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家族性腺瘤性息肉病中硬纤维瘤的全身细胞毒性化疗和放射治疗。

Systemic cytotoxic chemotherapy and radiation therapy for desmoid in familial adenomatous polyposis.

作者信息

Tsukada K, Church J M, Jagelman D G, Fazio V W, Lavery I C

机构信息

Department of Colorectal Surgery, Cleveland Clinic Foundation, Ohio.

出版信息

Dis Colon Rectum. 1991 Dec;34(12):1090-2. doi: 10.1007/BF02050067.

Abstract

Forty-two of 416 familial adenomatous polyposis (FAP) patients in the FAP registry at the Cleveland Clinic had desmoid tumors. The role of cytotoxic chemotherapy and radiation therapy in the management of these patients was investigated. Eight intra-abdominal desmoid tumors were treated by systemic cytotoxic chemotherapy. Two had complete remission, and one had partial remission. Five patients died as a result of the desmoid tumor or late complications of chemotherapy. Three intra-abdominal desmoids were treated by radiation therapy with no response. Neither cytotoxic chemotherapy nor radiation therapy is recommended as a first-choice treatment for intra-abdominal desmoid tumors in patients with FAP.

摘要

克利夫兰诊所FAP登记处的416例家族性腺瘤性息肉病(FAP)患者中,有42例患有硬纤维瘤。研究了细胞毒性化疗和放射治疗在这些患者治疗中的作用。8例腹腔内硬纤维瘤接受了全身细胞毒性化疗。2例完全缓解,1例部分缓解。5例患者死于硬纤维瘤或化疗的晚期并发症。3例腹腔内硬纤维瘤接受放射治疗,无反应。对于FAP患者的腹腔内硬纤维瘤,不建议将细胞毒性化疗和放射治疗作为首选治疗方法。

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