Федеральные клинические рекомендации по диагностике и лечению адренокортикального рака

Определение гормональной активности и злокачественного потенциала - актуальнейший вопрос диагностики и выбора лечебной тактики при опухолях надпочечников. Адренокортикальный рак (АКР) - достаточно редкое заболевание, которое характеризуется плохими прогностическими показателями. Встречаемость АКР 0,5-2 случая на миллион населения, в структуре инциденталом надпочечников не более чем в 2-4% наблюдений. Для широкого обсуждения предлагается проект клинических рекомендаций по диагностике и лечению АКР, предназначенного для онкологов, хирургов, эндокринологов, специалистов по лучевой диагностике, патоморфологов и др.

опухоли надпочечника, адренокортикальный рак, рак коры надпочечника, феохромоцитома, параганглиома, гиперкортицизм, митотан

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