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    Wyświetlanie 1-4 z 4
    Tytuł:
    Calcifying Fibrous Tumor of the Small Bowel Mesentery in a 27-Year Old Male Patient - Case Report
    Autorzy:
    Wesecki, Mariusz
    Radziuk, DaGmara
    Niemiec, Szymon
    Waniczek, Dariusz
    Lorenc, Zbigniew
    Powiązania:
    https://bibliotekanauki.pl/articles/1395834.pdf
    Data publikacji:
    2014-12-18
    Wydawca:
    Index Copernicus International
    Tematy:
    small bowel mesentery tumor
    CFT
    Opis:
    Calcifying fibrous tumor is a rare disease entity, usually concerning the soft tissues of the limbs, neck, trunk, or scrotum. Cases of the above-mentioned pathology have also been reported considering the pleural and peritoneal cavity, and small bowel mesentery. The essence of the disease, whose etiology and pathogenesis remains unclear, is the fibrous tissue infiltration and diffuse inflammation with focal calcifications. The study presented a case of a 27-year old male patient subjected to surgical intervention, due to an abdominal cavity tumor. The tumor was radically removed, and its character and definitive diagnosis were established postoperatively. After a seven-year follow-up period, recurrence was not observed.
    Źródło:
    Polish Journal of Surgery; 2014, 86, 9; 436-439
    0032-373X
    2299-2847
    Pojawia się w:
    Polish Journal of Surgery
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Primary Duodenal Carcinoma - Case Report
    Autorzy:
    Wesecki, Mariusz
    Niemiec, Szymon
    Radziuk, Dagmara
    Waniczek, Dariusz
    Lorenc, Zbigniew
    Powiązania:
    https://bibliotekanauki.pl/articles/1395990.pdf
    Data publikacji:
    2015-02-03
    Wydawca:
    Index Copernicus International
    Tematy:
    duodenal carcinoma
    weight loss
    chronic bleeding from the upper gastrointestinal tract
    Opis:
    Duodenal carcinoma is a rare tumor of the gastrointestinal tract of an insidious and secretive course, often diagnosed during the advanced stage of the disease. The study presented a case of a female patient diagnosed with duodenal carcinoma, subjected to two-staged surgery. The initial surgical intervention consisted in the implementation of a gastrointestinal anastomosis, followed by radical surgery by means of Whipple's method performed after three years.
    Źródło:
    Polish Journal of Surgery; 2014, 86, 11; 540-543
    0032-373X
    2299-2847
    Pojawia się w:
    Polish Journal of Surgery
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Carrier-state of D allele in ACE gene insertion/deletion polymorphism is associated with coronary artery disease, in contrast to the C677→T transition in the MTHFR gene.
    Autorzy:
    Żak, Iwona
    Niemiec, Paweł
    Sarecka, Beata
    Balcerzyk, Anna
    Ciemniewski, Zbigniew
    Rudowska, Ewa
    Dyląg, Stanisław
    Powiązania:
    https://bibliotekanauki.pl/articles/1043632.pdf
    Data publikacji:
    2003
    Wydawca:
    Polskie Towarzystwo Biochemiczne
    Tematy:
    angiotensin converting enzyme gene (ACE)
    coronary artery disease
    methylenetetrahydrofolate reductase gene (MTHFR)
    polymorphisms
    Opis:
    Angiotensin I-converting enzyme (ACE), which plays an important role in blood pressure regulation, and methylenetetrahydrofolate reductase (MTHFR) involved in homocysteine metabolism belong to a large group of polypeptides which may be potential risk factors for atherosclerosis and coronary artery disease (CAD). To assess whether polymorphisms of the genes encoding these peptides are associated with CAD in Silesian we conducted a study among 68 individuals suffering from CAD (including 52 cases after myocardial infarction), 51 subjects with positive family history of CAD and 111 controls. We analysed the distribution of genotypes and allele frequencies of the insertion/deletion (I/D) polymorphism in the ACE gene using PCR amplification, and the C677→T polymorphism in the MTHFR gene using PCR-RFLP analysis. We found that D allele frequency was significantly higher in CAD patients (61%) than in controls (43%) (P = 0.001, OR = 2.06). The D allele carriers (DD + ID genotypes) were more frequent in the CAD patients (85%) compared to control group (65%) (P = 0.003, OR = 3.14), whereas the familial CAD risk group shows the highest frequency of the ID genotype (57% vs 43% in controls). In contrast, the MTHFR polymorphism does not seem to be associated with the disease. Our data indicate that in Silesian CAD patients the disease is strongly associated with carrier-state of the ACE D allele, but not with the C677→T transition in the MTHFR gene.
    Źródło:
    Acta Biochimica Polonica; 2003, 50, 2; 527-534
    0001-527X
    Pojawia się w:
    Acta Biochimica Polonica
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
      Wyświetlanie 1-4 z 4

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