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918 Possible Causes for Autoimmune Thrombocytopenia

  • Gastrointestinal Hemorrhage

    2015 ICD-9-CM Diagnosis Code 578.9 Hemorrhage of gastrointestinal tract, unspecified 2015 Billable Thru Sept 30/2015 Non-Billable On/After Oct 1/2015 ICD-9-CM 578.9 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 578.9 should only be used for claims with a date of[…][]

  • Evan's Syndrome

    Evan's syndrome is a hematologic disorder characterized by autoimmune thrombocytopenia and autoimmune hemolytic anemia.[] We report a case of the plasma cell variant of Castleman's disease that was associated with autoimmune hemolytic anemia and autoimmune thrombocytopenia (Evan's syndrome),[] […] syndrome (disorder) Evan syndrome Autoimmune hemolytic anemia and autoimmune thrombocytopenia Immune pancytopenia Evans' syndrome edit English Evans' syndrome Human disease[]

  • Autoimmune Thrombocytopenia

    Autoimmune thrombocytopenia has been rarely reported in WM and its incidence is not known.[] Chemotherapy is the best treatment in many non-Hodgkin's lymphomas patients with autoimmune thrombocytopenia compared with standard treatment of autoimmune thrombocytopenia[] Abstract Autoimmune thrombocytopenia is a disorder characterized by antibody-mediated accelerated platelet destruction.[]

  • Eczema

    INTRODUCTION: Langerhans cell histiocytosis (LCH) is a multisystem disorder of unknown etiology and characterized by accumulation of histiocytes in various tissues. CASE REPORT: A 3-year-old, previously healthy girl presented with progressive flattening of the parietal convexity for 6 months and seborrheic eczema[…][]

  • Thrombocytopenia

    The chronic form of autoimmune thrombocytopenia has duration greater than six months, and is an organ-specific autoimmune disease.[] Chemotherapy is the best treatment in many non-Hodgkin’s lymphomas patients with autoimmune thrombocytopenia compared with standard treatment of autoimmune thrombocytopenia[] Refractory severe chronic autoimmune thrombocytopenia, with or without autoimmune hemolytic anemia (Evan's syndrome), with all the following: Platelet count frequently below[]

  • Pediatric Systemic Lupus Erythematosus

    thrombocytopenia and/or autoimmune hemolytic anemia and treated with rituximab.[] Three patients with pediatric systemic lupus erythematosus (PSLE) and autoimmune thrombocytopenia (AT), who developed unacceptable side effects (pseudotumor cerebri, hypertension[] Investigations revealed autoimmune hemolytic anemia and thrombocytopenia. Anti-dsDNA and anti-phospholipid antibodies were positive.[]

  • Hypersensitivity

    Another example is autoimmune thrombocytopenia, which fits in with our topics this quarter. Antibodies here bind to platelets, leading to their destruction.[] Testing can be done via skin test for specific IgE. [2] II Cytotoxic, antibody-dependent Autoimmune hemolytic anemia Rheumatic heart disease Thrombocytopenia Erythroblastosis[] ALPS can cause numerous autoimmune problems, such as anemia (low level of red blood cells), thrombocytopenia (low level of platelets), and neutropenia (low level of neutrophils[]

  • Anemia

    Microangiopathic hemolytic anemia, thrombocytopenia, normal coagulation test results, and renal and neurologic abnormalities should lead the physician to the diagnosis.[] Immune thrombocytopenic purpura (ITP) is an autoimmune disease often precipitated by viral infections. [2] IgG autoantibodies bind to platelets, which then undergo destruction[]

  • Immune Thrombocytopenic Purpura

    HO, Autoimmune thrombocytopenia, Journal of Thrombosis and Haemostasis, 3, 8, (1763-1772), (2005). Douglas B.[] Purpura, Immune, Immune Thrombocytopenia, Thrombocytopenia, Autoimmune, Immune Thrombocytopenic Purpuras, Autoimmune Thrombocytopenias, Idiopathic thrombocytopenic purpura[] Carol Alliot and Marta Barrios, Efficacy of Dapsone in an Adolescent with Chronic Autoimmune Thrombocytopenia, Therapies, 10.2515/therapie:2004081, 59, 4, (479-480), (2004[]

  • RAS-Associated Autoimmune Leukoproliferative Disease

    We highlight the potential for monthly administration of rituximab in a patient with autoimmune thrombocytopenia and hemolytic anemia associated with RALD.[] , neoplastic Phenotypes Autoimmune thrombocytopenia ; Autosomal dominant inheritance ; Decreased lymphocyte apoptosis ; Follicular hyperplasia ; Hemolytic anemia ; Hepatomegaly[] The patient was initially diagnosed as Evans syndrome based on the presence of hemolytic anemia and autoimmune thrombocytopenia.[]

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