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Prominent dyserythropoiesis in four cases of haemophagocytic lymphohistiocytosis

Haemophagocytic lymphohistiocytosis (HLH) is a disease characterised by peripheral blood pancytopenia secondary to haemophagocytosis of formed blood cells by activated histiocytes. The demonstration of haemophagocytosis may be difficult and the diagnosis may require repeated tissue sampling (includi...

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Bibliographic Details
Main Authors: Macheta, M, Will, A, Houghton, J, Wynn, R
Format: Artigo
Language:Inglês
Published: 2001
Subjects:
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1731338/
https://ncbi.nlm.nih.gov/pubmed/11729218
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