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- DOI 10.18231/j.ijos.2023.040
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Giant cell tumor of distal femur with pathological fracture: A case report
Introduction
Giant cell bone tumors are typically benign bone tumors, but they can be locally aggressive and occasionally malignant.[1], [2] Sir Astley Cooper described the first bone giant cell tumor (GCT) in 1818. GCT is most common in skeletally mature individuals, peaking in the 20-40 years of age, with slightly more common in female than males. Patients with open epiphyses account for less than 2% of cases, and patients over the age of 65 accounts for only about 10% of cases.[1], [3], [4] It makes up 20% of benign bone tumors and about 5% of primary bone tumors.[5], [6], [7], [8], [9], [10] GCTB is a benign skeletal tumor, but it is also well-known for its aggressive behavior in the local area and high recurrence rates, which range from 2.3% to 20% after curettage in combination with adjuvant therapy (i.e., additional debridement with a high-speed burr, cryotherapy using liquid nitrogen, chemical debridement with phenol, or bone cementing).[5], [6], [8], [9]
The epiphysial-metaphyseal region of the long bones is the most common location for GCTB (70–90%); the majority of this lesion extends within 1 cm of the subarticular region of the affected bone. Underlying trauma necessitates attention to the tumour, or it may result in pathological fracture. A pathological fracture is brought on by a tumour that entered the subarticular space. The distal femur is the most typical location for the GCTB, followed by the proximal tibia, distal radius, sacrum, and proximal humerus. [10], [11] The hands, feet, patella, and talus are examples of atypical GCT sites; atypical sites are common in multicentric GCT.[10], [11], [12], [13] Rare GCT sites include the mobile spine's vertebral bodies and posterior elements.
Case Presentation
Patient information
A 37-year-old female laborer presented with a history of pain and swelling over her left knee for 1 month and an inability to bear weight for 20 days. Pain is associated with swelling which was insidious in onset and gradually progressive in nature. The pain and swelling occurred without any prior trauma. It grew in size over time, becoming worse when standing or walking. Pain interferes with the patient's daily activities. The patient has no family history of a similar complaint, nor does she have an addiction. The patient described a 20-day history of knee aspiration.
Clinical examinations
On clinical examination, the patient has tenderness, swelling was seen on the anterolateral aspect of the knee extending from the distal part of the femur towards the knee it was well-defined, smooth, firm and uniform in consistency with dimensions of 12cm x 8 cm. Swelling was movable sideways with no attachment to the bone. It adhered to the underlying soft tissue and hence moved with the movement of the knee. Knee movement were restricted. Flexion is 40 degree. Normal capillary circulation was present. Paraesthesia was not noted. No Lymphadenopathy and the rest General examination were normal.

Diagnosis: On the basis of clinical history and examination we have taken Giant cell tumor of the bone as our preliminary diagnosis and moved for the radiological and pathological examination for confirmation.
Radiological examination: initially we have done x-ray left knee.
Anteroposterior (AP) and lateral view ([Figure 2]) showed soft tissue shadow over the anterolateral surface of the distal femur bone involvement with cortical destruction. Ultrasonography was done which revealed mass attached to the underlying soft tissue on the anterolateral surface of the distal femur. MRI ([Figure 2]) of left knee which shows cortical breach.

Classification of GCT
This GCTB of knee is high grade aggresssive tumor as per According to Jaffe histological classification of GCT,[14] Campanacci[15] radiographic classification of the GCT it is Grade 3 as cortical breach is present. Campanacci it also guides for the treatment: Grade 1 and 2 treated with intralesional curettage, and for grade 3 lesions with en block resection and reconstruction require if neccessary.[16]
Enneking a clinico-radiological classification: benign 3 stages[17]
Other investigations like complete blood counts, random blood sugar, liver function tests, and renal function tests were normal.
The patient was surgically fit and an extended curettage with bone grafting with bone cementing of the underlying tumor was planned. It was done under spinal anaesthesia. A curvilinear incision was taken over the swelling over anterolateral aspect of the knee and dissection done. ([Figure 3]). A cortical window made in the tumor. Tumor contains caecious material which was removed with help of a curette. Sample sent for the histopathological examination. Cortical breach unable to appreciate intraoperatively. Thus repeated cycles of thorough curettage and wash given and Curettage was extended by using a burr ([Figure 4]). Bone graft harvested from the inner cortical table of the same side iliac crest. Harvested graft followed by gel foam placed near articular and over intercondylar region and the cavity was prepared for cementing (Sandwich technique) but while handling the limb, an medial cortical breach occurred, due to unavailability of distal femur plates the cavity was packed and wound closure done.


