Caglar Kudret, Ozyönüm Hasan, Akalin Minel, Balci Sevim
Pediatric Oncology Unit, Dr. Burhan Nalbantoglu State Hospital, Nicosia, North Cyprus.
Turk J Pediatr. 2006 Oct-Dec;48(4):365-8.
Desmoid tumor (aggressive fibromatosis), as a member of a group of borderline neoplasms, is a rare tumor of fibroblastic origin that remains difficult to treat. Treatments with surgery, radiotherapy and different medical protocols including interferon (IFN)-alpha, hormonal agents such as tamoxifen (anti-estrogen) as well as non-steroidal anti-inflammatory drugs and low-dose antineoplastic agents have been reported. In this report we describe a new patient with multifocal aggressive fibromatosis who was successfully treated with low-dose chemotherapy consisting of methotrexate and vinblastine.
硬纤维瘤(侵袭性纤维瘤病)作为一组交界性肿瘤的成员,是一种起源于成纤维细胞的罕见肿瘤,治疗仍然困难。已有报道采用手术、放疗以及不同的医学方案进行治疗,包括α干扰素、他莫昔芬(抗雌激素)等激素药物、非甾体抗炎药以及低剂量抗肿瘤药物。在本报告中,我们描述了一名患有多灶性侵袭性纤维瘤病的新患者,他通过甲氨蝶呤和长春碱组成的低剂量化疗成功治愈。