medigraphic.com
SPANISH

Revista Cubana de Anestesiología y Reanimación

ISSN 1726-6718 (Electronic)
Revista Cubana de Anestesiología y Reanimación
  • Contents
  • View Archive
  • Information
    • General Information        
    • Directory
  • Publish
    • Instructions for authors        
  • medigraphic.com
    • Home
    • Journals index            
    • Register / Login
  • Mi perfil

2013, Number 1

<< Back Next >>

Revista Cubana de Anestesiología y Reanimación 2013; 12 (1)

Anaesthesia in Steinert Disease

Amores AT, Cantero DY, Marrero QJ
Full text How to cite this article

Language: Spanish
References: 11
Page: 52-56
PDF size: 26.92 Kb.


Key words:

Steinert´s disease, myotonic dystrophy, myotony.

ABSTRACT

Background: Steinert´s myotonic dystrophy is a hereditary chronic multisystemic process that principally affects skeletal muscles and presents with slowly progressive myotony and muscular atrophies. Patients suffering from this disease are very susceptible to anaesthetic agents and can present serious perioperative complications.
Objectives: To describe the surgical evolution of a patient suffering from Steinert´s disease.
Clinical case report: A 42-year-old female patient that has been presenting metrorrhagias and dysmenorrheas of more than two years of evolution was operated on uterine fibroma. She had personal pathological antecedents of Steinert´s disease of fifteen years evolution and symptoms that worsened after delivery.
Conclusions: The patients who suffer from Steinert´s disease represent a challenge for the anaesthesiologist; nevertheless, an individualized and detailed preoperative assessment in each case so as the benefits offered by the monitoring, anaesthetic and surgical techniques allow a satisfactory evolution.


REFERENCES

  1. Roca R, Smith V. Atrofias musculares. En: Temas de Medicina Interna. 4ta. ed. La Habana: Editorial Ciencias Médicas; 2002. p. 466-70.

  2. Mathieu J. Prevalencia de la enfermedad de Steinert. La Presse Médicale. 2007;36(6):2.

  3. Ropper AH, Brown RH. The muscular distrophies. En: Principles of Neurology. 8va. ed. New York: Mc Graw Hill Interamericana; 2005. p. 1213-29.

  4. Guimaraes AS, Suazo GI, Nagahashi Marie SK. Fenómeno miotónico orofacial en pacientes con distrofia muscular de Steinert. Rev Avances en Odontoestomatología. 2010;26(3):139-42.

  5. Bueno Lledó J, Ballester Ibáñez C. Perforación colónica secundaria a distrofia miotónica de Steinert. Rev Cir Esp. 2003;73(6):375-7.

  6. Milne L, Henter J, Anshus J, Rosen P. Gastric volvulus: two cases and a review of the literature. J Emerg Medic. 1994;12:299-306.

  7. Puertos Bordallo D. Afectación oftalmológica de la distrofia miotónica congénita. Rev Acta Estrabiológica. 2005;34(3):145-9.

  8. Pelargonio G, Dello Russo A, Sanna T. Myotonic dystrophy and the heart. Heart 2002;88:665-70.

  9. Muraoka H, Negoro N, Terasaki F. Re-entry circuit in ventricular tachycardia due to focal fatty-fibrosis in a patient with myotonic dystrophy. Intern Med. 2005;44:129-35.

  10. Huson S. Myotonic dystrophy-time to improve patient care and prepare for pathogenesis based treatments. European J Human Genetics. 2005;13(2):131-132.

  11. Barra Bisinotto FM. Anestesia para colecistectomía videolaparoscópica en paciente con enfermedad de Steinert. Rev Bras Anestesiol. 2010;60(2):13-4.




2020     |     www.medigraphic.com

Mi perfil

C?MO CITAR (Vancouver)

Revista Cubana de Anestesiología y Reanimación. 2013;12