Journals / Disiplinlerarası Yenilik Araştırmaları Dergisi / 2022 / Cilt: 2 - Sayı: 2

An eight-and-a-half syndrome case: a rare presentation of pontine lacunar infarction

Bir sekiz buçuk sendromu olgusu: pontin laküner infarktın nadir bir prezentasyonu

Pages
114–117
Publication Date
2022-07-31
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Although the eight-and-a-half syndrome is rare, it should be kept in mind with patients presenting diplopia and peripheral facial palsy simultaneously.

📌 3 Key Takeaways

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Objective & Hypothesis:The eight-and-a-half syndrome is a one-and-a-half syndrome [conjugated horizontal gaze palsy and internuclear ophthalmoplegia (INO)], plus an ipsilateral cranial nerve seventh (CN VII) palsy.
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Key Findings & Data:In this case, we report a 68-year-old male patient admitted to our hospital with binocular horizontal diplopia later diagnosed with the eight-and-a-half syndrome.
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Conclusion & Impact:Although the eight-and-a-half syndrome is rare, it should be kept in mind with patients presenting diplopia and peripheral facial palsy simultaneously.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:diplopi · internükleer oftalmopleji · fasiyal palsi

Abstract

The eight-and-a-half syndrome is a one-and-a-half syndrome [conjugated horizontal gaze palsy and internuclear ophthalmoplegia (INO)], plus an ipsilateral cranial nerve seventh (CN VII) palsy. This rare syndrome is caused by the pontine tegmentum's lesions involving the abducens nucleus, the ipsilateral medial longitudinal fasciculus (MLF), and the facial colliculus. In this case, we report a 68-year-old male patient admitted to our hospital with binocular horizontal diplopia later diagnosed with the eight-and-a-half syndrome. Although the eight-and-a-half syndrome is rare, it should be kept in mind with patients presenting diplopia and peripheral facial palsy simultaneously.

Özet

Sekiz buçuk sendromu, bir buçuk sendromu [konjuge yatay bakış felci ve internükleer oftalmopleji (INO)], artı ipsilateral kraniyal sinir yedinci (CN VII) felcidir. Bu nadir sendrom, abdusens nükleusu içeren, ipsilateral medial longitudinal fasciculus (MLF) ve fasiyal kollikulusu tutan pontin tegmentum lezyonları sebebiyle meydana gelir. Bu olguda binoküler horizontal diplopi ile hastanemize başvuran ve sonrasında sekiz buçuk sendromu tanısı alan 68 yaşında bir erkek hastayı sunmaktayız. Sekiz buçuk sendromu nadir olmakla birlikte, aynı anda hem diplopi hem de periferik yüz felci olan hastalar da akılda tutulmalıdır.

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Cite This Article

ÇINKIR, U., MERT, S., KÖKSAL, A. (2022). An eight-and-a-half syndrome case: a rare presentation of pontine lacunar infarction. Disiplinlerarası Yenilik Araştırmaları Dergisi, Cilt: 2 - Sayı: 2, 114–117. https://ajindex.com/articles/851086

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References (4)

  1. Kumar NSS, Raju CG, Kiran PR et al. “Eight-and-a-Half Syndrome: A Rare Presentation of Pontine Infarction”. Journal of Stroke and Cerebrovascular Diseases, 23(8), e389-e391, 2014
  2. Frohman TC, Galetta S, Fox R, et al. “Pearls & Oy-sters: The medial longitudinal fasciculus in ocular motor physiology”. Neurology, 70(17), e57-e67, 2008
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  4. Wu YT, Cafiero‐Chin M, Marques C. “Wall‐eyed bilateral internuclear ophthalmoplegia”. Clinical and Experimental Optometry, 98(1), 25-30, 2015.