Abstract
Duodenal leiomyosarcoma is a rare condition with a poor prognosis. Early diagnosis of duodenal leiomyosarcoma is challenging because it presents with nonspecific symptoms and endoscopic biopsies usually do not enable a definitive diagnosis. Duodenal leiomyosarcomas are diagnosed on the basis of the histopathological identification of a mesenchymal lesion composed of malignant tumor cells that on immunohistochemical examination is positive for smooth muscle actin and desmin. We report the case of a 38-year-old man who presented with gastrointestinal bleeding and obstruction who was diagnosed with duodenal leiomyosarcoma after surgical resection.
References
1. Kang HC, Menias CO, Gaballah AH, et al. Beyond the GIST: mesenchymal tumors of the stomach. Radiographics. 2013; 33:1673–1690.
2. Miettinen M, Lasota J. Gastrointestinal stromal tumors–definition, clinical, histological, immunohistochemical, and molecular genetic features and differential diagnosis. Virchows Arch. 2001; 438:1–12.
3. Diamond T, Danton MH, Parks TG. Smooth muscle tumours of the alimentary tract. Ann R Coll Surg Engl. 1990; 72:316–320.
4. Jerraya H, Guirat A, Frikha F, Beyrouti I. Leiomyosarcoma of the duodeno-jejunal angle: two case reports and literature review. Surg Sci. 2013; 4:313–316.
5. Owada Y, Haji S, Asakura R, et al. A case report of resectable leiomyosarcoma of the duodenum origin invading to the inferior vena cava. Gan To Kagaku Ryoho. 2018; 45:142–144.
6. Katz SC, DeMatteo RP. Gastrointestinal stromal tumors and leiomyosarcomas. J Surg Oncol. 2008; 97:350–359.
7. Yeo GE, Kwon HJ, Kim JH, Chang HK, Park JG. A incidentally diagnosed duodenal subepithelial mass: gangliocytic paraganglioma treated by endoscopic mucosal resection. Korean J Helicobacter Up Gastrointest Res. 2019; 19:132–136.
8. Olurin EO, Solanke TF. Case of leiomyosarcoma of the duodenum and a review of the literature. Gut. 1968; 9:672–677.