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Erschienen in: Maxillofacial Plastic and Reconstructive Surgery 1/2017

Open Access 01.12.2017 | Case report

Schwannoma of the tongue: a case report with review of literature

Erschienen in: Maxillofacial Plastic and Reconstructive Surgery | Ausgabe 1/2017

Abstract

Background

Schwannomas (or neurilemmomas) of the tongue are benign, usually solitary, encapsulated masses derived from Schwann cells. Clinical evidence indicates that schwannoma is painless and slow growing. In general, schwannoma is treated by surgical excision.
Here, we describe a case of schwannoma of the tongue, include a review of the literature from 1955 to 2016, and provide data on age, gender, location, presenting symptoms, size, and treatment methods.

Case presentation

A 71-year-old female patient presented with a swelling at the base of the tongue of unknown duration. Magnetic resonance images (MRI) showed a large well-circumscribed solid mass and no significant lymph node enlargement. The mass was excised without removing overlying mucosa.

Conclusions

The authors report a case of lingual schwannoma that was completely removed intraorally without preoperative biopsy. No sign or symptoms of recurrence were observed at 12 months postoperatively.

Background

Around 25–40% of schwannomas occur in the head and neck region, and of these, 1–12% affect the intraoral area [1], most frequently the tongue or mouth floor [2]. Because of their rarity, intraoral schwannomas are not generally part of the differential diagnosis of tongue mass which includes squamous cell carcinoma, sarcoma, granular cell tumor, salivary gland tumor, schwannoma, leiomyoma, rhabdomyoma, hemangioma, lipoma, lymphangioma, dermoid cysts, and inflammatory lesions [3].
Clinically, schwannomas are benign, usually solitary, encapsulated masses that originate from Schwann cells without pain or ulceration.
Here, we report a case of schwannoma of the tongue base and review the literature. A Google search of the terms “schwannoma (neurilemmoma) of the tongue” and “lingual Schwannoma” was performed from 1955 to 2016. Age, gender, location (anterior, posterior, base, ventral), presenting symptoms, size, and treatment methods were extracted from case reports.

Case presentation

A 71-year-old female patient presented with a firm swelling at the base of her tongue of unknown duration that had progressively increased in size. Her only symptom was distortion of the tongue. Medical history taking revealed controlled hypertension (duration X years) and thyroid grand tumor. A well-encapsulated nodular mass was evident at physical examination, but without any neurologic symptom or lymphadenopathy in the submandibular area. The mass was 3 × 2 cm sized without ulceration (Fig. 1). Magnetic resonance imaging (MRI) depicted a solid, soft, heterogeneously enhanced lesion (Figs. 2 and 3). Complete surgical excision was conducted under general anesthesia without preoperative biopsy. Blunt dissection was performed without rupturing the mass or causing dehiscence of superficial mucosa. The mass was completely excised under mucosa (Fig. 4). It had been infiltrated by a branch of the lingual nerve, and a portion of the nerve had to be removed to achieve complete resection. On gross examination, the mass was grayish-yellow and well encapsulated with exophytic lobules (Fig. 5). Microscopically, the lesion was characterized by a mixture of Antoni type A and B tissue growth patterns with hyalinized vessel walls (Fig. 6). No sign or symptoms of recurrence were detected 12 months after surgery (Fig. 7).
A review of the literature over the past 61 years that showed 84 cases, including the present case, has been reported (Table 1). Lingual schwannoma may arise at any age between 7 and 77 and shows no sex predilection (44 males and 40 females) [4, 5]. Despite the fact that it originates from nerve tissue, lingual schwannoma is usually painless.
Table 1
Patients and tumor characteristics of tongue schwannomas
Author
Year
Gender
Age
Size (cm)
Site
Presentation
Surgical approach
Mercantini and Mopper [21]
1959
M
22
1
Anterior
Intermitten pain
Transoral
Cameron [22]
1959
M
25
1.5
Anterior
Lump
Transoral
Chadwick [23]
1964
F
20
2.2
Posterior
Lump
Transoral
Craig [24]
1964
F
8
3
Posterior
Lump
Transoral
Pantazopoulos [25]
1965
F
45
4.5
Posterior
Dyshagia/change in voice
Transoral
 
