Small vestibular schwannoma presented with trigeminal neuralgia: illustrative case.

ABR = auditory brainstem response MR = magnetic resonance MRA = magnetic resonance angiogram MRC = magnetic resonance cisternogram MRI = magnetic resonance imaging NIM = nerve integrity monitor TN = trigeminal neuralgia VS = vestibular schwannomas surgery trigeminal nerve trigeminal neuralgia vestibular schwannoma

Journal

Journal of neurosurgery. Case lessons
ISSN: 2694-1902
Titre abrégé: J Neurosurg Case Lessons
Pays: United States
ID NLM: 9918227275606676

Informations de publication

Date de publication:
29 Aug 2022
Historique:
received: 21 06 2022
accepted: 27 07 2022
entrez: 2 9 2022
pubmed: 3 9 2022
medline: 3 9 2022
Statut: epublish

Résumé

A vestibular schwannoma (VS) presenting with paroxysmal facial electric shock pain, that is, trigeminal neuralgia (TN), is relatively rare. Furthermore, TN is extremely rare in small VSs. Herein, the authors report the case of a 52-year-old woman with a complaint of right TN. Magnetic resonance (MR) imaging revealed a right VS of 12-mm diameter that compressed the trigeminal nerve. Although she did not report any hearing impairment, audiometry revealed decreased high-frequency range on the right side. The tumor was excised using the right retrosigmoid approach, and TN was confirmed to be caused by direct compression of the trigeminal nerve by the VS. Sufficient decompression of trigeminal nerve was done. The proximity of the trigeminal nerve root to the vestibular nerve root was the cause of TN. TN disappeared immediately after surgery, and there was no worsening of hearing impairment and facial paralysis. It is important to remember that TN may occur with direct tumor compression, even in small VSs. A preoperative 3-dimensional MR cisternogram/angiogram fusion image clearly showed direct tumor compression of the trigeminal nerve and the absence of responsible vessels, which was useful for surgical planning.

Sections du résumé

BACKGROUND BACKGROUND
A vestibular schwannoma (VS) presenting with paroxysmal facial electric shock pain, that is, trigeminal neuralgia (TN), is relatively rare. Furthermore, TN is extremely rare in small VSs.
OBSERVATIONS METHODS
Herein, the authors report the case of a 52-year-old woman with a complaint of right TN. Magnetic resonance (MR) imaging revealed a right VS of 12-mm diameter that compressed the trigeminal nerve. Although she did not report any hearing impairment, audiometry revealed decreased high-frequency range on the right side. The tumor was excised using the right retrosigmoid approach, and TN was confirmed to be caused by direct compression of the trigeminal nerve by the VS. Sufficient decompression of trigeminal nerve was done. The proximity of the trigeminal nerve root to the vestibular nerve root was the cause of TN. TN disappeared immediately after surgery, and there was no worsening of hearing impairment and facial paralysis.
LESSONS CONCLUSIONS
It is important to remember that TN may occur with direct tumor compression, even in small VSs. A preoperative 3-dimensional MR cisternogram/angiogram fusion image clearly showed direct tumor compression of the trigeminal nerve and the absence of responsible vessels, which was useful for surgical planning.

Identifiants

pubmed: 36051778
doi: 10.3171/CASE22274
pii: CASE22274
pmc: PMC9426354
doi:
pii:

Types de publication

Case Reports

Langues

eng

Pagination

CASE22274

Informations de copyright

© 2022 The authors.

Déclaration de conflit d'intérêts

Disclosures The authors report no conflict of interest concerning the materials or methods used in this study or the findings specified in this paper.

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Auteurs

Keisuke Onoda (K)

1Department of Neurosurgery, International University of Health and Welfare, School of Medicine, Narita Hospital, Narita, Chiba, Japan; and.

Yoshifumi Ogasawara (Y)

2Department of Neurosurgery, Yuuai Medical Center, Tomishiro, Okinawa, Japan.

Yu Hirokawa (Y)

1Department of Neurosurgery, International University of Health and Welfare, School of Medicine, Narita Hospital, Narita, Chiba, Japan; and.

Ryohei Sashida (R)

1Department of Neurosurgery, International University of Health and Welfare, School of Medicine, Narita Hospital, Narita, Chiba, Japan; and.

Ren Fujiwara (R)

1Department of Neurosurgery, International University of Health and Welfare, School of Medicine, Narita Hospital, Narita, Chiba, Japan; and.

Tomihiro Wakamiya (T)

1Department of Neurosurgery, International University of Health and Welfare, School of Medicine, Narita Hospital, Narita, Chiba, Japan; and.

Yuhei Michiwaki (Y)

1Department of Neurosurgery, International University of Health and Welfare, School of Medicine, Narita Hospital, Narita, Chiba, Japan; and.

Tatsuya Tanaka (T)

1Department of Neurosurgery, International University of Health and Welfare, School of Medicine, Narita Hospital, Narita, Chiba, Japan; and.

Kazuaki Shimoji (K)

1Department of Neurosurgery, International University of Health and Welfare, School of Medicine, Narita Hospital, Narita, Chiba, Japan; and.

Eiichi Suehiro (E)

1Department of Neurosurgery, International University of Health and Welfare, School of Medicine, Narita Hospital, Narita, Chiba, Japan; and.

Fumitaka Yamane (F)

1Department of Neurosurgery, International University of Health and Welfare, School of Medicine, Narita Hospital, Narita, Chiba, Japan; and.

Masatou Kawashima (M)

1Department of Neurosurgery, International University of Health and Welfare, School of Medicine, Narita Hospital, Narita, Chiba, Japan; and.

Akira Matsuno (A)

1Department of Neurosurgery, International University of Health and Welfare, School of Medicine, Narita Hospital, Narita, Chiba, Japan; and.

Classifications MeSH