Download full-text PDF |
Source |
|---|
Publication Analysis
Top Keywords
Similar Publications
Risk factors for metastatic disease at presentation with chordoma and its prognostic value.
N Am Spine Soc J
March 2025
Department of Orthopaedics, Rutgers New Jersey Medical School, Newark, New Jersey, United States.
Background: Chordoma is a rare bone cancer arising from the embryonic notochord with special predilection to the axial skeleton. The locally destructive nature and metastatic potential of chordomas can lead to devastating outcomes in terms of survival. The purpose of this study was to examine potential risk factors predictive of metastatic disease at presentation and prognostic factors in patients with metastasis.
View Article and Find Full Text PDFDiagnostic Utility of Squash Smear Cytology in Chordoma: A Tertiary Care Center Experience.
J Cytol
November 2024
Department of Pathology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Background And Aims: Chordomas are rare notochordal tumors. They are suitable candidates for squash smear cytology (SSC) owing to their gelatinous consistency and destructive nature. SSC is an important tool for making a quick intra-operative preliminary diagnosis and taking real-time surgical and further management decisions.
View Article and Find Full Text PDFA rare case of primary chordoma of the nasopharynx mimicking nasopharyngeal carcinoma: A case report.
Int J Surg Case Rep
January 2025
Department of Internal medicine, Hawassa University Comprehensive Specialized Hospital, Hawassa, Sidama, Ethiopia.
Introduction And Importance: Chordoma is an uncommon malignant tumor that originates from the remnants of the primitive notochord in the embryo. They account for 1 % of intracranial tumors and 4 % of primary bone tumors. It is a locally aggressive tumor with a low risk of metastasis.
View Article and Find Full Text PDFChallenging the giant: A case report on a huge sacrococcygeal chordoma and its radiological insights.
Radiol Case Rep
February 2025
Department of Psychiatry, Datta Meghe Institute of Medical Sciences, Sawangi, Wardha, Maharashtra 442001, India.
Sacral chordoma is a rare osseous tumor of malignant origin. Remnants of the notochord in the region of sacrum and coccyx is said to be the origin of these tumors. Patients generally have delayed presentation, which is responsible for larger tumor size.
View Article and Find Full Text PDFBilateral Pedicled Superior Gluteal Artery Perforator (SGAP) Flap for Double-Layer Closure and Reconstruction of Sacrococcygeal Defect After Chordoma Resection: A Case Report.
Microsurgery
January 2025
Zentrum für Plastische Chirurgie, Pyramid Clinic, Zurich, Switzerland.
Article Synopsis
- Chordomas are rare, slow-growing cancers that often occur in the lower spine area and require surgical removal, which can leave significant defects.
- Traditional reconstruction methods often use musculocutaneous flaps, leading to higher complications at the donor site; hence, there is a need for better techniques that reduce these issues.
- This case report introduces a new reconstruction method using gluteus maximus muscle advancement and superior gluteal artery perforator flaps for a patient after chordoma removal, resulting in successful recovery and minimal complications at the donor site during follow-up.
Want 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!