Affiliation:
1. Department of Orthopaedics, First Affiliated Hospital of Jinan University, Tianhe District, Guangzhou City, Guangdong Province, China.
Abstract
Rationale:
Thalassemia combined with extramedullary hematopoietic spinal cord compression is extremely rare; its ideal treatment is still controversial. Herein, we present 2 cases of thalassemia combined with extramedullary hematopoietic compression of the spinal cord wherein satisfactory results were obtained using unilateral bi-portal endoscopy (UBE).
Patient concerns:
Case 1 was of a 43-year-old male who presented with a chief complaint of numbness of the left lower limb since 1-month. Case 2 involved a 23-year-old male who was admitted to the hospital with a chief complaint of numbness in both toes since 3 months and walking instability since 2 weeks. Both cases had a history of being diagnosed with thalassemia.
Diagnoses:
Computed tomography and magnetic resonance imaging showed spinal canal space-occupying lesions causing dural compression and spinal stenosis. Postoperative pathology confirmed the spinal canal lesions to be extramedullary hematopoietic tissue.
Interventions:
For spinal canal decompression, UBE supplemented by blood transfusion was performed for both cases.
Outcomes:
All preoperative symptoms were relieved postoperatively; no recurrence was noted at the 6-month follow-up.
Lessons:
Thalassemia combined with extramedullary hematopoiesis can lead to acute spinal cord compression. UBE significantly relieves spinal stenosis symptoms; furthermore, UBE combined with blood transfusion for spinal canal extramedullary hematopoiesis gives satisfactory results, is safe, and has a low risk of spinal cord injury.
Publisher
Ovid Technologies (Wolters Kluwer Health)
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