Abstract:Vitamin B12 deficiency can cause profound alterations in the bone marrow. These alterations can mimic the more serious diagnosis of acute leukemia. The two patients described in this report were originally suspected of having acute leukemia or myelodysplasia on the basis of the bone marrow smear, and induction chemotherapy was considered. However, after further studies, they were both found to have vitamin B12 deficiency, and parenteral vitamin B12 administration resulted in normalization of the bone marrow.
“…Aitelli et al had stated that Vitamin B12 deficiency can cause profound alterations in the bone marrow and may mimic acute leukaemia or myelodysplasia. 23 However, after further studies, they were both found to have vitamin B 12 deficiency, and parenteral vitamin B 12 administration resulted in normalization of the bone marrow. So, a trial of Vitamin B 12 and folic acid therapy should be given before labelling a case as myelodysplasia.…”
“…Aitelli et al had stated that Vitamin B12 deficiency can cause profound alterations in the bone marrow and may mimic acute leukaemia or myelodysplasia. 23 However, after further studies, they were both found to have vitamin B 12 deficiency, and parenteral vitamin B 12 administration resulted in normalization of the bone marrow. So, a trial of Vitamin B 12 and folic acid therapy should be given before labelling a case as myelodysplasia.…”
“…Megaloblastic anaemia which is due to impaired DNA synthesis is considered as panmyelosis and may progress to pancytopenia (Carmel, 2009). Megaloblastic anaemia presenting with pancytopenia may clinically mimic or simulate pancytopenia arising due to other causes including leukaemia (Aitelli, Wasson & Page, 2004). Bone marrow aspiration/trephine biopsy along with relevant laboratory investigations are generally required to distinguish such cases.…”
MPV has limited sensitivity and specificity to discriminate between megaloblastic and non-megaloblastic pancytopenia. Pancytopenia due to aplastic/hypocellular marrow and acute leukaemia has significantly lower MPV than megaloblastic group while other pancytopenic cases do not show any statistical difference in MPV from megaloblastic pancytopenia.
“…The BM of patients with MBA can display significant atypical features (e.g. hypercellularity, erythroid hyperplasia, increased nuclear to cytoplasmic ratios, and increased mitotic figures), 24 which may mislead the diagnostician into considering a neoplastic process 25 . Therefore, we would suggest excluding MBA before considering non‐acute myeloid neoplastic categories (i.e.…”
In complex BM cases, the presence of ≥30% CD34+ MKs constitutes a potentially useful diagnostic tool with which to distinguish non-acute myeloid neoplasms and MBA from non-MBA reactive conditions, for minimal additional cost.
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