1965
M
25
1
Anterior
Lump
Transoral
Chhatbar [26]
1965
M
29
5
Posterior
Throat discomfort
Transoral
Firfer et al. [27]
1966
F
28
3
Anterior
Lump
Transoral
Hatziotis and Aspride [28]
1967
M
25
Hazelnut
Posterior
Lump
Transoral
 
1967
F
60
Pea
Anterior
Lump
Transoral
Oles and Werthemier [29]
1967
M
52
1
Anterior
Lump
Transoral
Paliwal et al. [30]
1967
M
32
2.5
Anterior
Lump
Transoral
Crawford et al. [31]
1968
M
23
0.5
Anterior
Lump
Transoral
 
1968
M
24
1
Anterior
Lump
Transoral
Das Gupta et al. [32]
1969
F
21
5
Posterior
Pain
Transoral
Bitici [33]
1969
M
40
2.5
Anterior
Slight discomfort
Transoral
Sinha and Samuel [34]
1971
M
23
1.5
Posterior
Dysphagia
Transoral
Mosadomi [35]
1975
M
19
3
Anterior
Painful mass
Transoral
Swangsilpa et al. [36]
1976
M
26
3
Anterior
Lump
Transoral
Sharan and Akhtar [37]
1978
F
30
1.5
Anterior
Change in voice
Transoral
Akimoto et al. [38]
1987
M
15
1
Anterior
Lump
Transoral
Sira et al. [39]
1988
F
18
3
Posterior
Lump
Transoral
Flickinger et al. [40]
1989
F
28
3
Anterior
Lump
Transoral
Talmi et al. [41]
1991
F
75
1
Posterior
Lump
Transoral
Gallesio and Berrone [42]
1992
F
21
1.9
Anterior/base
Dysphonia/paresthesia/chewing difficulty
Transoral
Lopez and Ballistin [10]
1993
M
24
0.6
Anterior
Lump
Transoral
Haring [43]
1994
F
49
2
Anterior
Lump
Transoral
Nakayama et al. [44]
1996
F
40
5.5
Anterior
Lump
Transoral
Dreher et al. [15]
1997
F
31
3
Base
Dysphagia
Transoral
Spandow et al. [45]
1999
M
37
7.9
Posterior
Throat discomfort
Transoral
de Bree et al. [2]
2000
F
24
5
Posterolateral/base
Lump
Submandibular
Pfeifle et al. [46]
2001
F
30
0.3
Anterior
Lump
Transoral
 
2001
M
18
2
Anterior
Lump
Transoral
Cinar et al. [47]
2004
M
7
1
Anterior
Lump
Transoral
Bassichis and McMlay [48]
2004
M
9
2.3
Posterior/base
Snoring
Transoral
Nakasato et al. [49]
2005
F
9
2
Posterolateral/base
Bleeding/ulceration
Transoral
Hwang et al. [50]
2005
M
23
2.8
Anterior
Lump
Transoral
Lopez-Jornet and Bermejo-Fenoll [51]
2005
M
39
0.8
Posterolateral/base
Lump
Transoral
Vafiadis et al. [52]
2005
M
18
3.1
Anterior
Lump
Transoral
Bansal et al. [53]
2005
M
26
4
Posterolateral/ventral
Paresthesia/dysphonia
Transoral
Hsu et al. [7]
2006
M
20
5
Posterior/base
Bleeding
Transoral
 
2006
F
39
4
Posterior/base
Dysphagia
Transoral
 
2006
F
32
1.8
Posterior/base
Lump
Transoral
 
2006
M
38
3
Anterior
Lump
Transoral
 
2006
M
45
0.5
Anterior
Lump
Transoral
 
2006
M
25
0.9
Anterior
Lump
Transoral
 
2006
F
39
1
Anterior
Lump
Transoral
 
2006
M
9
1.2
Anterior
Lump
Transoral
 
2006
F
15
1.2
Anterior
Lump
Transoral
 
2006
F
12
1.6
Anterior
Lump
Transoral
Ying et al. [54]
2006
F
26
4
Posterior/base
Dysphagia/otalgia
Transoral
Enoz et al. [14]
2006
M
7
2.5
Anterior/base
Dysphagia/pain
Transoral
Mehrzad et al. [55]
2006
M
49
2.2
Posterior/ventral
Pain
CO2-transoral
Batra et al. [56]
2007
M
30
3
Posterolateral/base
Dysphagia, dyspnea, abscess
Transoral
 
