ArticleFrontiers in oncology2025
Atypical cartilaginous tumor imaging findings in the distal phalanx of the left thumb: case report and literature review.
Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Atypical cartilaginous tumors (ACTs) usually occur in long bones rather than in the hands or feet. To date, detailed imaging features of ACTs in the hands or feet were reported in only a few case reports. Case presentation: We report a case of an Asian woman in her early 80s who presented to our hospital with a painless mass in the distal phalanx of the left thumb. Radiography and computed tomography (CT) showed osteolytic destruction and cortex thickening in the distal phalanx with extension into soft tissue. Magnetic resonance imaging (MRI) demonstrated a local soft tissue signal mass with isosignal intensity in T1 and heterogeneous high-signal intensity in T2. Color Doppler ultrasound suggested that the tumor was hypovascularized. The patient underwent amputation, and histological analysis revealed an ACT. The patient's symptoms improved postoperatively, with no recurrence as of the 3-year follow-up. Conclusion: Meanwhile, this study also reviewed the comparable diagnostic methods of ACT and chondrosarcoma. The analysis of previous similar cases showed that preoperative imaging diagnosis of ACT can be challenging and multimodal imaging appears to be beneficial in diagnosing ACTs and malignant chondrosarcoma grade II/III in the hands and feet.
Indexed as
Identifiers
What OpenQuestion holds
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.