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Colegio de Medicos y Cirujanos República de Costa Rica
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2014, Number 612

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Rev Med Cos Cen 2014; 71 (612)

Acalasia (Revisión Clínica)

Vargas PN
Full text How to cite this article

Language: Spanish
References: 10
Page: 699-702
PDF size: 220.69 Kb.


Key words:

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ABSTRACT

Achalasia is a rare chronic disease, with an incidence of approximately 1.5 person per 100,000. This is characterized by irreversible destruction of neurons in the myenteric plexus at the level of the esophagus, and consequently a loss in esophageal motility and relaxation of lower esophageal sphincter causing symptoms such as dysphagia (main symptom), chest pain, vomiting, regurgitation, heartburn and weight loss. Current treatment consists of procedures such as pneumatic dilation, laparoscopic Heller myotomy and recently has begun with the perioral endoscopic myotomy.


REFERENCES

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  2. Gockel, I., Timm, S., George G. et al. Achalasia—If Surgical Treatment Fails: Analysis of Remedial Surgery. (2010). J Gastrointest Surg (2010) 14 (Suppl 1):S46–S57. DOI 10.1007/ s11605-009-1018-0.

  3. Henning, G., Schumacher, J., Gockel, I., et al. Achalasia: will genetic studies provide insights?. 2010. Hum Genet (2010) 128:353– 364.DOI 10.1007/s00439-010- 0874-8.

  4. Kee, S., Hua, C., Wei, W., et al. Current status in the treatment options for esophageal achalasia. World Journal of Gastroenterology. (2013). ISSN 2219-2840.

  5. Moonenn A., Boeckxstaens, G. Management of Achalasia. (2013). Elsevier. Gastroenterol Clin N Am 42 45–55.

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  7. Orla M O’Neill, Brian T Johnston, Helen G Coleman. Achalasia: A review of clinical diagnosis, epidemiology, treatment and outcomes. (2013) World Journal of Gastroenterology. ISSN 2219-2840.

  8. Patti, M., Pellegrini, C. Esophageal Achalasia 2011: Pneumatic Dilatation or Laparoscopic Myotomy? (2011). J Gastrointest Surg (2012) 16:870–873. DOI 10.1007/s11605-011-1694-4

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Rev Med Cos Cen. 2014;71