Modulation of macrocytosis in aplastic anemia

Alter, Blanche P.

doi:10.1002/(sici)1096-8652(199801)57:1<92::aid-ajh22>3.0.co;2-a

Am. J. Hematol.

1998

DOI: 10.1002/(sici)1096-8652(199801)57:1<92::aid-ajh22>3.0.co;2-a

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Modulation of macrocytosis in aplastic anemia

Blanche P. Alter

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2006

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“…Alter reported that macrocytic anemia may not be macrocytic in the face of microcytosis caused by genetic or acquired hematological diseases [9]. DBA may be overlooked when the MCV value is in the normal range in such patients.…”

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Diamond–Blackfan anemia associated with β-thalassemia trait

et al. 2006

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A 14-month-old boy was referred to our hospital for evaluation of severe anemia. In the bone marrow aspiration smear, normal cellularity with severe erythroblastopenia (3%) was observed. The hemoglobin electrophoresis of the patient and his father were compatible with the b-thalassemia trait. Because macrocytosis of DiamondBlackfan anemia (DBA) is masked by microcytosis of b-thalassemia trait, the diagnosis of DBA co-existing with b-thalassemia trait might be challenging. We report herein a case of DBA co-existing with b-thalassemia trait in a Turkish boy. Am.

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Diamond–Blackfan anemia associated with β-thalassemia trait

et al. 2006

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Modulation of macrocytosis in aplastic anemia

Cited by 1 publication

References 3 publications

Diamond–Blackfan anemia associated with β-thalassemia trait

Diamond–Blackfan anemia associated with β-thalassemia trait

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