Giant Cell Tumor of the Tendon Sheath Workup

  • Author: James R Verheyden, MD; Chief Editor: Harris Gellman, MD   more...
 
Updated: Feb 6, 2012
 

Imaging Studies

  • Plain radiography
    • Plain radiographs demonstrate a benign-appearing circumscribed soft-tissue shadow in 50% of cases. These radiographs also show cortical erosion of the bone due to a pressure effect of the adjacent mass on the cortex in 10-20% of cases (see the images below). Radiograph demonstrates cortical erosion from the Radiograph demonstrates cortical erosion from the pressure effect of the adjacent mass on the radial aspect of the proximal phalanx. Radiograph demonstrates the bony erosion associateRadiograph demonstrates the bony erosion associated with some giant cell tumors of the tendon sheath and shows the unmineralized soft-tissue shadow of the mass.
    • True bone invasion is not typical and is suggestive of an aggressive neoplasm.
    • Cortical erosion from these tumors is more common in the feet than elsewhere because the strong ligaments in this region frequently prevent outward tumor growth.
    • Occasionally, intralesional soft-tissue calcification is seen with giant cell tumors of the tendon sheath. This intralesional calcification can be confused with synovial chondromatosis, periosteal chondroma, or calcific tendinitis.
    • On rare occasions when extensive cortical erosion is present, the lesion may have a radiographic appearance suggestive of a periosteal chondroma (see the images below). Radiograph demonstrates cortical erosion from the Radiograph demonstrates cortical erosion from the pressure effect of the overlying giant cell tumor of the tendon sheath. This apple-core effect is indicative of a primary soft-tissue mass that is causing external erosion, which should not be confused with a primary bone process such as periosteal chondroma. Radiograph demonstrates cortical erosion from the Radiograph demonstrates cortical erosion from the pressure effect of the overlying giant cell tumor of the tendon sheath. Histologic findings of a giant cell tumor of the tHistologic findings of a giant cell tumor of the tendon sheath. High-power photomicrograph depicts the histologic High-power photomicrograph depicts the histologic findings of a giant cell tumor of the tendon sheath.
  • Magnetic resonance imaging (MRI)
    • Giant cell tumors of the tendon sheath frequently have a unique MRI appearance for an extra-articular soft-tissue mass.[23, 24] On both T1- and T2-weighted MRIs, at least some portions of the tumor have decreased signal intensity (see the images below) similar to that seen with PVNS. However, this appearance is not entirely specific to giant cell tumors of the tendon sheath. Typical T2-weighted MRI appearance of a giant cellTypical T2-weighted MRI appearance of a giant cell tumor of the tendon sheath. Most of the tumor has intermediate signal intensity, and portions of the tumor have low signal intensity; the latter finding likely reflects signal attenuation due to hemosiderin deposition. Typical T1-weighted MRI appearance of a giant cellTypical T1-weighted MRI appearance of a giant cell tumor of the tendon sheath. Portions of the tumor have decreased signal intensity. Typical T1-weighted MRI findings in a giant cell tTypical T1-weighted MRI findings in a giant cell tumor of the tendon sheath overlying the metacarpophalangeal joint. Note the low-signal-intensity areas. Corresponding T2-weighted MRI findings in the tumoCorresponding T2-weighted MRI findings in the tumor shown in the image above. Note the areas of low signal intensity.
    • The degree to which these low–signal-intensity areas are present depends on the amount of hemosiderin, which varies. PVNS often has more low–signal-intensity areas on T2-weighted images, secondary to its higher hemosiderin content resulting from characteristic intralesional bleeding.
  • Sonography: For the value of sonograms, see studies by Bancroft et al[24] and Wang et al[25]
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Histologic Findings

Gross pathologic findings

Giant cell tumors of the tendon sheath have a well-circumscribed multilobular appearance and often possess shallow grooves along their deep surfaces created by the underlying tendons. These tumors are usually small, with a diameter of 0.5-5 cm. Compared with other lesions, giant cell tumors in the hand digits are usually smaller and have a more regular appearance. Giant cell tumors in the feet and elsewhere are often larger and more irregular in appearance. On cut sections, these tumors have a mottled appearance, varying in color from grayish-brown to yellow-orange. The coloration depends on the amount of hemosiderin, collagen, and histiocytes in the sample. Tumors with more hemosiderin deposition due to bleeding have more of the yellow-orange or even reddish-brown color (see the images below).

