ArticleMedicine2025
From birth to triumph: A rare case report of rib chondrosarcoma with unprecedented growth patterns.
Article in Medicine, 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
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
rationalePrimary tumors of ribs are uncommon in clinical practice. These tumors can be benign or malignant and often present unique challenges in diagnosis and treatment. For instance, rib chondrosarcoma is a rare type of chondrosarcoma that occurs in the rib cage, representing a significant clinical diagnosis challenge due to its potential for local recurrence and metastasis. With rib chondrosarcoma being more or less common compared to other locations such as the long bones and pelvis. Generally, rib chondrosarcoma develops rapidly and mostly occurred in middle-aged or elderly crowds. Rib chondrosarcoma in children is a rare but significant clinical concern. PATIENT CONCERNS: A 30-year-old male patient, prior to marriage, sought surgical removal of a chest wall mass, which present from birth, to achieve an improved aesthetic appearance of the chest wall. DIAGNOSES: Preoperative chest computed tomography scans indicated the presence of a rib tumor, which was initially presumed to be benign. However, postoperative histopathological analysis revealed the mass to be a rib chondroma.
interventionsHe received resection of the tumor and reconstruction of chest wall. Considering the slow growth of the tumor, this patient did not receive any other adjuvant treatments after the surgery, including chemotherapy or targeted therapy. OUTCOMES: The symptoms disappeared after the operation, no other discomfort was appealed during the follow-up over the next 5 years, and no recurrence of the intrathoracic lesion was detected in the imaging examinations. LESSONS: Such a slow growth pattern of rib chondrosarcoma has not been reported in the previous literature. Considering the diagnosis of rib chondrosarcoma is crucial for assessing the extent of the tumor and planning surgical intervention, this case expands the knowledge of clinicians and radiologists in the diagnosis of rib chondrosarcoma.
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.