Histiocyte Society classification of histiocytoses

Changed by Francis Deng, 4 Sep 2019

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~~2016~~ Histiocyte Society classification of histiocytoses

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The ~~2016~~ ~~Histiocyte~~Histiocyte Society classification of histiocytoses and neoplasms of macrophage-dendritic cell lineages is ~~a proposed~~currently in its 2016 revision of the organisation's initial classification system from 1987.

Terminology

Histiocytes are mononuclear phagocytes that reside in tissues, including macrophages and dendritic cells. Histiocytoses are disorders characterized by the accumulation of cells derived from macrophages or dendritic cells.

Classification

L (Langerhans) group

Langerhans cell histiocytosis
Erdheim-Chester disease
indeterminate cell histiocytosis
mixed Langerhans cell histiocytosis and Erdheim-Chester disease

C group: cutaneous and mucocutaneous non-Langerhans cell histiocytoses

cutaneous non-Langerhans cell histiocytoses
- xanthogranuloma family
  - juvenile xanthogranuloma
  - adult xanthogranuloma
  - solitary reticulohistiocytoma
  - benign cephalic histiocytosis
  - generalized eruptive histiocytosis
  - progressive nodular histiocytosis
- non-xanthogranuloma family
  - cutaneous Rosai-Dorfman disease
  - necrobiotic xanthogranuloma
  - cutaneous histiocytoses not otherwise specified
cutaneous non-Langerhans cell histiocytoses with a major systemic component
- xanthogranuloma family
  - xanthoma disseminatum
- non-xanthogranuloma family
  - multicentric reticulohistiocytosis

M group: malignant histiocytoses

primary malignant histiocytoses
secondary malignant histiocytoses (following or associated with another haematologic neoplasia)
subtypes
- histiocytic
- interdigitating cell
- Langerhans cell
- indeterminate cell
- not specified

R group: Rosai-Dorfman disease and miscellaneous noncutaneous, non-Langerhans cell histiocytoses

familial Rosai-Dorfman disease
sporadic Rosai-Dorfman disease
- classical (nodal) Rosai-Dorfman disease
- extranodal Rosai-Dorfman disease
- neoplasia-associated Rosai-Dorfman disease
- immune disease-associated Rosai-Dorfman disease
other non-C non-L non-M non-H histiocytoses

H group: haemophagocytic lymphohistiocytosis and macrophage activation syndrome

primary haemophagocytic lymphohistiocytosis (Mendelian inherited conditions)
secondary haemophagocytic lymphohistiocytosis (apparently non-Mendelian)
haemophagocytic lymphohistiocytosis of unknown/uncertain origin

-<p>The <strong>2016</strong><strong> Histiocyte Society classification of histiocytoses and neoplasms of macrophage-dendritic cell lineages </strong>is a proposed revision of the organisation's initial classification system from 1987.</p><h4>Terminology</h4><p>Histiocytes are mononuclear phagocytes that reside in tissues, including macrophages and dendritic cells. Histiocytoses are disorders characterized by the accumulation of cells derived from macrophages or dendritic cells.</p><h4>Classification</h4><h5>L (Langerhans) group</h5><ul>
+<p>The <strong>Histiocyte Society classification of histiocytoses and neoplasms of macrophage-dendritic cell lineages </strong>is currently in its 2016 revision of the organisation's initial classification system from 1987.</p><h4>Terminology</h4><p>Histiocytes are mononuclear phagocytes that reside in tissues, including macrophages and dendritic cells. Histiocytoses are disorders characterized by the accumulation of cells derived from macrophages or dendritic cells.</p><h4>Classification</h4><h5>L (Langerhans) group</h5><ul>
~~-<li>primary <a title="Haemophagocytic lymphohistiocytosis" href="/articles/haemophagocytic-lymphohistiocytosis">haemophagocytic lymphohistiocytosis</a> (Mendelian inherited conditions)</li>~~
+<li>primary <a href="/articles/haemophagocytic-lymphohistiocytosis">haemophagocytic lymphohistiocytosis</a> (Mendelian inherited conditions)</li>