Introduction: Extraskeletal or soft-tissue chondroma is a rare benign cartilaginous neoplasm which usually affects hands and feet. Scientific literature only reports one previous case of this pathology in the preauricular region.
Presentation Of The Case: This report describes a rare case of extraskeletal chondroma surrounding the temporomandibular joint of a 55-year-old female patient.
Discussion And Conclusion: Diagnosis of extraskeletal chondroma is challenging since tissue swelling, diagnostic imaging and even histopathological features may be misleading for other joint or gland pathologies.
Download full-text PDF |
Source |
|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039882 | PMC |
| http://dx.doi.org/10.1016/j.ijscr.2018.06.012 | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Extraskeletal Chondromatosis in a 30-Year-Old Patient: A Rare Case Report.
Cureus
July 2024
Pathology, Dr. D. Y. Patil Medical College, Hospital and Research Centre, Dr. D. Y. Patil Vidyapeeth (Deemed to be University), Pune, IND.
The term chondroma refers to a slow-growing benign tumor. When the tumor arises from the medullary cavity, it is referred to as enchondroma, which is a very common bone tumor. However, if it arises from soft tissues, which is extremely rare, it is referred to as soft tissue chondroma or extraskeletal chondroma.
View Article and Find Full Text PDFExtraskeletal chondroma of the toe in a child with DICER1 tumor predisposition syndrome: support for a dominant negative mechanism.
Virchows Arch
June 2024
Department of Human Genetics, Medicine, McGill University, Montreal, QC, Canada.
Article Synopsis
- DICER1 tumor predisposition syndrome can cause different types of tumors, especially in kids.
- A child had a rare tumor called an extraskeletal chondroma in their toe and had a specific type of DICER1 gene change, different from what is usually found.
- This gene change messes up the process of making molecules that help control genes, showing that there are other ways the DICER1 gene can cause problems without completely stopping it from working.
Posttraumatic extraskeletal chondroma of the posterior neck: A systematic literature review on a rare finding and report of a case.
J Craniovertebr Junction Spine
September 2023
Department of Neurosurgery and Gamma Knife Radiosurgery, San Raffaele Scientific Institute, Vita-Salute University, Milan, Italy.
Article Synopsis
- - Extraskeletal chondromas (EC) are rare, benign tumors mainly found in the upper and lower extremities, with only four previous pediatric cases reported in the neck's anterior compartment, and this text discusses the first case in the posterior compartment.
- - Diagnosis of EC can be challenging as they may be mistaken for malignant tumors on imaging, highlighting the need for thorough diagnostic procedures prior to surgery.
- - The treatment primarily involves surgical excision, which shows promising results, as demonstrated by symptom improvement and no recurrence in the presented case after six months of follow-up.
Extremely Rare Case of Extra Skeletal Soft Tissue Chondroma of Masseteric Space: a Diagnostic Challengel.
Indian J Otolaryngol Head Neck Surg
September 2023
Department of Head Neck Oncology, Rajiv Gandhi Cancer Institute & Research Centre, New Delhi, 110085 India.
Unlabelled: Benign soft tissue chondroma is a rare type of extraskeletal chondrocytic tumour. It usually can be found in skeletal system in extremities. Head and neck region is one of the most uncommon sites for extraskeletal chondroma .
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!