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Updated: Jun 6, 2026

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Endoscopic Endonasal Trans-sphenoidal Approach: Minimally Invasive Surgery for Pituitary Adenomas
Published on: January 17, 2018
A silent nasal mass with ophthalmic presentation
Vanita Sarin1, Baldev Singh, Pawan Prasher
1Dept of Otolaryngology, SGRDIMSR, Vallah, Amritsar. vanitasarin@yahoo.co.in
Orbit (Amsterdam, Netherlands)
|December 17, 2010
Summary
Nasal chondromesenchymal hamartoma (NCMH) is a rare pediatric tumor that can mimic cancer. Early recognition and complete surgical removal are key to successful treatment and avoiding misdiagnosis.
Area of Science:
- Pediatric pathology
- Surgical oncology
- Medical genetics
Background:
- Nasal chondromesenchymal hamartoma (NCMH) is a rare benign tumor in children.
- NCMH can be misdiagnosed due to overlapping features with other soft tissue tumors.
- Accurate diagnosis is crucial to avoid unnecessary or harmful treatments.
Observation:
- A case of NCMH in a 2.5-year-old child is presented.
- Histological examination revealed a mix of mesenchymal elements, including spindle cells, collagen, and osseous/chondroid tissue.
- Immunohistochemistry showed sensitivity to SMA and calponin.
Findings:
- NCMH exhibits benign biological behavior.
- Complete surgical resection is the recommended treatment.
- Histological and immunohistochemical features aid in diagnosis.
Implications:
- Increased awareness of NCMH can improve diagnostic accuracy in pediatric cases.
- Correct diagnosis prevents misclassification as malignant, avoiding aggressive therapies.
- Complete resection ensures favorable outcomes for this benign condition.
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