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J Neurol Surg Rep 2015; 76(01): e65-e71
DOI: 10.1055/s-0034-1396656
Case Report
Georg Thieme Verlag KG Stuttgart · New York

Rare Presentation of Giant Cell Tumor in the Internal Auditory Canal: Case Report and Review of the Literature

Ajit S. Jada
1   Department of Neurosurgery, Montefiore Medical Center, Bronx, New York, United States
,
Raj K. Shrivastava
2   Department of Neurosurgery, The Mount Sinai Medical Center, New York, New York, United States
,
Abul Mannan
3   Department of Pathology, The Mount Sinai Medical Center Roosevelt Division, New York, New York, United States
,
Andrew Kobets
1   Department of Neurosurgery, Montefiore Medical Center, Bronx, New York, United States
,
Spiros Manolidis
4   Department of Otolaryngology, The Mount Sinai Medical Center Roosevelt Division, New York, New York, United States
› Author Affiliations
Further Information

Address for correspondence

Ajit S. Jada, MD
3316 Rochambeau Avenue
Bronx, NY 10467
United States   

Publication History

03 July 2014

22 October 2014

Publication Date:
18 February 2015 (online)

Also available ateRefMedOne
 
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Abstract

Giant cell tumor (GCT) is a benign but locally aggressive bone tumor that usually involves the end of long bones. It is a relatively common neoplasm in patients, constituting 5 to 10% of all benign bone tumors. Approximately 2% of GCTs occur in the craniofacial skeleton with a predilection for the ethmoid, sphenoid, and temporal bones. The skull base location is unique and not commonly described. Hearing loss, headache, tinnitus, and subcutaneous masses are the most commonly reported symptoms in GCTs of the skull base. In this case report we present the first description of a GCT within the internal auditory canal causing cranial neuropathy and review the recent pertinent literature.


 

Keywords

giant cell tumor - internal auditory canal - skull base tumor

Introduction

Giant cell tumor (GCT) is a benign but locally aggressive bone tumor that usually involves the end of long bones. It is a relatively common neoplasm in patients, constituting 5 to 10% of all benign bone tumors.[1] [2] Most of these tumors occur in the long bones in the epiphyseal segment within the bone marrow of the bone. In the long bones, they tend to occur at the distal femur, proximal tibia, proximal humerus, and distal radius.[3]

The pathologic hallmark of this lesion is a pattern of osteolytic destruction. There are, however, similar bony tumors that can mimic the clinical presentation of these lesions. The differential diagnosis of a GCT is therefore wide and consists of giant cell reparative granuloma, chondroblastoma, aneurysmal bone cyst, and enchondroma. Giant cell reparative granulomas are known to have a more benign course, with complete cure following surgical curettage alone. GCTs, in contrast, have a high recurrence rate of 40 to 60%[4] with a 10% risk for malignant transformation. Despite benign histology, 1 to 4% metastasize to the lungs.[5] Approximately 2% of GCTs occur in the craniofacial skeleton with a predilection for the ethmoid, sphenoid, and temporal bones.[6] The skull base location is unique and not commonly described.


 

Clinical Features: Signs and Symptoms of the Skull Base

Hearing loss, headache, tinnitus, and subcutaneous masses are the most commonly reported symptoms in GCTs of the skull base.[7] [8] Findings on examination are minimal including micro-otoscopy because these tumors originate in the deeper structures of the temporal/sphenoid bone. Facial nerve and lower cranial nerve involvement has been observed in advanced stages of the disease; pain is an uncommon complaint.[7] Hearing loss can be either conductive due to involvement of the middle ear or sensorineural due to involvement of the otic capsule.[8] Radiographically, these tumors occupy the middle cranial fossa, the temporomandibular joint, and the infratemporal fossa. Computed tomography (CT) and magnetic resonance imaging (MRI) are used to evaluate the extent of bony erosion and the extent of soft tissue involvement.[4] GCTs typically are hypointense on T1 and T2 and enhance with the administration of gadolinium.[4] GCTs rarely exhibit calcifications; however, when calcifications are present, other pathology should be considered such as chordoma, craniopharyngioma, meningioma, and chondrosarcoma.[9]

In this case report study, we report the first description of a GCT within the internal auditory canal (IAC) causing cranial neuropathy.


 

Case Report

Patient is a 47-year-old woman who presented to the neurosurgery clinic with significant headache, dizziness, and right ear pain. She reported complaints of a dramatic decrease in hearing in her right ear and disabling tinnitus over the course of the past year. She had no past medical history.

