Rare site giant cell tumors: report of two cases on phalanges of the finger and review of literature
© Springer-Verlag 2009
Received: 6 June 2008
Accepted: 20 January 2009
Published: 29 September 2009
Giant cell tumor (GCT) of bone arising from a phalanx of a finger is extremely rare. We report two cases of GCT arising from a phalanx of a finger. One case presented with recurrence following the amputation of the left ring finger (performed elsewhere). He was treated successfully with ray amputation. The other case was treated primarily by intralesional curettage and autogenous bone graft. At their most recent follow-ups (80 and 24 months, respectively), both were recurrence free and had returned to their previous occupational and recreational activities.
KeywordsGCT Phalanx Recurrent
Giant cell tumor (GCT) of a phalanx of a finger is extremely rare. Only 2% of all reported GCTs are found in the hand . The metaphyseal region of the metacarpals and phalanges has been found to be the common site of GCTs in most of the reported cases [2–4]. Though GCT is not a sarcoma, its relatively high recurrence rate  coupled with local aggressiveness after simple curettage often requires extensive en bloc excision. The recurrence of GCT of hand is higher than for other locations. Local recurrence following curettage and bone grafting has been reported to be as high as 90% [1, 4, 6, 7]. Wide resection and reconstruction with structural bone grafting is also reported to have a high local recurrence rate . Multiple procedures like excision (local or wide), ray amputation, and amputation are used to eradicate the disease completely. Even with single- or double-ray resection for primary or recurrent tumors, local tumor control may not be absolute.
Here, we report two cases of GCT on phalanges of the finger, noting the rarity of a lesion at this site.
A radiograph revealed partial amputation of the proximal phalanx through the proximal one-third, with an expansile lesion in the remaining part involving the articular surface that was associated with soft tissue swelling (Fig. 2b). CT scan clearly demonstrated an irregular expansile lytic lesion with cortical erosion (Fig. 2c). Evidence of new bone formation was prominent. A radiograph of the chest was normal. There were no signs of the disease elsewhere in the body. Results of laboratory studies were within normal limits.
At his most recent follow-up (80 months), neither clinical nor radiological evidence of local recurrence was seen. He was able to perform normal activities of daily life. There was no limitation on the strength or motion of the uninvolved digits or wrist.
A 26 year old female presented with a painless swelling of the left little finger of six months duration without any history of trauma or fever.
Under general anesthesia, curettage of the lesion was performed with cancellous bone grafting from the iliac crest. The recovery was uneventful. Histology confirmed the diagnosis of a GCT, demonstrating osteoclastic giant cells admixed with stromal cells.
The patient is undergoing regular check-ups for 24 months and has not shown any evidence of local recurrence clinically or radiologically (Fig. 5c). Her grip strength is normal, with good functional recovery.
Informed consent was obtained from both of the patients to publish their clinical cases.
GCT of the hand is rare and seems to be different from conventional GCT, which occurs at other sites in the skeleton. GCTs recur more rapidly in the hand than they do in other locations. It is even rarer to encounter a GCT arising from the phalanges. Of the more than 2,400 skeletal GCTs reported in the literature, less than 50 were found to involve the phalanges of the hand [7, 8]. Coley et al.  reported only two cases of GCT arising from the phalanges in their series of 108 cases. Goldenberg et al., in their analysis of 218 cases of GCT, reported six cases involving the phalanges . In another two large series of 568 and 327 cases of GCT, authors found only four and one cases of phalangeal involvement, respectively [11, 12]. Yasudal et al.  reported a multicentric giant cell tumor of the hand involving a finger and the wrist. Benign metastazing giant cell tumor of the hand has also been reported . In our series of 124 skeletal GCTs, we could find only two cases involving the phalanges.
Giant cell tumors of the hand have been treated with curettage and cancellous bone grafting, wide resection, and structural bone grafting or ray amputation [1, 4, 6, 7, 15]. High local recurrence rates have been reported with these treatment modalities [1, 4, 6, 7]. Daniel et al.  reported a GCT of the middle phalanx treated with curettage and bone grafting, which recurred at 9 months and was successfully treated by excision and allograft replacement. Wittig et al.  reported three cases of phalangeal GCT treated with curettage, cryosurgery and cementation. Resection–iliac graft and double arthrodesis for GCT of the proximal phalanx of the thumb has also been reported .
Our patient (case no. 2) with curettage and iliac bone grafting recovered uneventfully. To avoid stiffness of fingers and tendon adhesion, we started active finger rehabilitation measures as early as the second week. The patient was still disease free at the most recent follow-up, and was performing normal activities with a good grip strength.
Reported local recurrence after curettage, resection and amputation for GCT of the hand
No. of cases
Curettage ± bone graft
Resection or ray amputation
Averill et al. 
Wold et al. 
Patel et al. 
Athanasian et al. 
Daniel et al. 
Most of the GCT cases with recurrent tumors require ray amputation to prevent recurrence. There are reports of success with ray resection or amputation at the cost of the loss of a functional finger [7, 15]. We chose ray resection of the amputated ring finger with the aim of preventing recurrence. The recurrent tumor in our patient expanded eccentrically, leading to breakage of the surgical scar and ulcer formation. Contrary to malignant ulcers, the margin of the ulcer was not everted and did not bleed on touch. Histology of the lesion also revealed osteoid formation. Kumar and Tuli  and Dahlin et al.  reported similar histological findings in their series. Following ray resection of the ring finger, there was no functional loss of the hand in our patient. The patient was satisfied with a cosmetically improved hand.
In view of the comparative rarity of a tumor arising from the phalanges of the finger, the present two cases are considered worth reporting.
Conflict of interest statement
The authors declare that they have no conflict of interest related to the publication of this manuscript.
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