Okur Fatma Visal, Oguz Aynur, Karadeniz Ceyda, Citak Caglar, Bayik Pelin, Boyunaga Oznur
Department of Pediatric Oncology, Gazi University, Ankara, Turkey.
J Pediatr Hematol Oncol. 2006 Mar;28(3):173-6. doi: 10.1097/01.mph.0000201419.05182.29.
We report a 2-year-old boy who had a family history of neurofibromatosis, multiple cafe-au-lait spots on the trunk, tibial pseudarthrosis, and was diagnosed with a malignant triton tumor of the pelvis. To our knowledge our case is one of the youngest patients reported with a malignant triton tumor and the second pediatric case with a pelvic malignant triton tumor.
我们报告了一名2岁男孩，他有神经纤维瘤病家族史，躯干有多个咖啡牛奶斑，患有胫骨假关节，并被诊断为骨盆恶性蝾螈瘤。据我们所知，我们的病例是报告的最年轻的恶性蝾螈瘤患者之一，也是第二例患有骨盆恶性蝾螈瘤的儿科病例。
