Table 4.

Management of hematologic complications in the inherited bone marrow failure syndromes and responses.1

TreatmentFanconi anemiaDyskeratosis congenitaDiamond-Blackfan anemiaShwachman-Diamond syndromeSevere congenital neutropeniaAmegaThrombocytopenia absent radii
Abbreviations: Amega, amegakaryocytic thrombocytopenia; G-CSF, granulocyte colony-stimulating factor. Yes, proven role; —, used rarely, role uncertain; No, role not proven and may be detrimental. 
1Response rates and durations vary according to the disorder. 
2Transplantation regimens and successes depend on the disorder and the donor type. 
Androgens Yes Yes — — No Yes No 
Prednisone — — Yes — No — No 
G-CSF Rare Rare No Yes Yes — No 
Erythropoietin Rare Rare —     
Red cell transfusions As needed As needed First year; as needed Rare No As needed — 
Platelet transfusions As needed As needed No Rare No As needed First year; as needed 
Stem cell transplantation2 Yes Yes Yes Yes Yes Yes Yes 
“Spontaneous” remission Mosaicism Rare ~25% Pancreatic function may improve with age No No Yes 
TreatmentFanconi anemiaDyskeratosis congenitaDiamond-Blackfan anemiaShwachman-Diamond syndromeSevere congenital neutropeniaAmegaThrombocytopenia absent radii
Abbreviations: Amega, amegakaryocytic thrombocytopenia; G-CSF, granulocyte colony-stimulating factor. Yes, proven role; —, used rarely, role uncertain; No, role not proven and may be detrimental. 
1Response rates and durations vary according to the disorder. 
2Transplantation regimens and successes depend on the disorder and the donor type. 
Androgens Yes Yes — — No Yes No 
Prednisone — — Yes — No — No 
G-CSF Rare Rare No Yes Yes — No 
Erythropoietin Rare Rare —     
Red cell transfusions As needed As needed First year; as needed Rare No As needed — 
Platelet transfusions As needed As needed No Rare No As needed First year; as needed 
Stem cell transplantation2 Yes Yes Yes Yes Yes Yes Yes 
“Spontaneous” remission Mosaicism Rare ~25% Pancreatic function may improve with age No No Yes 

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