Unusual achalasic sigmoid esophagus
Achalasia cardia is a rare primary esophageal motility disorder with an incidence of about 1 in 100,000 individuals. If left untreated or inappropriately treated, the disease may progress to end-stage achalasia characterized by megaesophagus or sigmoid esophagus. The presentation as severe malnutri...
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Society of Surgeons of Nepal
2019
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oai:doaj.org-article:f501bedfccba44b197d60b81d0d738692021-12-05T19:15:47ZUnusual achalasic sigmoid esophagus10.3126/jssn.v22i2.287431815-39842392-4772https://doaj.org/article/f501bedfccba44b197d60b81d0d738692019-12-01T00:00:00Zhttps://www.nepjol.info/index.php/JSSN/article/view/28743https://doaj.org/toc/1815-3984https://doaj.org/toc/2392-4772 Achalasia cardia is a rare primary esophageal motility disorder with an incidence of about 1 in 100,000 individuals. If left untreated or inappropriately treated, the disease may progress to end-stage achalasia characterized by megaesophagus or sigmoid esophagus. The presentation as severe malnutrition, anemia, hypoalbuminemia, and asymptomatic tracheal compression has not been described in the setting of the sigmoid esophagus, in absence of underlying malignancy. Here we report an interesting case of a young male, who presented with the above features and managed excellently by open Heller’s myotomy under epidural anesthesia due to the poor performance status. Narendra PanditVijay ShresthaLaligen AwaleLokesh Shekher JaiswalSociety of Surgeons of NepalarticleAchalasia cardiaHeller's myotomyMalnutritionSigmoid esophagusSurgeryRD1-811ENJournal of Society of Surgeons of Nepal, Vol 22, Iss 2 (2019) |
| institution |
DOAJ |
| collection |
DOAJ |
| language |
EN |
| topic |
Achalasia cardia Heller's myotomy Malnutrition Sigmoid esophagus Surgery RD1-811 |
| spellingShingle |
Achalasia cardia Heller's myotomy Malnutrition Sigmoid esophagus Surgery RD1-811 Narendra Pandit Vijay Shrestha Laligen Awale Lokesh Shekher Jaiswal Unusual achalasic sigmoid esophagus |
| description |
Achalasia cardia is a rare primary esophageal motility disorder with an incidence of about 1 in 100,000 individuals. If left untreated or inappropriately treated, the disease may progress to end-stage achalasia characterized by megaesophagus or sigmoid esophagus. The presentation as severe malnutrition, anemia, hypoalbuminemia, and asymptomatic tracheal compression has not been described in the setting of the sigmoid esophagus, in absence of underlying malignancy. Here we report an interesting case of a young male, who presented with the above features and managed excellently by open Heller’s myotomy under epidural anesthesia due to the poor performance status.
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| format |
article |
| author |
Narendra Pandit Vijay Shrestha Laligen Awale Lokesh Shekher Jaiswal |
| author_facet |
Narendra Pandit Vijay Shrestha Laligen Awale Lokesh Shekher Jaiswal |
| author_sort |
Narendra Pandit |
| title |
Unusual achalasic sigmoid esophagus |
| title_short |
Unusual achalasic sigmoid esophagus |
| title_full |
Unusual achalasic sigmoid esophagus |
| title_fullStr |
Unusual achalasic sigmoid esophagus |
| title_full_unstemmed |
Unusual achalasic sigmoid esophagus |
| title_sort |
unusual achalasic sigmoid esophagus |
| publisher |
Society of Surgeons of Nepal |
| publishDate |
2019 |
| url |
https://doaj.org/article/f501bedfccba44b197d60b81d0d73869 |
| work_keys_str_mv |
AT narendrapandit unusualachalasicsigmoidesophagus AT vijayshrestha unusualachalasicsigmoidesophagus AT laligenawale unusualachalasicsigmoidesophagus AT lokeshshekherjaiswal unusualachalasicsigmoidesophagus |
| _version_ |
1718371097683951616 |