MacArthur C J, McGill T J, Healy G B
Children's Hospital, Boston, Massachusetts 02115.
Clin Pediatr (Phila). 1992 Feb;31(2):66-70. doi: 10.1177/000992289203100201.
Rhabdomyosarcoma (RMS), the most common malignant soft-tissue tumor in the pediatric population, occurs most often in the head and neck region. Major advancements in the management of these aggressive tumors have been achieved in the last 20 years on three fronts: chemotherapy, radiation therapy, and surgery. Surgery, with the advent of skull-base, craniofacial, and free-tissue-transfer reconstructive techniques, has once again become part of the primary management of these tumors. Prior to 1960, RMS was uniformly fatal; now, with the introduction of multimodality treatment regimens, two thirds of patients can expect long-term survival.
横纹肌肉瘤(RMS)是儿童群体中最常见的恶性软组织肿瘤,最常发生于头颈部区域。在过去20年里,这些侵袭性肿瘤的治疗在三个方面取得了重大进展:化疗、放疗和手术。随着颅底、颅面及游离组织移植重建技术的出现,手术再次成为这些肿瘤主要治疗手段的一部分。在1960年之前,RMS无一例外都是致命的;如今,随着多模式治疗方案的引入,三分之二的患者有望获得长期生存。