Physical Examination

Results of her general physical and neurologic examination were unremarkable, except for mild sensorineural hearing loss in her right ear and a positive Romberg sign. Her facial nerve function was intact with no signs of facial asymmetry. Her audiometric evaluation disclosed a 4% discrimination score and a 35 to 50 Db mild to moderate downsloping sensorineural hearing loss in her right ear with word recognition significantly lower than would be expected given her pure tone thresholds.


 

Laboratory Values

All preoperative basic chemistry and hematologic laboratory values were within normal limits. Calcium, magnesium, and phosphorus were also within normal limits.

An MRI was performed that revealed an enhancing lesion at the level of the right cerebellopontine angle cistern (CPA) with extension into the right IAC ([Fig. 1]). Our institution typically performs CT scans on CPA lesions to evaluate the bony anatomy, for preoperative planning, and we prefer to fuse the CT and MRI scans in stereotactic operative guidance systems. The CT scan of the right IAC demonstrated a lytic lesion involving the right temporal bone and the posterior wall of the right IAC. The lesion measured 1.3 × 1.2 × 0.8 cm. The lesion involved the medial aspect of the vestibular aqueduct but spared the vestibule, semicircular canals, and cochlea. The mass was inferior to the intracanalicular portions of cranial nerves VII and VIII complexes. The presumptive diagnosis based on imaging was meningioma, however; aneurysmal bone cyst, osteosarcoma, vestibular schwannoma, and brown tumor of hyperparathyroidism (lower suspicion based on normal serum calcium) were also considered in the differential diagnosis.

Zoom
Fig. 1 Axial contrast-enhanced magnetic resonance imaging demonstrating a uniformly enhancing lesion involving the right cerebellopontine angle cistern with extension into the right internal auditory canal. The imaging lead to a presumptive diagnosis of a meningioma. However, a dural tail was not identified, raising the suspicion for an alternative pathology.

Operation

Based on the patient's clinical deterioration in hearing, persistent headaches, and vertigo, and the atypical appearance of bony destruction on CT scan, a discussion with the patient outlined the necessity for operative intervention. A decision was made to proceed with skull base tumor resection. The surgery would entail a right presigmoid/retrolabyrinthine approach combined with posterior (retro) sigmoid approach. The patient was placed supine with a shoulder roll and placed in a Mayfield head holder. Somatosensory evoked potentials and motor potentials were attached as well. The combined retro/presigmoid craniectomy was performed, and the IAC was exposed. The inferior and superior aspect of the tumor was removed and the IAC was skeletonized from within the temporal bone. Intraoperatively it appeared that a gross total resection (GTR) was achieved. Neurophysiologic monitoring demonstrated a drop in facial motor potentials at the end of the case. The tumor had a soft and granular consistency. A frozen section was sent intraoperatively, and the preliminary report stated the tissue was consistent with a meningioma ([Fig. 2]).

Zoom
Fig. 2 Photomicrograph showing proliferation of monomorphic plump spindle cells, admixed with multinucleated giant cells (hematoxylin and eosin: magnification ×200). Inset shows immunoreactivity for CD68 in the multinucleated cells as well as the spindle cells (avidin-biotin-peroxidase magnification ×200). Findings were consistent with giant cell tumor.

 

Surgical Pathology

The surgical pathology report identified the specimen as consisting of multiple tan/brown soft tissue fragments aggregating up to 2.0 × 1.2 × 0.4 cm. Microscopy revealed the lesion to be composed of a proliferation of monomorphic spindle and plump epithelioid cell proliferation admixed with numerous multinucleated giant cells ([Fig. 2]). The mitotic rate was up to 4 per 10 high power fields. There was no significant atypia, coagulative tumor cell necrosis, or neoplastic osteoid, thus ruling out osteosarcoma. Also, microscopy did not demonstrate honeycombed blood-filled spaces that would have been consistent with an aneurysmal bone cyst. Immunohistochemistry showed immunoreactivity for CD 68 in both the multinucleated giant cells and a proportion of mononuclear cells (figure inset). The cells were negative for epithelial membrane antigen and progesterone receptor. Negative immunoreactivity for epithelial membrane antigen and progesterone receptor ruled out a meningioma. The morphological and immunophenotypic features were consistent with a giant cell rich fibrohistiocytic lesion. Furthermore, with normal parathyroid function and calcium levels, brown tumor of hyperparathyroidism was also ruled out.


