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Permanent thoracic myelopathy resulting from herniation of a calcified intervertebral disc in a child
Konrad Mahlfeld1, Ralph Kayser, Henning Grasshoff
1Orthopaedic University Clinic Magdeburg, Germany.
Insights
Juvenile intervertebral disc calcification (IDC) is typically benign. However, this case highlights rare permanent neurologic deficits from IDC, emphasizing the need for vigilance even in self-limiting conditions.
Area of Science:
- Pediatric Neurology
- Spinal Surgery
- Radiology
Background:
- Juvenile intervertebral disc calcification (IDC) is generally considered a benign condition with a favorable prognosis.
- Most cases of juvenile IDC resolve spontaneously with conservative management, showing excellent outcomes.
- Surgical intervention for juvenile IDC is rarely indicated, especially in cases without severe complications.
Observation:
- This study details a rare case of a child experiencing neurologic deficits attributed to intervertebral disc calcification.
- The patient presented with symptoms indicative of thoracic myelopathy secondary to IDC.
- Despite conservative treatment not being explicitly detailed as failed, the severity necessitated surgical intervention.
Findings:
- Urgent decompressive thoracic laminectomy was performed to address the myelopathy caused by juvenile IDC.
- At a 3-year follow-up, the patient exhibited persistent deficits in motor and sensory functions.
- This case represents one of the few documented instances of juvenile IDC leading to permanent myelopathy requiring surgery.
Implications:
- This case underscores that while typically benign, juvenile IDC can rarely result in severe and permanent neurologic damage.
- The findings suggest that urgent surgical decompression may be necessary in select cases of juvenile IDC with significant myelopathy.
- Further research into risk factors and optimal management strategies for severe juvenile IDC complications is warranted.
Abstract:
This retrospective study was made to illustrate the rare occurrence of neurologic deficits resulting from intervertebral disc calcification (IDC) in a child. Most authors agree that juvenile IDC is usually a benign, self-limiting disease with excellent prognosis. The symptoms subside spontaneously in 95% of patients. Conservative treatment is therefore usually sufficient. Reviewing the English-speaking literature, only two further cases of operated juvenile IDC with myelopathy have been published. In the current report, we describe a case of permanent thoracic myelopathy resulting from juvenile IDC treated by urgent decompressive thoracic laminectomy. At the 3-year follow-up examination, the patient had not recovered fully. Persisting deficits in motor and sensory function were observed.
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