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Chordoma: Site-Wise Predilections and Pathological Tenets.
Anshima Singh1, Ram Nawal Rao1, Yash Billore2
1Department of Pathology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.
Journal of the West African College of Surgeons
|June 30, 2025
Summary
This study analyzed 41 rare chordoma cases, finding that patient age and tumor size significantly vary by anatomical location. Understanding these clinico-pathological features is crucial for managing this axial skeleton neoplasm.
Area of Science:
- Oncology
- Pathology
- Radiology
Background:
- Chordomas are rare, slow-growing, locally invasive neoplasms originating from the notochordal remnants.
- They predominantly occur in the axial skeleton, including the skull base, spine, and sacrococcygeal region.
- Accurate diagnosis relies on integrated radiological, histopathological, and immunohistochemical criteria, with surgical resection aiming for negative margins.
Purpose of the Study:
- To analyze the clinico-pathological spectrum of chordoma cases.
- To investigate variations in clinical presentation and pathological features based on anatomical location.
- To contribute to the understanding of this rare tumor in a tertiary care setting in Northern India.
Main Methods:
- Retrospective analysis of 41 histopathologically confirmed chordoma cases from January 2013 to August 2023.
- Recording and review of clinico-radiological data and histopathological diagnoses by two pathologists.
- Statistical comparison of clinico-pathological parameters across different anatomical locations (spheno-occipital, sacrococcygeal, vertebral).
Main Results:
- A total of 41 chordomas were analyzed, with a mean age of 43.2 years and a male:female ratio of 1.2:1.
- Spheno-occipital chordomas were most frequent (27 cases), followed by sacrococcygeal (8) and vertebral (6). Pain was the most common symptom.
- Patient age (P=0.011) and tumor size (P=0.0004) showed statistically significant variations based on anatomical location.
Conclusions:
- Clinico-pathological parameters of chordomas exhibit significant variation depending on their anatomical location.
- Age and tumor size are key factors that differ significantly across anatomical sites.
- This study provides valuable insights into the clinico-radiopathological features of chordomas encountered in Northern India.
Keywords:
(1) Presents our experience with this rare tumour category in a tertiary care centre in northern India. (2) Clinico-pathological parameters vary with the anatomical location of chordoma. (3) Even though chordoma is a rare neoplasm, it should be considered in the differential diagnoses of the midline tumours manifesting with relevant clinical features, pertinent radiological picture, histopathological presence of tumour cells with vacuolated cytoplasm, physaliphorous cells, and abundant amount of extracellular myxoid matrix, along with the appropriate immunohistochemical profile. (4) Patients can be modestly treated with surgery with/without radiotherapy. Thus, surgical excision should be performed in all centres having technical expertise.Chordomaphysaliphorous cellssacrococcygeal regionskull basespheno-occipitalvertebralRelated Concept Videos
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