 

 

Postoperative Course

The patient awoke from anesthesia with a right-side facial nerve palsy, consistent with a House-Brackmann grade IV. She was started on high-dose dexamethasone that was tapered over a week. Her hearing postoperatively was stable, and she is pending formal audiometric evaluation. Of note, the patient's vertigo did improve postoperatively with abatement of her Romberg sign and dizziness. On postoperative follow-up 6 weeks later, the patient had improved to a House-Brackmann grade III with independent eye closure. There were no signs of postoperative cerebrospinal fluid leak, either clinically with clear fluid egress, or radiographically with air or fluid on imaging, 6 weeks postoperatively.


 

 

Discussion

GCTs commonly involve the sphenoid and temporal bones in the craniofacial skeleton.[6] We report here this first description of a GCT primarily affecting the IAC and causing cranial neuropathy. This skull base location and proximity to the cranial nerves presents several challenges in their surgical management. Because GCT is primarily a locally aggressive tumor and rarely metastasizes, the most common treatment paradigm involves local curettage and a wide excision. This becomes more difficult, however, when the bony margins involve the skull base and cranial nerves. This complicates treatment of the GCT in the craniofacial skeleton as opposed to GCTs in long bones. Despite GTR, GCTs still recur locally in 10 to 50% of patients as reported in some clinical series.[10]

Due to the location of these tumors and their propensity to recur locally, complete excision without damage to regional critical structures, especially cranial nerves, is challenging. Tumor removal in a complete fashion is the goal of the treatment because recurrence in these areas will necessitate revision surgery that increases the chance of cranial nerve injury as well as local recurrence. However, when the tumor is large, internal debulking is necessary.[11] Therefore it is imperative that the first surgical resection be directed at GTR with preservation of neurovascular structures. In the temporal bone this is particularly important given the sensitivity of the cochleovestibular nerve and the complex course of the facial nerve.


 

Staging

GCTs are often characterized by extent of invasion prior to operative planning. Stage I tumors are located within a small area in the bone; stage II tumors are expansile within the cortex. Stage III tumors are defined as having breached the cortex and extending into the adjacent soft tissues.[12]


 

Histopathology and Cell Biology

GCTs are characterized by uniform layers of ovoid mononuclear cells interspersed with multinucleated osteoclast-like giant cells, which is a pathognomonic histologic sign of this tumor.[11] [12] [13] GCTs consist mainly of three cell types[14]: spindle shaped cells, mononuclear cells,[15] and multinucleated osteoclast-like giant cells.[15] [16] The osteoclast-like giant cells and their precursors express a receptor activator of nuclear factor κB (RANK). The mononuclear cells express the RANK ligand (RANKL)[17] that is essential to osteoclast function, formation, and survival. It is theorized that the recruitment of osteoclast-like giant cells is related to the expression of RANKL and that the giant cells mediate the osteolytic nature of the tumor.[17] [18] [19] [20] [21] This finding has led to treatment paradigms targeting the RANKL.

Emphasis has been placed on the differentiation between the giant cell reparative granuloma and GCT due to the proposed differences in their nature and clinical course.[22] These differences are based mostly on the clinical behavior of GCTs in long bones. However, there have been case reports of giant cell reparative granulomas in the skull base mimicking intracranial tumors.[23] Hence it is necessary to understand the pathology and differences in the treatment of GCT and giant cell reparative granulomas. Giant cell reparative granulomas are known to have a more benign course, with complete cure following surgical curettage alone. GCTS, in contrast, have a high recurrence rate of 40 to 60% with a risk for malignant transformation and potential to metastasize ranging from 1% to 9%, with the lung the most common location for metastases.[4]

Although most literature is on GCTs of long bones, bisphosphonates and other antiosteoclastic drugs have shown efficacy in various trials for treating local and metastatic GCTs.[12] Tse et al administered two doses of intravenous bisphosphonate before surgery and at 3 to 4 weeks between each dose for three doses and 3 months of additional oral bisphosphonate therapy. In the treatment group, 4.2% developed local recurrence; in the control group, 30% developed recurrence.[12] It is hypothesized that bisphosphonate use results in apoptosis of GCT cells that can be used as an adjunct to surgical resection.[24]

Intraoperatively, it is difficult to distinguish GCT from other pathology based on gross appearance and texture. If GCT is suspected based on radiographic features, the pathologist should be notified before frozen sectioning.


