Hospital Sarah Brasília, Cirurgia Plástica e Cirurgia de Mão, Brasília, DF, Brazil
Introduction
Giant cell tumor (GCT) is defined as an aggressive benign bone tumor with uncertain biological behavior, characterized histologically by richly vascularized tissue with ovoid and fusiform cells and numerous osteoclastic giant cells, evenly distributed throughout the tumor tissue.1,2 GCT mainly affects young adults between the ages of 20–35 years, and the most frequent locations are the distal femur and proximal tibia. It is more common in females, and constitutes 8% of primary bone tumors.3 The main purpose of this report is to demonstrate the importance of resection following oncological principles for such lesions with involvement the femoral neck and whose treatment is mainly surgical, with radical replacement of the segment; in case of failure of other techniques, such as curettage and autologous or homologous bone grafts, prosthetic replacement (non-conventional endoprosthesis) is mandatory. Case report Female patient, aged 33 years, reported pain in the left hip and lower back for the last six months and had no history of trauma or physical effort and progressive worsening of the pain. At physical examination, the patient presented pain on palpation in the anterior aspect and during movement of the left hip, with normal range of motion.
The initial radiological study (pelvis radiograph) disclosed the presence of an extensive osteolytic lesion on the femoral neck and proximal third of the greater trochanter (Fig. 1).
Magnetic resonance imaging (MRI) revealed an expansile, destructive, insufflated bone lesion the epiphysismetaphyseal region of the left proximal femur, with regular and well-defined contours, which started on the femoral neck and extended to the anterior aspect of the femoral head. The lesion presented a homogeneous solid matrix, hypointense on T1, and with intermediate signal on T2, with intense uptake after intravenous contrast administration. Bone marrow edema was observed near the lesion, without signs of expansion to the adjacent soft tissue (Fig. 2).
In light of these findings, the possibility of GCT was considered and a bone biopsy was proposed; the biopsy was performed immediately, corroborating the primary diagnostic hypothesis. The authors decided to perform an intralesional resection, with local curettage and electrocauterization as an adjuvant treatment, as well as filling of the cavity with autologous bone graft from the fibula and bone cement (methylmethacrylate) (Fig. 3).
The patient had no significant clinical abnormalities. Full weight bearing was authorized after 120 days. One year after surgery, a control MRI was performed; although the patient is completely asymptomatic, nodular lesions of regular and well-defined borders were observed, with T1 and T2 isointensity, homogeneously capturing the intravenous contrast in the intertrochanteric region, in the lower portion of the surgical cavity. Bone marrow edema was observed adjacent to the lesion and to the bone graft/cement, as well as reactive periostitis, consistent with tumor recurrence (Fig. 4).
In light of these findings, a new surgical intervention was proposed; a block resection of the proximal third of the femur was performed, replaced with non-conventional modular titanium endoprosthesis and uncemented acetabular prosthesis (Figs. 5 and 6).
Discussion
The treatment of GCT is essentially surgical. There is evidence contrary to curettage, but there is a correlation with surgery and method, histologic type, tumor size, location, and age of the patient – these are factors that directly influence the prognosis, as well as lesion staging.4
In 1983, Enneking proposed a three-stage radiographic classification: stage I – tumor with well-defined edges and cortical integrity; stage II – expanded cortex with well-defined edges; stage III – non-defined edges with soft tissue invasion. Stage I is treated with curettage and adjuvant treatment (electrocauterization, methylmethacrylate, liquid nitrogen, and phenol). Stage II can also be treated by this method, but it presents worse functional outcomes when treated similarly to stage III (wide resection of the lesion and replacement).4–6
Bone cement has no biological properties and long-term results are very difficult to anticipate, especially when this method is used in the treatment of GCT.7,8 Although some authors have demonstrated excellent results with this method based on the clinical approach, no deleterious effects were directly related to the use of methylmethacrylate and other adjuvant treatments that have been recommended to reduce GCT recurrence were observed.9
Treatments involving substitution, such as reconstruction of the proximal femur with femoral prostheses, the use of proximal endoprosthesis for large replacements of proximal femoral neoplasms, modular titanium endoprosthesis, and conventional total hip arthroplasty are techniques used for GCT of the hip.10–13
Resection of the proximal third of the femur is defined as a surgery that removes the previously defined region of bone damage caused by GCT and the macroscopically affected local tissues. The proximal block of the femur is completely


re move d and a cementless prosthesis is used in acetabular preparation to ensure the durability and reliability of the system. Resection of the proximal third of the femur is a suitable surgical treatment for cases of femoral neck GCT. As in the present case, it is a viable surgical alternative to resection with curettage and other filling methods, which have been proven to be comparatively ineffective.
