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750 Possible Causes for Immune Thrombocytopenic Purpura

  • Thrombocytopenia

    What is immune thrombocytopenic purpura? Immune thrombocytopenic purpura (ITP) is an autoimmune disorder.[] Immune thrombocytopenic purpura (ITP) is a bleeding disorder in which the immune system destroys platelets, which are necessary for normal blood clotting.[] Our patient was initially diagnosed with immune thrombocytopenic purpura with no evidence of malignancy on bone marrow biopsy but presented shortly after with ALL.[]

  • Evan's Syndrome

    Evan's syndrome is a rare hematological condition defined as immune thrombocytopenic purpura and hemolytic anemia.[] Immune thrombocytopenic purpura is a condition in which platelets are destroyed by an autoimmune process.[] Evans' syndrome is a clinical syndrome characterized by autoimmune hemolytic anemia (AIHA) accompanied by immune thrombocytopenic purpura (ITP).[]

  • Chronic Hepatitis C

    Immune thrombocytopenic purpura in patients with chronic hepatitis C virus infection. Am J Gastroenterol. 2002;97:2040–5.[] Hepatitis C virus-related thrombocytopenia: clinical and laboratory characteristics compared with chronic immune thrombocytopenic purpura.[] Efficacy of romiplostim in patients with chronic immune thrombocytopenic purpura: a double-blind randomised controlled trial. Lancet. 2008:371:395–403.[]

  • Purpura

    Abstract Immunoglobulin G is used to both prevent infection in primary immunodeficiency diseases (PIDs) and prevent bleeding in immune thrombocytopenic purpura.[] Immune thrombocytopenic purpura Other names Idiopathic thrombocytopenic purpura, idiopathic immune thrombocytopenia, primary immune thrombocytopenia, idiopathic thrombocytopenic[] […] and other hemorrhagic conditions D69.0 Allergic purpura D69.1 Qualitative platelet defects D69.2 Other nonthrombocytopenic purpura D69.3 Immune thrombocytopenic purpura D69.4[]

  • Autoimmune Disease

    A 17-year-old woman with a history of immune thrombocytopenic purpura was referred to the adolescent medicine clinic for evaluation of oligomenorrhea with secondary amenorrhea[] Immune thrombocytopenic purpura after recombinant hepatitis B vaccine: retrospective study of seven cases.[] Examples of cytotoxic reaction are autoimmune hemolytic anemia, transfusion reaction, erthrobalstosis foetalis, idiopathic thrombocytopenic purpura (ITP) and myasthenia gravis[]

  • Sarcoidosis

    Sarcoidosis (Besnier-Boeck disease, Besnier-Boeck-Schaumann disease) is a multisystem inflammatory disease of unknown etiology, characterized by non-necrotizing granulomatous inflammation, predominantly in the lungs and intrathoracic lymph nodes. The presentation of the disease is highly dependent on the extent of[…][]

  • Castleman Disease

    thrombocytopenic purpura (ITP). [4] Last updated: 6/25/2015 In about half of people with multicentric Castleman disease (MCD), it is caused by human herpesvirus-8 (HHV-8)[] […] such as rashes and/or pemphigus Less commonly ( [4] Other conditions associated with MCD include amyloidosis , POEMS syndrome , autoimmune disease , hemolytic anemia , and immune[] […] abnormalities such as rashes and/or pemphigus Less commonly ( [4] Other conditions associated with MCD include amyloidosis, POEMS syndrome, autoimmune disease, hemolytic anemia, and immune[]

  • Acquired Immunodeficiency Syndrome

    Additional disorders that belong to the B category are immune thrombocytopenic purpura (ITP), cervical dysplasia (or cervical carcinoma in situ) and oral hairy leukoplakia[]

  • Chronic Immune Thrombocytopenic Purpura

    Hematuria is an uncommon manifestation of chronic immune thrombocytopenic purpura.[] thrombocytopenic purpura.[] Immune thrombocytopenic purpura is a disorder affecting all age groups.[]

  • Immune Thrombocytopenic Purpura

    Immune thrombocytopenic purpura (ITP), also called primary immune thrombocytopenia or idiopathic thrombocytopenic purpura, is an autoimmune disease affecting thrombocytes.[] Bone marrow aspiration findings and treatment response were suggestive for immune thrombocytopenic purpura.[] KEYWORDS: child; immune thrombocytopenic purpura; incidence[]

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