Abstract
Plexiform fibromyxoma (PF) is an exceptionally rare benign mesenchymal tumor of the gastrointestinal tract, primarily affecting the gastric antrum. We present a detailed case report of a 67-year-old female patient who underwent diagnostic and therapeutic endoscopic procedures for a suspected gastrointestinal stromal tumor (GIST) initially identified during an upper endoscopy. Subsequent examination and pathology confirmed a diagnosis of PF in the gastric body following endoscopic mucosal resection. This report discusses the clinical presentation, diagnostic approach, histological findings, management strategies, and review of current literature on PF.
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