TY - JOUR
T1 - Granulocyte transfusion as a treatment for enterococcal meningoencephalitis after allogeneic bone marrow transplantation from an unrelated donor
AU - Tsukada, Y.
AU - Nagayama, H.
AU - Mori, Takehiko
AU - Shimizu, T.
AU - Sato, N.
AU - Takayama, N.
AU - Ishida, A.
AU - Handa, Makoto
AU - Ikeda, Y.
AU - Okamoto, Shinichiro
PY - 2003/1
Y1 - 2003/1
N2 - Bacterial meningoencephalitis occurring in the pre-engraftment period after bone marrow transplantation (BMT) is a rare complication, and the feasibility of granulocyte transfusion (GTX) in such cases remains to be elucidated. A 37-year-old man developed enterococcal meningoencephalitis during a severely granulocytopenic pre-engraftment period after BMT. Despite therapy with appropriate antibiotics, cultures of blood and cerebrospinal fluid (CSF) continued to grow Enterococcus faecalis, and he developed rapid mental deterioration and seizure. Granulocytes were collected from his HLA-mismatched, ABO-matched sibling with subcutaneous injection of granulocyte colony-stimulating factor (G-CSF) and oral dexamethazone. Transfusion of 4.4 × 1010 granulocytes resulted in a 12-h post-transfusion granulocyte increment of 2.0 × 109/1, and maintained peripheral blood granulocyte counts above 0.5 × 109/l for 3 days. A rapid increase of granulocytes in CSF was also observed, and cultures of blood and CSF became negative after GTX. A transient worsening of seizure was observed as a potential side effect of GTX. The patient subsequently developed septic shock because of Pseudomonas aeruginosa and died. Further studies are warranted to evaluate the clinical efficacy of GTX for the treatment of uncontrolled infections in granulocytopenic stem cell transplant recipients.
AB - Bacterial meningoencephalitis occurring in the pre-engraftment period after bone marrow transplantation (BMT) is a rare complication, and the feasibility of granulocyte transfusion (GTX) in such cases remains to be elucidated. A 37-year-old man developed enterococcal meningoencephalitis during a severely granulocytopenic pre-engraftment period after BMT. Despite therapy with appropriate antibiotics, cultures of blood and cerebrospinal fluid (CSF) continued to grow Enterococcus faecalis, and he developed rapid mental deterioration and seizure. Granulocytes were collected from his HLA-mismatched, ABO-matched sibling with subcutaneous injection of granulocyte colony-stimulating factor (G-CSF) and oral dexamethazone. Transfusion of 4.4 × 1010 granulocytes resulted in a 12-h post-transfusion granulocyte increment of 2.0 × 109/1, and maintained peripheral blood granulocyte counts above 0.5 × 109/l for 3 days. A rapid increase of granulocytes in CSF was also observed, and cultures of blood and CSF became negative after GTX. A transient worsening of seizure was observed as a potential side effect of GTX. The patient subsequently developed septic shock because of Pseudomonas aeruginosa and died. Further studies are warranted to evaluate the clinical efficacy of GTX for the treatment of uncontrolled infections in granulocytopenic stem cell transplant recipients.
KW - Bone marrow transplantation
KW - Enterococcus
KW - G-CSF
KW - Granulocyte transfusion
KW - Meningoencephalitis
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U2 - 10.1038/sj.bmt.1703780
DO - 10.1038/sj.bmt.1703780
M3 - Article
C2 - 12621511
AN - SCOPUS:0037261449
SN - 0268-3369
VL - 31
SP - 69
EP - 72
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 1
ER -