Synovial Sarcoma of the Esophagus: A Case Report and Review of Literature

Middle East J Dig Dis. 2017 Apr;9(2):111-113. doi: 10.15171/mejdd.2017.60.

Abstract

Synovial sarcoma is an uncommon soft tissue tumor occurring mainly in the periarticular region of the extremities in young adults. It happens less frequently in the head and neck, mediastinum, lungs, heart, and digestive tract. A 28-year-old man two months after total esophagectomy with final diagnosis of esophageal synovial sarcoma was referred to our Positron Emission Tomography (PET-CT) department for the evaluation of treatment response and further treatment planning. To our knowledge this case is the 11th case of esophageal synovial sarcoma, being reported in the literature. We presented the 11th case of esophageal synovial sarcoma. Synovial sarcomas are very rare tumor entities, particularly in the gastrointestinal tract and are likely to be mistaken with other more common tumors such as gastrointestinal stromal tumors.

Keywords: Intestinal perforation; Non-Hodgkin lymphoma; T cell lymphoma.

Publication types

  • Case Reports