Langerhans cell histiocytosis in adults: Advances in pathophysiology and treatment
Langerhans cell histiocytosis in adults: Advances in pathophysiology and treatment
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Publisher
England: John Wiley & Sons, Inc
Journal title
Language
English
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Publisher
England: John Wiley & Sons, Inc
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Contents
Langerhans cell histiocytosis (LCH) is a rare systemic disorder characterized by the accumulation of CD1a+/Langerin+ LCH cells and wide‐ranging organ involvement. Langerhans cell histiocytosis was formerly referred to as histiocytosis X, until it was renamed in 1987. Langerhans cell histiocytosis β was named for its morphological similarity to skin...
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Full title
Langerhans cell histiocytosis in adults: Advances in pathophysiology and treatment
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6272080
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6272080
Other Identifiers
ISSN
1347-9032
E-ISSN
1349-7006
DOI
10.1111/cas.13817
