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Mousavi S R, Kalani N, Kazeminezhad A. Spinal Giant Cell Tumor in Neurospine Surgery: A Narrative Study. Iran J Neurosurg 2022; 8 :10-10
URL: http://irjns.org/article-1-281-en.html
1- Shiraz Neuroscience Research Center, Department of Neurosurgery, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran , moosavi_r@sums.ac.ir
2- Department of Anesthesiology, Critical Care and Pain Management Research Center, Jahrom University of Medical Sciences, Jahrom, Iran
3- Department of Neurosurgery, Peymanieh Hospital, Jahrom University of Medical Sciences, Jahrom, Iran
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1. Introduction
Giant Cell Tumor (GCT) is a complex clinical entity, and since 1818 when it was presented by Cooper and Travers, many new findings in multiple aspects of this tumor have been clarified [1]. GCT is a low-grade malignant aggressive tumor. The most prevalent sites of involvement are the femur, tibia, and radius, the involvement of the spine above the sacrum is rare, and the most common site of spinal involvement is the sacrum [23]. The most common region of involvement in the spine is in the vertebral body but is rarely confined to the vertebral body and may extend to the lamina, spinous process, and paravertebral site. Spinal GCTs destroy the vertebral body and neural arch and create expansile lytic lesions, with pain caused by a stretched periosteum followed by pathological fracture and neurologic symptoms [4, 5]. Because the most common manifestation of spinal GCTs is pain (back pain or low back pain), diagnosis may be delayed. Various treatment strategies, such as complete or incomplete operative resection and adjuvant therapies, such as cement injection, phenol ablation, cryotherapy, and radiotherapy have been described, but the treatment of choice for spinal GCTs is total spondylectomy with appropriate reconstruction for the preservation of spinal integrity [6, 7]. However, because of the proximity of the tumor to important neurovascular structures and vertebral cortex breakage with the tumor, usually complete extralesional resection cannot be done and incomplete partial resection following local radiotherapy is done [8, 9]. Radiation therapy can be given in cases of subtotal resection. For spinal reconstruction, cement or metallic cages are preferred and because of tumor recurrence in grafted bone, the bone graft is avoided. Tumor recurrence is frequently seen after intralesional or incomplete excision. In comparison to other areas, local recurrence in the spine is less, but as an invasive bone tumor, the postoperative recurrence rate of GCT is higher and distant metastasis may occur [10, 11, 12]. The main aim of this narrative study was to clarify and discuss these new aspects of GCT.
2. Methods and Materials/Patients
This study was a narrative study on the GCT of the spine. To provide up-to-date information on GCT of the spine, we concisely reviewed the spinal GCT incidence, manifestations, diagnosis, and management. Using the keywords of GCT, GCT manifestations, GCT complications, GCT management, and GCT incidence, all the relevant articles were retrieved from Google Scholar, Medline, and PubMed, reviewed, and critically analyzed.
3. Results
Based on the narrative study, the following results about incidence, manifestations, treatment, differential diagnosis, and outcome of this tumor were obtained. 
4. Discussion
About 6.5% of all GCTs occur in the spine with half occurring in the sacrum and about 7-10% of primary tumors of the spine are GCTs. The most common age for the occurrence of spinal GCTs is the third or fourth decades. The incidence of GCTs in females was twice as high as in males [13, 14].
Clinical manifestations
The onset of spinal GCT presentations is insidious and progression is slow over several months. The most prevalent presentation of spinal GCTs is pain. The expansile lesion with or without vertebral collapse and spinal instability causes pain. Following pain, with the encroachment of the tumor to the spinal canal, a neurological deficit occurs. Spinal GCT as an asymptomatic, incidental radiological finding is not common. Common clinical manifestations are as follows [15161718192021222324]: 
Pain: This is the most common manifestation because of vertebral destruction and periosteal stretching. In patients with sacral involvement, there is localized low-back pain that may radiate to one or both lower limbs.
Neurological deficit: This occurs because of canal encroachment and cord compression. Neurological symptoms are commonly subtle but bowel or bladder incontinence, leg weakness, or sexual dysfunction can occur. 
Structural deformity of the spine: Spinal GCT creates an expansile osteolytic lesion with the following mild vertebral collapse to a complete vertebra plane with blurring or loss of cortex and resultant structural deformity. Occasionally, a tumor can weaken a vertebra to such an extent that the vertebra breaks after relatively minor trauma. This is called a pathologic fracture.
