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Tenosynovial giant cell tumors of digits: MRI differentiation between localized types and diffuse types with pathology correlation

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Abstract

Objective

To compare the MRI findings between the localized- and diffuse-type tenosynovial giant cell tumors (TSGCTs) of digits with pathology correlation.

Methods

Twenty-eight patients with newly diagnosed TSGCTs of digits (22 localized and 6 diffuse types) who underwent preoperative MRI and surgical excision were included from Jan. 2015 to September 2021. MRI findings regarding nodularity, margins, morphology of hypointensity with pathology correlation, and disease extent (bone erosion, articular involvement, muscle involvement, tendon destruction, and neurovascular encasement) were assessed.

Results

Diffuse type was significantly larger (P = 0.006), more multinodular on both MRI and pathology (P = 0.038, both) with significant agreement, and infiltrative on both MRI and pathology (P < 0.001, both) with substantial agreement, and showed central granular on MRI and strong hemosiderin deposition on pathology (P = 0.022 and P = 0.021) with moderate agreement than localized type. Localized type showed significantly more frequent peripheral capsules on both MRI and pathology (P < 0.001, both) with moderate agreement than diffuse type. However, the septum on both MRI and pathology showed no statistically significant difference between the two groups (P = 0.529 and P = 0.372) without significant agreement. The disease extent was more severe in the diffuse type than the localized type regarding articular involvement (P < 0.001), muscle involvement (P < 0.001), and tendon destruction (P = 0.010). No statistically significant differences were found between the two groups regarding bone erosion (P = 0.196) or neurovascular bundle encasement (P = 0.165).

Conclusions

Diffuse-type TSGCTs of digits presented as locally aggressive lesions with larger, multinodular, infiltrative masses exhibiting stronger hemosiderin deposition and more severe disease extents of articular, muscle, and tendon involvement than the localized type.

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Abbreviations

AUC:

Areas under the curve

H&E:

Hematoxylin and eosin

MRI:

Magnetic resonance imaging

PIP:

Proximal interphalangeal

ROC:

Receiver operating characteristic

TSGCT:

Tenosynovial giant cell tumor

References

  1. World Health Organization WHO, Fletcher C, Bridge JA, Hogendoorn PCW, Mertens F, editors. WHO classification of tumours of soft tissue and bone: WHO classification of tumours, vol. 5. 4th ed. World Health Organization; 2013. p. 468.

  2. Somerhausen NS, Fletcher CD. Diffuse-type giant cell tumor: clinicopathologic and immunohistochemical analysis of 50 cases with extraarticular disease. Am J Surg Pathol. 2000;24:479–92.

    Article  CAS  Google Scholar 

  3. van der Heijden L, Gibbons CL, Dijkstra PD, et al. The management of diffuse-type giant cell tumour (pigmented villonodular synovitis) and giant cell tumour of tendon sheath (nodular tenosynovitis). J Bone Joint Surg Br. 2012;94:882–8.

    Article  Google Scholar 

  4. Gouin F, Noailles T. Localized and diffuse forms of tenosynovial giant cell tumor (formerly giant cell tumor of the tendon sheath and pigmented villonodular synovitis). Orthop Traumatol Surg Res. 2017;103:S91–7.

    Article  CAS  Google Scholar 

  5. Rateb K, Hassen BG, Leila A, Faten F, Med SD. Giant cell tumor of soft tissues: a case report of extra-articular diffuse-type giant cell tumor of the quadriceps. Int J Surg Case Rep. 2017;31:245–9.

    Article  Google Scholar 

  6. Verspoor FG, van der Geest IC, Vegt E, Veth RP, van der Graaf WT, Schreuder HW. Pigmented villonodular synovitis: current concepts about diagnosis and management. Future Oncol. 2013;9:1515–31.

    Article  CAS  Google Scholar 

  7. Al-Qattan MM. Giant cell tumours of tendon sheath: classification and recurrence rate. J Hand Surg Br. 2001;26:72–5.

    Article  CAS  Google Scholar 

  8. Ozben H, Coskun T. Giant cell tumor of tendon sheath in the hand: analysis of risk factors for recurrence in 50 cases. BMC Musculoskelet Disord. 2019;20:457.

