2020, Number 4
<< Back
Otorrinolaringología 2020; 65 (4)
Integral management of Meige’s syndrome
Valadez-Jiménez VM, Rodríguez-Mauricio AF, Santamaría-Molina SJ, García-Arango AV
Language: Spanish
References: 31
Page: 221-233
PDF size: 420.06 Kb.
ABSTRACT
Background: Meige’s syndrome is a type of cranial focal dystonia characterized
by blepharospasm and oromandibular dystonia, which is associated with complex
movements of the lower muscles of the face, mouth, jaw, tongue, pharynx and neck.
It is of unknown cause, but with a close relationship between a genetic predisposition
and environmental triggers. The treatment options are divided into four groups: oral
medications, botulinum toxin, rehabilitation and others advanced procedures, such as
deep brain stimulation and denervation surgery in refractory cases.
Clinical case: A 66-year-old female patient with oromandibular, pharyngeal and
laryngeal dystonia with blepharospasm, dysphonia, dyspnea and dysphagia, treated
with voice therapy, speech and swallowing and botulinum toxin with good results.
Conclusions: In the reported case, the importance of the clinical and instrumented
study and the speech therapy that includes pharmacological, rehabilitative intervention,
change of habits and safe swallowing measures becomes evident.
REFERENCES
Almedra R, Velon AG, Veiga A, Silva MR. Blepharospasm and Meige syndrome: are there any differences? Toxicon 2015; 93: S2-S67. doi: 10.1016/j.toxicon.2014.11.007
Ananth J, Edelmuth E, Dargan B. Meige’s syndrome associated with neuroleptic treatment. Am J Psychiatry 1988; 145 (4): 513-5. doi: 10.1176/ajp.145.4.513
Tolosa E, Martí MJ. Blepharospasm-oromandibular dystonia syndrome (Meige’s syndrome): clinical aspects. Adv Neurol 1988; 49: 73-84.
Defazio G, Hallet M, Jinnah HA, Conte A, Berardelli A. Blepharospasm 40 years later. Mov Disord 2017; 32 (4): 498-509. doi: 10.1002/mds.26934
Hallett M, Evinger C, Jankovic J, Stacy M. Update on blepharospasm: report from the BEBRF International Workshop. Neurol 2008; 71 (16): 1275-82. doi: 10.1212/01. wnl.0000327601.46315.85
Valls-Sole J, Defazio G. Blepharospasm: Update on epidemiology, clinical aspects, and pathophysiology. Front Neurol 2016; 7: 45. doi: 10.3389/fneur.2016.00045
Lee JM, Baek JS, Choi HS, Kim SJ, Jang JW. Clinical features of benign essential blepharospasm in Korean patients. Korean J Ophthalmol 2018; 32 (5): 339-343. doi: 10.3341/ kjo.2018.0038
Jahngir MU, Patel BC. Meige syndrome. StatPearls [Internet] 2019. Disponible en: https://www.ncbi.nlm.nih.gov/ books/NBK513358/
Jankovic J, Ford J. Blepharospasm and orofacial-cervical dystonia: Clinical and pharmacological findings in 100 patients. Ann Neurol 1983; 13 (4): 402-411. doi: 10.1002/ ana.410130406
Titi-Lartey O, Patel BC. Benign essential blepharospasm. StatPearls [Internet]. 2020. Disponible en: https://www. ncbi.nlm.nih.gov/books/NBK560833/
LeDoux MS. Meige syndrome: What’s in a name? Parkinsonism Relat Disord 2009; 15 (7): 483-9. doi: 10.1016/j. parkreldis.2009.04.006
Cersósimo MG, Juri S, Suárez de Chandler S, Clerici R, Micheli FE. Swallowing disorders in patients with blepharospasm. Medicina (B Aires) 2005; 65 (2): 117-20.
Verheyden J, Blitzer A. Laryngeal dystonia. Dystonia: etiology, clinical features, and treatment. Philadelphia: Lippincott Williams and Wilkins; 2004; 175-83.10.
