• Title/Summary/Keyword: Neuritis

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Sequential Vestibular Neuritis: Report of Four Cases and Literature Review

  • Comacchio, Francesco;Mion, Marta;Armato, Enrico;Castellucci, Andrea
    • Journal of Audiology & Otology
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    • v.25 no.2
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    • pp.89-97
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    • 2021
  • Background and Objectives: Bilateral sequential vestibular neuritis (BSVN) is a rare condition in which an inflammation or an ischemic damage of the vestibular nerve occurs bilaterally in a sequential pattern. We described four cases of BSVN. Subjects and Methods: Every patient underwent video-head impulse test during the first and the second episode of vestibular neuritis (VN), furthermore they have been studied with radiological imaging. Results: Contralateral VN occurred after a variable period from prior event. Vestibular function recovered from the first episode in one case. The other three patients developed contralateral VN. One case was due to a bilateral VN in association with a Ramsay-Hunt syndrome, in another patient clinical records strongly suggested an ischemic etiology, whereas in two cases aetiology remained uncertain. Two patients subsequently developed a benign paroxysmal positional vertigo involving the posterior canal on the side of the latest VN (Lindsay-Hemenway syndrome). Conclusions: Instrumental vestibular assessment represents a pivotal tool to confirm the diagnosis of VN and BSVN.

Sequential Vestibular Neuritis: Report of Four Cases and Literature Review

  • Comacchio, Francesco;Mion, Marta;Armato, Enrico;Castellucci, Andrea
    • Korean Journal of Audiology
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    • v.25 no.2
    • /
    • pp.89-97
    • /
    • 2021
  • Background and Objectives: Bilateral sequential vestibular neuritis (BSVN) is a rare condition in which an inflammation or an ischemic damage of the vestibular nerve occurs bilaterally in a sequential pattern. We described four cases of BSVN. Subjects and Methods: Every patient underwent video-head impulse test during the first and the second episode of vestibular neuritis (VN), furthermore they have been studied with radiological imaging. Results: Contralateral VN occurred after a variable period from prior event. Vestibular function recovered from the first episode in one case. The other three patients developed contralateral VN. One case was due to a bilateral VN in association with a Ramsay-Hunt syndrome, in another patient clinical records strongly suggested an ischemic etiology, whereas in two cases aetiology remained uncertain. Two patients subsequently developed a benign paroxysmal positional vertigo involving the posterior canal on the side of the latest VN (Lindsay-Hemenway syndrome). Conclusions: Instrumental vestibular assessment represents a pivotal tool to confirm the diagnosis of VN and BSVN.

Chronic recurrent trigeminal neuritis of the maxillary branch confirmed by magnetic resonance imaging

  • Hong, Soon-Ho;Kim, Yong-Duk;Na, Sang-Jun;Lee, Kee Ook;Park, Yun Kyung;Yoon, Bora
    • Annals of Clinical Neurophysiology
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    • v.19 no.2
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    • pp.145-147
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    • 2017
  • Trigeminal neuralgia (TN) is generally characterized by lancinating, unilateral, paroxysmal pain occurring in the distribution of the fifth cranial nerve. TN is diagnosed clinically based on the typical patient history, negative findings in a neurologic examination, and the response to medication. Idiopathic TN is the most common type, but TN can result from vascular malformation, compression, trauma, neoplasm, multiple sclerosis, or inflammation. We report a TN case diagnosed as recurrent trigeminal neuritis of the maxillary branch confirmed by magnetic resonance imaging.

A Case of Chiasmal Optic Neuritis with Bitemporal Hemianopsia in Multiple Sclerosis (다발성 경화증 환자에서 진단된 양관자쪽반맹을 보이는 시신경교차부염 1예)

  • Kim, Sung-Min;Kim, Min-Jeong;Cha, Jeong-In;Sung, Jung-Joon;Lee, Kwang-Woo
    • Annals of Clinical Neurophysiology
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    • v.8 no.2
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    • pp.199-202
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    • 2006
  • We report a case of chiasmal optic neuritis in a patient who had been diagnosed as multiple sclerosis, and was presented with bitemporal hemianopsia. The brain MRI revealed a high signal lesion with focal enhancement in optic chiasm, and the visual evoked potential functionally supported it. This is the first case of chiasmal optic neuritis in multiple sclerosis with temporally and spatially disseminated lesions.