Intraoperative excision of the giant cell tumor ofIntraoperative excision of the giant cell tumor of the tendon sheath, which has the typical golden-yellow color secondary to hemosiderin deposition. The radial digital nerve is dissected free and slightly volar to the mass. After excision, the bone is curetted, leaving the After excision, the bone is curetted, leaving the exposed radial aspect of the proximal phalanx, as shown here. Giant cell tumor of the tendon sheath after marginGiant cell tumor of the tendon sheath after marginal excision.

Microscopic findings

Most giant cell tumors of the tendon sheath are moderately cellular and composed of sheets of rounded or polygonal cells that blend with hypocellular collagenized zones. Variable numbers of giant cells are present (see the first image below). Hemosiderin-containing xanthoma cells are common and often localized at the periphery of the lesion (see the second image below).

Typical microscopic appearance of a giant cell tumTypical microscopic appearance of a giant cell tumor of the tendon sheath. Sheets of rounded or polygonal cells blend with hypocellular collagenized zones; variable numbers of giant cells are present. High-power photomicrograph of giant cell tumor of High-power photomicrograph of giant cell tumor of the tendon sheath shows occasional numerous mononuclear cells, scattered giant cells, and hemosiderin-containing xanthoma cells.

In the localized form of the disease, a mature collagen capsule often surrounds the tumor. This capsule is continuous, with fibrous septa within the substance of the tumor that divide it into vague nodules. In the diffuse form, the tumor is not surrounded by this capsule and instead grows in expansive sheets.

Giant cells are also less common in the diffuse form. The histologic features of the localized and diffuse forms of giant cell tumor of the tendon sheath and the localized and diffuse forms of PVNS are essentially the same; therefore, these diseases form a histopathologic spectrum in which the tumors range from benign lesions to more locally aggressive lesions.

Cytopathologic findings

The predominant cell type is the mononuclear cell. These round-to-polygonal cells are found alone or in papillary clusters and have eccentrically located nuclei that lack pleomorphism. Varying amounts of refractile golden-brown crystals of hemosiderin are characteristically found within the histiocytes.[26, 27]

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Contributor Information and Disclosures
Author

James R Verheyden, MD  Consulting Surgeon, Department of Orthopedic Surgery, The Orthopedic and Neurosurgical Center of the Cascades

James R Verheyden, MD is a member of the following medical societies: American Academy of Orthopaedic Surgeons, American Medical Association, and American Society for Surgery of the Hand

Disclosure: Nothing to disclose.

Coauthor(s)

Timothy A Damron, MD  David G Murray Endowed Professor, Department of Orthopedic Surgery, Professor, Orthopedic Oncology and Adult Reconstruction, Vice Chair, Department of Orthopedics, State University of New York Upstate Medical University at Syracuse

Timothy A Damron, MD is a member of the following medical societies: American Academy of Orthopaedic Surgeons, American College of Surgeons, American Medical Association, Children's Oncology Group, Connective Tissue Oncology Society, Musculoskeletal Tumor Society, Orthopaedic Research Society, and Society for Experimental Biology and Medicine

Disclosure: Lippincott, Williams, and Wilkins Royalty Editing/writing textbook; Genentech Grant/research funds Clinical research; Orthovita Grant/research funds Clinical research; National Institutes of Health Grant/research funds Clinical research

Specialty Editor Board

Timothy A Damron, MD  David G Murray Endowed Professor, Department of Orthopedic Surgery, Professor, Orthopedic Oncology and Adult Reconstruction, Vice Chair, Department of Orthopedics, State University of New York Upstate Medical University at Syracuse

Timothy A Damron, MD is a member of the following medical societies: American Academy of Orthopaedic Surgeons, American College of Surgeons, American Medical Association, Children's Oncology Group, Connective Tissue Oncology Society, Musculoskeletal Tumor Society, Orthopaedic Research Society, and Society for Experimental Biology and Medicine

Disclosure: Lippincott, Williams, and Wilkins Royalty Editing/writing textbook; Genentech Grant/research funds Clinical research; Orthovita Grant/research funds Clinical research; National Institutes of Health Grant/research funds Clinical research

Francisco Talavera, PharmD, PhD  Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Medscape Salary Employment

Sean P Scully, MD, PhD  Professor, Department of Orthopedics, University of Miami

Sean P Scully, MD, PhD is a member of the following medical societies: American Academy of Orthopaedic Surgeons, International Society on Thrombosis and Haemostasis, and Society of Surgical Oncology

Disclosure: Nothing to disclose.

