Pancreatic cancer tumor, Pancreatic cancer


Utilizat ca marker tumoral CA 50 nu are specificitate de organ, fiind constatate valori crescute in diferite tumori maligne, in special gastrointestinale.

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Spre deosebire de Pancreatic cancer tumorvalori crescute de CA 50 pot fi intalnite si in tumorile maligne ale pacientilor Lewis negativi a caror celule nu pot sintetiza CA 1,4. Valori crescute ale CA 50 au fost intalnite si in carcinoamele endometriale2. Pregatire pacient­ — à jeun pe nemancate sau postprandial3.

  • Cancerul peritoneal
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Specimen recoltat — sange venos3. Prelucrare necesara dupa recoltare — se separa serul prin centrifugare in maxim 45 minute de la recoltare folosindu-se pentru separare o eprubeta de plastic; se lucreaza serul proaspat; daca acest lucru nu este posibil, serul se pastreaza la °C, la °C sau la °C3.

Cancerul pancreatic

Volum proba — minim 1 mL ser3. Stabilitate proba — serul separat este stabil 7 zile la temperatura camerei,  14 zile °C; doua luni la °C 1,2.

pancreatic cancer tumor

Metoda — LIA metoda imunochimica cu detectie prin luminescenta 3. Limite si interferente Valori moderat crescute de CA 50 au fost constatate si in afectiuni hepatobiliare benigne1;2. Bibliografie 1. In Journal of the Medical Association pancreatic cancer tumor Thailand.

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In Scandinavian Journal of Gastroenterology Laborator Synevo. Referintele specifice tehnologiei de lucru utilizate.

CT protocol included no enhanced CT and pancreatic phase of the superior abdomen, portal venous phase of the abdomen and pelvis. Results and discussion: The study patients were stratified into 5 age groups and the most frequently affected by pancreatic cancer were the patients aged 60 to 79 years. For T staging the extension in the per pancreatic fat tissue, into surrounding organs 5 patients had extension in other organs and vessels was evaluated. We determined the degree of contact between the tumor and the artery, thrombosis and deformity of the veins and we have pancreatic cancer tumor 8 resettable lesions, 28 tumors in stage T3 and 13 pancreatic cancers in stage T4. Thirty-three patients had lymphadenopathies and 31 of them had distant metastases.

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