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Morton's Neuroma (Interdigital Neuritis) (모턴씨 신경종(족지간 신경염))

  • Park, Hyun-Woo
    • Journal of Korean Foot and Ankle Society
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    • v.15 no.2
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    • pp.58-61
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    • 2011
  • Morton's neuroma is a common cause of forefoot pain, and is also known to be a entrapment neuropathy rather than a true tumor. Precise physical examination is necessary to differentiate from other diagnoses of similar symptoms. If proper conservative treatment modalities fail for this neuritis, neurectomy of interdigital nerve is generally performed, with the results of up to 80% of patient's satisfaction. However the failure rate of 2% to 35% should be improved by proper diagnosis and careful surgery.

The Clinical Experiences and Complications of Percutaneous Neurolysis of Upper Thoracic Sympathetic Ganglion by Using Ethylalcohol -A report of three cases- (알코올을 이용한 흉부교감신경절차단술에 대한 임상경험 및 합병증 -증례 보고-)

  • Kwon, Ok-Hee;Kim, Jong-Il;Ban, Jong-Seock;Min, Byung-Woo
    • The Korean Journal of Pain
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    • v.8 no.2
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    • pp.374-377
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    • 1995
  • Percutaneous neurolysis of upper thoracic sympathetic ganglion was performed by simultaneously injecting 3 ml of pure alcohol into the $T_2$ and $T_3$ levels after testng with same amount of local anesthetics on the same sites. We experienced poor sympatholytic effect or intercostal neuritis and Horner's Syndrome as the result of complication of thoracic sympathetic ganglion block. In Case 1, in spite of the good testing result, neurolytic block effect was poor. In Case 2, intercostal neuritis occurred, but neuralgia subsided within 3 weeks. In Case 3, Horner's Syndrome occurred for 1 day. To increase the success rate of block and decrease the incidence of complications, good radio-opaque dye appearance and good test block effect should be obtained.

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Optic neuritis and multiple cranial neuropathies in patient with chronic inflammatory demyelinating polyneuropathy

  • Bae, Min-Jeong;Lee, Joonwon;Eun, Jeong Ik;Shin, Kyong Jin
    • Annals of Clinical Neurophysiology
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    • v.24 no.2
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    • pp.59-62
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    • 2022
  • Chronic inflammatory demyelinating polyneuropathy (CIDP) is a chronic recurrent acquired immune-mediated disease of the peripheral nerves that presents with progressive sensory and motor deficits in all four limbs. Cranial nerve involvement is not as common as in Guillain-Barre syndrome, and central nervous system involvement including optic neuritis has rarely been reported in patients with CIDP. We recently experienced a case with classic CIDP involving bilateral facial and trigeminal nerves, right lower cranial nerves, and the right optic nerve.

A Case of Isolated Nodular Infarction Mimicking Vestibular Neuritis on the Contralateral Side

  • Lee, Jun;Song, Kudamo;Yu, In Kyu;Lee, Ho Yun
    • Korean Journal of Audiology
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    • v.23 no.3
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    • pp.167-172
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    • 2019
  • Differentiating central vestibulopathy from more common vestibular disorders is crucial because it often necessitates different treatment strategies, and early detection can help to minimize potential complications. Isolated nodular infarct is one of the central brain lesions that can mimic peripheral vertigo. We present a case of isolated nodular infarct that had been misdiagnosed as vestibular neuritis on the contralateral side at the initial evaluation. The patient was successfully treated with anticoagulants and antihyperlipidemic agents. Clinicians should keep in mind that some causes of central vertigo mimic peripheral vestibulopathy at the early stage.

A Case of Isolated Nodular Infarction Mimicking Vestibular Neuritis on the Contralateral Side

  • Lee, Jun;Song, Kudamo;Yu, In Kyu;Lee, Ho Yun
    • Journal of Audiology & Otology
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    • v.23 no.3
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    • pp.167-172
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    • 2019
  • Differentiating central vestibulopathy from more common vestibular disorders is crucial because it often necessitates different treatment strategies, and early detection can help to minimize potential complications. Isolated nodular infarct is one of the central brain lesions that can mimic peripheral vertigo. We present a case of isolated nodular infarct that had been misdiagnosed as vestibular neuritis on the contralateral side at the initial evaluation. The patient was successfully treated with anticoagulants and antihyperlipidemic agents. Clinicians should keep in mind that some causes of central vertigo mimic peripheral vestibulopathy at the early stage.