Reticulohistiocytosis

Reticulohistiocytosis
Reticulohistiocytosis
Specialty	Dermatology

Reticulohistiocytosis is a cutaneous condition of which there are two distinct forms:^[1]^: 718–9

References

ISBN 978-0-7216-2921-6
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Histiocytosis
WHO-I/Langerhans cell histiocytosis/
X-type histiocytosis

Letterer–Siwe disease

Hand–Schüller–Christian disease

Eosinophilic granuloma

Congenital self-healing reticulohistiocytosis

WHO-II/non-Langerhans cell histiocytosis/
Non-X histiocytosis

Juvenile xanthogranuloma

Hemophagocytic lymphohistiocytosis

Erdheim-Chester disease

Niemann–Pick disease

Sea-blue histiocytosis

Benign cephalic histiocytosis

Generalized eruptive histiocytoma

Xanthoma disseminatum

Progressive nodular histiocytosis

Papular xanthoma

Hereditary progressive mucinous histiocytosis

Reticulohistiocytosis (Multicentric reticulohistiocytosis, Reticulohistiocytoma)

Indeterminate cell histiocytosis

WHO-III/malignant histiocytosis

Histiocytic sarcoma

Langerhans cell sarcoma

Interdigitating dendritic cell sarcoma

Follicular dendritic cell sarcoma

Ungrouped

Rosai–Dorfman disease

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Retrieved from "https://en.wikipedia.org/w/index.php?title=Reticulohistiocytosis&oldid=996186872"

[Andrews-1] ISBN 978-0-7216-2921-6
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[1]

See also

References