Dinesh Patel, MD, FACS  Associate Clinical Professor of Orthopedic Surgery, Harvard Medical School; Chief of Arthroscopic Surgery, Department of Orthopedic Surgery, Massachusetts General Hospital

Dinesh Patel, MD, FACS is a member of the following medical societies: American Academy of Orthopaedic Surgeons

Disclosure: Nothing to disclose.

Chief Editor

Harris Gellman, MD  Consulting Surgeon, Broward Hand Center; Voluntary Clinical Professor of Orthopedic Surgery and Plastic Surgery, Departments of Orthopedic Surgery and Surgery, University of Miami, Leonard M Miller School of Medicine

Harris Gellman, MD is a member of the following medical societies: American Academy of Medical Acupuncture, American Academy of Orthopaedic Surgeons, American Orthopaedic Association, American Society for Surgery of the Hand, and Arkansas Medical Society

Disclosure: Nothing to disclose.

References
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Image in a 44-year-old right hand–dominant man who presented with a mass on the volar radial aspect of his left index finger. The mass was painless and had been slowly growing for 1.5 years.
Radiograph demonstrates cortical erosion from the pressure effect of the adjacent mass on the radial aspect of the proximal phalanx.
Radiograph demonstrates the bony erosion associated with some giant cell tumors of the tendon sheath and shows the unmineralized soft-tissue shadow of the mass.
Radiograph demonstrates cortical erosion from the pressure effect of the overlying giant cell tumor of the tendon sheath. This apple-core effect is indicative of a primary soft-tissue mass that is causing external erosion, which should not be confused with a primary bone process such as periosteal chondroma.
Radiograph demonstrates cortical erosion from the pressure effect of the overlying giant cell tumor of the tendon sheath.
Histologic findings of a giant cell tumor of the tendon sheath.
High-power photomicrograph depicts the histologic findings of a giant cell tumor of the tendon sheath.
Typical T2-weighted MRI appearance of a giant cell tumor of the tendon sheath. Most of the tumor has intermediate signal intensity, and portions of the tumor have low signal intensity; the latter finding likely reflects signal attenuation due to hemosiderin deposition.
Typical T1-weighted MRI appearance of a giant cell tumor of the tendon sheath. Portions of the tumor have decreased signal intensity.
Typical T1-weighted MRI findings in a giant cell tumor of the tendon sheath overlying the metacarpophalangeal joint. Note the low-signal-intensity areas.
Corresponding T2-weighted MRI findings in the tumor shown in the image above. Note the areas of low signal intensity.
Intraoperative excision of the giant cell tumor of the tendon sheath, which has the typical golden-yellow color secondary to hemosiderin deposition. The radial digital nerve is dissected free and slightly volar to the mass.
After excision, the bone is curetted, leaving the exposed radial aspect of the proximal phalanx, as shown here.
Giant cell tumor of the tendon sheath after marginal excision.
Typical microscopic appearance of a giant cell tumor of the tendon sheath. Sheets of rounded or polygonal cells blend with hypocellular collagenized zones; variable numbers of giant cells are present.
High-power photomicrograph of giant cell tumor of the tendon sheath shows occasional numerous mononuclear cells, scattered giant cells, and hemosiderin-containing xanthoma cells.
An 11-year-old girl presented with this firm nonfluctuant mass over her posterior medial left ankle that had been present for 5 months and had not increased in size. The mass was not transilluminating. Findings on frozen section were consistent with a benign giant cell tumor of the tendon sheath. The mass was marginally excised.
Giant cell tumor of the tendon sheath after marginal excision from an 11-year-old girl who presented with a firm nonfluctuant mass over her posterior medial left ankle that had been present for 5 months and had not increased in size.
 
 
 
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