The excised tumour was sent for histopathological examination, which showed polygonal to round histiocytes surrounded by multinucleated giant cells, fibro-fatty tissue ([Figure 5]) suggestive of GCTB.

After 8 days, incision taken over previous surgical scar, Bone exposed fracture reduction thorough wash given graft and gel foam reinserted. Fresh bone cement was prepared with the cement in semi solid state. Semisolid was inserted to plug the defect and through the semi solid cement a lateral distal femur plate was placed and screws were passed through the semi-solid cement. Open reduction internal fixation with plating with bone cement performed for the medial cortical breach.

Discussion
The case presented to the hospital as a high grade giant cell tumour of the left knee, which was diagnosed and confirmed on histopathological examination after surgical excision of the tumour. The patient has no clinical or radiological signs of recurrence after 12 weeks of follow-up. In addition, the patient requests a one-year follow-up visit.
Only curettage was the mainstay of treatment for GCT, particularly for grades 1 and 2, but it was associated with a high recurrence rate (35-40%).[16], [18], [19], [20] To reduce recurrence, adjuvants such as bone cement, phenol, hydrogen peroxide (H2O2), cryosurgery, and argon beam are used. To reduce the risk of local recurrence, systemic treatments such as bisphosphonates, interferon alpha (IFN-a), and denosumab can be used.[20]
Grade 3 patients are primarily treated with en bloc resection and reconstruction. Other reconstruction methods, such as CC screws and steinmen pins, are available, but plating provides greater stability and stiffness. Jeremy Ruskin et al. concluded in their 2016 study on Steinmann pin augmentation versus locking plate constructs that locking plate constructs had greater stiffness than tibial constructs fixed with Steinmann pins.[21]
In their 2009 paper, Distal femur defects reconstructed with polymethylmethacrylate and internal fixation devices: a biomechanical study, Anthony D Uglialoro et al concluded that locking plate constructs were stronger (P=.028) than Steinmann pin constructs. Constructions with crossed screws were significantly weaker (P.001) than constructions with locking plates. Crossed screw constructs failed due to defect bulging, articular impaction, and minimal fracture propagation, whereas Steinmann pin constructs failed due to severe intra-articular fractures.[22] Using locking plates in other orthopaedic oncology reconstructions has been shown in other studies to be an effective treatment. Locking-plate systems may provide better purchase in poor quality bone and equivalent purchase with fewer screws, as well as limit screw pullout.[23]
Post-operatively follow-up was held every 6 weekly. The patient had complete relief of pain, with improvement in the range of movement, knee flexion till 80 degree with full extension without any surgical site complications evident. The patient was able to perform her activities of daily living. No evidence of recurrence was noted on clinical and radiological examination.

