Create issue ticket

438 Possible Causes for Bleeding Diathesis, Thrombocytopenia, Thrombocytopenic Purpura

  • Immune Thrombocytopenic Purpura

    A controversy soon emerged regarding the pathologic mechanisms responsible for the thrombocytopenia.[] 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.[]

  • Kasabach Merritt Syndrome

    Title Other Names: Kasabach Merritt syndrome; Thrombocytopenia-hemangioma syndrome; Kasabach Merritt phenomenon; Kasabach Merritt syndrome; Thrombocytopenia-hemangioma 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[]

  • Disseminated Intravascular Coagulation

    Both initially received antibiotic treatment for suspected infection-associated thrombocytopenia.[] Bleeding diathesis must be corrected before surgery in order to prevent massive intraoperative bleeding.[] In contrast, disseminated intravascular microthrombosis (DIT) occurs in thrombotic thrombocytopenic purpura (TTP) and TTP-like syndrome due to ADAMTS13 deficiency or insufficiency[]

  • Bernard-Soulier Syndrome

    The first woman presented with platelet-associated autoantibodies and thrombocytopenia, but her three newborn infants showed normal platelet count and function.[] Immune thrombocytopenic purpura is a diagnosis of exclusion.[] The propositus was a 39-year-old Japanese female with life-long bleeding diathesis.[]

  • Glanzmann Thrombasthenia

    Heikal, Rare complication of treated immune thrombocytopenia, American Journal of Hematology, 92, 11, (1262-1266), (2017). John E. Zvijac, Sharhabil S.[] 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.[]

  • Thrombocytopathy

    A patient is described who presented a thrombocytopenia with thrombocytopathy followed by the development of a leukaemia.[] Thrombocytopenic purpura thrombocytopenic purpura n. See idiopathic thrombocytopenic purpura.[] Patients with thrombocytopathy due to storage pool disease mostly suffer from mild bleeding diathesis. However surgical interventions can lead to excess bleeding.[]

  • Bleeding Diathesis

    A complete blood count (CBC) can detect anemia and more importantly thrombocytopenia (defined as platelet count 150,000/μL), which may occur either as a result of impaired[] purpura.[] A 6-year-old girl presented with presumed relapse of childhood immune thrombocytopenia.[]

  • Aspirin-induced Platelet Defect

    Thrombocytopenia /absent radii (TAR syndrome) - radial aplasia or hypoplasia and thrombocytopenia. Bernard-Soulier syndrome (BSS).[] [top] Thrombotic Thrombocytopenic Purpura (TTP) and the VWF-Cleaving Protease (ADAMTS-13) Assay Thrombotic thrombocytopenic purpura (TTP) is caused by ultra-high molecular[] Acquired platelet dysfunction as a cause of bleeding diathesis: two case studies. Hematol Transfus Int J. 2017;4(1):31‒34.[]

  • Platelet-Type Bleeding Disorder 17

    GPS is an α-granule defect associated with the development of myelofibrosis and mild to moderate thrombocytopenia.[] This patient had long-term thrombocytopenia which had been initially misdiagnosed as idiopathic thrombocytopenic purpura (ITP).[] Splenectomy was followed by normalization of platelet count but the bleeding diathesis continued.[]

  • Platelet Storage Pool Deficiency

    A new inherited thrombocytopenia the Paris-Trousseau syndrome associated with dysmegakaryopoiesis, giant platelet alpha granules, congenital abnormalities and mental retardation[] In myeloproliferative disorders, disseminated intravascular coagulation (DIC), following cardiopulmonary bypass, Thrombotic Thrombocytopenic Purpura (TTP), and Hemolytic Uremic[] Abstract Delta-granule platelet storage pool deficiency (δ-PSPD) is a poorly studied bleeding diathesis resulting from either decreased granule content or decreased average[]

Similar symptoms