Revisiting the hematological manifestations of vitamin B12 deficiency.
This article reviews the hematologic manifestations of vitamin B12 deficiency, including pediatric pancytopenia and pseudothrombotic microangiopathy that can mimic marrow failure, myelodysplasia, or hematologic malignancy, and notes recovery following vitamin B12 replacement.
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This article reviews the hematologic manifestations of vitamin B12 deficiency, including pediatric pancytopenia and pseudothrombotic microangiopathy that can mimic marrow failure, myelodysplasia, or hematologic malignancy, and notes recovery following vitamin B12 replacement.
Research significance
The record states that timely vitamin B12 replacement often produces rapid and complete hematologic recovery; by inference, systematically evaluating cobalamin deficiency in children with unexplained cytopenias could identify a reversible condition and help avoid inappropriate oncologic or marrow-failure treatment, although no comparative intervention data are supplied.
Source abstract
Vitamin B12 (cobalamin) deficiency remains a significant problem affecting both children and adults and is associated with a wide range of hematological manifestations that are largely preventable with timely diagnosis and treatment. Vitamin B12 deficiency can present with variable hematological, neuropsychiatric, and mucocutaneous changes. Hematological abnormalities are among the most common presentations. The classical peripheral blood smear shows macrocytosis with oval macrocytes, anisopoikilocytosis, and hypersegmented neutrophils. Anemia may be accompanied by leukopenia and thrombocytopenia due to ineffective hematopoiesis. Bone marrow examination typically reveals hypercellularity with erythroid hyperplasia and large megaloblasts exhibiting open chromatin and nuclear-cytoplasmic asynchrony as a result of defective DNA synthesis. Ineffective erythropoiesis leads to intramedullary destruction of hematopoietic precursors, resulting in elevated lactate dehydrogenase, indirect hyperbilirubinemia, and reduced haptoglobin, thereby mimicking hemolytic anemias. Abnormal red cells and megaloblasts that enter the circulation have a shortened lifespan, leading to megaloblastic anemia, with reticulocyte counts that are inappropriately low for the degree of anemia. In pediatric patients, manifestations may be severe, particularly in infants born to cobalamin-deficient mothers. Presentations include profound anemia, pancytopenia, failure to thrive, recurrent infections, and bleeding manifestations due to thrombocytopenia, often misdiagnosed as aplastic anemia or myelodysplasias. Pigmentary changes in the form of hyperpigmentation of knuckles, oral mucosa and rarely Addisonian pigmentation have been described. In older children, isolated anemia or bicytopenia with subtle macrocytosis may delay diagnosis. Severe presentations, seen in approximately 10% of cases, include pancytopenia, hemolytic anemia, and pseudothrombotic microangiopathy, which may mimic hematological malignancies or thrombotic microangiopathies. Early recognition is crucial, as vitamin B12 replacement leads to rapid and often complete hematological recovery.