Cml. Ho et al., SUCCESSFUL BONE-MARROW TRANSPLANTATION IN A CHILD WITH X-LINKED CHRONIC GRANULOMATOUS-DISEASE, Bone marrow transplantation, 18(1), 1996, pp. 213-215
A 16-month-old Aboriginal boy was diagnosed with chronic granulomatous
disease (CGD) when he presented with frequent significant infections
from the age of 12 months, BMT was performed from a HLA-matched siblin
g after conditioning with busulphan, cyclophosphamide, etoposide and a
ntithymocyte globulin. A small bowel obstruction developed in the firs
t week and settled with conservative treatment, VOD occurred in the th
ird week, resolving after treatment with tissue plasminogen activator,
Sustained engraftment has occurred, as indicated by return of the nit
roblue tetrazolium (NET) test to normal when performed at 11 weeks and
7 months post-BMT. No further infections have occurred, BMT can be su
ccessfully performed for CGD. Complications occurring post-BMT may be
related to the underlying disease (CGD), BMT remains an attractive opt
ion for CGD in children who have a matched sibling donor.