Michal Studniarek

Prof. Dr. Michal Studniarek

orcid

Research Focus & Metrics

Academic Career Length

42Years (1985-Present)

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

Representative Publications

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15 October 2014 in European Radiology
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Journal Article
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JRJonathan Richenberg
Jonathan Richenberg
JBJane Belfield
Jane Belfield
PRParvati Ramchandani
Parvati Ramchandani
LRLaurence Rocher
Laurence Rocher
SFSimon Freeman
Simon Freeman
LDLorenzo E. Derchi
Lorenzo E. Derchi

22 July 2019 in European Radiology
Verified
Journal Article
Closed access
MWMembers Of The Esur-Spiwg Wg
Members Of The Esur-Spiwg Wg
SFSimon Freeman
Simon Freeman
MBMichele Bertolotto
Michele Bertolotto
JRJonathan Richenberg
Jonathan Richenberg
JBJane Belfield
Jane Belfield
LDLorenzo E. Derchi
Lorenzo E. Derchi

11 July 2017 in European Radiology
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Journal Article
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ATAthina C Tsili
Athina C Tsili
MBMichele Bertolotto
Michele Bertolotto
ATAhmet Tuncay Turgut
Ahmet Tuncay Turgut
VDVikram Dogra
Vikram Dogra
SFSimon Freeman
Simon Freeman
JRJonathan Richenberg
Jonathan Richenberg

2 February 2018 in Polish Journal of Radiology
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Journal Article
Open access
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PPPaulina Pałasz
Paulina Pałasz
ŁAŁukasz Adamski
Łukasz Adamski
MGMagdalena Górska-Chrząstek
Magdalena Górska-Chrząstek
Anna StarzyńskaAnna Starzyńska
Anna Starzyńska
MSMichal Studniarek
Michal Studniarek
Oral squamous cell carcinoma (OSCC) is the most common cancer of the oral cavity and constitutes 95% of all cancers of this area. Men are affected twice as commonly as women, primarily if they are over 50 years of age. Forty percent of the lesions are localized in the tongue and 30% in the floor of the oral cavity. OSCC often affects upper and lower gingiva, buccal mucous membrane, the retromolar triangle and the palate. The prognosis is poor and the five-year survival rate ranges from 20% (OSCC in the floor of the mouth) to 60% (OSCC in the alveolar part of the mandible). Treatment is difficult, because of the localization and the invasiveness of the available methods. The diagnosis is made based on a histopathological examination of a biopsy sample. The low detection rate of early oral SCC is a considerable clinical issue. Although the oral cavity can be easily examined, in the majority of cases oral SCC is diagnosed in its late stages. It is difficult to diagnose metastases in local lymph nodes and distant organs, which is important for planning the scope of resection and further treatment, graft implantation, and differentiation between reactive and metastatic lymph nodes as well as between disease recurrence and scars or adverse reactions after surgery or radiation therapy. Imaging studies are performed as part of the routine work-up in oral SCC. However, it is difficult to interpret the results at the early stages of the disease. The following imaging methods are used – dental radiographs, panoramic radiographs, magnetic resonance imaging with diffusion-weighted and dynamic sequences, perfusion computed tomography, cone beam computed tomography, single-photon emission computed tomography, hybrid methods (PET/CT, PET/MRI, SPECT/CT) and ultrasound. Some important clinical problems can be resolved with the use of novel modalities such as MRI with ADC sequences and PET. The aim of this article is to describe oral squamous cell carcinoma as it appears in different imaging methods considering both their advantages and limitations.

1 April 2003 in European Radiology
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Journal Article
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JZJ. Zielonko
J. Zielonko
MSMichal Studniarek
Michal Studniarek
MMM. Markuszewski
M. Markuszewski

19 January 2016 in PLOS ONE
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Open access
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JPJoanna Pienkowska
Joanna Pienkowska
KGKatarzyna Gwoździewicz
Katarzyna Gwoździewicz
Katarzyna SkrobiszKatarzyna Skrobisz
Katarzyna Skrobisz
IMIwona Marek
Iwona Marek
JKJustyna Kostro
Justyna Kostro
MSMichal Studniarek
Michal Studniarek
Severe acute pancreatitis (AP) is still a significant clinical problem which is associated with a highly mortality. The aim of this study was the evaluation of prognostic value of CT regional perfusion measurement performed on the first day of onset of symptoms of AP, in assessing the risk of developing severe form of acute pancreatitis. 79 patients with clinical symptoms and biochemical criteria indicative of acute pancreatitis (acute upper abdominal pain, elevated levels of serum amylase and lipase) underwent perfusion CT within 24 hours after onset of symptoms. The follow-up examinations were performed after 4–6 days to detect progression of the disease. Perfusion parameters were compared in 41 people who developed severe form of AP (pancreatic and/or peripancreatic tissue necrosis) with parameters in 38 consecutive patients in whom course of AP was mild. Blood flow, blood volume, mean transit time and permeability surface area product were calculated in the three anatomic pancreatic subdivisions (head, body and tail). At the same time the patient's clinical status was assessed by APACHE II score and laboratory parameters such as CRP, serum lipase and amylase, AST, ALT, GGT, ALP and bilirubin were compared. Statistical differences in the perfusion parameters between the group of patients with mild and severe AP were shown. Blood flow, blood volume and mean transit time were significantly lower and permeability surface area product was significantly higher in patients who develop severe acute pancreatitis and presence of pancreatic and/or peripancreatic necrosis due to pancreatic ischemia. There were no statistically significant differences between the two groups in terms of evaluated on admission severity of pancreatitis assessed using APACHE II score and laboratory tests. CT perfusion is a very useful indicator for prediction and selection patients in early stages of acute pancreatitis who are at risk of developing pancreatic and/or peripancreatic necrosis already on the first day of the onset of symptoms and can be used for treatment planning and monitoring of therapy of acute pancreatitis. Early suspicion of possible pancreatic necrosis both on the basis of scores based on clinical status and laboratory tests have low predictive value.