Journals / Türk Nöroloji Dergisi / 2017 / Cilt: 23 - Sayı: 2

A Rare Pontine Neuro-ophthalmic Syndrome: Eight-and-a-Half Syndrome

Nadir Bir Pontin Nöro-oftalmolojik Sendrom: Sekiz Buçuk Sendromu

Pages
67–69
Publication Date
2022-11-05
DOI
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AI Summary & Key Takeaways

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

We wanted to present this case to emphasize this rare situation

📌 3 Key Takeaways

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Objective & Hypothesis:One-and-a half syndrome is seen in paramedian pontine lesions, and may also co-exist with cranial nerve paralysis.
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Key Findings & Data:A man aged 38 years was admitted with symptoms of sudden-onset binocular diplopia and dizziness.
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Conclusion & Impact:We wanted to present this case to emphasize this rare situation
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

One-and-a half syndrome is seen in paramedian pontine lesions, and may also co-exist with cranial nerve paralysis. This clinical situation is called eight-anda-half syndrome when facial nerve paralysis also accompanies this manifestation. A man aged 38 years was admitted with symptoms of sudden-onset binocular diplopia and dizziness. The patient had no known co-morbidities. Cranial magnetic resonance imaging showed a small-sized infarct in the left paramedian pontine tegmentum posterior area. In his neuro-ophthalmologic examination, total paresis of left eye horizontal movements, mild lateral deviation, and monocular nystagmus during abduction of the right eye were observed. The patient also had peripheral facial paralysis on the left side; therefore, no signs of motor deficit of his extremities were examined. Eight-and-a-half syndrome is a rare disorder that is seen in localized-small pons lesions, mostly accompanied by infarcts. This clinical manifestation is called eight-and-a-half syndrome and arises within lesions in both the parapontine reticular formation and the medial longitudinal fasciculus in the inferior pons tegmentum where horizontal eye movements are controlled, and facial axons adjacent to the nucleus of the sixth nerve. We wanted to present this case to emphasize this rare situation

Özet

Paramedyan pontin lezyonlarında görülen bir buçuk sendromu, kraniyal sinir paralizileri ile birlikte de görülebilir. Fasiyal sinir paralizisi ile birlikte görülen klinik tablo sekiz buçuk sendromu olarak adlandırılır. Otuz sekiz yaşında erkek hasta, ani başlayan çift görme, baş dönmesi şikayetleriyle başvurdu. Bilinen komorbiditesi olmayan hastanın çekilen kraniyal manyetik rezonans görüntülerinde difüzyon ağırlıklı kesitlerinde sol paramedyan pontin tegmentum posterior kesimde küçük bir enfarkt alanı görüldü. Nöro-oftalmolojik muayenesinde sol göz horizontal göz hareketlerinde tam parezi, sağ göz primer pozisyonda hafif laterale deviasyon ile addüksiyon kısıtlılığı ve dışa bakış sırasında ortaya çıkan nistagmus görüldü. Ekstremitelerinde motor defisite rastlanmayan hastada solda periferik tipte fasiyal paralizi saptandı. Bir buçuk sendromu iyi lokalize küçük pons lezyonlarında, en sık olarak enfarktlar ile birlikte tanımlanmış nadir bir tablodur. Horizontal göz hareketlerinin düzenlendiği inferior pons tegmentumundaki paramedyan pontin retiküler formasyon, mediyal longitidunal fasikül ve altıncı kraniyal sinir nükleusu ile hemen komşuluğundaki fasiyal sinir aksonlarını tutan lezyonlar ile ortaya çıkan klinik tablo sekiz buçuk sendromu olarak adlandırılır. Literatürde nadir olarak bildirilmiş bu durumu vurgulamak için olguyu sunmak istedik

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Cite This Article

BİLEN, Ş., TİTİZ, A. P., MÜHÜRDAROĞLU, M., TOPKAN, T. A., ERUYAR, E., AK, F. (2022). A Rare Pontine Neuro-ophthalmic Syndrome: Eight-and-a-Half Syndrome. Türk Nöroloji Dergisi, Cilt: 23 - Sayı: 2, 67–69. https://ajindex.com/articles/636876

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References (8)

  1. Eggenberger E. Eight-and-a-half syndrome: one-and-a-half syndrome plus cranial nerve VII palsy. J Neuroophthalmol 1998;18:114-116
  2. Kakar P, Brown Z, Banerjee S. Eight-and-a-half syndrome: an unusual presentation of brainstem infarction. QJM 2013;106:273-276
  3. Kataoka S, Hori A, Shirakawa T, Hirose G. Paramedian pontine infarction. Stroke 1997;28:809-815
  4. Johkura K, Komiyama A, Kuroiwa Y. Eye deviation in patients with oneand-a-half syndrome. Eur Neurol 2000;44:210-215
  5. Duss P. Nöroloji. Tanıda Lokalizasyon. Palme Yayıncılık, Ankara 2001;109
  6. Sampath Kumar NS, Raju CG, Kiran PR, Kumar TA, Gopal BV, Khaseem DB. Eight-and-a-half syndrome: a rare presentation of pontine infarction. J Stroke Cerebrovasc Dis 2014;23:e389-391
  7. Gold JJ, Crawford JR. An unusual cause of pediatric stroke secondary to congenital basilar artery fenestration. Case Rep Crit Care 2013
  8. Cooke DL, Stout CE, Kim WT, Kansagra AP, Yu JP, Gu A, Jewell NP, Hetts SW, Higashida RT, Dowd CF, Halbach VV. Cerebral arterial fenestrations. Interv Neuroradiol 2014;20:261-274.