Metastatic manifestations: About 10% of GCTs are malignant and metastatic involvement occurs in about 1%-6% of these tumors. The most common site of metastasis is the lung. Solitary metastases to regional lymph nodes, the mediastinum, and the pelvis have been reported nonspecific abdominal pain, early satiety, and change in bowel/bladder habits. 
Imaging studies
X-ray: In spinal GCT radiology, there is an expansile osteolytic lesion with the vertebral body in association with blurring or loss of cortex and associated soft-tissue mass. Because of the destructive effect of this tumor, the vertebral pedicle is deformed or completely disappeared [25].
Computed Tomography (CT) scan: The tumor has a soft-tissue density with no evidence of mineralized matrix. CT scan shows the tumor to be totally hypodense (areas of hemorrhage or necrosis) and hyperdense areas with a sclerotic rim at the periphery of the tumor. In the lytic areas of the cortex with an associated soft tissue mass, the cortex may be thinned, penetrated, or disappeared. The CT finding of GCT that is helpful in the diagnosis of this tumor is paradoxical appearance as the sclerotic border at one side of the tumor and expansile remodeling and breakthrough of the cortex at the opposite side because when the lesion is eccentrically distributed, the sclerotic rim appears at the opposite side of eccentric extension and remodeling at the same side of the eccentric extension. A radiographic “soap bubble” appearance, especially at the border of the tumor opposite the eccentric side is created because of some bony septa arising from the border of the tumor extending inside the lesion. This appearance is demonstrated in the axial image [26272829, 30, 31].
Magnetic Resonance Imaging (MRI): Spine GCT has heterogeneous signal intensity on all MR sequences. The following MRI findings can be observed that are helpful in differential diagnosis [3233, 34, 35]:
• Low-to-intermediate signal intensity of solid parts of tumor are observed in T2-Weighted (T2W) MRI. Because of the high signal intensity on T2W MRI in most other spinal neoplasms, such as metastases, lymphoma, and chordoma, this will be useful in the differential diagnosis of this tumor.
• Hemosiderin deposition in GCT shows low signal intensity on all sequence images with the nodular, zonal, whorled, or diffuse pattern. Because of the sensitivity of gradient-recalled echo images to hemosiderin, the areas of low signal intensity are exaggerated on T2W images.
• Because of the multiloculated lesion with thickened trabeculae, fibrous septa, or hemosiderin deposit, there are curvilinear low-signal areas on both T1W and T2W images on MRI of spinal GCT. 
• There are some focal cystic regions with low intensity in T1W images and high intensity in T2W images without enhancement.
• Bleeding areas with high intensity on T1W and T2W images and fluid-fluid levels may be visible.
The above findings are not specific and are common in Aneurismal Bone Cyst (ABC). Occasionally there is a fibrous capsule around the margin of the tumor as a thin sclerotic border with a band of low-signal intensity around the margin of the tumor. Because of the rich vascular supply of these tumors, there is a marked enhancement in contrast-enhanced CT and MRI. If there is the enhancement of solid components on T1W MRI with contrast, this is in favor of GCT with an ABC (secondary ABC) rather than pure ABC (primary ABC) [3233, 34, 35].
Differential diagnoses
ABC: The most prevalent lesion associated with secondary ABC is GCT and must be differentiated from primary ABC. ABC of the spine usually involves the posterior parts of the spine, the age range is below 20 years, and on MRI, has a purely cystic appearance If there is the enhancement of solid components on T1W MRI with contrast, this is in favor of GCT with an ABC (secondary ABC) rather than pure ABC (primary ABC) [26, 3637].
Plasmacytoma: Plasmacytomas are tumors in cases with an age range of above 40 years. Cystic change is not usual, and there are bony septa on CT scans and curvilinear low-signal intensity on MRI causes an appearance of sulci of the brain (minibrain appearance) [30].
Symptomatic hemangiomas: These tumors show irregular vertical trabeculae but marked pathological compression of vertebral bodies is infrequent in hemangioma. For symptomatic hemangiomas, there are the following helpful diagnostic findings: marked hyperintensity on T2W images and an undamaged cortex in the vicinity to a paraspinal or epidural mass [31].