 

Origin in the Skull Base

The skull is an uncommon location for GCTs. The GCTs arise from nonosteogenic stromal cells of bone marrow at the epiphysis in cartilaginous bone.[25] The temporal bone consists of squamous and petromastoid components. GCTs are found to develop from petromastoid temporal bone more so than the squamous temporal bone.[26] The radiologic and clinical features in our case favor the origin from the petrous portion of the temporal bone. It is still the belief of some authors that GCTs and giant cell reparative granulomas (GCRGs) encompass a single disease process that is influenced by both the age of the patient and the site of occurrence.[27]

The first case of GCRG in the temporal bone was reported by Hirschl and Katz.[28] [29] Some specimens have distinct histologic features of either GCT or GCRG, but there may be similarities in the microscopic appearances of others.[30] These overlapping lesions reconfirm the hypothesis that GCT and GCRG may be a single spectrum of pathology. Trauma has been implicated in the etiology of both GCTs and GCRGs, as in the present case, and suggests a correlation between the two lesions.[31] Few GCTs have been reclassified as GCRGs due to the confusion in these lesions in the head and neck region. It is still a possibility that lesions following trauma are not true neoplasms and those giant cell granulomas that lack the history of trauma are true neoplastic lesions.

GCTs are uncommon in the skull and comprise <1% of all reported bone tumors.[32] [33] Moreover, GCTs commonly involve the sphenoid and temporal bones of the middle cranial fossa that are formed by the enchondral bone.[26] From a histologic perspective, GCTs are a benign lesion; however, when located in the skull base or sphenoid bone, these locally aggressive tumors can be clinically devastating due to their aggressive local destruction and their proximity to vital neurologic structures.[34] [35] [36] GCTs that present in the skull base are surgically challenging lesions, and the use of adjuvant therapy with external-beam radiotherapy has been reported without clear benefit and without obvious radiologic regression.[37] More research is needed in radiation as a treatment for GCT. As reported in the literature, the lack of efficacy of radiation on GCT has led authors toward surgical management as their primary modality of treatment for GCT, despite the morbidity as noted in our case presentation.

As an alternative to radiotherapy, bisphosphonate treatment for GCTs has been proposed in the literature as well, with data showing lower local recurrence and promising outcomes.[12] [24] However, this modality needs further clinical evaluation.


 

Treatment

In a review of the head and neck/skull base literature, surgery is still the definitive treatment modality for GCTs. Approximately 80% of patients with primary GCTs (craniofacial and long bone) have surgically amenable lesions; however, the morbidity associated with surgery is substantial, especially with regard to GCTs of the skull base. The reported recurrence rate is 10 to 75% depending on the location and size of the lesion, as well as the extent of surgical resection.[38] [39] There is a paucity of literature on recurrence of skull patients with GCT lesions who are not amenable to surgical resection and have limited treatment options. Arterial embolization and radiation therapy are treatment possibilities, although radiation can lead to transformation of GCTs to high-grade sarcomas, or it can lead to development of secondary malignancies.[40] Reports have shown that patients with pulmonary GCT metastases have favorable life expectancies; however, distant metastases of GCTs have not been shown to respond to chemotherapy and carry a poor prognosis.[41]


 

Causative Factors

Although the etiology of GCTs is uncertain, current theories for the origin of GCTs include neoplastic, toxic, allergic, genetic, inflammatory, and traumatic causes.[42] [43] True neoplastic lesions are thought to originate from the connective tissue of bone, whereas inflammatory lesions are thought to arise from the periosteum. Differentiating periosteal lesions from marrow or soft tissue lesions, either clinically or radiographically, is challenging due to the size of the tumor at diagnosis.[44] Thus there is debate on the etiology of GCTs and whether they are inflammatory reactions as opposed to a true neoplastic lesion.[45] Haque and Moatasim describes GCTs as a nonneoplastic condition that is a reactive process resulting from weak local vasculature in the bone.[45]


 

Radiology

Radiologic features of GCT can help establish a diagnosis. GCTs typically demonstrate a meta-epiphyseal location with an extension into subchondral bone.[4] On temporal bone CT, GCTs are identified as osteolytic lesions with a soft tissue component resulting in bony erosion and distinct margins.[46] GCTs have been described as having a “soap bubble appearance” on CT scan as well.[47] Although CT scan is essential for the delineation of bony anatomy and erosion, MRI is the diagnostic modality of choice for GCTs. Both cystic and solid components of the lesion can be observed on MRI. Lesions are typically isointense on T1 and low to intermediate intensity on T2, with heterogeneous enhancement after administration of intravenous gadolinium.[4] [48]

The CT scan in our patient revealed smooth expansion of bone with areas of bone destruction and a characteristic soap bubble matrix.[47] Also the lesion was isointense to the surrounding brain parenchyma on both T1- and T2-weighted images with intense postcontrast enhancement.

