Giant cell tumours of the tendon sheath (GCTTS) are uncommon and usually benign lesions that arise from the tendon sheath. It is unclear whether these lesions represent neoplasms or simply reactive masses 2.
It is also known as pigmented villonodular tumour of the tendon sheath (PVNTS) or extra-articular pigmented villonodular tumor of the tendon sheath 4.
Typically, they present in 3rd-5thdecades and have a slight female predilection with a M:F ratio of 1.5-2.1:1 4.
Clinically these masses typically present in the hand (although they are found elsewhere also) with localised swelling with or without pain. They are slow growing.
They have been divided macroscopically into localised or diffuse forms, and appear as rubbery multinodular masses that are well circumscribed. They have an enveloping fibrous capsule, and the cut surface is variably coloured depending on the relative proportions of fibrous tissue, haemosiderin and pigmented foam cells 2.
The tumour is histologically identical to pigmented villonodular synovitis (PVNS) and is composed of fibroblasts and multinucleated giant cells, foamy histiocytes and inflammatory cells on a background fibrous matrix 1-2.
As these masses arise from tendons, commonly of the hand, they may cause pressure erosions on the underlying bone. This is only seen in 10-20% of cases. More commonly these masses arise from the palmar tendons. The mass itself is of soft tissue density. Calcification is uncommon 5.
Ultrasound is useful as it allows not only characterisation of the lesion but also is able to demonstrate the relationship with the adjacent tendon. On dynamic scan, there is free movement of the tendon within the lesion (case 5).
These masses are typically homogeneously hypoechoic, although some heterogeneity may be seen in echo-texture in a minority of cases 1. Most will have some internal vascularity.
Not surprisingly, given the histological similarity to PVNS, giant cell tumours of the tendon sheaths also share the same finding on MRI, mainly on account of hemosiderin accumulation.
Signal characteristics include:
- low signal
- variable enhancement
- T2: low signal
Treatment and prognosis
Local surgical excision usually suffices, with local recurrence (seen in 10-20% of cases) requiring more extensive surgery with or without radiotherapy being uncommon 1.
General imaging differential considerations include:
- cystic component
- if previously ruptured may appear similar 1
pignented villonodular synovitis (PVNS)
- histologically identical
- involves larger joints
- desmoid tumour
If in the hand consider:
- glomangioma: has high T2 signal on MRI
- 1. Middleton WD, Patel V, Teefey SA et-al. Giant cell tumors of the tendon sheath: analysis of sonographic findings. AJR Am J Roentgenol. 2004;183 (2): 337-9. AJR Am J Roentgenol (full text) - Pubmed citation
- 2. Ly JQ, Carlson CL, Lagatta LM et-al. Giant cell tumor of the peroneus tendon sheath. AJR Am J Roentgenol. 2003;180 (5): 1442. AJR Am J Roentgenol (full text) - Pubmed citation
- 3. Jelinek JS, Kransdorf MJ, Shmookler BM et-al. Giant cell tumor of the tendon sheath: MR findings in nine cases. AJR Am J Roentgenol. 1994;162 (4): 919-22. AJR Am J Roentgenol (abstract) - Pubmed citation
- 4. Murphey MD, Rhee JH, Lewis RB et-al. Pigmented villonodular synovitis: radiologic-pathologic correlation. Radiographics. 28 (5): 1493-518. doi:10.1148/rg.285085134 - Pubmed citation
- 5. Peh WC, Shek TW, Ip WY. Growing wrist mass. Ann. Rheum. Dis. 2001;60 (6): 550-3. doi:10.1136/ard.60.6.550 - Pubmed citation
Synonyms & Alternative Spellings
|Synonyms or Alternative Spelling||Include in Listings?|
|Giant cell tumour of the tendon sheath||✗|
|Giant cell tumour of the tendon sheath (GCTTS)||✗|
|Giant cell tumour of tendon sheath||✗|
|Pigmented villonodular tenosynovitis||✓|
|Xanthomatous giant cell tumour of the tendon sheath||✗|
|Giant cell tumor of the tendon sheath||✗|
|Xanthomatous giant cell tumor of the tendon sheath||✗|
|Extra-articular pigmented villonodular tumor of the tendon sheath||✗|