Blood and immunity

• lymphocytophagocytosis
  11 March 2004

  Etiology
  macrophagic activation syndrome

• leukocytes
  9 March 2004

  leucocytes

• dendritic cells
  9 March 2004

  DCs

• T lymphocytes trafficking
  9 March 2004

  T cell migration

• T lymphocytes
  9 March 2004

  T-cells

• X-linked thrombocytopenia
  7 March 2004

  XLT

• thrombocytopenia
  7 March 2004
• multicentric reticulohistiocytosis
  6 February 2004

  Multicentric reticulohistiocytosis is a rare disorder with proliferating histiocytes that develop into multinucleated giant cells with "ground-glass" cytoplasm. The disease presents with a rapidly destructive, sometimes permanently debilitating, polyarthritis and a papulonodular eruption, generally of the face and hands.
  Localization
  skin
  articulations
  References
  Bogle MA, Tschen JA, Sairam S, McNearney T, Orsak G, Knox JM. Multicentric reticulohistiocytosis with pulmonary (...)

• systemic histiocytoses
  6 February 2004

  Types
  Langerhans histiocytosis
  non-Langerhans histiocytoses Erdheim-Chester disease systemic juvenile xanthogranuloma generalized eruptive histiocytoma multicentric reticulohistiocytosis (#14639398#, #2192569#) xanthoma disseminatum
  References
  Weitzman S, Jaffe R. Uncommon histiocytic disorders: the non-Langerhans cell histiocytoses. Pediatr Blood Cancer. 2005 Sep;45(3):256-64. PMID: #15547923#
  Jaffe R. The other histiocytosis. Pediatr Dev Pathol. 2004 Jan-Feb;7(1):2-4. PMID: (...)

• reticular dysgenesis
  21 January 2004

  Reticular dysgenesis is a very rare congenital immunodeficiency classified within the severe combined immunodeficiencies (SCID) and characterized by impairment of both lymphoid and myeloid cell development. It is characterized by congenital agranulocytosis, lymphopenia, and lymphoid and thymic hypoplasia with absent cellular and humoral immunity functions. MIM.267500

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