Achalasia is an important esophageal motor disorder that causes dysphagia, disrupting patients’ nutrition and decreasing their quality of life. The pathophysiological basis of this disorder is the loss of peristalsis in the esophagus and insufficient relaxation of the lower esophageal sphincter (LES). Major clinical signs; Dysphagia against both solids and liquids, regurgitation of the esophageal contents, heartburn, retrosternal chest pain, cough, aspiration, and weight loss. Achalasia was first described and named by Sir Thomas Willis in 1674. (1)
Esophageal manometry is the gold standard for diagnosis. It usually starts insidiously. Swallowing disorder, chest pain may even manifest with symptoms. Diagnosis can usually take 2-3 years. (2)
Pharmacotherapy: calcium channel blockers and long acting nitrates;
Botulinum toxin injections into LOS
Pneumatic expansion of LOS
peroral endoscopic myotomy (POEM);
laparoscopic Heller cardiomyotomy (LHC) (3)
It is known as Heller myotomy (Esopageal myotomy), a procedure in which the muscles around the esophagus are opened and cut. (4)
Studies have reported that Laparoscopic Heller Myotomy surgery is effective in 85% of children. (5)
For example, our patient, E.K, was 23 years old and had only been fed with liquid for the last 3 years. Before the operation, endoscopy, chest X-ray and tomography examinations were performed. Heller myotomy was applied laparoscopic.
Per-oral endoscopic myotomy can be applied in patients whose Heller myotomy operation is ineffective. (6)
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