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Intramedullary tumoral calcinosis
Vivek A Mehta1, Chetan Bettegowda, George I Jallo
1Division of Pediatric Neurosurgery, Department of Neurosurgery, The Johns Hopkins Hospital, Baltimore, Maryland 21287, USA.
Journal of Neurosurgery. Pediatrics
|June 3, 2010
Summary
Tumoral calcinosis (TC), a rare spinal cord mass, was successfully treated in a young boy. This case highlights the importance of considering TC in spinal cord lesion diagnoses.
Area of Science:
- Neurosurgery
- Orthopedics
- Radiology
Background:
- Tumoral calcinosis (TC) typically presents as calcium hydroxyapatite masses in the extremities and hips.
- TC is rarely found in the spine and has never been reported within the spinal cord.
- TC can occur sporadically, run in families, or result from conditions causing soft-tissue calcification.
Observation:
- A 20-month-old boy presented with lower-extremity spasticity due to an intramedullary mass at the T-5 level.
- The mass was identified as tumoral calcinosis, a rare spinal cord occurrence.
- Pre-operative diagnosis of TC was not considered.
Findings:
- The study details the first reported case of intramedullary tumoral calcinosis within the spinal cord.
- Gross-total resection was performed, appearing curative for the patient.
- The report discusses diagnostic features, radiological and histological findings, and treatment outcomes.
Implications:
- This case expands the known anatomical locations for tumoral calcinosis.
- It emphasizes the need to include TC in the differential diagnosis of spinal cord lesions, especially in pediatric patients.
- Early consideration of TC could lead to more accurate pre-surgical diagnoses and potentially improved management strategies.
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