Intracranial extramedullary hematopoiesis in a patient with beta-thalassemia presenting with head trauma

0Citations
Citations of this article
10Readers
Mendeley users who have this article in their library.

Abstract

Background: Beta-thalassemia is an inherited hemoglobinopathy, whereby reduced or absent expression of beta-globin genes causes impaired erythropoiesis. Extramedullary hematopoiesis (EMH) occurs in 1% of all patients with beta-thalassemia major receiving regular transfusions and is exceedingly rare intracranially. Case Description: We report a case of a male in his 20s with beta thalassemia who presented with head trauma found to have intracranial EMH mimicking multiple extra-axial hematomas. Making the correct diagnosis was critical in avoiding prolonged neuromonitoring and unnecessary interventions. Conclusion: Intracranial extramedullary hematopoietic pseudotumor is an exceedingly rare entity and seldom appears in a neurosurgeon's differential diagnosis. This case illustrates how this condition can easily mimic an acute intracranial hemorrhage in a patient with beta-thalassemia who presents with head trauma. We review the topic to further inform clinicians who may encounter this condition in their practice.

Cite

CITATION STYLE

APA

Nichols, N. M., Hackett, A. M., Carrasquilla, A., Solodnik, P., Byun, H., Jones, S., & Hickman, Z. L. (2022). Intracranial extramedullary hematopoiesis in a patient with beta-thalassemia presenting with head trauma. Surgical Neurology International, 13. https://doi.org/10.25259/SNI_730_2022

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free