CC BY-NC-ND 4.0 · Asian J Neurosurg 2017; 12(01): 78-81
DOI: 10.4103/1793-5482.145112
CASE REPORT

Clival giant cell tumor - A rare case report and review of literature with respect to current line of management

Mohana Patibandla
Department of Neurosurgery, Nizam's Institute of Medical Sciences, Hyderabad
,
Amit Thotakura
Department of Neurosurgery, Nizam's Institute of Medical Sciences, Hyderabad
,
Marabathina Rao
1   Department of Neurosurgery, NRI Medical College, Mangalagiri, Guntur, Andhra Pradesh
,
Gokul Addagada
5   Department of Radiology, NRI Medical College, Mangalagiri, Guntur, Andhra Pradesh
,
Manisha Nukavarapu
5   Department of Radiology, NRI Medical College, Mangalagiri, Guntur, Andhra Pradesh
,
Manas Panigrahi
2   Guntur Medical College, Guntur, Andhra Pradesh
,
Shantiveer Uppin
3   Krishna Institute of Medical Sciences, Secunderabad, Telangana
,
Sundaram Challa
3   Krishna Institute of Medical Sciences, Secunderabad, Telangana
,
Srinivas Dandamudi
4   Department of Pathology, Nizam's Institute of Medical Sciences, Hyderabad
› Author Affiliations

Giant-cell tumor (GCT) involving the skull base is rare. Sphenoid bone is the most commonly involved bone followed by petrous temporal bone. Histopathology and radiological features of these lesions are similar to GCT involving bone elsewhere. Unlike other sites, skull base is not an ideal site for the radical surgery. Hence adjuvant treatment has pivotal role. Radiation therapy with intensity-modulated radiation therapy, stereotactic radiosurgery or chemotherapy with adriamycin are promising as described in some case reports. Bisphosphonates showed good control in local recurrence. In vitro studies with Zolendronate loaded bone cement and phase 2 trials of Denosumab showed hopeful results, may be useful in future.



Publication History

Article published online:
20 September 2022

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