There are many types of benign esophageal tumors; many are found incidentally, remain asymptomatic, and warrant only observation. Some can cause swallowing symptoms and rarely ulceration or bleeding.
Although relatively rare overall, benign esophageal tumors include a variety of histologic types. Some of the more common types include the following (1):
Leiomyoma
Schwannoma (or other neurogenic tumors)
Lipoma
Papilloma
Hemangioma
Fibrovascular polyp
Duplication cyst
Granular cell tumor
Reference
1. Ha C, Regan J, Cetindag IB, Ali A, Mellinger JD. Benign esophageal tumors. Surg Clin North Am. 2015;95(3):491-514. doi:10.1016/j.suc.2015.02.005
Symptoms and Signs of Benign Esophageal Tumors
The clinical presentation of benign esophageal tumors vary widely and depend on the type. The majority are asymptomatic and are discovered incidentally. However, symptoms can include dysphagia, retrosternal or epigastric discomfort, bleeding, and/or weight loss.
Diagnosis of Benign Esophageal Tumors
Barium esophagram or upper GI endoscopy
Initial evaluation typically mirrors that of dysphagia, beginning with a barium esophagram or upper GI endoscopy (with or without endoscopic ultrasound).
Once a lesion is visualized, tissue samples can be obtained with upper endoscopy.
A CT scan or MRI may be helpful in some cases for initial characterization, extent of involvement, and monitoring of changes over time.
Treatment of Benign Esophageal Tumors
Surgical or endoscopic removal
Generally, treatment is recommended when benign tumors continue to enlarge or patients become symptomatic.
Leiomyoma, the most common benign esophageal tumor, may be multiple and can become large. Depending on its size and location, the tumor can be excised or enucleated. Minimally invasive approaches such as endoscopic submucosal dissection and video-assisted thoracoscopic surgery (VATS) have increasingly replaced open thoracotomy in many cases, thus reducing operative morbidity. With treatment, this tumor usually has an excellent prognosis (1).
Esophageal papillomas and granular cell tumors, although rare, may become malignant and their complete endoscopic removal is recommended.
Treatment reference
1. Mutrie CJ, Donahue DM, Wain JC, Wright CD, Gaissert HA, Grillo HC, Mathisen DJ, Allan JS. Esophageal leiomyoma: a 40-year experience. Ann Thorac Surg. 2005 Apr;79(4):1122-5. doi: 10.1016/j.athoracsur.2004.08.029