A 55-year-old woman presented with pain in the left groin region.
An expansile geographic lytic lesion with a narrow zone of transition and cortical thinning was found involving the left acetabulum.
On MR images, the lesion showed predominantly low signal intensity at the T1 and T2-weighted images. No cystic component nor fluid-fluid levels were noted. Solid enhancement was seen after Gadolinium-Based Contrast Media administration.
Giant cell tumour of bone (CGTB) is a relatively rare, usually benign, bone tumour, that can be locally aggressive and even metastasize to the lungs. They are typically solitary [1].
The vast majority of lesions occur after physeal closure and are typically seen in young adults, between 20 and 50 years of age [1].
Most of the tumours develop at the end of the long bones but may also occur in flat bones and apophysis [2].
Pelvic location is relatively rare, with the acetabulum appearing the commonest site [3].
CGTB consists of numerous multinucleated osteoclastic giant cells uniformly distributed amongst a proliferation of mononuclear stromal cells that express RANKL, which appears to be play an important role in the pathogenesis of these lesions. Tumours often contain haemorrhagic areas [2].
The typical imaging appearance is a geographic lytic lesion with a well-defined margin without surrounding sclerosis, often with mild bone expansion. The lesion typically abuts the articular surface. More aggressive features such as broader zone of transition, cortical thinning, cortical break-through and soft-tissue mass can also be present. There is no matrix calcification [1].
The degree of aggressiveness by imaging does not correlate with histology and does not appear to predict well either the risk of local recurrence or the development of lung metastases.
On T2-weighted images areas of low signal intensity are typically seen due to large amounts of haemosiderin, fibrosis or high cellularity [1].
Fluid-fluid levels might be seen due to secondary aneurysmal bone cyst (ABC) component, which has been reported in 14% of cases [4].
The presence of enhancing solid components helps differentiate CGTB with secondary ABC from primary ABC [1].
Surgery is the treatment of choice for resectable tumours. In general, intralesional curettage is usually recommended. Combination of curettage with bone cement (polymethylmethacrylate, PMMA) increases local control [5, 6].
In conclusion, GCTB shoud be considered in the differential diagnosis of pelvic bone lytic lesions, particularly when meeting the aforementioned epidemiologic and imaging features.
Pelvic bone giant cell tumour
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1. X-ray (Pelvic AP View): A relatively well-defined, lytic “geographic” lesion is observed in the left acetabulum (iliac bone). There is only slight expansion, with no obvious sclerotic rim, and no notable calcification or intraosseous formation.
2. CT (Coronal View): A large, low-density bone defect is seen in the left acetabular region. The lesion has a well-defined contour, locally thinned cortical bone, and mildly compressed adjacent soft tissue. There may be a slight protrusion of soft tissue component, but no obvious calcification.
3. MRI: On T1-weighted images, the lesion appears as medium to slightly low signal intensity in the left acetabulum. On T2-weighted images, parts of the lesion show low signal intensity, suggesting possible hemorrhage, hemosiderin, or fibrous content. A small amount of fluid-fluid levels is visible, suggesting changes similar to aneurysmal bone cyst (ABC) internally.
4. Post-contrast enhancement shows marked enhancement in the solid portion of the lesion, consistent with a lesion predominantly composed of mononuclear stromal cells mixed with vascularized or cystic areas. No significant evidence of distant metastasis is identified.
1. Giant Cell Tumor of Bone (GCTB):
2. Aneurysmal Bone Cyst (ABC):
3. Metastatic Lesions, Osteosarcoma, or Other Malignant Bone Tumors:
Considering the imaging and clinical features in this case, a giant cell tumor of bone (GCTB) is the most likely.
Based on the patient’s age (55), the presence of a lytic lesion in the left acetabulum, lesion morphology, and the findings on contrast-enhanced MRI, the most probable diagnosis is: Giant Cell Tumor of Bone (GCTB).
If uncertainties remain, a biopsy is recommended to confirm the pathological diagnosis and rule out other malignancies.
Treatment Plan:
Rehabilitation and Exercise Prescription:
Postoperative rehabilitation should follow a gradual progression (FITT-VP principle) and be individualized:
If the patient presents with fragile bones or other comorbidities, training intensity and pace should be adjusted under guidance from specialists and rehabilitation therapists. Regular monitoring of bone healing and soft tissue status is recommended to assess risks in a timely manner.
Disclaimer:
This report is based solely on the provided imaging and brief clinical information, serving as a reference for analysis. It cannot replace in-person consultations or professional medical advice. Final diagnosis and treatment should be determined by integrating the patient’s complete medical history, pathological examination, and specialty assessments.
Pelvic bone giant cell tumour