Abstract
INTRODUCTION AND IMPORTANCE: Telangiectatic osteosarcoma (TOS) is a rare and aggressive subtype of osteosarcoma that is often misdiagnosed as more benign lesions, such as aneurysmal bone cysts (ABCs) or giant cell tumors (GCTs). The accurate differentiation between these conditions is crucial to ensure timely and appropriate treatment, as misdiagnosis can lead to delayed management and poor prognoses. CASE PRESENTATION: We present the case of a 12-year-old girl who initially presented with left hip and proximal thigh pain, with imaging studies suggesting an ABC. Following curettage and grafting, the initial pathology report confirmed the diagnosis of ABC. However, the patient experienced rapid recurrence within two months, leading to further surgical intervention. A thorough re-evaluation of the pathological specimen revealed characteristics consistent with TOS, confirmed by immunohistochemical staining and molecular tests. The patient received four cycles of chemotherapy after the second surgery and underwent limb - salvage surgery 3 months after the operation. CLINICAL DISCUSSION: This case highlights the challenges in diagnosing TOS due to its histological similarity to other giant cell-rich lesions. The initial misdiagnosis delayed the commencement of appropriate treatment. However, upon correct identification, the patient was treated with an effective chemotherapy regimen, including cisplatin, doxorubicin, and ifosfamide, resulting in significant tumor regression and control of lung metastases. CONCLUSION: This case underscores the necessity for clinicians to maintain a high index of suspicion for TOS when evaluating aggressive bone lesions, particularly in pediatric patients. The importance of comprehensive pathological assessment, including immunohistochemistry and molecular analysis, cannot be overstated, as early and accurate diagnosis significantly influences treatment outcomes and prognosis.