TY - JOUR
T1 - Primary central nervous system Burkitt's lymphoma presenting as Guillain‐Barré syndrome
AU - Toren, A.
AU - Mandel, M.
AU - Shahar, E.
AU - Rimmoni, E.
AU - Roizin, H.
AU - Neuman, Y.
AU - Brok‐Simoni, F.
AU - Mark, Z.
AU - Biniaminov, M.
AU - Rosenthal, E.
AU - Segal, M.
AU - Frand, M.
AU - Ben‐Bassat, I.
AU - Rechavi, G.
PY - 1994
Y1 - 1994
N2 - A rare case of CNS Burkitt's lymphoma presenting as acute Guillain‐Barré syndrome is presented. A 6‐year‐old previously healthy female presented with acute onset of limb and truncal weakness, involvement of ocular and bulbar nerves, and areflexia. The clinical diagnosis of Guillain‐Barré syndrome prompted treatment with intravenous gammaglobulin with no response. A lumbar puncture following revealed marked pleocytosis, elevated protein, and decreased glucose. Immunological, cytological, and molecular studies of these cells confirmed the diagnosis of Burkitt's lymphoma IgM, kappa with t(8;14) and rearrangement of the J and kappa immunoglobulin chains. Aggressive systemic and intrathecal chemotherapy were started and within 5 days remission was achieved. The child is in complete remission 2 years from diagnosis. Although very rare, CNS lymphoma should be taken into account in every patient presenting with the clinical features of acute polyneuropathy. © 1994 Wiley‐Liss, Inc.
AB - A rare case of CNS Burkitt's lymphoma presenting as acute Guillain‐Barré syndrome is presented. A 6‐year‐old previously healthy female presented with acute onset of limb and truncal weakness, involvement of ocular and bulbar nerves, and areflexia. The clinical diagnosis of Guillain‐Barré syndrome prompted treatment with intravenous gammaglobulin with no response. A lumbar puncture following revealed marked pleocytosis, elevated protein, and decreased glucose. Immunological, cytological, and molecular studies of these cells confirmed the diagnosis of Burkitt's lymphoma IgM, kappa with t(8;14) and rearrangement of the J and kappa immunoglobulin chains. Aggressive systemic and intrathecal chemotherapy were started and within 5 days remission was achieved. The child is in complete remission 2 years from diagnosis. Although very rare, CNS lymphoma should be taken into account in every patient presenting with the clinical features of acute polyneuropathy. © 1994 Wiley‐Liss, Inc.
KW - chemotherapy
KW - gammaglobulin
KW - lumbar puncture
UR - http://www.scopus.com/inward/record.url?scp=0028108106&partnerID=8YFLogxK
U2 - 10.1002/mpo.2950230410
DO - 10.1002/mpo.2950230410
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
AN - SCOPUS:0028108106
SN - 0098-1532
VL - 23
SP - 372
EP - 375
JO - Medical and Pediatric Oncology
JF - Medical and Pediatric Oncology
IS - 4
ER -