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Histiocyte Society information


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The Histiocyte Society is an international network of people that co-ordinate studies of the histiocytoses, which it has divided into Langerhans cell histiocytosis (class I) (previously known as Hand–Schüller–Christian disease and histocytosis-X), non-Langerhans cell histiocytoses (class II), and malignant histiocytosis (class III).[1][2][3][4] They provided the criteria to definitively diagnose Langerhans cell histiocytosis.[5]

  1. ^ Tebbi, Cameron K. (16 September 2020). Kanwar, Vikramjit S (ed.). "What is the Histiocyte Society classification of histiocytosis syndromes?". Medscape. Retrieved 4 December 2020.
  2. ^ H. A. Harfi; F. B. Stapleton; H. Nazer (2012). Textbook of Clinical Pediatrics. Springer Science & Business Media. p. 3215. ISBN 978-3-642-02202-9.
  3. ^ Chang, Karen L.; Snyder, David S. (2007). "17. Langerhans Cell Histiocytosis". In Stephen M. Ansell (ed.). Rare Hematological Malignancies. Springer Science & Business Media. p. 383. ISBN 978-0-387-73743-0.
  4. ^ Satter, Elizabeth K.; High, Whitney A. (May 2008). "Langerhans cell histiocytosis: a review of the current recommendations of the Histiocyte Society". Pediatric Dermatology. 25 (3): 291–295. doi:10.1111/j.1525-1470.2008.00669.x. ISSN 1525-1470. PMID 18577030. S2CID 20024618.
  5. ^ Ajithkumar, Thankamma V; Barrett, Ann; Hatcher, Helen; Cook, Natalie (2011). "4. Site specific cancer management". Oxford Desk Reference: Oncology. Oxford University Press. p. 523. ISBN 978-0-19-923563-6.

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Histiocyte Society

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The Histiocyte Society is an international network of people that co-ordinate studies of the histiocytoses, which it has divided into Langerhans cell histiocytosis...

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Langerhans cell histiocytosis

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at birth) and histiocytosis X, until it was renamed in 1985 by the Histiocyte Society. The disease spectrum results from clonal accumulation and proliferation...

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Histiocytosis

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In medicine, histiocytosis is an excessive number of histiocytes (tissue macrophages), and the term is also often used to refer to a group of rare diseases...

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Chronic multifocal Langerhans cell histiocytosis

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internationally recognised. In 1987, the Histiocyte Society published their classification of the histiocyte disorders together with criteria for diagnosis...

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Hemophagocytic lymphohistiocytosis

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look deeply for various underlying contributors. The International Histiocyte Society has collected the published consensus management documents for the...

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Canine histiocytic diseases

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cells of histiocytoma frequently occurs and intra-epidermal nests of histiocytes resemble Pautrier's aggregates, characteristically found in epidermotropic...

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Tumors of the hematopoietic and lymphoid tissues

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(DLBCL), NOS Germinal centre B-cell subtype Activated B-cell subtype T-cell/histiocyte-rich large B-cell lymphoma Primary DLBCL of the CNS Primary cutaneous...

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Aphthous stomatitis

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vascularity and a mixed inflammatory infiltrate composed of lymphocytes, histiocytes and polymorphonuclear leukocytes. The epithelium on the margins of the...

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Lymphoma

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contours of the medium-sized lymphoma cells and the presence of a pink histiocyte. By immunohistochemistry, the lymphoma cells expressed CD20, CD5, and...

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Toxoplasmosis

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germinal centers, clusters of monocytoid B cells, and scattered epithelioid histiocytes.[citation needed] The classic triad of congenital toxoplasmosis includes:...

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Syphilis

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"Mercury as an Antisyphilitic Chemotherapeutic Agent". Journal of the Royal Society of Medicine. 83 (June 1990): 392–395. doi:10.1177/014107689008300619. PMC 1292694...

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Histoplasmosis

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showing organisms surrounded by halos, in a granuloma of epithelioid histiocytes. Histopathology of Histoplasma capsulatum, GMS stain, showing narrow...

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Granuloma inguinale

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organisms that can be seen in the cytoplasm of mononuclear phagocytes or histiocytes in tissue samples from patients with granuloma inguinale. They appear...

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Hodgkin lymphoma

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reactive cell infiltrate composed of variable proportions of lymphocytes, histiocytes, eosinophils, and plasma cells. The Reed–Sternberg cells are identified...

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GM1 gangliosidoses

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mucopolysaccharidoses) 10–80% of peripheral lymphocytes are vacuolated; foamy histiocytes in bone marrow; visceral mucopolysaccharide storage similar to that in...

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Mantle cell lymphoma

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allogeneic stem cell transplant). A presentation at the December 2007 American Society of Hematology (ASH) conference by Christian Geisler, chairman of the Nordic...

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Hypophyseal portal system

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state. In Erdheim–Chester disease, cells of the immune system called histiocytes proliferate at an abnormal rate causing a plethora of symptoms and, in...

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Vaginal epithelium

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ten-layer cell layer. The parabasal cells can also differentiate into histiocytes or glandular cells. Estrogen also influences the changing ratios of nuclear...

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Acral myxoinflammatory fibroblastic sarcoma

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the tumors may contain degenerated, dying, and or dead cells and large histiocyte-like cells that have engulfed other cells, usually neutrophils (this cell-engulfing...

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Fibroblastic and myofibroblastic tumors

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metastasizing infantile fibrosarcoma. Myxofibrosarcoma, once classified as a histiocyte-derived histiocytoma now reclassified as a fibroblastic/myofibroblastic...

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Dendritic cell

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seen here efficiently taking up at least four conidia in its vicinity. Histiocyte Macrophage List of human clusters of differentiation for a list of CD...

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