2007
M
33
3
Posterolateral/base
Dysphonia
Transoral
Ballesteros et al. [57]
2007
F
31
2
Base
Pain
CO2-transoral
Sawhney et al. [19]
2008
F
37
4.6
Posterolateral/base
Dysphagia/snoring
Submandibular
Sethi et al. [58]
2008
F
28
1
Anterolateral/ventral
Lump
Transoral
Pereira et al. [59]
2008
M
12
1.5
Posterolateral/ventral
Lump
 
Cohen and Wang [17]
2009
M
77
0.7
Posterolateral/ventral
Lump
Transoral
 
2009
F
19
1.8
Posterolateral/ventral
Lump
Transoral
Gupta et al. [60]
2009
F
18
1
Anterior/ventral
Lump
Transoral
Mardanpour and Rahbar [61]
2009
M
18
2
Posterior
Dysphagia/change of voice
Transoral
Karaca et al. [62]
2010
F
13
2
Posterolateral/ventral
Dysphagia
Transoral
Cigdem et al. [63]
2010
M
13
2
Anterior/ventral
Lump
Transoral
Jeffcoat et al. [64]
2010
M
68
1.5
Lateral
Lump
Transoral
Naidu and Sinha [65]
2010
M
12
2
Anterolateral/base
Paresthesia/bleeding/ulceration
Transoral
Lukšić et al. [66]
2011
M
10
1.5
Posterolateral/ventral
Lump
Transoral
Batra et al. [67]
2011
F
38
4.2
Posterior/ventral
Dysphagia/change of voice
Transoral
Nisa et al. [68]
2011
F
38
8.5
Posterolateral/ventral
Dysphagia/dysphonia/dyspnea
Transoral
Monga et al. [69]
2013
M
20
2
Posterolateral/base
Lump
Transoral
Lira et al. [5]
2013
F
26
2.5
Posterior/ventral
Cervical pain
Transoral
Erkul et al. [70]
2013
M
21
3
Posterolateral/ventral
Chewing difficulty
Transoral
 
2013
M
21
2
Anterolateral/ventral/tip
Lump
Transoral
Jayaraman et al. [71]
2013
F
25
3
Anterolateral/base
Lump
Transoral
George et al. [4]
2014
M
26
4
Posterolateral/base
Dysphagia/dysphonia
Transoral
Bhola et al. [11]
2014
F
14
1.5
Anterolateral/ventral
Lump
Transoral
Moreno-García et al. [16]
2014
F
13
2
Anterior/ventral
Lump
Lip split/mandibulotomy
Nibhoria et al. [72]
2015
F
18
1.5
Posterolateral/ventral
Lump
Transoral
Gopalakrishnan et al. [73]
2016
M
32
3
Posterolateral/ventral
Dysphagia
Transoral
Sharma and Rai [74]
2016
F
20
4
Posterolateral/ventral
Dysphagia/dysphonia
Transoral
Kavčič and Božič [75]
2016
F
20
1.3
Anterolateral/ventral/tip
Lump
Transoral
Lee et al. [76]
2016
M
28
4
Posterior/ventral
Lump
Transoral
Lee
Present case
F
71
3.5
Anterior/base
Lump
Transoral
       
Transoral
       
Transoral
MRI magnetic resonance images, CT computed tomography
In 51 cases, the only presenting symptom was an enlarging lump. Other symptoms were dysphagia (15 cases), pain (or discomfort, 10 cases), dysphonia (6 cases), voice change (5 cases), paresthesia (3 cases), snoring (2 cases), bleeding (2 cases), ulceration (2 cases), and abscess (1 case). Masses were located in any part of the tongue. Average size at removal was 2.4 cm (range, 0.3–8.5 cm), and all were treated by transoral excision except 3 cases. The submandibular approach was used in 2 cases and lip splint and mandibulectomy in 1 case. In all three of these cases, masses were located in posterolateral bases.

