Journal of cancer research and clinical oncology · 2025
A clinical report and analysis of metachronous multiple primary cancers occurred in four sites.
Клинический случайСтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Sun Rongze, Xie Hongxia, He Sijia, Li Qi
Аннотация
PURPOSE: This case report describes a rare occurrence of quadruple primary malignancies-specifically, bilateral primary breast cancer, ovarian cancer, and pleomorphic malignant fibrous histiocytoma/undifferentiated high-grade pleomorphic sarcoma-and explores its potential association with hereditary tumor syndromes.
METHODS: We conducted a detailed clinical and histopathological analysis of the case. Repeated imaging and pathological examinations were performed to confirm the diagnosis of each primary malignancy.
RESULTS: The patient was diagnosed with four distinct primary tumors, and pathological evaluation confirmed each malignancy.
CONCLUSION: This case emphasizes the importance of comprehensive pathological and genetic evaluation in patients with multiple primary malignancies. It highlights the growing incidence of such tumors among long-term cancer survivors and provides valuable insights for diagnosis and management in the context of hereditary cancer syndromes.
METHODS: We conducted a detailed clinical and histopathological analysis of the case. Repeated imaging and pathological examinations were performed to confirm the diagnosis of each primary malignancy.
RESULTS: The patient was diagnosed with four distinct primary tumors, and pathological evaluation confirmed each malignancy.
CONCLUSION: This case emphasizes the importance of comprehensive pathological and genetic evaluation in patients with multiple primary malignancies. It highlights the growing incidence of such tumors among long-term cancer survivors and provides valuable insights for diagnosis and management in the context of hereditary cancer syndromes.