ArticleCureus2024
Nasal Osteochondromyxoma Without Carney Complex: A Case Report and a Literature Review.
Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 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
2 citing papers in PubMed.
- Fibrous dysplasia in a patient with Carney complex.Hormones (Athens, Greece) · 2026Review
- Sinonasal Tract Osteochondromyxoma: An Underrecognized Tumor Easily Mistaken for Nasal Chondromesenchymal Hamartoma.Head and neck pathology · 2025Article
Corrections and comments
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Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Osteochondromyxoma (OMX) is an extremely rare bone tumor and has been classified by the World Health Organization as a benign chondrogenic bone tumor. The tumor can be associated with Carney complex which is a rare autosomal dominant syndrome. The clinical presentation of the patient depends primarily on the location and the size of the tumor. It has an excellent prognosis with complete surgical excision. Here, in this case, we present a young female patient diagnosed with OMX without carney complex and underwent complete endoscopic surgical excision.
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Registered trials
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