Conclusion
The femoral neck is not the most common region for the presence of GCT. In the present case, the authors concluded that the femoral neck GCT should be widely resected, pursuant to all the criteria and principles of oncological surgery. Block resection of the entire lesion with a safety margin for the removal of the entire affected area, as well as the underlying tissue that presented contaminated macroscopic features, followed by a non-conventional prosthetic replacement was opted. The authors emphasize the need for complete and safe resection to prevent recurrence of the lesion.
Conflicts of interest
The authors declare no conflicts of interest.
1. Schajowicz F. Tumores y lesiones pseudotumorales de huesos y articulaciones. Buenos Aires: Panamericana; 1982. 2. Camargo OP, Croci AT, Oliveira CRG, Baptista AM, Caiero MT, Giannotti MA. Tumor de células gigantes – evoluc¸ão histórica do seu diagnóstico e tratamento junto ao Instituto de Ortopedia e Traumatologia da FMUSP. Acta Ortop Bras. 2001;9(4):46–52. 3. Catalan J, Fonte AC, Lusa JRB, Melo ES, Justino Júnior RO, Min TT, et al. Tumor de células gigantes ósseo: aspectos clínicos e radiográficos de 115 casos. Radiol Bras. 2006;39(2):119–22. 4. Filho RJG, Korukian M, Ishirara HI, Miceno Filho NM, Figueiredo MTB, Seixas MT. É a curetagem um método eficiente no tratamento dos tumores ósseos? Rev Bras Ortop. 1993;28(11/12):813–6. 5. Camargo OPO. Estado da arte no diagnóstico e tratamento do tumor de células gigantes. Rev Bras Ortop. 2002;37(10):424–9. 6. Oda Y, Miura H, Tsuneyoshi M, Iwamoto Y. Giant cell tumor of bone: oncological and functional results of long-term follow-up. Jpn J Clin Oncol. 1998;28(5):323–8. 7. Shih HN, Cheng CY, Chen YJ, Huang TJ, Hsu RW. Treatent of the femoral neck amd trochanteric benign lesions. Clin Orthop Relat Res. 1996;(328):220–6. 8. Camargo OP, Croci AT, Oliveira CRGMC, Baptista AM, Caiero MT. Avaliac¸ão radiográfica e funcional de 214 lesões ósseas benignas agressivas tratadas com curetagem, cauterizac¸ão e cimentac¸ão: 24 anos de seguimento. Clinics. 2005;60(6):439–44, 60. 9. Prosser GH, Baloch KG, Tillman RM, Carter SR, Grimer RJ. Does curettage without adjuvant therapy provide low recurrence rates in giant-cell tumors of bone? Clin Orthop Relat Res. 2005;(435):211–8. 10. Menendez LR, Ahlmann ER, Kermani C, Gotha H. Endoprosthetic reconstruction for neoplasms of the proximal femur. Clin Orthop Relat Res. 2006;450:46–51. 11. Croci AT, Camargo OP, Baptista AM, Caiero MT. The use of a modular titanium endoprosthesis in skeletal reconstructions after bone tumor resections: method presentation and analysis of 37 cases. Rev Hosp Clin Fac Med São Paulo. 2000;55(5):169–76. 12. Donati D, Giacomini S, Gozzi E, Mercuri M. Proximal femur reconstruction by an allograft prosthesis composite. Clin Orthop Relat Res. 2002;(394):192–200. 13. Kulkarni SS, Dogra AS, Bhosale PB. Total hip arthroplasty for giant cell tumour. J Postgrad Med. 1996;42(3):82–4.