Low grade central osteosarcoma dedifferentiating into a high grade leiomyosarcoma in a young adult

L. D. Silva, S. Wijetunge, S. Hameed
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引用次数: 1

Abstract

An 18 –year-old male patient presented with left knee joint pain of seven month duration. The initial MRI scan was suggestive of an infective process, while the subsequent scan revealed radiological features suggestive of an osteosarcoma in the left distal femur. The biopsy was reported as an osteosarcoma in a different institution. Following neoadjuvant chemotherapy wide local excision of the tumour was performed.  On histologic evaluation, a low grade central osteosarcoma was diagnosed with progression to high grade leiomyosarcoma. Low grade central osteosarcoma is an uncommon bone forming tumour which occasionally dedifferentiate into a highgrade sarcoma, most commonly to conventional osteosarcoma. The young age of the patient and dedifferntiation into a leiomyosarcoma are unusual features encountered in this case. Furthermore, we discuss the challenges encountered in diagnosing a low grade central osteosarcoma which has deceptively benign features radiologically and histologically.
年轻成人低级别中枢性骨肉瘤向高级别平滑肌肉瘤去分化
一名18岁男性患者表现为左膝关节疼痛7个月。最初的MRI扫描提示感染过程,而随后的扫描显示放射学特征提示左侧股骨远端骨肉瘤。活检报告为骨肉瘤在不同的机构。新辅助化疗后,行肿瘤局部广泛切除。在组织学评估中,低级别中央骨肉瘤被诊断为进展为高级别平滑肌肉瘤。低级别中枢性骨肉瘤是一种罕见的骨形成肿瘤,偶尔会退分化为高级别肉瘤,最常见的是常规骨肉瘤。患者年龄小且向平滑肌肉瘤的去分化是本病例不常见的特征。此外,我们还讨论了在诊断低级别中枢性骨肉瘤时遇到的挑战,这种肉瘤在放射学和组织学上具有欺骗性的良性特征。
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