Achalasia.
Achalasia is a rare neurogenic motility disorder of the esophagus, occurring in approximately 0.11 cases per 100,000 children.
APA
Islam S (2017). Achalasia.. Seminars in pediatric surgery, 26(2), 116-120. https://doi.org/10.1053/j.sempedsurg.2017.02.001
MLA
Islam S. "Achalasia.." Seminars in pediatric surgery, vol. 26, no. 2, 2017, pp. 116-120.
PMID
28550869
Abstract
Achalasia is a rare neurogenic motility disorder of the esophagus, occurring in approximately 0.11 cases per 100,000 children. The combination of problems (aperistalsis, hypertensive lower esophageal sphincter (LES), and lack of receptive LES relaxation) results in patients having symptoms of progressive dysphagia, weight loss, and regurgitation. Treatment modalities have evolved over the past few decades from balloon dilation and botulinum toxin injection to laparoscopic Heller myotomy and endoscopic myotomy. Most data on achalasia management is extrapolated to children from adult experience. This article describes understanding of the pathogenesis and discusses newer therapeutic techniques as well as controversies in management.
추출된 의학 개체 (NER)
| 유형 | 영어 표현 | 한국어 / 풀이 | UMLS CUI | 출처 | 등장 |
|---|---|---|---|---|---|
| 시술 | botulinum toxin
|
보툴리눔독소 주사 | dict | 1 | |
| 기법 | endoscopic
|
내시경 | dict | 1 |
MeSH Terms
Child; Digestive System Surgical Procedures; Esophageal Achalasia; Humans
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