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Wyszukujesz frazę "Sajdak, Piotr" wg kryterium: Autor


Wyświetlanie 1-2 z 2
Tytuł:
Anomalous origin of the left vertebral artery from the arch of the aorta
Autorzy:
Jasiewicz, Maria
Sajdak, Piotr
Sopel, Aleksandra
Strzępek, Kamil
Ziajor, Seweryn
Pliszka, Anna
Balawender, Krzysztof
Powiązania:
https://bibliotekanauki.pl/articles/2040185.pdf
Data publikacji:
2021-09-30
Wydawca:
Uniwersytet Rzeszowski. Wydawnictwo Uniwersytetu Rzeszowskiego
Tematy:
anatomy
dissection
vertebral artery
Opis:
Introduction. Although there are lots of varieties of aorta arch, they seem to appear relatively rarely. Anomalies of aortic arch departures are mainly concerned with its location, course, the place of departure and number of its main branches. However, they warrant attention due to their importance in operative, diagnostic, and endovascular procedures. Aim. We want to present here a case of a female cadaver with rare aortic arch origin of the left vertebral artery. The aim of this article is to complete the frame of anomalies in aortic arch and to explore rare variability shown in this specific case. Description of the case. The present report describes an anomalous case of the left vertebral artery arising from the aortic arch between the left common carotid artery and the left subclavian artery in a female cadaver during dissection in an anatomical laboratory. Aortic origin of the vertebral artery is a rare anatomic variant. Conclusion. Thorough knowledge of anomalous origin is important for patients who undergo operation of an aortic arch or inferior part of the neck. Normally, the vertebral artery arises from the first part of the subclavian artery on both sides.
Źródło:
European Journal of Clinical and Experimental Medicine; 2021, 3; 277-279
2544-2406
2544-1361
Pojawia się w:
European Journal of Clinical and Experimental Medicine
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Unmasking the nature of granulomatosis with polyangiitis – a diagnostic odyssey revealed through a compelling case report
Autorzy:
Sajdak, Piotr
Krużel, Aleksandra
Stodolak, Marcel
Bednarski, Artur
Ziajor, Seweryn
Turski, Mikołaj
Żurowska, Klaudia
Kłos, Kamil
Tomasik, Justyna
Dębik, Marika
Szydłowski, Łukasz
Powiązania:
https://bibliotekanauki.pl/articles/40614541.pdf
Data publikacji:
2024-06-30
Wydawca:
Uniwersytet Rzeszowski. Wydawnictwo Uniwersytetu Rzeszowskiego
Tematy:
autoimmune diseases
granulomatosis with polyangiitis
vasculitis
Opis:
Introduction and aim. Granulomatosis with polyangiitis (GPA), formerly known as Wegener’s granulomatosis, presents a formidable challenge in the realm of autoimmune diseases. Granulomatosis, characterized by vasculitis and granuloma formation, exhibits diverse clinical manifestations. The rarity of GPA is evident, with an estimated incidence between 0.4 and 11.9 cases per 1 million person-years. The aim of this report is to show the complex diagnostic challenges inherent in GPA, demonstrating the diagnostic process from initial symptoms. Description of the case. This case report unfolds the diagnostic journey of a 52-year-old Caucasian male. The presented case, initially suspected as a respiratory infection, led to a comprehensive investigation owing to persistent symptoms, abnormal blood counts, and elevated inflammatory markers. This narrative aims to depict the patient’s diagnostic journey. Key diagnostic tools include ANCA testing, imaging studies, and tissue biopsy. Pulmonary nodules, lymphangitic changes, and renal involvement culminating in a GPA diagnosis confirmed by positive ANCA and anti-PR3 antibodies. The successful management of this case involved a tailored therapeutic regimen, including cyclophosphamide and methylprednisolone, addressing both vasculitic and renal components. Conclusion. This case contributes to the understanding of atypical presentations of GPA, emphasizing the importance of a holistic and dynamic diagnostic approach.
Źródło:
European Journal of Clinical and Experimental Medicine; 2024, 22, 2; 462-468
2544-2406
2544-1361
Pojawia się w:
European Journal of Clinical and Experimental Medicine
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-2 z 2

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