Conclusion
Our case is an example of GCTB in a left knee with iatrogenic complication without considering the intra operative complication and probable bail out plan.
Proper preoperative planning with probable complications is very crucial. Also, bail-out plan must be made prior by keeping in mind the probable complications. After 1 year of follow-up, the patient is able to resume his duty and daily activity without pain. Thus, proper implant size and type selection are also crucial. In this case we identify the complication and rectified it with proper close followup.
Source of Funding
None.
Conflict of Interest
None.
References
- DC Dahlin, RE Cupps, EW Johnson. Giant-cell tumor: a study of 195 cases. Cancer 1970. [Google Scholar]
- HD Dorfman, B Czerniak. Bone cancers. Cancer 1995. [Google Scholar]
- RR Goldenberg, CJ Campbell, M Bonfiglio. Giant-cell tumor of bone. An analysis of two hundred and eighteen cases. J Bone Joint Surg Am 1970. [Google Scholar]
- GS Kulkarni, S Babhulkar. . Textbook of Orthopedics and Trauma 2015. [Google Scholar]
- KK Uni, CY Inwards. Giant cell tumor (osteteoclastoma). Dahlin’s bone tumors 2010. [Google Scholar]
- NA Athanasou, M Bansal, R Forsyth, RP Reid, Z Sapi, CDM Fletcher, JA Bridge, PCW Hogendoorn, F Mertens. Giant cell tumour of bone. WHO classification of tumours of soft tissue and bone 2013. [Google Scholar]
- N Hammas, C Laila, ALM Youssef, E F Hind, T Harmouch, T Siham. Can p63 serve as a biomarker for giant cell tumor of bone? A Moroccan experience. Diagn Pathol 2012. [Google Scholar] [Crossref]
- SF Xu, B Adams, XC Yu, M Xu. Denosumab and giant cell tumour of bone-a review and future management considerations. Curr Oncol 2013. [Google Scholar]
- CJ Chakarun, DM Forrester, CJ Gottsegen, DB Patel, EA White, GR Matcuk. Giant cell tumor of bone: review, mimics, and new developments in treatment. Radiographics 2013. [Google Scholar]
- RE Turcotte. Giant cell tumor of bone. Orthop Clin North Am 2006. [Google Scholar]
- M Kransdorf, M Murphey. Giant cell tumor. The imaging of bone tumors and tumor-like lesions. Davies M, Sundaram M, James S 2009. [Google Scholar]
- KK Unni. . Dahlin’s bone tumors: general aspects and data on 11,087 cases 1996. [Google Scholar]
- D Resnick, M Kyriakos, G Greenway, D Resnick. Imaging and pathology of specific lesions, in the diagnosis of bone and joint disorders. Tumors and tumor-like lesions of bone 2002. [Google Scholar]
- HL Jaffe, L Lichtenstein, RB Portis. Giant cell tumor of bone. Its pathologic appearance, grading, supposed variants and treatment. Arch Pathol 1940. [Google Scholar]
- M Campanacci, N Baldini, S Boriani, A Sudanese. Giantcell tumor of bone. J Bone Joint Surg Am 1987. [Google Scholar]
- F Abat, M Almenara, A Peiro, L Trullols, S Bague, I Gracia. Giant cell tumour of bone: a series of 97 cases with a mean follow-up of 12 years. Rev Esp Cir Ortop Traumatol 2015. [Google Scholar]
- WF Enneking, SS Spanier, MA Goodman. A system for the surgical staging of musculoskeletal sarcoma. Clin Orthop Relat Res 1980. [Google Scholar]
- HD Dorfman, B Czerniak. . Bone tumors 1998. [Google Scholar]
- RL Randall. Giant cell tumor of the sacrum. Neurosurg Focus 2003. [Google Scholar]
- P Ruggieri, AF Mavrogenis, G Ussia, A Angelini, PJ Papagelopoulos, M Mercuri. Recurrence after and complications associated with adjuvant treatments for sacral giant cell tumor. Clin Orthop Relat Res 2010. [Google Scholar]
- J Ruskin, P Caravaggi, KS Beebe, S Corgan, L Chen, RS Yoon. Steinmann pin augmentation versus locking plate constructs. J Orthop Traumatol 2016. [Google Scholar]
- AD Uglialoro, M Maceroli, KS Beebe, J Benevenia, FR Patterson. Distal femur defects reconstructed with polymethylmethacrylate and internal fixation devices: a biomechanical study. Orthopedics 2009. [Google Scholar] [Crossref]
- WW Virkus, BJ Miller, PC Chye, S Gitelis. The use of locking plates in orthopedic oncology reconstructions. Orthopedics 2008. [Google Scholar]
How to Cite This Article
Vancouver
Vaidya SP, Mankar S, Sakhare R, Deshpande S, Daware A. Giant cell tumor of distal femur with pathological fracture: A case report [Internet]. Indian J Orthop Surg. 2023 [cited 2025 Sep 13];9(3):206-210. Available from: https://doi.org/10.18231/j.ijos.2023.040
APA
Vaidya, S. P., Mankar, S., Sakhare, R., Deshpande, S., Daware, A. (2023). Giant cell tumor of distal femur with pathological fracture: A case report. Indian J Orthop Surg, 9(3), 206-210. https://doi.org/10.18231/j.ijos.2023.040
MLA
Vaidya, Shubham Prakashrao, Mankar, Sushil, Sakhare, Rahul, Deshpande, Satyajeet, Daware, Ambar. "Giant cell tumor of distal femur with pathological fracture: A case report." Indian J Orthop Surg, vol. 9, no. 3, 2023, pp. 206-210. https://doi.org/10.18231/j.ijos.2023.040
Chicago
Vaidya, S. P., Mankar, S., Sakhare, R., Deshpande, S., Daware, A.. "Giant cell tumor of distal femur with pathological fracture: A case report." Indian J Orthop Surg 9, no. 3 (2023): 206-210. https://doi.org/10.18231/j.ijos.2023.040