Abstract
Histiocytosis or histiocytic disorders comprise a large and diverse group of entities that have as common denominator infiltration and/or abnormal accumulation of histiocytes within blood and other tissues. In many of these disorders, the skin plays a key role in diagnosis, and may be the only organ involved. In skin of color, histiocytic disorders can present with different characteristics and look different than in lighter skin tones. The purpose of this chapter is to review some of the histiocytic disorders that affect mainly the pediatric population and highlight differences that might be present in the different skin tones of children of color.
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Abbreviations
- BCH:
-
Benign cephalic histiocytosis
- CSHRH:
-
Congenital self-healing reticulohistiocytosis
- GEH:
-
Generalized eruptive histiocytoma
- HLH:
-
Hemophagocytic lymphohistiocytosis
- ICH:
-
Indeterminate-cell histiocytosis
- JXG:
-
Juvenile xanthogranuloma
- LC:
-
Langerhans cells
- LCH:
-
Langerhans cell histiocytosis
- MPS:
-
Mononuclear phagocytic system
- MRH:
-
Multicentric reticulohistiocytosis
- MS:
-
Multisystem
- PNH:
-
Progressive nodular histiocytosis
- RDD:
-
RosaiāDorfman disease
- SHML:
-
Sinus histiocytosis with massive lymphadenopathy
- SS:
-
Single-system
- XD:
-
Xanthoma disseminatum
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Del Pozzo-MagaƱa, B., Lara-Corrales, I. (2015). Histiocytosis. In: Silverberg, N., DurƔn-McKinster, C., Tay, YK. (eds) Pediatric Skin of Color. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-6654-3_23
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