Babin-Boilletot A, Flamant F, Terrier-Lacombe M J, Marsden H B, van Unnik A, Deméocq F, Zucker J M, Voûte P A, Otten J, Behar C
Service d'Onco-Hematologie, Centre Hospitalier Régional, Strasbourg, France.
Med Pediatr Oncol. 1993;21(9):634-9. doi: 10.1002/mpo.2950210905.
Primary intrahepatic malignant nonepithelial tumors are very rare in children and account for 2% of all malignant mesenchymatous tumors under the age of 15 years. Clinical presentation, radiologic features, and histologic types are not unequivocal. The predominant role of surgery takes place either initially in small localized tumors or later, after initial reductive chemotherapy. In all cases, complete resection is the necessary but not sufficient condition for cure. Additional radiotherapy seems ineffective. High-dose chemotherapy and/or liver transplantation can be proposed for resistant cases. The disease-free survival rate is 37% at 2 years for the whole series.
原发性肝内恶性非上皮性肿瘤在儿童中非常罕见,占15岁以下所有恶性间叶性肿瘤的2%。临床表现、放射学特征和组织学类型并不明确。手术的主要作用要么在最初用于小的局限性肿瘤,要么在初始的减瘤化疗后用于后期。在所有病例中,完整切除是治愈的必要但不充分条件。额外的放疗似乎无效。对于耐药病例,可以考虑高剂量化疗和/或肝移植。整个系列的2年无病生存率为37%。