Complete surgical excision is the treatment of choice in spinal GCT. Radiotherapy as a therapeutic option in unrespectable cases of GCT is not satisfactory for vertebral lesions because of possible spinal cord myelitis and malignant transformation of the tumor. Chemotherapy is another therapeutic option. Because of overexpression of the Receptor Activator of NF-KB Ligand (RANKL)and its receptor in GCTs, denosumab may be an effective alternative therapy. However, this is not a suitable therapeutic option for the treatment of GCT due to its toxic effects and normally benign nature of GCT. Therefore, there is no standard chemotherapy protocol for GCTs [383940, 4142, 4344].
As mentioned above, the ideal treatment for spinal GCT is complete extralesional/en bloc resection, which is usually not possible for two reasons: adjacent important neurovascular structures and vertebral cortex breakage. Therefore, the usual treatment option is marginal or intralesional resection, with complete intralesional curettage and excision followed by local radiotherapy. For increasing the yield of the diagnostic features in the histology/frozen section, it is better to take the sample from the tumor wall rather than the tumor substance. With modern radiotherapy techniques, there is no chance for malignant transformation of GCT, especially by keeping the total radiation dose under 50Gy. Preoperative embolization about 24 hours before the operation, because of the rich vascular supply of the tumor, decreases blood loss and creates a dry surgical field for meticulous resection of tumor and hemostasis. Because of the risk of infarction of the cord, if there is a common feeder between the cord and the tumor in DSA, embolization cannot be carried out. After complete surgical tumor removal, reconstruction surgery must be done by cement or metallic cages with avoidance of bone graft because of the high recurrence rate of tumor in the grafted bone. Postoperative radiotherapy also decreases graft fusion rate.
The prognosis of spinal GCT is better than non-spine types. Local recurrences and metastasis are less observed in spinal GCTs than GCTs in other locations. In spinal GCTs, recurrence rates are higher in the following conditions: operation is done in the first center after arrival without referral to a tertiary center, involvement of vertebral body and posterior elements by GCTs in contrast to GCTs limited to the vertebral body, and tumoral involvement of spinal canal and paraspinal musculature. For diagnosis of recurrences in the GCTs, the physician must have a high index of suspicion. If there is any suspicion of recurrence, a biopsy must be done to prove this, unless it is very obvious on the CT/MRI. For monitoring the postoperative status of a tumor, a CT scan over a one-year period, and for minimizing postoperative recurrence rates, postoperative irradiation are recommended [9, 10, 11, 12, 15, 36, 45464748].
5. Conclusion
Spinal GCTs are complex clinical disorders. They rarely present as incidental asymptomatic radiologic findings. Imaging studies, especially CT and MRI have a paramount role in the diagnosis of this tumor and for definitive diagnosis, a biopsy from the wall of the tumor is diagnostic. Surgical treatment as extralesional/en bloc resection is the ideal treatment. For effective early diagnosis and prevention of recurrence, close follow-up with a high index of suspicion is important. Adjuvant treatments, including radiotherapy and chemotherapy, need more conclusive detailed studies.

Ethical Considerations
Compliance with ethical guidelines

No human or animal subjects participated in this study. There were no ethical considerations to be considered in this research.

This research did not receive any grant from funding agencies in the public, commercial, or non-profit sectors.

Authors' contributions
All authors equally contributed to preparing this article.

Conflict of interest
The authors declared no conflict of interest.

We would like to thank the Clinical Research Development Unit of Peymanieh Educational and Research and Therapeutic Center of Jahrom University of Medical Sciences for providing facilities for this work.

