ArticleJournal of orthopaedics2016
Liposclerosing myxofibrous tumor: A series of 9 cases and review of the literature.
Article in Journal of orthopaedics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
5 citing papers in PubMed, 18 citations in OpenAlex.
- From Setback to Success: A Case Report of Secondary Surgical Strategies for Liposclerosing Myxofibrous Tumor-Related Fractures.Clinical case reports · 2026Article
- Liposclerosing myxofibrous tumor: radiographic reporting frequency, pathologic correlation, and malignant transformation.Skeletal radiology · 2026Article
- Malignant Transformation of Musculoskeletal Lesions with Imaging-Pathology Correlation-Part 1: Bone Lesions.Diagnostics (Basel, Switzerland) · 2025Review
- Liposclerosing Myxofibrous Tumor: A Separated Clinical Entity?Diagnostics (Basel, Switzerland) · 2025Article
- Liposclerosing myxofibrous tumor of the distal femur: A case report.Frontiers in surgery · 2022Article
Corrections and comments
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Authors and funding
7 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundLiposclerosing myxofibrous primary bone tumor is a rare benign bone lesion that was characterized by complex mixture of various histological elements.
methodsWe have studied the radiological, clinical and pathological features of nine patients with this disorder. Pain and limping were the main symptoms.
resultsRadiographic images typically showed a geographic lytic lesion with thick sclerotic margin, reflecting a pattern of slow growth. Histological sections revealed a polymorphic neoplasia characterized by predominant proliferation of stellate and fusiform cells aimed the myxoid matrix.
conclusionsThese features suggest that the lesion may represent a variant of fibrous dysplasia with a high risk of malignant transformation.
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