Discussion

Although the etiology of schwannoma is not clear, it is known to be derived from nerve sheath Schwann cells, which surround cranial, peripheral, and autonomic nerves [6, 7]. The head and neck are rather common location of this neoplasm. Intraoral schwannomas mainly arise from the tongue, followed by the palate, mouth floor, buccal mucosa, gingiva, lip, and vestibule [8, 9], though the tongue is most commonly involved [10]. The lesion is slow growing, and thus, its onset is usually long before presentation. Lingual schwannoma shows no age or gender predisposition [11]. Usually, it is presented as a painless lump in any part of the tongue of average size 2.4 cm. However, when the mass exceeds 3.0 cm, dysphagia, pain (or discomfort), dysphonia, and voice change are usually presented (Table 1).
Computed tomography (CT) usually shows well-defined homologous lesions. When a heterogeneous lesion is observed by CT, malignant change may be suspected [12]. However, MRI is superior to CT at depicting lingual schwannoma, as it is not degraded by dental artifacts that plague CT in the intraoral area. Lesion signals are isointense versus muscle on T1-weighted images, but hyperintense on T2-weighted images [13]. MRI also allows mass size to be accurately measured and mass localization in relation to other structures. Characteristically, these tumors usually appear to be smooth and well demarcated and do not invade the surrounding structures.
In our case, MRI ruled out the possibility of malignancy and invasion. Enoz et al. [14] reported a malignant transformation rate for head and neck schwannoma of 8–10%. In general, schwannoma does not undergo malignant transformation [15, 16]. However, several cases of malignant transformation of head and neck schwannomas have been reported, although only one involved the tongue [17]. One malignant transformation was evident in our patient.
Histologically, all schwannomas are encapsulated, and beneath capsules, two main patterns are observed, that is, Antoni type A, which is highly cellular and is composed of elongated Schwann cells, which exhibit a palisading nuclear pattern, and Antoni type B, which is also composed of elongated Schwann cells, but cells are arranged in a less dense myxoid manner and are more disorganized than Antoni type A (Fig. 6).
Schwannomas are usually treated by surgical excision with involved originating nerve [18]. In the literature, transoral excision is the most common approach used (Table 1), although some other approaches have been reported to produce success results, such as the submandibular, which is adopted to address lingual schwannoma of the posterolateral base. More recently, CO2 laser excision has also been used to treat base of tongue Schwannomas [5, 17]. On the other hand, if a mass is located at the posterolateral base, is inaccessible via the mouth, and has a size >4.0 cm, open techniques, such as the submandibular or lip split approach, are used [2, 4, 19]. Schwannomas are not responsive to radiotherapy [9], and incomplete surgical excision may result in recurrence, although recurrence is uncommon after complete surgical excision [20]. Because masses are encapsulated, their complete removal is straightforward. In our patient, overlying mucosa was preserved to minimize postoperative complications and promote rapid healing without inflammation, and during follow-up, she reported little inconvenience.

Conclusions

Lingual schwannoma is a relatively rare tumor of the head and neck and may occur anywhere in the tongue. At presentation, the majority of patients complain an asymptomatic mass and slight ulceration. Transoral resection preserving overlying mucosa allowed us to remove the tumor in a manner that precluded recurrence and prevented tongue dysfunction.

Acknowledgements

This work was supported by the research grant of the Chungbuk National University Hospital in 2016.

Authors’ contributions

All the authors contributed to the work described in the paper, and all take responsibility for it. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.
Written informed consent was obtained from the patient for publication of this case report and accompanying images.

Publisher’s Note

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Metadaten
Titel
Schwannoma of the tongue: a case report with review of literature
Publikationsdatum
01.12.2017
Erschienen in
Maxillofacial Plastic and Reconstructive Surgery / Ausgabe 1/2017
Elektronische ISSN: 2288-8586
DOI
https://doi.org/10.1186/s40902-017-0116-2

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