ArticleJournal of cytology2014
A rare case of giant soft tissue chondroma of the wrist: A cytopathological study with review of the literature.
Article in Journal of cytology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 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
4 citing papers in PubMed, 8 citations in OpenAlex.
- Soft-tissue Chondroma Masquerading as Chondroid Syringoma - A Case Report.Journal of orthopaedic case reports · 2024Article
- Extraskeletal Chondroma: A Rare Cause of Trigger Finger in Children.Case reports in orthopedics · 2020Article
- A rare presentation of soft tissue chondroma: A case report.International journal of surgery case reports · 2020Article
- Para-articular extraskeletal chondroma mimicking first metatarsophalangeal synovitis.Radiology case reports · 2017Article
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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
Giant soft tissue chondromas (STCs) of the wrist are seldom encountered in clinical practice. Precise diagnosis of benign STC may pose diagnostic difficulties on clinical and radiological findings alone. We encountered a slowly growing soft tissue neoplasm in the radial aspect of the wrist joint of the right hand in a 52-year-old male, masquerading as a calcified hematoma, as suggested by magnetic resonance imaging. On cytohistopathological examination, it turned out to be a rare giant STC. The variable cellularity, in conjunction with cellular immaturity and atypia, could mislead one to a malignant pathological interpretation. Diagnosis is based on both radiological and cytohistological evaluation, which is indispensable for determining the tumor type. The detailed clinical, radiological, cytomorphological, and immune-histopathological study was carried out, which has prompted us to report this case along with a review of the literature.
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