GCTs have shown increased uptake of technetium-99m; however, it is both a nonspecific and unreliable marker in defining extent of tumor, and its use is limited to metastatic or multicentric GCTs.[49] Positron emission tomography (PET) scans have demonstrated utility in the diagnosis of malignant and recurring GCTs, in addition to surveillance imaging for monitoring response to therapy.[49]


 

Emerging Treatments

As described earlier, the expression of the RANKL has been implicated in giant cell recruitment and the osteolytic nature of GCTs. New therapy has been directed at inhibiting the RANKL.

Denosumab is a fully human monoclonal antibody that specifically inhibits RANKL, thus inhibiting osteoclast-mediated bone destruction.[13] Denosumab has demonstrated suppression of bone turnover in patients with multiple myeloma, breast and prostate cancer, bone metastases, and osteolytic bone disease.[50] [51] [52] [53] Current studies are investigating the efficacy of denosumab in patients with GCT. With its mechanism of inhibition of RANKL, it may inhibit bone destruction and eliminate giant cells.[13] PET/CT may be the ideal imaging study to ascertain serial progression to treatment.


 

Surgical Management

Surgical resection remains the mainstay and primary treatment modality of GCTs of the head, neck, and long bones. GCTs of the skull base present a challenge due to the complex anatomy and intimate nature of the neurovascular elements. GTR with preservation of the facial nerve and lower cranial nerves is the goal of surgery, although with GCTs of the temporal bone, GTR may not possible. In our case, GTR was attempted; however, there was compromise of the facial nerve. The surgical approach to the tumor must be evaluated on a case-by-case basis. For tumors involving the temporal bone, some authors have advocated an infratemporal fossa approach, and for tumors involving the middle cranial fossa, a combined middle fossa and infratemporal approach has been suggested.[7] The surgical treatment of choice is intralesional curettage, burring with a high-speed drill, and packing with bone cement (polymethyl methacrylate). Furthermore, some authors suggest chemical adjuncts, if applicable, such a hydrogen peroxide or phenol.[38] Balke et al reports a reduction of recurrence rate by a factor of 28 with the addition of a chemical adjunct.[54]


 

Radiation

Postoperative radiation for subtotal resection remains controversial.[55] In a case series by Roeder et al, the authors concluded intensity-modulated radiotherapy (IMRT) is a feasible option for subtotal resection of GCTs, noting 4 of 5 patients with symptom relief and local control.[56] Furthermore, in a review of GCT of the sphenoid and temporal bones, Glasscock and Hunt noted recurrence rates of 60 to 70% when radiotherapy was used as a single modality.[57] Typically, radiation should be reserved for those patients who are not surgical candidates, have GCTs not amenable to surgery due to location and procedural risk, or have multiple recurrences after surgical resection. More research is needed to delineate the role of radiation in the management of GCTs.


 

Conclusion

In this case report study we report the first description of a GCT within the IAC causing cranial neuropathy. GCTs are locally aggressive benign lesions that occur in long bones, with 2% occurring in the craniofacial skeleton, most commonly within the sphenoid and temporal bones. Patients may present with facial nerve symptoms and hearing loss late in the presentation of the disease. GTR remains the mainstay of treatment; however, in lesions of the temporal bone this may not be feasible. Postoperative cranial neuropathy and/or weakness may occur from the extensive bony involvement. This may happen even in a delayed fashion. Local recurrence correlates with the size of the lesion and the extent of resection and curettage. Although controversial, IMRT may be a possible treatment modality for subtotal resection and should be investigated further. Emerging technologies for treatment are being developed and may provide improved patient outcomes.


 

 

Address for correspondence

Ajit S. Jada, MD
3316 Rochambeau Avenue
Bronx, NY 10467
United States   


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Zoom
Fig. 1 Axial contrast-enhanced magnetic resonance imaging demonstrating a uniformly enhancing lesion involving the right cerebellopontine angle cistern with extension into the right internal auditory canal. The imaging lead to a presumptive diagnosis of a meningioma. However, a dural tail was not identified, raising the suspicion for an alternative pathology.
Zoom
Fig. 2 Photomicrograph showing proliferation of monomorphic plump spindle cells, admixed with multinucleated giant cells (hematoxylin and eosin: magnification ×200). Inset shows immunoreactivity for CD68 in the multinucleated cells as well as the spindle cells (avidin-biotin-peroxidase magnification ×200). Findings were consistent with giant cell tumor.