• 沒有找到結果。

Vestibular Schwannoma Presenting as Oral Dysgeusia:

N/A
N/A
Protected

Academic year: 2022

Share "Vestibular Schwannoma Presenting as Oral Dysgeusia:"

Copied!
7
0
0

加載中.... (立即查看全文)

全文

(1)

Case Report

Vestibular Schwannoma Presenting as Oral Dysgeusia:

An Easily Missed Diagnosis

Emma Brown

1

and Konrad Staines

2

1Oral Medicine Department, Bristol Dental Hospital, Lower Maudlin Street, Bristol BS1 2LY, UK

2Oral Medicine Department, University of Bristol Dental School, Lower Maudlin Street, Bristol BS1 2LY, UK

Correspondence should be addressed to Emma Brown; elbrown7@hotmail.co.uk Received 27 October 2015; Revised 4 January 2016; Accepted 27 January 2016 Academic Editor: Miguel Pe˜narrocha

Copyright © 2016 E. Brown and K. Staines. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

We present a case of a fifty-year-old male patient who was referred to the Oral Medicine Department with a complaint of a salty taste.

History taking subsequently revealed that the patient was also experiencing intermittent numbness of his left lower lip, tinnitus, and a feeling of fullness in the left ear. Magnetic resonance imaging was performed which revealed a large vestibular schwannoma affecting the left vestibulocochlear nerve, which was treated surgically. This case shows the importance of taking a detailed history in a patient presenting with an initial complaint of oral dysgeusia. It also highlights the possibility of significant underlying pathology, presenting with initial low level, nonspecific complaints such as an altered taste, and the rationale for imaging patients who report unilateral facial hypoesthesia.

1. Introduction

Oral dysgeusia is defined as a gustatory disturbance relating to a distorted taste perception, or to a persistent taste sensa- tion in the absence of stimulation [1], and can be very dis- tressing for the patient. Patients with taste disturbances are commonly referred to and investigated within Oral Medicine Departments in the UK. Identifiable causes of dysgeusia can include local factors, drugs, systemic disease, and peripheral or central neurological conditions; see Table 1 [1–5].

Local factors influencing taste include infections of the oral cavity, such as candidiasis or dental abscess, trauma, or hyposalivation [1–3]. Over 250 drugs have been associated with oral dysgeusia, of which the most common are outlined in Table 1 [3–5]. Dysgeusia can also be a manifestation of a systemic disease such as an underlying haematinic deficiency, diabetes mellitus, Crohn’s disease, or Sj¨ogren’s syndrome [1, 3]. Rarely, damage to the peripheral or central nervous system can be the cause. Tumours affecting the cerebellopontine angle, such as a schwannoma or meningioma, can cause taste disturbances. Central neurological causes such as ischaemia, haemorrhage, or demyelination affecting the gustatory path- way in the brain, or temporal lobe epilepsy, also require exclusion [1].

In a significant number of cases, the taste disturbance cannot be attributed to an identifiable cause and therefore a diagnosis of idiopathic oral dysgeusia is made. Although altered taste is a rare symptom of vestibular schwannoma, this case illustrates the need for a high index of clinical suspicion when assessing patients with seemingly low level symptoms, such as oral dysgeusia.

2. Case Presentation

2.1. History. A fifty-year-old male patient was referred to the Oral Medicine Department by his General Dental Prac- titioner with a primary complaint of an altered taste. The taste disturbance had been affecting the patient for six months and manifested as a constant salty taste. His General Medical Practitioner had empirically prescribed omeprazole to exclude gastric oesophageal reflux disease as a potential cause. However, this was ineffective and therefore the patient had discontinued the treatment.

Additionally, the patient also complained of a cracked tongue surface and intermittent numbness of his lower left lip and chin. He had experienced three episodes of facial hypoesthesia affecting the mandibular division of the left

(2)

Table1:Possiblecausesoforaldysgeusia[1–5]. LocalfactorsDentalabscess,candidainfection,traumatotheoralcavity,hyposalivation,removableprostheses,andgastricoesophagealrefluxdisease Drugs

