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An intracranial extramedullary hematopoiesis in a 34-year-old man with beta thalassemia: a case report

INTRODUCTION: Extramedullary hematopoiesis occurs in approximately 15% of cases of thalassemia. Intracranial deposits of extramedullary hematopoiesis are an extremely rare compensatory process in intermediate and severe thalassemia. CASE PRESENTATION: We present an unusual case of an intracranial ex...

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Detalles Bibliográficos
Autores principales: Tabesh, Homayoun, Shekarchizadeh, Ahmad, Mahzouni, Parvin, Mokhtari, Mojgan, Abrishamkar, Saeid, Abbasi Fard, Salman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3285055/
https://www.ncbi.nlm.nih.gov/pubmed/22182855
http://dx.doi.org/10.1186/1752-1947-5-580
Descripción
Sumario:INTRODUCTION: Extramedullary hematopoiesis occurs in approximately 15% of cases of thalassemia. Intracranial deposits of extramedullary hematopoiesis are an extremely rare compensatory process in intermediate and severe thalassemia. CASE PRESENTATION: We present an unusual case of an intracranial extramedullary hematopoiesis with a choroid plexus origin in a 34-year-old Caucasian man with beta thalassemia intermedia, who presented with the complaints of chronic headache and rapid progressive visual loss. CONCLUSION: An intracranial extramedullary hematopoiesis, although extremely rare, should be considered as a potential ancillary diagnosis in any thalassemic patient and therefore appropriate studies should be performed to investigate the probable intracranial ectopic marrow before any surgical intervention.