Histiocytosis, Non-Langerhans-Cell
"Histiocytosis, Non-Langerhans-Cell" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Group of disorders which feature accumulations of active HISTIOCYTES and LYMPHOCYTES, but where the histiocytes are not LANGERHANS CELLS. The group includes HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; SINUS HISTIOCYTOSIS; xanthogranuloma; reticulohistiocytoma; JUVENILE XANTHOGRANULOMA; xanthoma disseminatum; as well as the lipid storage diseases (SEA-BLUE HISTIOCYTE SYNDROME; and NIEMANN-PICK DISEASES).
| Descriptor ID |
D015616
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| MeSH Number(s) |
C15.604.250.410
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Histiocytosis, Non-Langerhans-Cell".
Below are MeSH descriptors whose meaning is more specific than "Histiocytosis, Non-Langerhans-Cell".
This graph shows the total number of publications written about "Histiocytosis, Non-Langerhans-Cell" by people in this website by year, and whether "Histiocytosis, Non-Langerhans-Cell" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2005 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Histiocytosis, Non-Langerhans-Cell" by people in Profiles.
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The color of skin: orange diseases of the skin, nails, and mucosa. Clin Dermatol. 2019 Sep - Oct; 37(5):520-527.
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High prevalence of myeloid neoplasms in adults with non-Langerhans cell histiocytosis. Blood. 2017 08 24; 130(8):1007-1013.
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Benign cephalic histiocytosis with S-100 protein positivity. J Cutan Pathol. 2011 Oct; 38(10):842-3.
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Multicentric reticulohistiocytosis and urologic carcinomas: a possible paraneoplastic association. J Cutan Pathol. 2011 Jan; 38(1):43-8.
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Epstein-Barr virus-associated peripheral T-cell lymphoma and hemophagocytic syndrome arising after liver transplantation: case report and review of the literature. Pediatr Blood Cancer. 2005 Mar; 44(3):270-6.
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Haemophagocytosis in hereditary fructose intolerance: a diagnostic dilemma. J Inherit Metab Dis. 1990; 13(3):267-9.