Antimicrobials Antibacterials:cephalosporins,ciprofloxacin,clarithromycin,clindamycin,co-trimoxazole,doxycycline,imipenemwithcilastatin,metronidazole,ofloxacin, penicillins,trimethoprim,tetracycline,andvancomycin Antivirals:aciclovir,ganciclovir,indinavir,ritonavir,andzidovudine Antifungals:fluconazoleandgriseofulvin Centralnervoussystem Antiparkinsonians:bromocriptine,levodopa,andpergolide Migrainemedications:naratriptanandsumatriptan Musclerelaxants:baclofenandmethocarbamol Tricyclicantidepressants:amitriptyline,clomipramine,desipramine,doxepin,imipramine,nortriptyline,andtrimipramine Selectiveserotoninreuptakeinhibitors:citalopram,fluoxetine,fluvoxamine,andsertraline Antipsychotics:clozapine,olanzapine,andrisperidone Benzodiazepines:alprazolam,clonazepam,flurazepam,andmidazolam Moodstabilisers:lithium Cardiovascular Angiotensin-convertingenzymeinhibitors:captopril,enalapril,lisinopril,andperindopril Beta-adrenoreceptorblockers:labetalol,metoprolol,propranolol,andtimolol Calcium-channelblockers:amlodipine,diltiazem,andnifedipine Potassium-sparingdiuretics:amilorideandtriamterene Statins:atorvastatin,fluvastatin,andsimvastatin Antiarrhythmics:amiodarone,flecainide,andprocainamide Endocrine Diabeticmedications:glibenclamide,metformin,andtolbutamide Other Antineoplastics:busulfan,dacarbazine,vinblastine,andvincristine Antimalarials:hydroxychloroquine,pyrimethamine,andquinine Bisphosphonates:alendronicacid,etidronicacid,andpamidronicacid Bronchodilators:salbutamolandterbutaline Nonsteroidalanti-inflammatories:celecoxib,diclofenac,ketoprofen,andketorolac SystemicdiseaseDiabetesmellitus,haematinicdeficiency(ferritin,folate,orvitaminB12),Sj¨ogren’ssyndrome,Crohn’sdisease,andchronickidneydisease PeripheralnervoussystemSyndromesaffectingthefacial,glossopharyngeal,orvagalnerves(e.g.,Bell’spalsy)andtumoursoftheskullbaseorcerebellopontineangle(meningioma, schwannoma,epidermoidtumour,andbrainmetastasis) CentralnervoussystemIschaemia,haemorrhage,ordemyelinationaffectingthebrainstem,thalamusorcorticalcomponentsofthegustatorypathway,andtemporallobeepilepsy

(3)

resolved spontaneously.

Medical history was clear except for tinnitus and a feeling of fullness affecting the left ear for the past three years. This had been diagnosed by the General Medical Practitioner as Eustachian tube dysfunction and treated with fluticasone nasal spray. This had no benefit in relieving the symptoms and was discontinued. The patient therefore took no regular medication.

Socially, the patient was a semiretired office based worker.

He was a nonsmoker and had a low alcohol intake.

2.2. Examination. Cranial nerve examination at the initial clinic appointment did not reveal any sensory disturbance along the trigeminal nerves or motor deficit of the facial nerves. The eyes were unaffected, with no lacrimation abnor- malities identified. Swallow and phonation were not affected.

The uvula was not deviated, and the movement of the palate and tongue was normal. Extra oral examination of the head and neck showed normal anatomy, with no facial swelling and no cervical lymphadenopathy. Intraorally the soft tissues of the mouth were healthy with no mucosal lesions detected and no obvious source of infection that could cause the oral dysgeusia. The cracked tongue surface was deemed to be a variation of normal anatomy termed a fissured tongue.

2.3. Investigations. An orthopantomogram radiograph was completed, which confirmed the absence of dental or bony pathology. Blood investigations, including a full blood count, blood glucose, serum ferritin, folate, and vitamin B12 levels, all resulted as normal.

Due to the reported facial hypoesthesia, magnetic reso- nance imaging of the head was performed. This identified a large vestibular schwannoma of the left vestibulocochlear nerve (eighth cranial nerve). This measured 2.7 cm by 2.4 cm by 2.3 cm and was located in the left cerebellopontine angle, involving the left internal auditory meatus. There was asso- ciated compression of the brainstem and distortion of the fourth ventricle, without hydrocephalus (see Figures 1–4).

2.4. Treatment. The patient was referred to the Ear, Nose, and Throat Team for further management. They identified 45 to 50 decibels of sensorineural hearing loss in the left ear on audiogram. There was also some instability on stand- ing, particularly when the patient’s eyes were closed. The hypoesthesia of the left trigeminal nerve had worsened, with a constant tingling affecting the maxillary and mandibular divisions and reduced pin prick sensation in these regions.

