Polypoid leiomyosarcoma of the esophagus treated by endoscopic submucosal dissection

• Published in: Digestive endoscopy Vol. 27; no. 6; pp. 700 - 703
• Main Authors: Yamamoto, Yoshinobu, Nishisaki, Hogara, Koma, Yu‐ichiro, Sawai, Hiroaki, Sakai, Aya, Mimura, Takuya, Kushida, Saeko, Tsumura, Hidetaka, Sakamoto, Takeshi, Tobimatsu, Kazutoshi, Miki, Ikuya, Sakuma, Toshiko, Tsuda, Masahiro, Mano, Masayuki, Hirose, Takanori, Inokuchi, Hideto
• Format: Journal Article
• Language: English
• Published: Australia 01.09.2015
• Subjects: Biopsy, Needle; Deglutition Disorders - diagnosis; Deglutition Disorders - etiology; dissection; endoscopic; Esophageal Neoplasms - diagnostic imaging; Esophageal Neoplasms - pathology; Esophageal Neoplasms - surgery; Esophagoscopy - methods; esophagus; Follow-Up Studies; Humans; Immunohistochemistry; leiomyosarcoma; Leiomyosarcoma - diagnostic imaging; Leiomyosarcoma - pathology; Leiomyosarcoma - surgery; Male; Middle Aged; Minimally Invasive Surgical Procedures - methods; Mucous Membrane - pathology; Mucous Membrane - surgery; Polyps - diagnostic imaging; Polyps - pathology; Polyps - surgery; Risk Assessment; submucosal; Time Factors; Tomography, X-Ray Computed - methods; Treatment Outcome; endoscopic; leiomyosarcoma; esophagus; submucosal; dissection
• ISSN: 0915-5635; 1443-1661
• DOI: 10.1111/den.12437

We report a rare case of polypoid leiomyosarcoma of the esophagus that was treated by endoscopic submucosal dissection (ESD). A 63‐year‐old man with complaints of progressive dysphagia was referred to Hyogo Cancer Center for treatment of esophageal tumor. Esophagoscopy revealed a polypoid tumor 25 mm in diameter on the left side of the upper esophagus. Despite several biopsy specimens, the diagnosis could not be confirmed. Computed tomography showed a protruded, homogeneously enhancing mass in the upper esophagus, but no lymph node enlargement or metastasis. After 1.5 months, the esophagogram showed a filling defect 47 mm in diameter in the upper esophagus. Given this rapid tumor growth, en bloc resection was done by ESD for therapeutic diagnosis. After this treatment, the tumor seemed to grow larger, showing a short stalk and occupying the esophageal lumen. Histopathologically, the tumor comprised pleomorphic spindle cells with mitosis. Tumor invasion involved the lumina propria mucosae and contact with the muscularis mucosae, but not involving the submucosa. Immunohistochemical examination showed positive staining for smooth muscle actin and HHF35, but negative for desmin, caldesmon, CD34, c‐kit, DOG1, ALK, S‐100 protein and cytokeratin. These histopathological findings were compatible with a diagnosis of esophageal leiomyosarcoma derived from the muscularis mucosae.