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326 Possible Causes for Bleeding Diathesis, Hematuria, Thrombocytopenic Purpura

  • Disseminated Intravascular Coagulation

    Two weeks later, he was transferred to the West China Hospital with nasal hemorrhage for 1 week, hematochezia, hematuria, and petechiae for 5 days.[] We report on 3 male neonates with hereditary ADAMTS13 deficiency (Upshaw Schulman syndrome, USS), the inherited form of thrombotic thrombocytopenic purpura (TTP). 2 presented[] Bleeding diathesis must be corrected before surgery in order to prevent massive intraoperative bleeding.[]

  • Glanzmann Thrombasthenia

    We report a six day old newborn presenting with hematuria following suprapubic aspiration, who was diagnosed as Glanzmann thrombasthenia.[] Acquired Glanzmann's thrombasthenia (GT) is an uncommon accompaniment to immune thrombocytopenic purpura.[] Patients with Glanzmann thrombasthenia experience lifelong spontaneous and post-traumatic mucocutaneous bleeding diathesis.[]

  • Coagulation Abnormalities

    INCREASED VASCULAR FRAGILITY seldom serious skin bruises, dependent petechiae, gum bleeding, hematuria, nosebleeds, GI bleeds.[] Cancer patients may also suffer from the impediment of hemolytic uremic syndrome or thrombotic thrombocytopenic purpura (HUS/TTP).[] diathesis.[]

  • Acquired Hemophilia A

    The woman presented to the emergency room with hematuria. Coagulation screening tests showed a prolonged APTT.[] ., idiopathic thrombocytopenic purpura, thrombotic thrombocytopenic purpura, connective tissue disorders and autoimmune hemolytic anemia) in which it has been used with the[] In any elderly patient with a bleeding diathesis and an abnormality in intrinsic coagulation, the presence of inhibitors to factor VIII should be suspected.[]

  • Acquired Coagulation Factor Deficiency

    […] at birth abnormal bleeding during or after injury, surgery, or childbirth Rare symptoms bleeding in the central nervous system (the brain and spinal cord) blood in urine (hematuria[] ( D47.3 ) purpura fulminans ( D65 ) thrombotic thrombocytopenic purpura ( M31.1 ) D69.0 Allergic purpura Purpura: · anaphylactoid · Henoch(-Schönlein) · nonthrombocytopenic[] They did not require any plasma or plasma product for the control of their bleeding diathesis and decreased factor IX activity returned to normal in a relatively short period[]

  • Kasabach Merritt Syndrome

    A neonate that had a forearm hemangioma, gross hematuria, and a renal parenchymal hematoma was found to have Kasabach-Merritt syndrome.[] purpura or hypersplenism.Placental chorioangiomas are the most widespread non-trophoblastic benign tumor-like lesions of placenta.[] A patient can lose up to 70% of their coagulation factors before developing a clinical bleeding diathesis, so the goal is the ensure the levels of coagulation factors remain[]

  • Immune Thrombocytopenic Purpura

    Severe visceral bleeding (hematuria, gastrointestinal hemorrhage or cerebromeningeal bleeding) is mainly observed when thrombocytopenia is below 10,000/microL.[] Immune thrombocytopenic purpura (ITP), also called primary immune thrombocytopenia or idiopathic thrombocytopenic purpura, is an autoimmune disease affecting thrombocytes.[] A year later she presented with bleeding diathesis and was diagnosed as ITP.[]

  • Hemophilia

    Hematuria is frequent in hemophilia.[] Rituximab chimeric anti-CD20 monoclonal antibody treatment for adults with chronic idiopathic thrombocytopenic purpura. Blood 2001; 98: 952-957. 84 Wiestner A. et al.[] Results We showed that platelet-FVIII expression was sustained and the bleeding diathesis was restored in FVIII null mice after 2bF8LV gene therapy.[]

  • Acquired Hemophilia

    KEYWORDS: Factor 8 deficiency, acquired [Supplementary Concept] ; Hematuria; Nephrolithiasis[] Is immune thrombocytopenic purpura less common among black Americans? Blood 2005; 105:1368–1369. 21. Landgren O, Gridley G, Fears TR, Caporaso N.[] diathesis that does not require any personal or family history of bleeding or clotting disorder.[]

  • Essential Thrombocythemia

    […] pain to ischemia and gangrene of the distal portions of toes and fingers. 15 The most frequent bleeding events are hemorrhages from the gastrointestinal tract followed by hematuria[] ( D47.3 ) hemorrhagic thrombocythemia ( D47.3 ) purpura fulminans ( D65 ) thrombotic thrombocytopenic purpura ( M31.1 ) Waldenström hypergammaglobulinemic purpura ( D89.0[] diathesis 30 .[]

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