Difference between revisions of "Esophageal web"
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Latest revision as of 22:10, 7 February 2019
Synonyms and Keywords: Oesophageal web
Esophageal webs are mucosal folds that partially obstructs the esophageal lumen. The exact pathogenesis of esophageal webs is not known but it is thought to be due to either esophageal inflammation, congenital anomaly, or iron deficiency. They can be classified into type A, B, and C according to their site and extent; type B being the most common. The most common causes are Plummer-Vinson syndrome, celiac sprue and Zenker’s diverticulum. Esophageal webs most commonly present with dysphagia that has a slow onset and is rarely complicated with weight loss. Esophageal webs must be differentiated from other causes of dysphagia such esophageal strictures and achalasia. In barium esophagogram, esophageal webs appear as a uniform narrowing of the esophagus and on endoscopy, esophageal webs appear as a smooth narrowing of the esophagus that is not present in the whole circumference of the lumen. Esophageal dilation is the cornerstone of treatment and it is effective in relieving the symptoms but with high recurrence rate.
- In 1944, esophageal webs were first described by Templeton and it was thought to be a congenital disease because most of the patients were children.
- In 1953, a series of case reports of patients having dysphagia and radiological signs denoting esophageal narrowing made the diagnosis of esophageal rings not confined to the pediatric population.
- In 1968, histological examination of specimens from the esophageal rings proved that none of them had muscle involvement.
- Type A esophageal rings describe webs that involve the muscle layer of the esophageal wall and lies in close proximity to the squamo-columnar junction.
- It is less common than type B esophageal webs.
- Type B esophageal rings describe the webs that involve only the mucosa and submucosa of the esophagus.
- It is often named “Schatzki ring”.
- It is located exactly at the squamo-columnar junction.
- Type C esophageal rings refer to wall invaginations due to pressure from the diaphragm.
- It is rare with no clinical significance.
There are multiple theories explaining the origin of esophageal webs.
- Esophageal webs are thought to be due to the chronic damage to the esophageal mucosa.
- This is supported by the presence of inflammatory cells in the wall of the web.
- In eosinophilic esophagitis, eosinophils were found while in cases of chronic inflammation as GERD, lymphocytes prevailed.
- Esophageal webs are thought to be due to failure of the esophagus to recanalize.
- Specimens showed that the esophageal webs contained respiratory epithelium supporting this theory.
- The webs mostly remain asymptomatic for long times and that is why it is not correlated with being congenital.
- The esophageal webs of Plummer-Vinson syndrome have been associated with iron deficiency anemia in many studies.
- The exact mechanism by which iron deficiency causes esophageal webs is not known, but it was hypothesized that iron deficiency starts a sequence of events in the esophageal epithelium that ends in its damage and formation of a web.
- Moreover, treatment of iron deficiency in Plummer-Vinson syndrome patients leads to resolution of dysphagia even before the laboratory results become normal.
- Esophageal webs appear as an eccentric narrowing of the esophageal lumen (while rings cause circumferential narrowing).
- Esophageal webs are covered normally by mucosa and submucosa.
- It is characterized by the presence of basal cell hyperplasia.
- The tissue is often heavily infiltrated with chronic inflammatory cells.
- Eosinophilic esophagitis is characterized by the presence of eosinophil infiltration.
More common causes
Less common causes
Differentiating esophageal webs from other diseases
|Disease||Signs and Symptoms||Barium esophagogram||Endoscopy||Other imaging and laboratory findings||Gold Standard|
|Onset||Dysphagia||Weight loss||Heartburn||Other findings||Mental status|
|Diffuse esophageal spasm||
||Positive serology for|
- Webs are diagnosed in 5-15% of patients doing barium esophagogram for diagnosing the cause of dysphagia.
- Congenital esophageal webs are estimated to be 1 in 25,000 to 1 in 50,000 live births.
- Esophageal webs affects the whites more than other population.
- Esophageal webs tend to be more common in females.
- This may be due to the increased prevalence of iron deficiency anemia.
- Esophageal has no predilection for an age group, however, it is usually not symptomatic until after the age of 40.
According to USPSTF, there are no screening measures recommended for esophageal webs.
Natural history, complications and prognosis
- The disease can start at any age but symptoms usually start in the fifth decade of life.
- The dysphagia is usually to solids at the beginning then it progresses to both solids and liquids.
- If left untreated, the webs may progress causing esophageal strictures and esophageal carcinoma.
- Progression to esophageal carcinoma.
- Choking spells.
- Esophagitis from chronic injury of the mucosa.
- Progression to esophageal stricture.
- The prognosis of esophageal webs is generally good especially with treatment of the underlying cause.
- One of out of ten patients with Plummer-Vinson syndrome will develop esophageal carcinoma.
History and symptoms
- Patients are usually older than 40 years because it can be asymptomatic for a long time.
- The patient may give a history of the cause such as iron deficiency anemia, GERD, or autoimmune disease.
- There may be a history of excessive food chewing to facilitate swallowing.
- Most of the esophageal webs are asymptomatic.
- The major symptom of esophageal webs is dysphagia.
- Dysphagia is usually more for solid food.
- Esophageal webs do not usually result in malnutrition nor to weight loss.
Esophageal webs do not have significant physical exam findings, however, it might show the signs of the cause such as:
- Koilonychia and glossitis in the cases of Plummer-Vinson syndrome.
- It might also show the findings in in the cases of skin disorders such as epidermolysis bullosa, bullous pemphigoid, and pemphigus vulgaris.
- A Laboratory workup is not necessary for the diagnosis of esophageal webs because the diagnosis is dependent on the symptoms and radiological tests.
- CBC might show microcytic hypochromic anemia in cases of Plummer-Vinson syndrome as it is the primary cause of the esophageal web.
- Antibody panel might be done to screen for the primary cause.
- Barium esophagogram is more sensitive in detecting esophageal webs than endoscopy.
- Webs appear as a uniform narrowing of the esophageal lumen.
Other diagnostic tests
- Endoscopy is less sensitive in detecting webs than barium esophagram.
- Esophageal webs appear as a smooth membrane that is not encircling the whole lumen.
- It allows obtaining a biopsy from the lesion in addition to excluding other causes of dysphagia.
- Esophageal webs can go unnoticed during the esophagram as it is only a mucous membrane fold with no muscle support.
- Patients should be educated to change their diet and food habits, especially in the cases when esophageal webs are secondary to GERD.
- H2 blockers or proton pump inhibitors can be used for managing the symptoms of GERD and the prevention of progression to webs.
- Proper management of acid reflux after esophageal dilation is associated with decreased recurrence of symptoms.
- Esophageal dilation is the cornerstone of treating esophageal webs especially in cases refractory to medical treatment.
- In cases of eosinophilic esophagitis, dilation should be gradual as sudden forced dilation is associated with muscle tears.
- In cases of non-eosinophilic esophagitis, dilation using a single dilator is more effective than graded dilation.
- Esophageal dilation is associated with improved dysphagia.
- Esophageal dilation is associated with symptom recurrence in about 89% at five years and often requires redoing of the procedure.
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