J Korean Ophthalmol Soc.  2017 Feb;58(2):197-202. 10.3341/jkos.2017.58.2.197.

The Characteristics and Prognosis of Miller Fisher Syndrome

Affiliations
  • 1Department of Ophthalmology, Pusan National University Yangsan Hospital, Pusan National University School of Medicine, Yangsan, Korea. jungjaeho@pusan.ac.kr

Abstract

PURPOSE
In the present study, the clinical characteristics and prognosis of patients clinically diagnosed with classic Miller Fisher syndrome were evaluated.
METHODS
We retrospectively investigated the clinical and laboratory findings as well as treatment outcomes using the medical records of patients diagnosed with Miller Fisher syndrome. Symptom triad including acute ophthalmoplegia, ataxia, and areflexia were evaluated.
RESULTS
This study included 10 patients. Nine patients had antecedent infectious illness which took an average of 11 ± 9.7 days for onset of diplopia from antecedent infectious systemic illness. Seven patients showed bilateral paralytic strabismus. Specifically, 5 patients showed the involvement of vertical and horizontal extraocular muscles. Pupil impairment and blepharoptosis were observed in 4 patients, limb weakness in 3 patients, dysarthria in 3 patients and facial palsy in 1 patient. Two patients showed contrast enhancement of the abducens nerve on brain magnetic resonance imaging (MRI) and 2 patients showed albumin-cell dissociation on cerebrospinal fluid (CSF) analysis. Eight patients had anti-GQ1b antibodies in their blood serum analysis. Six patients were treated with intravenous immunoglobulins and the other patients were observed with regular follow-ups. The duration of diplopia was 2.9 ± 1.2 months in the treatment group and 3.1 ± 1.7 months in the control group (p > 0.05). The duration of ataxia was 1 ± 0.4 months in the treatment group and 1 ± 0.9 months in the control group (p > 0.05).
CONCLUSIONS
Miller Fisher syndrome should be considered in patients with antecedent infection; acute ophthalmoplegia, ataxia and areflexia as well as anti-GQ1b antibody can be helpful for diagnosis. Final outcomes in the treated group were not significantly different from the control group and all patients showed good final outcomes.

Keyword

Anti-GQ1b; Bickerstaff's brain stem encephalitis; Miller Fisher syndrome; Ophthalmoplegia

MeSH Terms

Abducens Nerve
Antibodies
Ataxia
Blepharoptosis
Brain
Cerebrospinal Fluid
Diagnosis
Diplopia
Dysarthria
Extremities
Facial Paralysis
Follow-Up Studies
Humans
Immunoglobulins, Intravenous
Magnetic Resonance Imaging
Medical Records
Miller Fisher Syndrome*
Muscles
Ophthalmoplegia
Prognosis*
Pupil
Retrospective Studies
Serum
Strabismus
Antibodies
Immunoglobulins, Intravenous

Figure

  • Figure 1. Case 7. Contrast enhancement of the left sixth cra-nial nerve in orbit magnetic resonance image (white arrow).


