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  2. Histiocytosis - Wikipedia

    en.wikipedia.org/wiki/Histiocytosis

    Sinus histiocytosis, a common feature in lymph node biopsies, is characterized by dilated sinuses containing variable numbers of histiocytes. [ 4 ] Histiocytosis is a rare disease, thus its diagnosis may be challenging.

  3. Langerhans cell histiocytosis - Wikipedia

    en.wikipedia.org/wiki/Langerhans_cell_histiocytosis

    Langerhans cell histiocytosis (LCH) is an abnormal clonal proliferation of Langerhans cells, abnormal cells deriving from bone marrow and capable of migrating from skin to lymph nodes. Symptoms range from isolated bone lesions to multisystem disease . [ 1 ]

  4. Chronic multifocal Langerhans cell histiocytosis - Wikipedia

    en.wikipedia.org/wiki/Chronic_multifocal_Langer...

    Before the Histiocyte Society classified histiocytoses in the 1980s, the condition was also known as "Histiocytosis X", where "X" denoted the then unknown cause. [9] [10] [11] It is now known as chronic multifocal Langerhans cell histiocytosis, a subtype of LCH. [3] The disease is rare. [12] Most present between the ages of two and six. [2]

  5. Non-Langerhans cell histiocytosis - Wikipedia

    en.wikipedia.org/wiki/Non-Langerhans_cell...

    Non-Langerhans cell histiocytosis, also known as rare histiocytoses, comprise all histiocyte, macrophage, and dendritic cell proliferative disorders that are not categorized as hemophagocytic lymphohistiocytosis (HLH) or Langerhans cell histiocytosis (LCH). [1] The spectrum of non-langerhans cell histiocytoses include: Benign cephalic histiocytosis

  6. Rosai–Dorfman disease - Wikipedia

    en.wikipedia.org/wiki/Rosai–Dorfman_disease

    Rosai–Dorfman disease, also known as sinus histiocytosis with massive lymphadenopathy or sometimes as Destombes–Rosai–Dorfman disease, [1] [2] [3] is a rare disorder of unknown cause that is characterized by abundant histiocytes in lymph nodes or other locations including the skin, sinuses, brain and heart. Individuals with the disorder ...

  7. X-type histiocytosis - Wikipedia

    en.wikipedia.org/wiki/X-type_histiocytosis

    X-type histiocytoses are a clinically well-defined group of cutaneous syndromes characterized by infiltrates of Langerhans cells, as opposed to Non-X histiocytosis in which the infiltrates contain monocytes/macrophages. [1]: 720 Conditions included in this group are: [1]: 720–4 Congenital self-healing reticulohistiocytosis

  8. Crystal-storing histiocytosis - Wikipedia

    en.wikipedia.org/wiki/Crystal-storing_histiocytosis

    Crystal-storing histiocytosis is a form of histiocytosis that mostly occurs in people with monoclonal gammopathies. [ 1 ] [ 2 ] Histiocytosis is an excessive number of histiocytes (an immune cell type which is part of the mononuclear phagocyte system ).

  9. Malignant histiocytosis - Wikipedia

    en.wikipedia.org/wiki/Malignant_histiocytosis

    Malignant histiocytosis is a rare hereditary disease found in the Bernese Mountain Dog and humans, characterized by histiocytic infiltration of the lungs and lymph nodes. The liver, spleen, and central nervous system can also be affected. Histiocytes are a component of the immune system that proliferate abnormally in this disease. In addition ...