Department of Medical Oncology, Institut Paoli-Calmettes, 13009 Marseille, France.
BMC Cancer. 2010 Nov 24;10:645. doi: 10.1186/1471-2407-10-645.
Low-grade extraskeletal osteosarcomas (ESOS) are extremely rare.
We present the first case of low-grade ESOS of the chest wall, which occurred in a 30-year-old man. Because of initial misdiagnosis and patient's refusal of surgery, the diagnosis was done after a 4-year history of a slowly growing mass in soft tissues, leading to a huge (30-cm diameter) calcified mass locally extended over the left chest wall. Final diagnosis was helped by molecular analysis of MDM2 and CDK4 oncogenes. Unfortunately, at this time, no surgical treatment was possible due to loco-regional extension, and despite chemotherapy, the patient died one year after diagnosis, five years after the first symptoms.
We describe the clinical, radiological and bio-pathological features of this unique case, and review the literature concerning low-grade ESOS. Our case highlights the diagnostic difficulties for such very rare tumours and the interest of molecular analysis in ambiguous cases.
低度骨外骨肉瘤(ESOS)极为罕见。
我们报告首例发生于胸壁的低度 ESOS,患者为 30 岁男性。由于最初误诊及患者拒绝手术,在经历了 4 年缓慢生长的软组织肿块病史后,才明确诊断,导致局部广泛延伸的巨大(直径 30 厘米)钙化肿块。通过 MDM2 和 CDK4 癌基因的分子分析有助于明确诊断。不幸的是,此时由于局部区域的扩展,无法进行手术治疗,尽管进行了化疗,但患者在诊断后 1 年,即首次出现症状后 5 年死亡。
我们描述了这例独特病例的临床、放射学和生物病理学特征,并回顾了关于低度 ESOS 的文献。我们的病例强调了此类非常罕见肿瘤的诊断困难,以及在疑难病例中进行分子分析的重要性。