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Unbounded Medicine is a medical weblog intented to share medical information with other colleagues and make opinions about diagnostic procedures and medicine-related topics including suggested readings, links and presenting original clinical cases. Please read my Bio

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I always enjoy the Image Challenge Contest at The New England Journal of Medicine, time ago there was a similar picture of this:

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U P D A T E: A nice comment and correct answer by Drmikeunoe

We can see generalized osteopenia, widening of the diploetic space, and thinning of the outer table.

This characteristic “hair on end” appearance of the outer table is compatible with the presence of massive hyperplasia of the bone marrow, as can be seen in the homozygous state of beta-thalassemia (i.e. thalassemia major).

Beta thalassemia syndromes are a group of hereditary disorders characterized by a genetic deficiency in the synthesis of beta-globin chains (adult hemoglobin usually is α2β2) resulting in excess α-chains and severe transfusion-dependent anemia, thus causing bone marrow hyperplasia.




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