Kakigi R, Shibasaki H, Kuroda Y, Shin T, Maeyama T, Oono S. Meige’s syndrome associated with spasmodic dysphagia. J Neurol Neurosurg Psychiatry 1983; 46 (6): 589-90. doi: 10.1136/jnnp.46.6.589
Hwang, CJ, Eftekhari K. Benign essential blepharospasm. Internat Ophthalmol Clin 2018; 58 (1): 11-24. doi:10.1097/ iio.0000000000000207
Pedrero-Escalas MF, García-López I, Santiago-Pérez S, Vivancos F, Gavilán J. Clinical experience with patients with spasmodic dysphonia and primary Meige syndrome. Acta Otorrinolaringol Esp 2019; 70 (1):1-5. doi: 10.1016/j. otorri.2017.11.007
Aramideh M, Bour LJ, Koelman JH, Speelman JD, Ongerboer de Visser BW. Abnormal eye movements in blepharospasm and involuntary levator palpebrae inhibition. Clinical and pathophysiological considerations. Brain 1994; 117 (Pt 6): 1457-74. doi: 10.1093/brain/117.6.1457
Cobeta I, Núñez F, Fernández S. Patología de la voz. 1ª ed. Barcelona, España. Marge Médica Books, 2013.
Khooshnoodi MA, Factor SA, Jinnah HA. Secondary blepharospasm associated with structural lesions of the brain. J Neurol Sci 2013; 331: 98-101. doi: 10.1016/j. jns.2013.05.022
Horovitz SG, Ford A, Najee-Ullah MA, Ostuni JL, Hallett M. Anatomical correlates of blepharospasm. Transl Neurodegener 2012; 1: 12. doi: 10.1186/2047-9158-1-12
Kerrison JB, Lancaster JL, Zamarripa FE, Richardson LA, Morrison JC, Holck DE. Positron emission tomography scanning in essential blepharospasm. Am J Ophthalmol 2003; 136: 846-52. doi:10.1016/S0002-9394(03)00895-X
Smith EE. Leukoaraiosis and stroke. Stroke 2010; 41 (10 Suppl): S139-43. doi: 10.1161/STROKEAHA.110.596056
Chan LK, Ho HY, Yu CS. Dementia with Lewy bodies in Meige syndrome. Innov Clin Neurosci 2012; 9 (7-8): 39-41.
Jinnah HA, Factor SA. Diagnosis and treatment of dystonia. Neurol Clin 2015; 33: 77-100. doi: 10.1016/j. ncl.2014.09.002
Markaki E, Kefalopoulou Z, Georgiopoulos M, Paschali A, Constantoyannis C. Meige’s syndrome: A cranial dystonia treated with bilateral pallidal deep brain stimulation. Clin Neurol Neurosurg 2010; 112 (4): 344-6. doi: 10.1016/j. clineuro.2009.12.005
Houser M, Waltz T. Meige syndrome and pallidal deep brain stimulation. Mov Disord 2005; 20 (9): 1203-5. doi: 10.1002/mds.20522
Sabesan T. Meige syndrome: a rare form of cranial dystonia that was treated successfully with botulinum toxin. Br J Oral Maxillofac Surg 2008; 46 (7): 588-90. doi: 10.1016/j. bjoms.2008.02.002
Ababneh OH, Cetinkaya A, Kulwin DR. Long-term efficacy and safety of botulinum toxin A injections to treat blepharospasm and hemifacial spasm. Clin. Experiment Ophthalmol 2014; 42 (3): 254-61.
Kwek ABE, Tan EK, Luman W. Dysphagia as a side effect of botulinum toxin injection. Med J Malaysia 2004; 59 (4): 544-6.
Dutton JJ. Botulinum-A toxin in the treatment of craniocervical muscle spasms: short- and long-term, local and systemic effects. Surv Ophthalmol 1996; 41 (1): 51-65. doi: 10.1016/s0039-6257(97)81995-9
Borodic GE, Ferrante R, Pearce B, Smith K. Histologic assessment of dose-related diffusion and muscle fiber response after therapeutic botulinum A toxin injections. Mov Disord 1994; 88 (9): 31-39. doi: 10.1002/mds.870090106