Duodenal leiomyoma: a case report of upper gastrointestinal hemorrhage from a giant duodenal tumor

Introduction: Duodenal leiomyoma is a rare tumor, originating in the intestinal wall smooth muscle, making up <0.1% of all gastrointestinal tumors. The majority are discovered incidentally on endoscopy due to the small size of tumors at presentation. Larger duodenal leiomyomas may present with anemia from gastrointestinal hemorrhage. Case presentation: A 67-year-old male presented with life-threatening upper gastrointestinal hemorrhage. Magnetic resonance imaging identified an 11.9 × 8.7 cm submucosal mass in the second portion of the duodenum adjacent to the pancreatic head. An urgent upper endoscopy confirmed active hemorrhage, which was controlled with endoscopic clips. The patient underwent a successful resection of the tumor with no postoperative complications. Discussion: The diagnosis of duodenal leiomyomas remains challenging due to the lack of symptom manifestations. The differential diagnosis for a duodenal soft tissue mass includes gastrointestinal stromal tumor, solitary fibrous tumors, schwannoma, lymphoma, duodenal adenocarcinoma, and leiomyosarcoma. Radiographically, leiomyomas have typical imaging characteristics similar to skeletal muscle with marked T2 hypointensity, gradual enhancement on post contrast images, and the absence of extensive lesional necrosis. Surgical resection allows pathological confirmation of tissue diagnosis. Histopathologically, leiomyoma exhibits bland smooth muscle cells, with a low Ki67 proliferative index and absence of mitotic figures. Leiomyoma immunohistochemistry profile is positive for smooth muscle antigen and desmin. Conclusion: Reported is the largest case of an 11.9 cm giant duodenal leiomyoma with life-threatening gastrointestinal hemorrhage, providing the first comprehensive radiological-histopathological correlation for a giant duodenal leiomyoma. Surgical resection remains the primary treatment to confirm the pathological diagnosis of benign leiomyoma and manage symptoms.

Authors

Institutions

Publication Details

Journal
International Journal of Surgery Case Reports
Published
2026-03-12
DOI
https://doi.org/10.1097/rc9.0000000000000354
Primary Topic
Gastrointestinal Tumor Research and Treatment
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Duodenal leiomyoma: a case report of upper gastrointestinal hemorrhage from a giant duodenal tumor

Chien‐Hung Chen, Shawn MacKenzie, Morgan MacKenzie, Wan Wan Yap et al.
International Journal of Surgery Case Reports
Gastrointestinal Tumor Research and Treatment
article

Duodenal leiomyoma: a case report of upper gastrointestinal hemorrhage from a giant duodenal tumor

Chien‐Hung Chen, Shawn MacKenzie, Morgan MacKenzie, Wan Wan Yap, Benjamin MacKenzie, Amanda Yee-Kum Kwan
article en

Abstract

Introduction: Duodenal leiomyoma is a rare tumor, originating in the intestinal wall smooth muscle, making up <0.1% of all gastrointestinal tumors. The majority are discovered incidentally on endoscopy due to the small size of tumors at presentation. Larger duodenal leiomyomas may present with anemia from gastrointestinal hemorrhage. Case presentation: A 67-year-old male presented with life-threatening upper gastrointestinal hemorrhage. Magnetic resonance imaging identified an 11.9 × 8.7 cm submucosal mass in the second portion of the duodenum adjacent to the pancreatic head. An urgent upper endoscopy confirmed active hemorrhage, which was controlled with endoscopic clips. The patient underwent a successful resection of the tumor with no postoperative complications. Discussion: The diagnosis of duodenal leiomyomas remains challenging due to the lack of symptom manifestations. The differential diagnosis for a duodenal soft tissue mass includes gastrointestinal stromal tumor, solitary fibrous tumors, schwannoma, lymphoma, duodenal adenocarcinoma, and leiomyosarcoma. Radiographically, leiomyomas have typical imaging characteristics similar to skeletal muscle with marked T2 hypointensity, gradual enhancement on post contrast images, and the absence of extensive lesional necrosis. Surgical resection allows pathological confirmation of tissue diagnosis. Histopathologically, leiomyoma exhibits bland smooth muscle cells, with a low Ki67 proliferative index and absence of mitotic figures. Leiomyoma immunohistochemistry profile is positive for smooth muscle antigen and desmin. Conclusion: Reported is the largest case of an 11.9 cm giant duodenal leiomyoma with life-threatening gastrointestinal hemorrhage, providing the first comprehensive radiological-histopathological correlation for a giant duodenal leiomyoma. Surgical resection remains the primary treatment to confirm the pathological diagnosis of benign leiomyoma and manage symptoms.

International Journal of Surgery Case Reports
Royal Columbian Hospital (CA), University of British Columbia (CA), Fraser Health (CA), Surrey Memorial Hospital (CA)
Openalex Percentile: Top 25%
Gastrointestinal Tumor Research and Treatment
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.