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Cauda equina syndrome with beta thalassemia: a case report
Ahmed Almoallem1, Saud Alhamad2, Nayef Bin Dajim2
1Spine Department, Neuroscience Center, King Fahad Specialist Hospital- Dammam. 6830 Ammar Bin Thabet St, Al Muraikabat, Dammam, 32253-3202, Saudi Arabia. a_mm2005@hotmail.com.
Cauda equina syndrome (CES) in beta thalassemia patients with extramedullary hematopoiesis is rare. Surgical decompression improved symptoms, but ongoing management is needed for persistent deficits.
Area of Science:
- Neurology
- Hematology
- Spinal Surgery
Background:
- Cauda equina syndrome (CES) associated with extramedullary hematopoiesis in beta thalassemia is exceptionally rare.
- Limited case reports exist, highlighting varied treatment approaches and outcomes.
Observation:
- A 29-year-old male with beta thalassemia presented with acute back pain, lower limb numbness, and urinary incontinence.
- Physical examination revealed decreased anal tone and perianal sensation.
- Spinal MRI showed extramedullary hematopoiesis, disc protrusion, and cauda equina compression.
Findings:
- Surgical decompression and laminectomy led to symptom improvement in back pain and lower limbs over one year.
- Persistent sensory deficits and neurogenic bladder required continued urological care.
Implications:
- This case highlights the complex management of CES in beta thalassemia patients with extramedullary hematopoiesis.
- Further research and data collection are crucial due to the lack of established treatment guidelines.
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