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- W4386006422 abstract "Abstract Skin involvement is common in all forms of histiocytic disorders and is seen at all ages. In general, the histiocytoses can be divided into those involving dendritic cells and those involving the macrophage–monocyte lineage. Langerhans cell histiocytosis is the most common dendritic cell disorder and haemophagocytic lymphohistiocytosis the most common non‐dendritic disorder. Rarer disorders, the non‐Langerhans cell histiocytoses, can be divided into dendritic and non‐dendritic origin and each group further subdivided into those that mainly involve skin but occasionally have a systemic component and those that may include skin but in which the systemic component predominates. This chapter will provide an overview of histiocytic disorders including a brief discussion of possible pathogenetic mechanisms, followed by a more in‐depth discussion of the skin manifestations, pathology and therapy. The similarities and differences between childhood and adult forms of the diseases will be highlighted." @default.
- W4386006422 created "2023-08-20" @default.
- W4386006422 creator A5011133381 @default.
- W4386006422 creator A5048012532 @default.
- W4386006422 creator A5073802507 @default.
- W4386006422 date "2016-10-09" @default.
- W4386006422 modified "2023-10-12" @default.
- W4386006422 title "Cutaneous Histiocytoses" @default.
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