|Congenital self-healing reticulohistiocytosis|
|Other names||Hashimoto–Pritzker disease, and Hashimoto–Pritzker syndrome|
Congenital self-healing reticulohistiocytosis is a condition that is a self-limited form of Langerhans cell histiocytosis.:720
Non-specific inflammatory response, which includes fever, lethargy, and weight loss. This is suspected of being a genetic disorder, and as the name implies, is self healing.
- Skin: Commonly seen are a rash which varies from scaly erythematous lesions to red papules pronounced in intertriginous areas. Up to 80% of patients have extensive eruptions on the scalp.
- Lymph node: Enlargement of the lymph nodes in 50% of Histiocytosis cases.
It was first described by Ken Hashimoto and M. S. Pritzkar in 1973.
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