Computed tomography and pathological findings of five nasal neurilemmomas

Neurilemmomas are benign tumors deriving from Schwann cells of the nerve sheath. They occur in all parts of the body. The highest incidence of neurilemmoma is in the head and neck region (38–45%) [1, 2], but involvement of the nose and paranasal sinus is quite rare, with only sporadic cases having been reported in the world literature. Fewer than 4% of these tumors involve the nasal cavity and paranasal sinuses [3].

The clinical symptomatology of nasal neurilemmomas is varied and nonspecific. The signs and symptoms usually depend upon the location or size of the tumor and subsequent involvement of surrounding structures. Preoperative diagnosis is facilitated by endoscopy, CT, and magnetic resonance imaging (MRI) [1‐6]. CT reveals a unilateral nasal mass that may be expansile [6]. Some features of CT is helpful in differentiating neurilemmomas from malignancies. Schwannomas can cause bone remodeling by pressure and this behavior can lead to misdiagnosis as a malignant process [6]. Preoperative correct judgement can aid to perform appropriate surgical approach [1]. To our knowledge, there are few reports more than five cases of CT features of nasal schwannoma . In this study, we describe the clinical, pathologic, and CT features of five nasal neurilemmomas.

From March 2001 to Deotcember 2011, five cases of nasal neurilemmomas were surgically removed and pathologically confirmed at our hospital. The study was performed with approval of the institutional review board of institution. Informed consent was not required. We retrospectively reviewed the CT, clinical manifestations and pathological findings.

The routine CT studies, with and without intravenous contrast agent injection, were performed with contiguous 3.2 mm sections from the anterior edge of frontal sinus to the posterior edge of sphenoid sinus. CT findings were analyzed by three radiologists. All histologic slides were reviewed independently by two pathologists. The clinical data were obtained from an archive. Immunohistochemistry was performed using a streptavidin-peroxidase (SP) immunohistochemical staining technique. The primary antibodies consisted of S100 protein (polyclonal, dilution 1:300; Dako, Trappes, France).

Pathologic specimens, CT findings and clinical histories were reviewed.

Neurilemmomas are usually composed of Schwann cells and are consequently also called schwannomas. Neurilemmomas can basically develop anywhere in the body, arising from the myelin sheaths of peripheral motor, sensory, sympathetic, and cranial nerves. The optic and olfactory cranial nerves are not potential sites of origin because they lack sheaths that contain Schwann cells [3]. The most common neurilemmoma in the head and neck is an acoustic neuroma arising from the eighth cranial nerve [4]. Only 4% involve the nasal cavity and paranasal sinuses. Neurilemmomas are predominantly benign, and the English literature only contains isolated cases of malignant schwannomas [5, 6]. Tumor incidence in the sinonasal tract is not related to sex or age, with cases occurring in children and the elderly[4, 7‐15].In our present study, all five cases occurred in the nasal cavity, with two in the nasal vestibule and three in the nasal septum. The female/male ratio was 2:3, with an age range from 27 to 59 years and a median age of 48 years. Localization to the nasal septum and the nasal vestibule is exceedingly rare. The occurrence in the nasal septum is rare, with only 18 reported cases in the English literature. Malignant neurilemmoma of the nasal septum is extremely rare [8].

The clinical symptomatology is varied and nonspecific. The signs and symptoms usually depend upon the location or size of the tumor and subsequent involvement of surrounding structures, often in relation to signs of chronic nasal obstruction, such as rhinorrhea, epistaxis, and anosmia, and facial swelling [10]. Exophthalmos, facial swelling, and epiphora are less frequently observed [11]. In our present cases, the main symptom was nasal obstruction; only one other compliant, nasal bleeding, was recorded. All tumors were limited to the nasal cavity. However, these masses were easily misdiagnosed as other tumors, such as an inverted papilloma.

In general, benign neurilemmomas are well differentiated by a characteristic capsule derived from perineural cells in other locations. However, some authors have reported that neurilemmomas in the nasal cavity have been described as nonencapsulated masses [4, 12, 13]. These authors have suggested that this peculiarity could be explained by the development of these tumors from sinonasal mucosa autonomic nervous system fibers, which are devoid of perineural cells, similar to the case of gastric neurilemmoma. The absence of a capsule could be responsible for the lack of a cleavage plane and thus complicates surgical resection [14]. In our cases, however, we observed encapsulated tumors in four cases; only one case had a nonencapsulated tumor. Consequently, our cases were not consistent with the authors’ speculation. From our cases, we suggest that the lack of encapsulation does not imply malignancy.

Microscopically, neurilemmomas typically exhibit a biphasic histologic pattern of Antoni A and Antoni B areas. Antoni A areas are regions of high cellularity with spindle-shaped cells; the cells are often arranged in bundles, palisades, or whirls. Groups of compact parallel nuclei are also seen and are known as “Verocay bodies.” Antoni B areas are less cellular and do not exhibit a distinctive pattern. Additionally, neurilemmomas usually show intense immunostaining for S100 (particularly Antoni A areas), which may help to distinguish peripheral nerve sheath neoplasms from other tumors [16].We noted that the five benign nasal neurilemmomas had a mixed appearance, with Antoni A and B areas intermingled. A benign neurilemmoma of the paranasal sinuses should be differentiated from a malignant peripheral nerve sheath tumor, which is rarely described in this location.

Some findings have been reported on the special CT manifestations of neurilemmomas at other sites due to the varied pathologic changes [16, 17]. In general, Antoni A and collagen have been attributed to high density areas on CT. Antoni B, obsolete bleeding, and cystic changes have been attributed to areas of low density on CT. From this set of data and an analysis of the literature, we suggest that nasal cavity neurilemmomas have the following characteristics [3, 18, 19]:

As documented by previous reports [1‐4] and also by our observations, nasal neurilemmoma commonly displays a soft-tissue mass without any distinctive features; therefore, the differential diagnosis includes a broad spectrum of lesions ranging from a neurofibroma cyst or hemangioma to malignant tumors such as melanoma and olfactory neuroblastoma.

In our present series, Case 3 was misdiagnosed as a nasal inverted papilloma. Cases 1,2, 4 and 5 were diagnosed as benign nasal tumors.

Differentiating between a neurilemmoma and neurofibroma can be particularly difficult because of the presence of overlapping histological features. Basically, neurilemmomas are often solitary and tender, with degenerative changes. Neurofibromas are more frequently multiple and associated with Von Recklinghausen’s disease; they are usually non-tender and less commonly present regressive changes. Neurofibromas are not encapsulated and are formed by a combined proliferation of all the elements of a peripheral nerve: axons, Schwann cells, fibroblasts, and probably perineural cells [23]. Malignant transformation of a neurilemmoma is exceedingly rare, but the risk increases in patients with Von Recklinghausen’s disease in whom the incidence of malignant transformation is about 10–15% [24]. On CT, neurofibromas show unclear boundaries or mild infiltration.

Neurilemmoma should be considered in the differential of unusual nasal masses. Certain clinical and CT patterns (i.e., a mottled central lucency with peripheral intensification on contrast-enhanced CT scans) may be of use in the differential diagnosis.