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Primary spinal Burkitt’s lymphoma: Case report and literature review

BACKGROUND: Burkitt’s lymphoma is a non-Hodgkin B-cell lymphoma, occurring mostly in Equatorial Africa. According to the WHO, classification is three different variants: sporadic, endemic, and immunodeficient-associated. Here, we present a patient with “sporadic” primary epidural Burkitt’s lymphoma...

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Detalles Bibliográficos
Autores principales: Costanzo, Roberta, Scalia, Gianluca, Marrone, Salvatore, Umana, Giuseppe Emmanuele, Giuffrida, Massimiliano, Furnari, Massimo, Salerno, Marilena, Consoli, Ugo, Iacopino, Domenico Gerardo, Nicoletti, Giovanni Federico, Ponzo, Giancarlo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8422475/
https://www.ncbi.nlm.nih.gov/pubmed/34513154
http://dx.doi.org/10.25259/SNI_649_2021
Descripción
Sumario:BACKGROUND: Burkitt’s lymphoma is a non-Hodgkin B-cell lymphoma, occurring mostly in Equatorial Africa. According to the WHO, classification is three different variants: sporadic, endemic, and immunodeficient-associated. Here, we present a patient with “sporadic” primary epidural Burkitt’s lymphoma resulting in chronic low back pain (LBP). CASE DESCRIPTION: A 63-year-old female presented with a 2-month history of LBP and the left lower extremity sciatica. The thoracolumbar MRI showed a L5 irregular, osteolytic epidural lesion that was hypointense on T1-weighted images, hyperintense on STIR studies, and inhomogeneously enhanced with contrast. Additional hypointense lesions were also seen at the L2, L3, and L4 levels. The patient underwent a L4-L5 laminectomy for piecemeal epidural resection of tumor, and a L4-S1 transpedicular screws/rod fusion. In addition, a L2-L3 radiofrequency ablation was performed. The histological examination documented a primary “sporadic” spinal Burkitt’s lymphoma. The patient subsequently was treated with both radiotherapy/chemoradiotherapy CONCLUSION: Primary “sporadic” spinal Burkitt’s lymphoma is rare. Following tumor resection, adjunctive radiation and chemotherapy are typically warranted.