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106 Possible Causes for Bicytopenia, Purpura

  • Severe Aplastic Anemia

    This initial indication was for adult patients with chronic immune thrombocytopenic purpura (ITP) following an insufficient response to corticosteroids, immunoglobulins, or[] Mild anemia and macrocytosis may indicate SAA in patients otherwise possibly diagnosed with immune thrombocytopenic purpura.[]

  • Thrombocytopenia

    HIV post exposure prophylaxis induced bicytopenia: a case report. AIDS Res Ther . 2014; 11 :11. [ PubMed ] [ DOI ] 8. Visentin GP , Liu CY.[] MMR vaccine and idiopathic thrombocytopaenic purpura Alter HJ, et al. Thrombocytopenic purpura following vaccination with attenuated measles virus.[] Abstract The treatment of refractory immune-mediated thrombocytopenia purpura (ITP) can be challenging.[]

  • Disseminated Intravascular Coagulation

    Acute perturbations in the hemostatic balance of anticoagulation and procoagulation antecede the manifestation of purpura fulminans, a rare syndrome of intravascular thrombosis[] We report on 3 male neonates with hereditary ADAMTS13 deficiency (Upshaw Schulman syndrome, USS), the inherited form of thrombotic thrombocytopenic purpura (TTP). 2 presented[] The DIC was rapidly improved; however, the purpura and coagulopathy recurred after two months, and repeated rhsTM treatments were required.[]

  • Pancytopenia

    […] of bicytopenia and pancytopenia.[] Three of the 11 patients had severe thrombocytopenia, and they were admitted with complaints of epistaxis, gingival bleeding, petechiae, and purpura.[] Symptoms at presentation included: oral mucositis (n 37); fever (n 24); diarrhea (n 12), bleeding gums (n 5) and purpura (n 3).[]

  • Evan's Syndrome

    The pattern of occurrence of bicytopenia can delay the diagnosis since it may be coincidental, sequential, or separate, and the time frame between episodes can range from[] […] 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[] Immune-mediated thrombocytopenia (ITP) often manifests as petechiae, purpura, ecchymoses, epistaxis and mucocutaneous hemorrhage.[]

  • Acute Leukemia

    A 43-year-old female presented with leukocytosis and bicytopenia.[] Initial CBC showed bicytopenia, elevated blood urea, creatinine, and serum uric acid, while abdominal ultrasonography revealed bilateral renal enlargement.[]

  • Acute Myelocytic Leukemia

    In contrast to patients with RA and only dyserythropoiesis, patients with multilineage dysplasia have bicytopenia or pancytopenia, a higher incidence of cytogenetic abnormalities[] Petechiae are small dots, purpura is larger and ecchymoses are larger bruises. Hepatomegaly and splenomegaly may be found. Lymphadenopathy is less common.[] Extensive purpura is present on the soles of a patient with acute promyelocytic leukemia and DIC 47.[]

  • Gaucher Disease

    Niemann-Pick disease (lipid histiocytosis) (splenomegaly) 272.7 Pick's disease Pick-Niemann disease (lipid histiocytosis) 272.7 Pseudo-Hurler's disease (mucolipidosis III) 272.7 Purpura[] (1) 確定診断のついた特発性血小板減少性紫斑 病(ITP)の患者 (2) 確定診断のついた再生不良性貧血の患者 (3) その他、研究責任(担当)医師が本研究の対象として不適当と判断した患者 1.Patients who were definitively diagnosed as idiopathic thrombocytopenic purpura[]

  • Colchicine Poisoning

    Effects of long-term colchicine toxicity include agranulocytosis, thrombocytopenia, low white blood cell counts, aplastic anemia, alopecia, rash, purpura, vesicular dermatitis[] […] the Psychiatric Department of our hospital after recovering from a suicide attempt, apparently taking 40 pills of colchicine (40 mg), which led to severe pancreatitis and bicytopenia[] Inflammatory Reaction / Severe or persistent diarrhea / Type 2 Diabetes Mellitus / White Blood Cell 1 2 Recruiting Treatment Cutaneous Polyarteritis Nodosa / Henoch-Schönlein Purpura[]

  • Vitamin B12 Deficiency

    Laboratory data revealed bicytopenia with macrocytic anemia and methylmalonic acid in the urine, consistent with vitamin B12 deficient anemia.[] As a subset of microangiopathic hemolytic anemia, thrombotic thrombocytopenic purpura can present with a constellation of symptoms similar to the hemolytic anemia attributed[] Although thrombotic thrombocytopenic purpura (TTP) is rare, early diagnosis and treatment are important for decreasing the mortality rate.[]

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