scholarly journals Denosumab Chemotherapy for Recurrent Giant-Cell Tumor of Bone: A Case Report of Neoadjuvant Use Enabling Complete Surgical Resection

2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
Amit Agarwal ◽  
Brandon T. Larsen ◽  
Lawrence D. Buadu ◽  
Jack Dunn ◽  
Russell Crawford ◽  
...  

Giant-cell tumor of the bone (GCTB) is a rare neoplasm that affects young adults. The tumor is generally benign but sometimes can be locally aggressive. There are no standardized approaches to the treatment of GCTB. Recently, the RANKL inhibitor denosumab has shown activity in this tumor type. We present the case of a young female who presented with locally advanced disease and was successfully managed with the neoadjuvant use of denosumab allowing for surgical resection of the tumor that was previously deemed unresectable. Following surgery, the patient is being managed with continued use of denosumab as ‘maintenance,’ and she continues to be free of disease. Our case highlights a novel approach for the management of locally advanced and aggressive giant cell tumor of the bone.

2021 ◽  
Vol 61 (4) ◽  
pp. 1057-1065
Author(s):  
Mara Jidveian Popescu ◽  
◽  
Mihai Ciprian Stoicea ◽  
Ileana Marinescu ◽  
Răzvan Silviu Cismaşiu ◽  
...  

2005 ◽  
Vol 84 (7) ◽  
pp. 432-434 ◽  
Author(s):  
Marcus M. Lessa ◽  
Flavio A. Sakae ◽  
Robinson K. Tsuji ◽  
Bernardo C. Araújo Filho ◽  
Richard L. Voegels ◽  
...  

Brown tumor, an uncommon focal giant-cell lesion, arises as a direct result of the effect of parathyroid hormone on bone tissue in patients with hyperparathyroidism. The initial treatment involves the correction of hyperparathyroidism, which usually leads to tumor regression. We report a case of brown tumor of the right nasal fossa in a 71-year-old woman. The tumor had caused nasal obstruction and epistaxis. Laboratory evaluation revealed that the patient had primary hyperparathyroidism. Anatomicopathologic investigation revealed the presence of a giant-cell tumor. We performed a partial parathyroidectomy, but the tumor in the right nasal fossa failed to regress. One year later, we performed surgical resection of the lesion. The patient recovered uneventfully, and she remained asymptomatic and recurrence-free at the 1-year follow-up. Facial lesions with histologic features of a giant-cell tumor should be evaluated from a systemic standpoint. Hyperparathyroidism should always be investigated by laboratory tests because most affected patients are asymptomatic. Surgical resection of a brown tumor should be considered if the mass does not regress after correction of the inciting hyperparathyroidism or if the patient is highly symptomatic.


2019 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Kiranmye Reddy ◽  
Lorimar Ramirez ◽  
Kamlesh Kukreja ◽  
Rajkumar Venkatramani

2018 ◽  
Vol 8 (1) ◽  
pp. e15-e15 ◽  
Author(s):  
Michael K. Bokemper ◽  
Edgar T. Araiza ◽  
Kimberly J. Templeton ◽  
Tyler J. Fox

2012 ◽  
Vol 27 (4) ◽  
pp. 262 ◽  
Author(s):  
BhagwantRai Mittal ◽  
Ramesh Sen ◽  
Anish Bhattacharya ◽  
Kuruva Manohar

1997 ◽  
Vol 39 (6) ◽  
pp. 659-661 ◽  
Author(s):  
Jeffrey Weinzweig ◽  
H. Kirk Watson

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