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Resection of an esophageal schwannoma with thoracoscopic surgery: a case report

BACKGROUND: Esophageal schwannomas are rare primary submucosal esophageal tumors. We herein report a case of an esophageal schwannoma that was difficult to diagnose. CASE PRESENTATION: A 39-year-old woman presented with chief complaints of difficulty swallowing and epigastric pain. Enhanced computed...

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Detalles Bibliográficos
Autores principales: Watanabe, Takayoshi, Miyazaki, Tatsuya, Saito, Hideyuki, Yoshida, Tomonori, Kumakura, Yuji, Honjyo, Hiroaki, Yokobori, Takehiko, Sakai, Makoto, Sohda, Makoto, Kuwano, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5099309/
https://www.ncbi.nlm.nih.gov/pubmed/27822873
http://dx.doi.org/10.1186/s40792-016-0256-0
Descripción
Sumario:BACKGROUND: Esophageal schwannomas are rare primary submucosal esophageal tumors. We herein report a case of an esophageal schwannoma that was difficult to diagnose. CASE PRESENTATION: A 39-year-old woman presented with chief complaints of difficulty swallowing and epigastric pain. Enhanced computed tomography of her chest revealed a tumor mass at the upper thoracic esophagus with internal heterogeneity. 18-Fluorodeoxyglucose positron emission tomography/computed tomography showed a hypermetabolic appearance matching the tumor mass; the accumulation had a maximum standardized uptake value of 5.5. We performed endoscopic ultrasound-guided fine-needle aspiration biopsy under general anesthesia, but the small specimens obtained prevented a definitive diagnosis. Thoracoscopic esophagectomy was performed due to the large size of the tumor, suspicion of its malignant potential, and the patient’s symptoms. Histopathological examination revealed spindle-shaped cells in a fasciculated and disarrayed architecture in the proper muscle layer. Immunohistochemical studies showed S100 protein positivity and the absence of CD34 and c-kit. We diagnosed the tumor as a benign schwannoma. CONCLUSIONS: We herein report a relatively rare case of schwannoma of the esophagus that was diagnosed with difficulty.