  1. Kim HS, Lee JE, Jung SS, Chon J, Yoon DH, Park YK, et al. Spinal cord injury due to the giant cell tumor of the second thoracic vertebra: A case report. Annals of Rehabilitation Medicine. 2013; 37:269-73. [DOI:10.5535/arm.2013.37.2.269] [PMID] [PMCID]
  2. Balke M, Henrichs MP, Gosheger G, Ahrens H, Streitbuerger A, Koehler M, et al. Giant cell tumors of the axial skeleton. Sarcoma. 2012; 2012:410973. [DOI:10.1155/2012/410973] [PMID] [PMCID]
  3. Ben Nsir A, Said IB, Badri M, Boughamoura M, Jemel H. Giant cell tumor of the sixth thoracic vertebra: Case report. Turkish Neurosurgery. 2015; 25:475-8. [DOI:10.5137/1019-5149.JTN.8361-13.0] [PMID]
  4. van der Heijden L, Dijkstra PD, van de Sande MA. The clinical approach toward giant cell tumor of bone. Oncologist. 2014; 19:550-61. [DOI:10.1634/theoncologist.2013-0432] [PMID] [PMCID]
  5. Inci S, Akbay A, Bertan V. Giant-cell tumour of the lumbar spine. Case report. Spinal Cord. 1993; 31:412-4. [DOI:10.1038/sc.1993.69] [PMID]
  6. Martin C, Mccarthy EF. Giant cell tumor of the sacrum and spine: Series of 23 cases and a review of the literature. Iowa Orthopedic Journal. 2010; 30:69-75. [PMID] [PMCID]
  7. Patil S, Shah KC, Bhojraj SY, Nene AM. Recurrent spinal giant cell tumors: A study of risk factors and recurrence patterns. Asian Spine Journal. 2016; 10:129-35. [DOI:10.4184/asj.2016.10.1.129] [PMID] [PMCID]
  8. Charest-Morin R, Fisher CG, Varga PP, Gokaslan ZL, Rhines LD, Reynolds JJ, et al. En bloc resection versus intralesional surgery in the treatment of giant cell tumor of the spine. Spine. 2017; 42:1383-90. [DOI:10.1097/BRS.0000000000002094] [PMID]
  9. Savini R, Gherlinzoni F, Morandi M, Neff JR, Picci P. Surgical treatment of giant cell tumor of the spine: The experience at the Istituto Ortopedico Rizzoli. The Journal of Bone & Joint Surgery. 1983; 65:1283-9. [DOI:10.2106/00004623-198365090-00009] [PMID]
  10. Boriani S, Weinstein JN, Biagini R. Primary bone tumors of the spine: Terminology and surgical staging. Spine. 1997; 22:1036-44. [DOI:10.1097/00007632-199705010-00020] [PMID]
  11. Di Lorenzo ND, Spallone A, Nolletti A, Nardi P. Giant cell tumors of the spine: A clinical study of six cases, with emphasis on the radiological features, treatment and follow-up. Neurosurgery. 1980; 6:29-34. [DOI:10.1097/00006123-198001000-00003] [PMID]
  12. Fidler MW. Surgical treatment of giant cell tumours of the thoracic and lumbar spine: Report of nine patients. European Spine Journal. 2001; 10:69-77. [DOI:10.1007/s005860000206] [PMID] [PMCID]
  13. Hitchon P W, Bilsky M H, Ebersold MJ. Primary bony spinal lesions. In: Benzel EC, editor. Spine surgery:Techniques, complications, avoidance,and management. Houston: Gulf Professional Publishing; 2005. [Link]
  14. Hacbem LD, Scbneider L, Hawryluk G WF, Feblings MG. Phatophysiology and treatment of of spinal cord injury. In; H R Winn, editor. Youmans and Winn Neurological Surgery. Amsterdam: Elsevier Health Sciences; 2022. [Link]
  15. Biagini R, De Cristofaro R, Ruggieri P, Boriani S. Giant-cell tumor of the spine: A case report. The Journal of Bone and Joint Surgery. 1990; 72:1102-7. [DOI:10.2106/00004623-199072070-00025]
  16. Shikata J, Yamamuro T, Shimizu K, Shimizu K, Kotoura Y. Surgical treatment of giant-cell tumors of the spine. Clinical Orthopaedics and Related Research. 1992; 278:29-36. [DOI:10.1097/00003086-199205000-00005]