    Article  Google Scholar 

  9. Serhal A, Samet J, Shah C, Omar I, Youngner J. MRI evaluation of solid soft tissue masses of the fingers with pathology correlation. Eur J Radiol. 2021;135:109465.

    Article  Google Scholar 

  10. Ge Y, Guo G, You Y, et al. Magnetic resonance imaging features of fibromas and giant cell tumors of the tendon sheath: differential diagnosis. Eur Radiol. 2019;29:3441–9.

    Article  Google Scholar 

  11. Ho CY, Maleki Z. Giant cell tumor of tendon sheath: cytomorphologic and radiologic findings in 41 patients. Diagn Cytopathol. 2012;40(Suppl 2):E94–8.

    Article  Google Scholar 

  12. Chiari C, Pirich C, Brannath W, Kotz R, Trieb K. What affects the recurrence and clinical outcome of pigmented villonodular synovitis? Clin Orthop Relat Res. 2006;450:172–8.

    Article  Google Scholar 

  13. Kim DE, Kim JM, Lee BS, Kim NK, Lee SH, Bin SI. Distinct extra-articular invasion patterns of diffuse pigmented villonodular synovitis/tenosynovial giant cell tumor in the knee joints. Knee Surg Sports Traumatol Arthrosc. 2018;26:3508–14.

    Article  Google Scholar 

  14. van der Heijden L, Mastboom MJ, Dijkstra PD, van de Sande MA. Functional outcome and quality of life after the surgical treatment for diffuse-type giant-cell tumour around the knee: a retrospective analysis of 30 patients. Bone Joint J. 2014;96-B(8):1111–8.

  15. Ota T, Nishida Y, Ikuta K, et al. Tumor location and type affect local recurrence and joint damage in tenosynovial giant cell tumor: a multi-center study. Sci Rep. 2021;11:17384.

    Article  CAS  Google Scholar 

  16. Murphey MD, Rhee JH, Lewis RB, Fanburg-Smith JC, Flemming DJ, Walker EA. Pigmented villonodular synovitis: radiologic-pathologic correlation. Radiographics. 2008;28:1493–518.

    Article  Google Scholar 

  17. Dundar A, Young JR, Wenger DE, Inwards CY, Broski SM. Unusual manifestations of diffuse-type tenosynovial giant cell tumor in two patients: importance of radiologic-pathologic correlation. Skeletal Radiol. 2020;49:483–9.

    Article  Google Scholar 

  18. Wang C, Song RR, Kuang PD, Wang LH, Zhang MM. Giant cell tumor of the tendon sheath: Magnetic resonance imaging findings in 38 patients. Oncol Lett. 2017;13:4459–62.

    Article  Google Scholar 

  19. Crim J, Dyroff SL, Stensby JD, Evenski A, Layfield LJ. Limited usefulness of classic MR findings in the diagnosis of tenosynovial giant cell tumor. Skeletal Radiol. 2021;50:1585–91.

    Article  Google Scholar 

  20. Mastboom MJL, Verspoor FGM, Hanff DF, et al. Severity classification of Tenosynovial Giant Cell Tumours on MR imaging. Surg Oncol. 2018;27:544–50.

    Article  CAS  Google Scholar 

  21. Palmerini E, Staals EL, Maki RG, et al. Tenosynovial giant cell tumour/pigmented villonodular synovitis: outcome of 294 patients before the era of kinase inhibitors. Eur J Cancer. 2015;51:210–7.

    Article  Google Scholar 

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Correspondence to Seul Ki Lee.

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Jeong, H.S., Lee, S.K., Kim, JY. et al. Tenosynovial giant cell tumors of digits: MRI differentiation between localized types and diffuse types with pathology correlation. Skeletal Radiol 52, 593–603 (2023). https://doi.org/10.1007/s00256-022-04170-x

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