Çiftdemir Mert, Ünyilmaz Cihan, Ustabaşioğlu Fethi Emre, Usta Ufuk
Department of Orthopedics and Traumatology, Trakya University Faculty of Medicine, Edirne, Türkiye.
Department of Orthopedics and Traumatology, Orthopedic Resident, Trakya University Faculty of Medicine, Edirne, Türkiye.
Acta Orthop Traumatol Turc. 2025 May 28;59(3):179-184. doi: 10.5152/j.aott.2025.24076.
Giant cell-rich osteosarcoma (GCRO) is a rare variant of osteosarcoma with unusual radiological and histopathological features that make its diagnosis challenging. The most critical and unusual feature of GCRO is that it has a purely osteolytic appearance. Therefore, GCRO cases are frequently subject to delayed diagnosis or incorrect treatment owing to misdiagnosis. This negatively affects the prognosis of these patients. In this study, 3 young adult cases are presented. The first case describes a young female patient who underwent repeated curettages due to a misdiagnosis of a giant-cell bone tumor, and the second case describes a delay in diagnosis in a young male patient who was misdiagnosed with an aneurysmal bone cyst. The final case report describes a young woman who was diagnosed early, treated promptly, and had a good prognosis. One of the poor prognosis cases in this report was treated with amputation, and the other was alive with multiple metastases. Misdiagnosis or delayed diagnosis leads to a poor prognosis in such cases. To make a diagnosis, it is necessary to have knowledge and to be suspicious of the radiological features of this rare variant. Giant cell-rich osteosarcoma should be among the differential diagnosis options when dealing with pure metaphysiodiaphyseal osteolytic bone lesions in young adults. To avoid misdiagnosis or delay, it is necessary to have knowledge and to be suspicious of this rare variant. Level of Evidence: Level IV, Therapeutic study.
富含巨细胞的骨肉瘤(GCRO)是骨肉瘤的一种罕见变体,具有不寻常的放射学和组织病理学特征,这使得其诊断具有挑战性。GCRO最关键和不寻常的特征是它具有纯粹的溶骨性表现。因此,GCRO病例由于误诊经常会出现诊断延迟或治疗不当的情况。这对这些患者的预后产生负面影响。在本研究中,展示了3例年轻成人病例。第一例描述了一名年轻女性患者,因被误诊为巨细胞骨肿瘤而接受了多次刮除术,第二例描述了一名年轻男性患者被误诊为骨囊肿而导致诊断延迟。最后一例病例报告描述了一名年轻女性,早期被诊断,及时接受治疗,预后良好。本报告中预后较差的病例之一接受了截肢治疗,另一例有多处转移但仍存活。在这类病例中,误诊或诊断延迟会导致预后不良。为了做出诊断,有必要了解并怀疑这种罕见变体的放射学特征。在处理年轻成人单纯干骺端溶骨性骨病变时,富含巨细胞的骨肉瘤应作为鉴别诊断选项之一。为避免误诊或诊断延迟,有必要了解并怀疑这种罕见变体。证据级别:四级,治疗性研究。