  17. Saikia B, Goel A, Gupta SK. Fine-needle aspiration cytologic diagnosis of giant-cell tumor of the sacrum presenting as a rectal mass: A case report. Diagnostic Cytopathology. 2001; 24(1):39-41. [DOI:10.1002/1097-0339(200101)24:1<39::aid-dc1006>3.0.co;2-6] [PMID]
  18. Dahlin DC. Giant-cell tumor of bone: Highlights of 407 cases. American Journal of Roentgenology. 1985; 144(6):955-60. [DOI:10.2214/ajr.144.5.955] [PMID]
  19. Goldenberg RR, Campbell CJ, Bonfiglio M. Giant-cell tumor of bone. An analysis of two hundred and eighteen cases. The Journal of Bone and Joint Surgery American Volume. 1970; 52(4):619-64. [PMID]
  20. Murphy WR, Ackerman LV. Benign and maligngiant-cell tumors of bone. Cancer. 1956; 9:317-39. [Link]
  21. Rock MG, Pritchard DJ, Unni KK. Metastases from histologically benign giant-cell tumor of bone. The Journal of Bone & Joint Surgery. 1984; 66(A):269-73. [DOI:10.2106/00004623-198466020-00014]
  22. Bertoni F, Present D, Sudanese A, Baldini N, Bacchini P, Campanacci M. Giant-cell tumor of bone with pulmonary metastasis. Clinical Orthopaedics and Related Research. 1988; 237:275-85. [DOI:10.1097/00003086-198812000-00040]
  23. Gresen AA, Dahlin DC, Peterson LFA, Payne WS. Benign giant-cell tumor of bone metastasizing to lung. The Annals of Thoracic Surgery. 1973; 16:531-5. [DOI:10.1016/S0003-4975(10)65030-8] [PMID]
  24. Stargardtes FL, Cooperman LR. Giant-cell tumor of sacrum with multiple pulmonary metastases and long term survival. The British Journal of Radiology. 1971; 44(528):976-9. [DOI:10.1259/0007-1285-44-528-976] [PMID]
  25. Shi LS, Li YQ, Wu WJ, Zhang ZK, Gao F, Latif M. Imaging appearance of giant cell tumour of the spine above the sacrum. The British Journal of Radiology. 2015; 88(1051):20140566.[DOI:10.1259/bjr.20140566] [PMID] [PMCID]
  26. Si MJ, Wang CG, Wang CS, Du LJ, Ding XY, Zhang WB, et al. Giant cell tumours of the mobile spine: Characteristic imaging features and differential diagnosis. La Radiologia Medica. 2014; 119(9):681-93. [DOI:10.1007/s11547-013-0352-1] [PMID]
  27. Murphey MD, Andrews CL, Flemming DJ, Temple HT, Smith WS, Smirniotopoulos JG. From the archives of the AFIP. Primary tumors of the spine: Radiologic pathologic correlation. Radiographics. 1996; 16(5):1131-58. [DOI:10.1148/radiographics.16.5.8888395] [PMID]
  28. Junming M, Cheng Y, Dong C, Jianru X, Xinghai Y, Quan H, et al. Giant cell tumor of the cervical spine: A series of 22 cases and outcomes. Spine (Phila Pa 1976). 2008; 33:280-8. [DOI:10.1097/BRS.0b013e318162454f] [PMID]
  29. Murphey MD, Nomikos GC, Flemming DJ, Gannon FH, Temple HT, Kransdorf MJ. From the archives of AFIP. Imaging of giant cell tumor and giant cell reparative granuloma of bone: Radiologic-pathologic correlation. Radiographics. 2001; 21(5):1283-309. [DOI:10.1148/radiographics.21.5.g01se251283] [PMID]
  30. Major NM, Helms CA, Richardson WJ. The mini brain: Plasmacytoma in a vertebral body on MR imaging. American Journal of Roentgenology. 2000; 175:261-3. [DOI:10.2214/ajr.175.1.1750261] [PMID]
  31. Friedman DP. Symptomatic vertebral hemangiomas: MR findings. American Journal of Roentgenology. 1996; 167:359-64. [DOI:10.2214/ajr.167.2.8686604] [PMID]
  32. Kwon JW, Chung HW, Cho EY, Hong SH, Choi SH, Yoon YC, et al. MRI findings of giant cell tumors of the spine. American Journal of Roentgenology. 2007; 189:246-50. [DOI:10.2214/AJR.06.1472] [PMID]
  33. Aoki J, Tanikawa H, Ishii K, Seo GS, Karakida O, Sone S, et al. MR findings indicative of hemosiderin in giant-cell tumor of bone: Frequency, cause, and diagnostic significance. American Journal of Roentgenology. 1996; 166:145-8. [DOI:10.2214/ajr.166.1.8571864] [PMID]