Treatment options for vestibular schwannoma include monitoring with serial scanning to determine extent of tumour growth, microsurgery to remove or debulk the tumour, or stereotactic radiosurgery [6]. Following discus- sion at the Skull Base Multidisciplinary Team Meeting, which included a Clinical Oncologist, Neuroradiologist, Ear, Nose, and Throat Surgeon, and Neurosurgeon, a decision was made that microsurgery would be the best treatment option. This was due to the large size of the vestibular schwannoma, the neurological symptoms, and the associated compression of the brain stem. Therefore, the patient underwent surgical

Figure 1: Coronal MR image (T1 weighted) showing the vestibular schwannoma affecting the left vestibulocochlear nerve.

Figure 2: Axial MR image (T2 weighted, fat saturated) showing the vestibular schwannoma affecting the left vestibulocochlear nerve.

excision to remove the tumour and decompress the brain- stem. This was undertaken in a joint case with the Ear, Nose, and Throat and Neurosurgery Teams. A translabyrinthine approach was used, which leads to complete hearing loss on the affected side but aims to preserve the facial nerve.

2.5. Outcome. Surgical treatment was successful and the histology showed a schwannoma comprising densely cel- lular Antoni A areas with less densely cellular Antoni B areas. There was no significant mitotic activity or necrosis.

Immunohistochemistry showed that it was strongly positive for S100. The conclusion was that it was a benign schwan- noma of the left cerebellopontine angle, WHO Grade I.

These results were discussed postoperatively at the Skull Base

(4)

Figure 3: Coronal MR image (T2 weighted, fat saturated) showing the vestibular schwannoma affecting the left vestibulocochlear nerve.

Figure 4: Axial MR image (T2 diffusion-weighted image) showing the vestibular schwannoma affecting the left vestibulocochlear nerve.

Multidisciplinary Team Meeting and it was agreed that the patient would be followed up by the Neurosurgery Team.

The patient is doing well postoperatively. The aural fullness in the left ear has now completely resolved, and the tinnitus is barely noticeable. The facial hypoesthesia that affected the maxillary and mandibular divisions of the left trigeminal nerve preoperatively has also completely resolved.

There was some minor facial weakness, House-Brackmann Grade II, which was present immediately after surgery and has now returned to normal. Furthermore, the oral dysgeusia has improved since the surgery, with an occasional salty taste still noticed. The patient is now awaiting CROS hearing aids to help with his hearing loss on the left side. His balance

Figure 5: Axial MR image (T2 weighted, 3D DRIVE CLEAR) showing the postoperative changes.

Figure 6: Axial MR image (T2 weighted) showing the postoperative changes.

was severely affected from the surgery but this has now significantly improved.

Postoperative magnetic resonance imaging was per- formed at six months postoperatively (see Figures 5–7).

The figures show normal postsurgical changes involving the petrous bone and cerebellopontine angle. The left sided vestibular schwannoma has been resected. There is a cavity in the left middle cerebellar peduncle which is likely to represent an area of perioperative ischaemia. There is a thin cuff of residual tissue anterior to the site of the cerebellopontine angle tumour. The remnant of the schwannoma will be mon- itored by the Neurosurgery Team with a further magnetic resonance imaging in one year.

3. Discussion

Vestibular schwannomas, also termed acoustic neuromas, are benign tumours of the vestibulocochlear nerve [7–14]. They arise from the Schwann cells which comprise the myelin

(5)

Figure 7: Coronal MR image (T2 weighted) showing the postoper- ative changes.

sheath surrounding the vestibular branch of the eighth cranial nerve [14] and account for 80–90% of cerebellopontine angle tumours [7, 8, 11, 12]. The aetiology of vestibular schwannoma is unknown. The most common symptoms are unilateral hearing loss, tinnitus, or unsteadiness [7–13]. As the tumour grows it compresses surrounding intracranial structures.

Compression of the trigeminal nerve can lead to facial hypoesthesia, which is found in 7–26% of patients with vestibular schwannoma [9, 15], and usually begins in the region of the anterior mandible [9]. In 2.2–17% of patients the facial nerve is affected, due to the close anatomical relationship of the facial nerve to the vestibulocochlear nerve in the region of the cerebellopontine angle [9, 11, 15].

Pressure on the motor fibres can lead to facial weakness; and involvement of the sensory branch, the nervus intermedius which receives special sensory taste information from the anterior two-thirds of the tongue, via the chorda tympani, can have an impact on taste [15, 16]. There are a number of studies reporting facial numbness as the presenting feature of a vestibular schwannoma [7, 8, 12]. In another case, the patient presented with a burning sensation of the tongue [14], but no other report has described oral dysgeusia as the symptom prompting referral to secondary care.

