Yeh Shu-Nin, Lu Meng-Yao
Department of Pediatrics, Koo Foundation Sun Yat-Sen Cancer Center, 125 Lih-Der Road, Pei-Tou, Taipei, Taiwan.
Acta Paediatr Taiwan. 2005 Jul-Aug;46(4):230-4.
We describe a rare case of peritoneal metastasis in osteosarcoma. A 14-year-old boy was diagnosed with osteosarcoma of the femur. Although initial treatment with surgical resection and chemotherapy was successful, a large inoperable pulmonary metastasis was detected 27 months after diagnosis of the primary tumor. At 38 months, whilst still receiving salvage chemotherapy, malignant ascites with peritoneal metastasis was detected. The patient died two months later from disease progression. This is probably the 6th case and youngest patient with peritoneal metastasis of osteosarcoma reported in the literature. For early diagnosis, patients with a history of osteosarcoma having persistent abdominal symptoms or signs should be offered a CT scan of the abdomen, and examination of the ascitic fluid when present. With advances in treatments, unusual sites of metastasis may become more prevalent.
我们描述了一例骨肉瘤腹膜转移的罕见病例。一名14岁男孩被诊断为股骨骨肉瘤。尽管最初采用手术切除和化疗的治疗方法取得了成功,但在原发性肿瘤诊断27个月后,发现了一个无法手术切除的巨大肺转移灶。在38个月时,患者仍在接受挽救性化疗,此时检测到伴有腹膜转移的恶性腹水。患者两个月后因疾病进展死亡。这可能是文献报道的第6例骨肉瘤腹膜转移病例,也是最年轻的患者。为了早期诊断,有骨肉瘤病史且持续出现腹部症状或体征的患者应接受腹部CT扫描,并在有腹水时进行腹水检查。随着治疗方法的进步,不常见的转移部位可能会变得更加普遍。