Division of Orthopaedic Oncology, Kyushu Cancer Center, 3-1-1, Notame, Minami-ku, Fukuoka, 811-1395, Japan.
Department of Anatomic Pathology, Pathological Sciences, Graduate School of Medical Sciences, Kyushu University, 3-1-1, Maidashi, Higashi-ku, Fukuoka, 815-8582, Japan.
Pathol Res Pract. 2020 Apr;216(4):152832. doi: 10.1016/j.prp.2020.152832. Epub 2020 Jan 20.
Low-grade central osteosarcoma (LG-COS) is an uncommon variant of osteosarcoma (OS) that sometimes progresses to high-grade OS post-recurrence. We herein present a case of dedifferentiated LG-COS with extensive cystic change arising in the right iliac bone of a 26-year-old man. The LG-COS was initially diagnosed and managed as a simple bone cyst. The lesion recurred thrice, and high-grade OS was diagnosed during the third recurrence. The first lesion appeared as a typical benign cystic mass on radiography. However, a huge malignant osteoblastic mass subsequently developed in the right pelvis at the third recurrence. Extended hemipelvectomy with ipsilateral hemisacral resection was performed. Histologic analysis showed tumor necrosis and irregular neoplastic tumor osteoid, while immunohistochemistry revealed that the tumor was diffusely positive for MDM2 and CDK4. The histologic diagnosis was high-grade OS dedifferentiated from a preceding cystic lesion. Our final diagnosis of the primary lesion was LG-COS with extensive cystic change.
低度中央性骨肉瘤(LG-COS)是一种少见的骨肉瘤(OS)变异型,有时在复发后进展为高级别 OS。本文报告了一例 26 岁男性右髂骨发生的去分化 LG-COS 伴广泛囊性变。LG-COS 最初被诊断和治疗为单纯性骨囊肿。该病变复发了 3 次,第 3 次复发时诊断为高级别 OS。第一次病变在影像学上表现为典型的良性囊性肿块。然而,在第 3 次复发时,右侧骨盆随后出现了巨大的恶性成骨样肿块。行半骨盆切除术和同侧半骶骨切除术。组织学分析显示肿瘤坏死和不规则的肿瘤性成骨样组织,免疫组化显示肿瘤弥漫性表达 MDM2 和 CDK4。组织学诊断为从先前囊性病变分化而来的高级别 OS。我们对原发性病变的最终诊断是伴有广泛囊性变的低度中央性骨肉瘤。