ArticleRadiology case reports2022
Giant mesenteric myxoid liposarcoma: Challenges of diagnosis and treatment.
Article in Radiology case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 8 citations in OpenAlex.
- Synchronous retroperitoneal and mesenteric dedifferentiated liposarcoma: case report of a challenging rare disease and literature review.Journal of surgical case reports · 2026Article
- Perihepatic dedifferentiated liposarcoma mimicking IgG4-related disease.Clinical journal of gastroenterology · 2026Article
- Clinicopathological Characteristics and Survival Analysis of Primary Mesenteric Liposarcoma: A Retrospective Study.Medicina (Kaunas, Lithuania) · 2025Article
- Deep Introspection Regarding Cumulative Prognostic Factors in Liposarcoma and Atypical Lipomatous Tumor.Medicina (Kaunas, Lithuania) · 2025Article
- Giant transverse colonic mesenteric mucinous liposarcoma combined with rectal cancer and aortic coarctation: A case report and review of literature.World journal of gastrointestinal surgery · 2025Article
- Article
- Article
- Extraskeletal myxoid chondrosarcoma of the gingival: a rare case report and review of the literature.Diagnostic pathology · 2023Review
- A Rare Case of Primary Mesenteric Liposarcoma.Cureus · 2023Article
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Myxoid liposarcoma is the most frequent form of liposarcoma, frequently localized in the extremities. Abdominal liposarcomas more commonly arise from the retroperitoneum. However, primary mesenteric localization is extremely rare. To the best of our knowledge, 22 cases have been reported in English literature. The diagnosis is often delayed by the insidious evolution of this tumor. On radiological examination, primary mesenteric liposarcoma presents as a large mass that entrapped the small bowel loops. The treatment requires complete tumor resection. We report an observation of mesenteric myxoid liposarcoma in a 64-year-old female patient, revealed by an abdominal mass associated with abdominal pain. The treatment consisted of complete tumor removal. Histologically, the tumor proved to be a myxoid liposarcoma. No adjuvant treatment was considered necessary. The patient recovered well after the operation. The aim of reporting this case is to present an uncommon clinical entity because of its huge dimensions, the rarity of the site, and histological pattern.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.