Facial nerve dysfunction is rarely the presenting symptom of vestibular schwannoma [13]. However, literature shows that, in up to 17% of patients, the facial nerve is affected [15]. When the facial nerve is compressed by the tumour, taste disturbances appear earlier than facial palsy. This is because sensory nerves are more sensitive to compression than motor fibres [16]. A study by Watanabe et al. [17] found that preoperative taste disturbances were found in 28.7% of patients undergoing surgery for a vestibular schwannoma.

Another study by Sahu et al. [16] tested 142 patients with vestibular schwannoma and found taste disturbances present in 40.8% of patients preoperatively. Matthies and Samii [15]

found that taste disturbances were only reported in 1.8%

of 1000 patients diagnosed with vestibular schwannoma, although they did not formally test this and assumed that the actual incidence would be higher. They also established

facial nerve compromise and impending paresis.

Although oral dysgeusia is rarely the presenting symp- tom, it is clear that a significant proportion of patients with vestibular schwannoma do experience taste disturbances.

It is therefore imperative that for patients presenting with altered taste a detailed history is taken. The history should specifically include questions relating to sensory loss, and the appropriate investigations should be performed to rule out any significant underlying pathology.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

References

[1] J. G. Heckmann, S. M. Heckmann, C. J. G. Lang, and T. Hum- mel, “Neurological aspects of taste disorders,” Archives of Neu- rology, vol. 60, no. 5, pp. 667–671, 2003.

[2] N. Su, V. Ching, and M. Grushka, “Taste disorders: a review,”

Journal of the Canadian Dental Association, vol. 79, article d86, 2013.

[3] T. Maheswaran, P. Abikshyeet, G. Sitra, S. Gokulanathan, V.

Vaithiyanadane, and S. Jeelani, “Gustatory dysfunction,” Journal of Pharmacy and Bioallied Sciences, vol. 6, no. 5, pp. 30–33, 2014.

[4] R. Douglass and D. Heckman, “Drug-related taste disturb- ance—a contributing factor in geriatric syndromes,” Canadian Family Physician, vol. 56, no. 11, pp. 1142–1147, 2010.

[5] M. Abdollahi and M. Radfar, “A review of drug-induced oral reactions,” Journal of Contemporary Dental Practice, vol. 4, no.

1, pp. 10–31, 2003.

[6] E. Myrseth, P.-H. Pedersen, P. Møller, and M. Lund-Johansen,

“Treatment of vestibular schwannomas. Why, when and how?”

Acta Neurochirurgica, vol. 149, no. 7, pp. 647–660, 2007.

[7] D. J. Holt, P. M. Foy, and E. A. Field, “Orofacial paraesthesia: an unusual presentation of acoustic neuroma,” Dental Update, vol.

29, no. 3, pp. 141–142, 2002.

[8] R. P´erusse, “Acoustic neuroma presenting as orofacial anesthe- sia,” International Journal of Oral and Maxillofacial Surgery, vol.

23, no. 3, pp. 156–160, 1994.

[9] S. G. Harner and E. R. Laws Jr., “Clinical findings in patients with acoustic neurinoma,” Mayo Clinic Proceedings, vol. 58, no.

11, pp. 721–728, 1983.

[10] S. Berrettini, F. Ravecca, F. Russo, P. Bruschini, and S. Sellari- Franceschini, “Some uncharacteristic clinical signs and symp- toms of acoustic neuroma,” Journal of Otolaryngology, vol. 26, no. 2, pp. 97–103, 1997.

[11] R. F. Bento, M. H. Pinna, and R. V. De Brito Neto, “Vestibular schwannoma: 825 cases from a 25-year experience,” Interna- tional Archives of Otorhinolaryngology, vol. 16, no. 4, pp. 466–

475, 2012.

[12] R. C. Swensson, R. P. Swensson, F. E. C. Pizzini, P. R. Boldorini, and J. J. Jorge Jr., “An uncommon presentation of an VIII nerve tumor,” Brazilian Journal of Otorhinolaryngology, vol. 74, no. 4, pp. 628–631, 2008.

[13] T. D. Erson, L. A. Loevner, D. C. Bigelow, and N. Mirza, “Preva- lence of unsuspected acoustic neuroma found by magnetic resonance imaging,” Otolaryngology—Head and Neck Surgery, vol. 122, no. 5, pp. 643–646, 2000.

