scholarly journals Malignant giant cell tumor of the sphenoid bone and its differential diagnosis

Cancer ◽  
1970 ◽  
Vol 25 (1) ◽  
pp. 167-170 ◽  
Author(s):  
Guy D. Potter ◽  
Bruce L. McClennan
Author(s):  
Rasikbala Doshi ◽  
Abdul Basit Chaudhari ◽  
Gordon Thomson

SUMMARY:The clinical and histological features of two cases of giant cell tumor of the sphenoid bone are described. Both presented with similar symptoms and signs, comparable to previously described cases. The problems in histological differential diagnosis are discussed and radiotherapy as the treatment of choice is suggested.


1983 ◽  
Vol 59 (2) ◽  
pp. 322-327 ◽  
Author(s):  
James T. Wolfe ◽  
Bernd W. Scheithauer ◽  
David C. Dahlin

✓ Giant-cell tumor rarely affects the sphenoid bone. Ten cases of this tumor seen at the Mayo Clinic are reviewed, bringing the number of cases in the world literature to 31. These tumors, which present in the second and third decades of life and are slightly more frequent in women than in men, may present with various symptoms, including headache, visual field defects, blindness, and diplopia. The symptom complex and roentgenographic findings are seldom, if ever, sufficiently characteristic to allow preoperative diagnosis. The microscopic differential diagnosis of giant-cell tumor of the sphenoid region includes giant-cell reparative granuloma, aneurysmal bone cyst, fibrous dysplasia, and “brown tumor” of hyperparathyroidism. Interesting features of this series include the presence of multifocal giant-cell tumor in one case, and the absence of Paget's disease of bone in every case. Complete follow-up review in these cases allowed a discussion of therapy and prognosis; it appears that subtotal excision with postoperative radiation therapy is the treatment of choice. While the histological appearance of giant-cell tumor is characteristic, caution must be exercised in interpreting small samples, and various reparative and metabolic disorders must be considered in the differential diagnosis.


2005 ◽  
Vol 76 (2) ◽  
pp. 149-152 ◽  
Author(s):  
Faruk Zorlu ◽  
Ugur Selek ◽  
Figen Soylemezoglu ◽  
Kamil Oge

Orthopedics ◽  
1984 ◽  
Vol 7 (5) ◽  
pp. 909-913
Author(s):  
Michael G Rock ◽  
John W Beabout ◽  
Krishnan K Unni ◽  
Franklin H Sim

2019 ◽  
Vol 03 (03) ◽  
pp. 83-86
Author(s):  
Emmanouil Neonakis ◽  
Georgia Antoniou ◽  
Ioannis K. Triantafyllopoulos

1975 ◽  
Vol 12 (5-6) ◽  
pp. 428-433 ◽  
Author(s):  
G. H. Ford ◽  
R. N. Empson ◽  
C. G. Plopper ◽  
P. H. Brown

Masses removed from the superficial fascia of the jugular groove of a 12-year-old Arabian mare and from the femoral canal of a 7 1/2-year-old female cat appeared to be counterparts of the human malignant giant cell tumor of soft parts, even recapitulating the clinical behavior of the respective subgroups. Histologically, both neoplasms contained the characteristic features of the malignant giant cell tumor of soft parts: large multinucleate giant cells, pleomorphic mononuclear giant cells, histiocytes, fibroblasts and fibrocytes that were sometimes sarcomatous, and foci of hemorrhage and necrosis. Ultrastructural characteristics of the giant cells suggest mesenchymal origin with osteoblastic or chondroblastic differentiation.


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