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Thrombocytopenic Purpura
Author(s) -
Flessa Herberct C.
Publication year - 1995
Publication title -
academic emergency medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.221
H-Index - 124
eISSN - 1553-2712
pISSN - 1069-6563
DOI - 10.1111/j.1553-2712.1995.tb03266.x
Subject(s) - medicine , citation , family medicine , library science , computer science
Thrombocytopenic purpura (idiopathic thrombocytopenic purpura, Verlgofa disease) and hemophilia (A, B, C) belong to the group of hemorrhagic diseases and syndromes (hemorrhagic diathesis), a common feature of which is the manifestation of bleeding from the lungs "visual" form to fatal bleeding who require immediate action. Hemorrhagic diathesis clinical conditions when diagnosed symptoms associated with the release of blood vessels: bleeding in the skin, mucous membranes, joints, tissues, profuse bleeding that is not the result of random (aggressive) traumatic surgery. Classification: Hemorrhagic diathesis: 1. Thrombocytopenia and Thrombocytopathy (amegakariocytic): A. Thrombocytopenia (TP) I. Reduced produced: Innate Acquired (hypo, aplasia of bone marrow, myelotoxic drug / chemical / viral infections, cancers, radiation effects) II. Enhanced degradation (megakariocytic): Immune (autho-, allo-, medication), formerly known as: idiopathic TC disease Verlgofa; Microangiopathic (TTP thrombotic thrombocytopenic purpura, hemolytic uremic syndrome, disseminated intravascular coagulation); Other (infection, massive transfusion). III. Redistributive: In splenomegaly In syndrome of "hypersplenism" IV. Psudotrombocytopenic: In hemodilution "platelet satelizm"