恶性腹膜间皮瘤的细胞减少手术加腹腔内高温化疗。

Aaron U Blackham, Edward A Levine
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引用次数: 0

摘要

恶性腹膜间皮瘤(MPM)是一种罕见的侵袭性肿瘤,对传统的抗癌疗法有很大的耐药性。多年来,它一直被认为是一种绝症,一旦确诊,尽管进行了积极的治疗,患者通常存活不到一年。虽然罕见,但世界范围内MPM的发病率继续上升,部分原因是其与石棉接触有关。患者通常表现为腹胀和疼痛等非特异性症状,使诊断具有挑战性。近年来,在世界各地的多个中心,积极的细胞减少手术加上热腹腔化疗(HIPEC)提高了MPM患者的生存率。这篇综述文章简要介绍了MPM的表现、诊断和自然史。然后,我们探讨可用的治疗方案,主要侧重于细胞减少手术和腹腔内高温化疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytoreductive Surgery with Hyperthermic Intraperitoneal Chemotherapy for Malignant Peritoneal Mesothelioma.

Malignant peritoneal mesothelioma (MPM) is a rare and aggressive neoplasm that is largely resistant to traditional anti-cancer therapies. For years it has been considered a terminal condition and once diagnosed, patients generally survived less than a year despite aggressive treatment. Although rare, the worldwide incidence of MPM continues to rise, in part due to its association with asbestos exposure. Patients usually present with non-specific symptoms of abdominal distension and pain making the diagnosis challenging. In recent years, aggressive cytoreductive surgery with the administration of hyperthermic intraperitoneal chemotherapy (HIPEC) has improved survival in patients with MPM treated at multiple centers worldwide. This review article briefly highlights the presentation, diagnosis, and natural history of MPM. We then explore the available treatment options with primary focus on cytoreductive surgery and hyperthermic intraperitoneal chemotherapy.

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