  34. Stacy GS, Peabody TD, Dixon LB. Mimics on radiography of giant cell tumor of bone. American Journal of Roentgenolog. 2003; 181(6):1583-9. [DOI:10.2214/ajr.181.6.1811583] [PMID]
  35. Meyers SP. MRI of bone and soft tissue tumors and tumorlike lesions, differential diagnosis and atlas. New York: Thieme; 2011. [DOI:10.1055/b-002-66244]
  36. Sanjay BK, Sim FH, Unni KK, McLeod RA, Klassen RA. Giant-cell tumours of the spine. The Journal of Bone and Joint Surgery. British volume. 1993; 75-B(1):148-54. [DOI:10.1302/0301-620X.75B1.8421014] [PMID]
  37. Boriani S, Bandiera S, Casadei R, Boriani L, Donthineni R, Gasbarrini A, et al. Giant cell tumor of the mobile spine: A review of 49 cases. Spine (Phila Pa 1976). 2012; 37:E37-45.  [DOI:10.1097/BRS.0b013e3182233ccd] [PMID]
  38. Niu X, Zhang Q, Hao L, Ding Y, Li Y, Xu H, et al. Giant cell tumor of the extremity: Retrospective analysis of 621 Chinese patients from one institution. The Journal of Bone & Joint Surgery. 2012; 94:461-7. [DOI:10.2106/JBJS.J.01922] [PMID]
  39. Bhatia S, Miszczyk L, Roelandts M, Nguyen TD, Boterberg T, Poortmans P, et al. Radiotherapy for marginally resected, unresectable or recurrent giant cell tumor of the bone: A rare cancer network study. Rare Tumors. 3(4):e48. [DOI:10.4081/rt.2011.e48] [PMID] [PMCID]
  40. Khan DC, Malhotra S, Stevens RE, Steinfeld AD. Radiotherapy for the treatment of giant cell tumor of the spine: A report of six cases and review of the literature. Cancer Investigation. 1999; 17(2):110-3. [DOI:10.1080/07357909909011724] [PMID]
  41. Chen ZX, Yu ZH, Qian TN, Huang YR, Hu YH, Zhi GZ. Radiation therapy of giant cell tumor of bone: Analysis of 35 patients. International Journal of Radiation Oncology* Biology* Physics. 1986; 12(3):329-34. [DOI:10.1016/0360-3016(86)90346-9]
  42. Cheng YY, Huang L, Lee KM, Xu JK, Zheng MH, Kumta SM. Bisphosphonates induce apoptosis of stromal tumor cells in giant cell tumor of bone. Calcified Tissue International. 2004; 75:71-7. [DOI:10.1007/s00223-004-0120-2] [PMID]
  43. Thomas D, Henshaw R, Skubitz K, Chawla S, Staddon A, Blay JY, et al. Denosumab in patients with giant-cell tumour of bone: An open-label, phase 2 study.The Lancet Oncology. 2010; 11(3):275-80. [DOI:10.1016/S1470-2045(10)70010-3]
  44. Klenke FM, Wenger DE, Inwards CY, Rose PS, Sim FH. Recurrent giant cell tumor of long bones: Aanalysis of surgical management. Clinical Orthopaedics and Related Research. 2011; 469(4):1181-7. [DOI:10.1007/s11999-010-1560-9] [PMID] [PMCID]
  45. Guzman R, Dubach-Schwizer S, Heini P, Lovblad KO, Kalbermatten D, Schroth G, et al. Preoperative transarterial embolization of vertebral metastases. European Spine Journal. 2005; 14:263-8. [DOI:10.1007/s00586-004-0757-6] [PMID] [PMCID]
  46. Dahlin DC. Giant cell tumor of vertebrae above the sacrum: A review of 31 cases. Cancer. 1977; 39:1350-6.[DOI:10.1002/1097-0142(197703)39:33.0.CO;2-1] [PMID]
  47. Ozaki T, Liljenqvist U, Halm H, Hillmann A, Gosheger G, Winkelmann W. Giant cell tumor of the spine. Clinical Orthopaedics and Related Research. 2002; 401:194-201. [DOI:10.1097/00003086-200208000-00022] [PMID]
  48. Dahlin DC, Cupps RE, Johnson EW. Giant cell tumor: A study of 195 cases. Cancer. 1970; 25:1061-70. [DOI:10.1002/1097-0142(197005)25:5<1061::aid-cncr2820250509>3.0.co;2-e] [PMID].
Type of Study: Review | Subject: Neuroscience

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