2013, Number 1
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Revista Cubana de Anestesiología y Reanimación 2013; 12 (1)
Anaesthesia in Steinert Disease
Amores AT, Cantero DY, Marrero QJ
Language: Spanish
References: 11
Page: 52-56
PDF size: 26.92 Kb.
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
Roca R, Smith V. Atrofias musculares. En: Temas de Medicina Interna. 4ta. ed. La Habana: Editorial Ciencias Médicas; 2002. p. 466-70.
Mathieu J. Prevalencia de la enfermedad de Steinert. La Presse Médicale. 2007;36(6):2.
Ropper AH, Brown RH. The muscular distrophies. En: Principles of Neurology. 8va. ed. New York: Mc Graw Hill Interamericana; 2005. p. 1213-29.
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.
Bueno Lledó J, Ballester Ibáñez C. Perforación colónica secundaria a distrofia miotónica de Steinert. Rev Cir Esp. 2003;73(6):375-7.
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.
Puertos Bordallo D. Afectación oftalmológica de la distrofia miotónica congénita. Rev Acta Estrabiológica. 2005;34(3):145-9.
Pelargonio G, Dello Russo A, Sanna T. Myotonic dystrophy and the heart. Heart 2002;88:665-70.
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.
Huson S. Myotonic dystrophy-time to improve patient care and prepare for pathogenesis based treatments. European J Human Genetics. 2005;13(2):131-132.
Barra Bisinotto FM. Anestesia para colecistectomía videolaparoscópica en paciente con enfermedad de Steinert. Rev Bras Anestesiol. 2010;60(2):13-4.