J Neurol Surg A Cent Eur Neurosurg 2016; 77(03): 239-246
DOI: 10.1055/s-0035-1554808
Review Article
Georg Thieme Verlag KG Stuttgart · New York

Giant Cell Tumor of the Skull: Review of the Literature

Ryota Tamura
1   Department of Neurosurgery, Ashikaga Red Cross Hospital, Ashikaga City, Japan
,
Tomoru Miwa
1   Department of Neurosurgery, Ashikaga Red Cross Hospital, Ashikaga City, Japan
,
Kazuhiko Shimizu
2   Department of Pathology, Ashikaga Red Cross Hospital, Ashikaga City, Japan
,
Katsuhiro Mizutani
1   Department of Neurosurgery, Ashikaga Red Cross Hospital, Ashikaga City, Japan
,
Hideyuki Tomita
1   Department of Neurosurgery, Ashikaga Red Cross Hospital, Ashikaga City, Japan
,
Nobuo Yamane
3   Department of Oral Surgery, Ashikaga Red Cross Hospital, Ashikaga City, Japan
,
Takehiro Tominaga
4   Department of Otorhinolaryngology, Ashikaga Red Cross Hospital, Ashikaga City, Japan
,
Shunichi Sasaki
4   Department of Otorhinolaryngology, Ashikaga Red Cross Hospital, Ashikaga City, Japan
› Author Affiliations
Further Information

Publication History

28 April 2014

10 March 2015

Publication Date:
19 June 2015 (online)

Abstract

Background Giant cell tumors (GCTs) are rare in the skull. The present report describes a case with a primary GCT located in the temporal bone and reviews the relevant literature. We also propose a treatment strategy for GCT of the skull.

Clinical Presentation A 41-year-old man presented with headache and auditory disturbance. Radiologic images showed a lytic expansive extradural lesion originating primarily from the right temporal bone and expanding into the middle cranial fossa and the infratemporal fossa. A biopsy specimen of the lesion was obtained from the external auditory meatus. Total removal was performed with temporal craniectomy, mandibular condylar process removal, tympanoplasty, and mastoidectomy.

Discussion The rate of recurrence of GCTs is related to complete resection and location of the GCT rather than to the degree of invasiveness. Some of the mononuclear cells and stromal cells in GCT express receptor activator of nuclear factor κ-β ligand (RANKL). Because inhibition of RANKL and bisphosphonate therapy might eliminate giant cells, this approach might be useful for recurrent or unresectable GCTs of the skull.

Conclusions Preoperative diagnosis by biopsy is important in determining the therapeutic strategy of GCTs. Complete resection is important to reduce the recurrence rate of GCTs in the skull.

 
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