Published online Jan 28, 2014. doi: 10.3748/wjg.v20.i4.1114
Revised: September 7, 2013
Accepted: September 16, 2013
Published online: January 28, 2014
Processing time: 181 Days and 20.9 Hours
Achalasia cardia is an idiopathic disease that occurs as a result of inflammation and degeneration of myenteric plexi leading to the loss of postganglionic inhibitory neurons required for relaxation of the lower esophageal sphincter and peristalsis of the esophagus. The main symptoms of achalasia are dysphagia, regurgitation, chest pain and weight loss. At present, there are three main hypotheses regarding etiology of achalasia cardia which are under consideration, these are genetic, infectious and autoimmune. Genetic theory is one of the most widely discussed. Case report given below represents an inheritable case of achalasia cardia which was not diagnosed for a long time in an 81-year-old woman and her 58-year-old daughter.
Core tip: We report an inheritable case of achalasia cardia in an 81-year-old woman and her 58-year-old daughter with early manifestation of the disease at 23 and 25 years of age, respectively, and further progression of achalasia cardia which led to its decompensation and resulted in gastrostomy in the woman which was performed when she was 79-year-old.