Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1016/j.asjsur.2023.11.142 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Mesenteric extraskeletal osteosarcoma developed in a patient status-post gastric cancer surgery.
Asian J Surg
March 2024
Department of Urology, The First Affiliated Hospital of Gannan Medical University Ganzhou, China. Electronic address:
Primary Extraskeletal Ewing Sarcoma of the Duodenum Revealed by 18 F-FDG PET/CT.
Clin Nucl Med
August 2023
From the Departments of Nuclear Medicine.
Extraskeletal Ewing sarcoma of the duodenum is a relatively uncommon entity tumor. We report a case of extraskeletal Ewing sarcoma in a 21-year-old woman. She complained of abdomen pain and melena.
View Article and Find Full Text PDFHeterotopic Mesenteric Ossification With Trilineage Hematopoiesis.
Cureus
April 2022
Department of Pathology and Laboratory Medicine, Loyola University Medical Center, Maywood, USA.
Heterotopic ossification (HO) histologically refers to extraskeletal bone formation in non-ossifying tissues, most commonly noted in the extremities, buttocks, abdominal wall, and hip joints. HO developing in the mesentery (heterotopic mesenteric ossification, HMO) is very rare, with fewer than 100 cases reported in the literature. It usually occurs in adult male patients with a history of repeated abdominal trauma.
View Article and Find Full Text PDFPrimary extraskeletal osteosarcoma of small bowel mesentery presenting with acute bowel obstruction.
J Radiol Case Rep
December 2021
Department of Pathology, National University Hospital, Singapore.
Extraskeletal osteosarcoma of the small bowel mesentery is an exceedingly rare condition. It is an aggressive malignant neoplasm of mesenchymal origin characterized by osteoid formation. Final diagnosis is often made by histopathological analysis.
View Article and Find Full Text PDFEwing Sarcoma/Primitive Neuroectodermal Tumor Involving the Duodenum.
Ochsner J
January 2022
Department of Radiology, Brooke Army Medical Center, Fort Sam Houston, San Antonio, TX.
Ewing sarcoma/primitive neuroectodermal tumor (ES/PNET) is a soft tissue malignancy arising from the neuroectoderm. While the locations of these extraskeletal manifestations are diverse, origin from the small bowel and small bowel mesentery is extremely rare. Intra-abdominal manifestations of ES/PNETs are nonspecific, and patients present with a wide range of symptoms, most frequently vague abdominal pain.
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!