(6)

[14] J. W. Ferguson and J. F. Burton, “Clinical presentation of acoustic nerve neuroma in the oral and maxillofacial region,”

Oral Surgery, Oral Medicine, Oral Pathology, vol. 69, no. 6, pp.

672–675, 1990.

[15] C. Matthies and M. Samii, “Management of 1000 vestibular schwannomas (acoustic neuromas): clinical presentation,” Neu- rosurgery, vol. 40, no. 1, pp. 1–9, 1997.

[16] R. N. Sahu, S. Behari, V. K. Agarwal, P. Giri, and V. Jain, “Taste dysfunction in vestibular schwannomas,” Neurology India, vol.

56, no. 1, pp. 42–46, 2008.

[17] K. Watanabe, N. Saito, M. Taniguchi, T. Kirino, and T. Sasaki,

“Analysis of taste disturbance before and after surgery in patients with vestibular schwannoma,” Journal of Neurosurgery, vol. 99, no. 6, pp. 999–1003, 2003.

(7)

Submit your manuscripts at http://www.hindawi.com

Hindawi Publishing Corporation

http://www.hindawi.com Volume 2014

Oral Oncology

Journal of

Dentistry

International Journal of

Hindawi Publishing Corporation

http://www.hindawi.com Volume 2014

Hindawi Publishing Corporation

http://www.hindawi.com Volume 2014

International Journal of

Biomaterials

Hindawi Publishing Corporation

http://www.hindawi.com Volume 2014

BioMed

Research International

Hindawi Publishing Corporation

http://www.hindawi.com Volume 2014

Case Reports in Dentistry

Hindawi Publishing Corporation

http://www.hindawi.com Volume 2014

Oral Implants

Journal of

Hindawi Publishing Corporation

http://www.hindawi.com Volume 2014

Anesthesiology Research and Practice

Hindawi Publishing Corporation

http://www.hindawi.com Volume 2014

Radiology

Research and Practice Environmental and

Public Health

Journal of

Hindawi Publishing Corporation

http://www.hindawi.com Volume 2014

The Scientific World Journal

Hindawi Publishing Corporation

http://www.hindawi.com Volume 2014

Hindawi Publishing Corporation

http://www.hindawi.com Volume 2014

Dental Surgery

Journal of

Drug Delivery

Journal of

Hindawi Publishing Corporation

http://www.hindawi.com Volume 2014

Hindawi Publishing Corporation

http://www.hindawi.com Volume 2014

Oral Diseases

Journal of

Hindawi Publishing Corporation

http://www.hindawi.com Volume 2014

Computational and Mathematical Methods in Medicine

Scientifica

Hindawi Publishing Corporation

http://www.hindawi.com Volume 2014

Pain

Research and Treatment

Hindawi Publishing Corporation

http://www.hindawi.com Volume 2014

Hindawi Publishing Corporation

http://www.hindawi.com Volume 2014

Endocrinology

International Journal of

Hindawi Publishing Corporation

http://www.hindawi.com Volume 2014

Hindawi Publishing Corporation

http://www.hindawi.com Volume 2014

Orthopedics

Advances in

參考文獻

相關文件

In this report, we describe a rare case of bilateral symmetric ectopic oral tonsillar tissue located at the ventral surface of the tongue along with two solitary cases arising from

A large extra-axial mass involving right cerebellopontine angle .The aim of this case report is to show a tumor of cerebellopontine angle, presenting clinically as

 In conclusion, this report has described a case of an intraosseous LGFMS of the maxilla, adding another facet to the colorful clinical picture of this rare soft tissue tumor.

Case Presentation: In this clinical case report, it is described a case of a 16-year-old male patient with an asymptomatic osteolytic lesion at first upper left molar apical level,

We report a rare case of brown tumor occurring in mandible of a 40-year-old female patient that was the first clinical manifestation and presented as a multilocular radio-

原文題目(出處): A Rare Report of Two Cases: Ancient Schwannoma of Infratemporal Fossa and Verocay Schwannoma of Buccal Mucosa(Annals of Maxillofacial Surgery 2017;7;140-2)

15,16 Although ESFT diagnosis in this case was supported by the patients ’ age, when gnathic bones are involved, the mandible is the most affected site, with the neoplasm only

Although osteolipoma is a very rare entity in the oral cavity, it should be considered when a patient presents with a peripheral lesion that has a hard consistency on palpation,