Reference

References

1. Fisher M. An unusual variant of acute idiopathic polyneuritis (syndrome of ophthalmoplegia, ataxia and areflexia). N Engl J Med. 1956; 255:57–65.
Article
2. Bickerstaff ER, Cloake PC. Mesencephalitis and rhombencephalitis. Br Med J. 1951; 2:77–81.
Article
3. Ropper AH. Unusual clinical variants and signs in Guillain-Barré syndrome. Arch Neurol. 1986; 43:1150–2.
4. Ropper AH. Further regional variants of acute immune polyneuropathy. Bifacial weakness or sixth nerve paresis with paresthesias, lumbar polyradiculopathy, and ataxia with pharyngeal-cervical-brachial weakness. Arch Neurol. 1994; 51:671–5.
5. Shuaib A, Becker WJ. Variants of Guillain-Barré syndrome: Miller Fisher syndrome, facial diplegia and multiple cranial nerve palsies. Can J Neurol Sci. 1987; 14:611–6.
6. Chiba A, Kusunoki S, Shimizu T, Kanazawa I. Serum IgG antibody to ganglioside GQ1b is a possible marker of Miller Fisher syndrome. Ann Neurol. 1992; 31:677–9.
Article
7. Yuki N, Sato S, Tsuji S. . An immunologic abnormality com-mon to Bickerstaff’s brain stem encephalitis and Fisher’s syndrome. J Neurol Sci. 1993; 118:83–7.
Article
8. Odaka M, Yuki N, Hirata K. Anti-GQ1b IgG antibody syndrome: clinical and immunological range. J Neurol Neurosurg Psychiatry. 2001; 70:50–5.
Article
9. Sohn HJ, Lee JH, Paik HJ, Chi MJ. A case of atypical Miller Fisher sndrome. J Korean Ophthalmol Soc. 2007; 48:878–82.
10. Ahn JH, Lee SG. A case of anti-GQ1b-positive atypical Miller Fisher syndrome with pupil involvement. J Korean Ophthalmol Soc. 2009; 50:645–8.
Article
11. Park IK, Moon SW, Han JS, Shin JH. A case of Miller Fischer syn-drome with optic nerve involvement. J Korean Ophthalmol Soc. 2010; 51:1676–80.
Article
12. Kim EJ, Ha SG, Kim SH. A case of Miller Fisher syndrome in a pe-diatric patient with positive anti-GQ1b IgG. J Korean Ophthalmol Soc. 2016; 57:528–31.
Article
13. Son MG, Ahn HS. Miller Fisher syndrome. J Korean Ophthalmol Soc. 1997; 38:1470–9.
14. Holmes JM, Liebermann L, Hatt SR. . Quantifying diplopia with a questionnaire. Ophthalmology. 2013; 120:1492–6.
Article
15. Goffette S, Sindic CJ. Acute isolated ophthalmoplegia associated with high levels of anti-GQ 1b antibodies. Eur Neurol. 2000; 43:120–1.
16. Goffette S, Jeanjean A, Pierret F. . Clinical relevance of the de-termination of anti-GQ1b antibodies in Miller Fisher and Guillain-Barré syndromes. Acta Neurol Belg. 1998; 98:322–6.
17. Koga M, Gilbert M, Li J. . Antecedent infection in Fisher syn-drome: a common pathogenesis of molecular mimicry. Neurology. 2005; 64:1605–11.
18. Yuki N, Koga M. Bacterial infections in Guillain-Barré and Fisher syndromes. Curr Opin Neurol. 2006; 19:451–7.
Article
19. Saul RF. Neuro-ophthalmology and the Anti-GQ1b antibody syndromes. Curr Neurol Neurosci Rep. 2009; 9:379–83.
Article
20. Yuki N, Odaka M, Hirata K. Acute ophthalmoparesis (without ataxia) associated with anti-GQ1b IgG antibody: clinical features. Ophthalmology. 2001; 108:196–200.
21. Tatsumoto M, Odaka M, Hirata K, Yuki N. Isolated abducens nerve palsy as a regional variant of Guillain-Barré syndrome. J Neurol Sci. 2006; 243:35–8.
Article
22. Koo DL, Park LH, Kim HT. . Acute monocular ophthalmoplegia associated with anti-GQ1b IgG antibody. J Korean Neurol Assoc. 2004; 22:663–5.
23. Lo YL. Clinical and immunological spectrum of the Miller Fisher syndrome. Muscle Nerve. 2007; 36:615–27.
Article
24. Sugita A, Yanagisawa T, Kamo T. . Internal ophthalmoplegia with anti-GQ1b IgG antibody. J Neurol. 2002; 249:1475–6.
Article
25. Chiba A, Kusunoki S, Obata H. . Ganglioside composition of the human cranial nerves, with special reference to pathophysiol-ogy of Miller Fisher syndrome. Brain Res. 1997; 745:32–6.
Article
26. Ilyas AA, Willison HJ, Quarles RH. . Serum antibodies to gan-gliosides in Guillain-Barré syndrome. Ann Neurol. 1988; 23:440–7.
Article
27. Kim JK, Bae JS, Kim DS. . Prevalance of anti-ganglioside anti-bodies and their clinical correlates with gullain-barré syndrome in Korea: a nationwide multicenter study. J Clin Neurol. 2014; 10:94–100.
28. Svennerholm L, Boström K, Fredman P. . Gangliosides and al-lied glycosphingolipids in human peripheral nerve and spinal cord. Biochim Biophys Acta. 1994; 1214:115–23.
Article
29. Neisser A, Bernheimer H, Berger T. . Serum antibodies against gangliosides and Campylobacter jejuni lipopolysaccharides in Miller Fisher syndrome. Infect Immun. 1997; 65:4038–42.
Article
30. Chiba A, Kusunoki S, Obata H. . Serum anti-GQ1b IgG anti-body is associated with ophthalmoplegia in Miller Fisher syndrome and Guillain-Barré syndrome: clinical and immunohistochemical studies. Neurology. 1993; 43:1911–7.
31. Kusunoki S. Diagnosis, pathogenesis and treatment of Miller Fisher syndrome and related disorders: clinical significance of antiGQ1b IgG antibody. Expert Rev Neurother. 2003; 3:133–40.
Article
32. Kaida K, Kanzaki M, Morita D. . Anti-ganglioside complex antibodies in Miller Fisher syndrome. J Neurol Neurosurg Psychiatry. 2006; 77:1043–6.
Article
33. Na JG, Jung WY, Won K, Lim GH. Brainstem encephalitis mim-icking Miller Fisher syndrome. J Korean Neurol Assoc. 1994; 12:758–63.
34. Kim BJ, Seo YL. Relapsing sensory ataxia initially manifested by miller-fisher syndrome. J Korean Neurol Assoc. 1997; 15:216–21.
35. Hong SN, Koo JS, Kim BK. . A case of Miller Fisher syndrome presenting as sudden vertigo. J Korean Neurol Assoc. 2000; 18:486–9.
36. Mori M, Kuwabara S, Fukutake T. . Clinical features and prog-nosis of Miller Fisher syndrome. Neurology. 2001; 56:1104–6.
Article
37. Mori M, Kuwabara S, Fukutake T, Hattori T. Intravenous im-munoglobulin therapy for Miller Fisher syndrome. Neurology. 2007; 68:1144–6.
Article
Full Text Links
  • JKOS
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr