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Giant cell tumor of the distal ulna: a case report
© Vanni et al.; licensee BioMed Central Ltd. 2012
Received: 29 November 2011
Accepted: 1 June 2012
Published: 1 June 2012
Several cases of long bone giant cell tumor have been reported in the literature. We report the case of a patient with a giant cell tumor in the distal ulna. This is very unusual, with a reported incidence of 0.45 to 6%.
A 17-year-old Colombian man presented with a painful swelling of the left wrist. After performing an instrumental examination, a diagnosis of distal ulna giant cell tumor was made. The tumor was treated with an intralesional curettage, phenol application and bone grafting.
This tumor may have a good prognosis if it is diagnosed early and radically treated. It is important to be aware of atypical cancer localizations in order to perform a proper diagnosis.
Bone giant cell tumor (GCT) is a rare, generally benign and locally aggressive tumor. It represents approximately 3% to 5% of all primary bone cancers. It generally occurs in adults between the ages of 20 and 40 years. GCT of bone is very rarely seen in children or in adults older than 65 years of age. GCT tumors occur in approximately one person per million per year. Usually, the tumor site is at the long bone meta-epiphysis, especially the distal radius and femur, proximal humerus and tibia. The ulna distal extremity is an unusual site (0.45% to 3.2%) for a primary bone GCT. We report the case of a distal ulna GCT diagnosed in a 17-year-old man. It was treated with intralesional curettage, adjuvant therapy with 5% phenol and a synthetic bone graft reconstruction.
After an incisional biopsy, the diagnosis of GCT was finally made, although it was in an atypical site.
Subsequently, the patient was surgically treated with intralesional curettage, adjuvant therapy with 5% phenol and a synthetic bone graft reconstruction.
A cortical bone rawplug was removed through a skin incision at the dorsomedial side of the deformity. Accessing the cystic cavity revealed a gelatinous ‘chocolate brown’ material, with many areas of darker color.
A clinical and radiographic follow-up was performed one, three, six, 12, 24 and 48 months post-operatively to evaluate the bone consolidation. Chest radiographs were performed every six months. Within the first post-operative month, the patient completely recovered the wrist ROM. After 3 years, there have been no signs of recurrence.
The bone GCT was first described in 1818 by Cooper and Travers. Its local aggression has been highlighted by Nelaton and its malignant potential by Virchow.
It is a rare tumor, essentially benign, but it may behave unexpectedly, regardless of the results of radiological or histological examinations.
It is usually located in the long bone meta-epiphysis and it frequently involves the subchondral bone without involvement of the articular surface; however, larger tumors may extend into the metaphysis and, more rarely, into the diaphysis. Proximal tibia, humerus, distal femur and radius are typical sites.
In 70% of cases, it involves women in the third to fourth decade of life.
The distal epiphysis of the ulna is an unusual place for a primary bone GCT; in fact, this occurs in only 0.45% to 3.2% of all primary bone GCT’s .
In the past, these tumors were treated with amputation or large resections and ulterior reconstructions. Currently, surgical treatments are:
· Intralesional curettage
· Curettage and bone grafting
· Cryotherapy of the cavity after curettage
· Application of phenol after curettage
· Insertion of methyl methacrylate cement in the cavity after curettage
· Resection followed by allograft
· En-bloc resection with or without reconstruction or stabilization of the ulna and prosthetic reconstruction
· Embolization of the feeding vessels
The variables related to the tumor, such as size, location, biological activity, cortical bone destruction or pathologic fracture evidence, determine the treatment .
Although an en-bloc resection radically assaults the tumor, significantly reducing the risk of recurrence, functional outcome is very bad. A simple curettage provides an excellent functional outcome, but with a higher recurrence rate of approximately 40% [1–5] if compared with the patients who received adjuvant therapy (45% versus 18%).
However, it needs to be mentioned that a multicenter study of the Canadian Sarcoma Group  reported an overall recurrence rate of 17% and claimed that the filling material or the type of adjuvant would not have an absolute impact on recurrence.
Furthermore, some studies show that the use of an adjuvant would not be necessary in some cases, such as intraosseous GCT .
According to Schajowicz , curettage alone is an inadequate oncological procedure, but when it is combined with an adjuvant therapy, it globally provides a better result with respect to one-block excision, especially in terms of functionality.
Curettage associated with bone grafting has been shown to be effective in many cases . In this study it is used with phenol as an adjuvant, because it is capable of causing protein and DNA coagulation, inducing cell necrosis.
In the present case intralesional curettage was possible because the tumor was a grade II and the reconstruction was carried out with synthetic cancellous bone, due to the young age of the patient.
Neoformation bone diagnosis is difficult and requires a great deal of experience, especially in young patients. Osteolytic lesions incidentally found at a long bone epiphysis, can be misinterpreted. This tumor may have a good prognosis if treated early and radically. It is important to know atypical cancer locations in order to perform a proper diagnosis.
Written informed consent was obtained from the patient’s next-of-kin for publication of this case report and any accompanying images.
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