AHAna Hećimović
Ana Hećimović
DPDijana Perković
Dijana Perković
BABranimir Anić
Branimir Anić
The aim of this study was to develop a Croatian Delphi-based expert consensus for screening interstitial lung disease (ILD) associated with connective tissue disease (CTD). A systematic literature review was conducted on risk factors for the development of ILD, prevalence and incidence of ILD, diagnostic and screening methods for ILD, and prognosis of ILD in idiopathic inflammatory myopathy (IIM), mixed connective tissue disease (MCTD), primary Sjögren’s syndrome (pSS), rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), and systemic sclerosis (SSc) were performed. Based on the evidence found, experts developed questionnaires for screening and monitoring ILD in each CTD, which were provided via an online survey. Following the electronic survey, two screening algorithms were developed based on the consensus opinions. The detection strategy for ILD included high-resolution computed tomography (HRCT) in addition to pulmonary function testing for IIM, MCTD, and SSc. and pulmonary function testing for newly diagnosed pSS, RA and SLE. However, in patients with identified risk factors for ILD HRCT, these tests should also be performed. A screening strategy for early identification of patients with various CTD-ILD was first developed by a multidisciplinary team of rheumatologists, pulmonologists, and radiologists to identify early CTD patients at risk of ILD, a severe extra-articular manifestation of CTD.

1 January 2009 in Internal Medicine
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Journal Article
Open access
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MBMarko Barešić
Marko Barešić
IGIvan Gornik
Ivan Gornik
RRRadovan Radonic
Radovan Radonic
OZOzrenka Zlopaša
Ozrenka Zlopaša
NGNina Gubarev
Nina Gubarev
VGVladimir Gašparovic
Vladimir Gašparovic
Chromic acid is a strong metal acid and acute poisoning is very rare, but very serious with severe skin injury, renal and liver failure. The majority of published cases were suicide attempts with lethal outcomes. We describe the case of a 55-year-old man who had accidentally taken a sip of 20% chromic acid (estimated chromium intake: 2.3 g). Renal and liver failure were not present at presentation, but appeared later in the course of disease. He was treated with hemodialysis, no chelating agents or other methods for enhancing elimination were used. Liver and renal function improved over the next 30 days and the patient was discharged after 45 days of hospitalization with no need for dialysis. In the follow-up period of eight months his renal function remained depressed, but stable.

17 June 2015 in Lupus
Verified
Journal Article
Closed access
MBMarko Barešić
Marko Barešić
KSK B Sreter
K B Sreter
LBL Brčić
L Brčić
AHA Hećimović
A Hećimović
ZJZ Janevski
Z Janevski
BABranimir Anić
Branimir Anić
Localized amyloid deposits (tumoral amyloidosis or amyloidoma) are uncommon form of amyloidosis and nodular pulmonary amyloidomas are rarely found. This incidental finding can mimic a bronchopulmonary neoplasm and may occur secondarily to an infectious, inflammatory or lymphoproliferative disease. We report a case of a 62-year-old female with long-standing systemic lupus erythematosus (SLE) with low compliance who presented with radiologically-verified solitary pulmonary nodule. Work-up included positron emission tomography–computed tomography (PET-CT) scan, which revealed hypermetabolic uptake of 18F-fluorodeoxyglucose, and lobectomy was performed. Staining of the tissue was positive for Congo red and was green birefringent under polarized light. Immunohistochemical methods excluded lymphoproliferative disease and confirmed amyloidoma. SLE was controlled with antimalarials and glucocorticoids. Pulmonary amyloidoma should be considered in the differential diagnosis of solitary lung nodules.

1 July 2023 in Clinical Rheumatology
Verified
Journal Article
Closed access
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MBMarko Barešić
Marko Barešić
SNSrđan Novak
Srđan Novak
DPDijana Perković
Dijana Perković
BKBoris Karanovic
Boris Karanovic
FMFilip Mirić
Filip Mirić
BABranimir Anić
Branimir Anić

30 December 2016 in Rheumatology
Verified
Journal Article
Open access
DBDubravka Bosnić
Dubravka Bosnić
BŽBranimir Žarković
Branimir Žarković
MBMarko Barešić
Marko Barešić
MZMaja Zarkovic
Maja Zarkovic
BABranimir Anić
Branimir Anić
Hidradenitis suppurativa is a chronic inflammatory disorder characterized by occlusion of the follicular pilosebaceous units of the skin. The treatment options are sometimes very limited and unpleasant odor and abundant drainage complicate the disease. Ankylosing spondylitis is a form of seronegative spondyloarthritis with predominantly axial but also peripheral joint involvement. Both of the conditions lower the patient’s quality of life and affect everyday activities. We describe a 39-year-old male patient with both diseases treated with different medications with only a modest result. After the initiation of a tumor necrosis factor α (TNF-α) inhibitor (adalimumab) the patient experienced first the musculoskeletal and later on the skin improvement. The introduction of TNF- inhibitors should be considered early in the treatment of overlapping hidradenitis suppurativa and the spondyloarthritis spectrum of conditions. Available medical data confirm the positive results and beneficial effect on disease course, activity and, most importantly, quality of life.

17 May 2018 in Rheumatology International
Verified
Journal Article
Closed access
PDF file
MBMarko Barešić
Marko Barešić
MRMirna Reihl
Mirna Reihl
Mario HabekMario Habek
Mario Habek
NVNenad Vukojević
Nenad Vukojević
BABranimir Anić
Branimir Anić