Purpura and other hemorrhagic conditions (D69)
ICD-10 Index
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50–D89)
Coagulation defects, purpura and other hemorrhagic conditions (D65-D69)
- D69 - Purpura and other hemorrhagic conditions NON-BILLABLE CODE
- D69.0 - Allergic purpura BILLABLE CODE
- D69.1 - Qualitative platelet defects BILLABLE CODE
- D69.2 - Other nonthrombocytopenic purpura BILLABLE CODE
- D69.3 - Immune thrombocytopenic purpura BILLABLE CODE
- D69.4 - Other primary thrombocytopenia NON-BILLABLE CODE
- D69.41 - Evans syndrome BILLABLE CODE
- D69.42 - Congenital and hereditary thrombocytopenia purpura BILLABLE CODE
- D69.49 - Other primary thrombocytopenia BILLABLE CODE
- D69.5 - Secondary thrombocytopenia NON-BILLABLE CODE
- D69.51 - Posttransfusion purpura BILLABLE CODE
- D69.59 - Other secondary thrombocytopenia BILLABLE CODE
- D69.6 - Thrombocytopenia, unspecified BILLABLE CODE
- D69.8 - Other specified hemorrhagic conditions BILLABLE CODE
- D69.9 - Hemorrhagic condition, unspecified BILLABLE CODE
Purpura and other hemorrhagic conditions (D69)
Clinical Information for Purpura and other hemorrhagic conditions (D69)
Jacobsen Distal 11q Deletion Syndrome - A clinically recognized congenital malformation condition caused by a distal 11q deletion. The features of the syndrome are growth retardation, psychomotor retardation, trigonocephaly, divergent intermittent strabismus, epicanthus, telecanthus, broad nasal bridge, short nose with anteverted nostrils, carp-shaped upper lip, retrognathia, low-set dysmorphic ears, bilateral camptodactyly, and hammertoes. Platelet dysfunction is a feature in Paris-Trousseau type thrombocytopenia.
Kasabach-Merritt Syndrome - Rapidly growing vascular lesion along the midline axis of the neck, upper trunk, and extremities that is characterized by CONSUMPTION COAGULOPATHY; THROMBOCYTOPENIA; and HEMOLYTIC ANEMIA. It is often associated with infantile Kaposiform HEMANGIOENDOTHELIOMA and other vascular tumors such as tufted ANGIOMA.
Purpura, Thrombocytopenic, Idiopathic - Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases IMMUNOGLOBULIN G autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute (affecting children) and chronic (adult) forms.
Thrombocytopenia - A subnormal level of BLOOD PLATELETS.
Thrombocytopenia, Neonatal Alloimmune - A condition in newborns caused by immunity of the mother to PLATELET ALLOANTIGENS on the fetal platelets. The PLATELETS, coated with maternal ANTIBODIES, are destroyed and removed by the fetal MONONUCLEAR PHAGOCYTE SYSTEM. Affected infants may have INTRACRANIAL HEMORRHAGES.
Murexide - 5,5'-Nitrilodibarbituric acid ammonium derivative. Used as an indicator for complexometric titrations.
Purpura - Purplish or brownish red discoloration, easily visible through the epidermis, caused by hemorrhage into the tissues. When the size of the discolorization is >2-3 cm it is generally called Ecchymoses (ECCHYMOSIS).
Purpura Fulminans - A severe, rapidly fatal reaction occurring most commonly in children following an infectious illness. It is characterized by large, rapidly spreading skin hemorrhages, fever, or shock. Purpura fulminans often accompanies or is triggered by DISSEMINATED INTRAVASCULAR COAGULATION.
Purpura, Hyperglobulinemic - Purplish or brownish red discoloration of the skin associated with increase in circulating polyclonal globulins, usually GAMMA-GLOBULINS. This syndrome often occurs on the legs of women aged 20 to 40 years.
Purpura, Thrombocytopenic - Any form of purpura in which the PLATELET COUNT is decreased. Many forms are thought to be caused by immunological mechanisms.
Purpura, Thrombocytopenic, Idiopathic - Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases IMMUNOGLOBULIN G autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute (affecting children) and chronic (adult) forms.
Purpura, Thrombotic Thrombocytopenic - An acquired, congenital, or familial disorder caused by PLATELET AGGREGATION with THROMBOSIS in terminal arterioles and capillaries. Clinical features include THROMBOCYTOPENIA; HEMOLYTIC ANEMIA; AZOTEMIA; FEVER; and thrombotic microangiopathy. The classical form also includes neurological symptoms and end-organ damage, such as RENAL FAILURE. Mutations in the ADAMTS13 PROTEIN gene have been identified in familial cases.
Transfusion Reaction - Complications of BLOOD TRANSFUSION. Included adverse reactions are common allergic and febrile reactions; hemolytic (delayed and acute) reactions; and other non-hemolytic adverse reactions such as infections and adverse immune reactions related to immunocompatibility.
Waterhouse-Friderichsen Syndrome - A condition of HEMORRHAGE and NECROSIS of the ADRENAL GLAND. It is characterized by rapidly developing ADRENAL INSUFFICIENCY; HYPOTENSION; and widespread cutaneous PURPURA.
Gray Platelet Syndrome - A rare, inherited platelet disorder characterized by a selective deficiency in the number and contents of platelet alpha-granules. It is associated with THROMBOCYTOPENIA, enlarged platelets, and prolonged bleeding time.
Thrombocytopenia - A subnormal level of BLOOD PLATELETS.
Blood Platelets - Non-nucleated disk-shaped cells formed in the megakaryocyte and found in the blood of all mammals. They are mainly involved in blood coagulation.
Ecchymosis - Extravasation of blood into the skin, resulting in a nonelevated, rounded or irregular, blue or purplish patch, larger than a petechia.
Disseminated Intravascular Coagulation - A disorder characterized by procoagulant substances entering the general circulation causing a systemic thrombotic process. The activation of the clotting mechanism may arise from any of a number of disorders. A majority of the patients manifest skin lesions, sometimes leading to PURPURA FULMINANS.
gamma-Globulins - Serum globulins that migrate to the gamma region (most positively charged) upon ELECTROPHORESIS. At one time, gamma-globulins came to be used as a synonym for immunoglobulins since most immunoglobulins are gamma globulins and conversely most gamma globulins are immunoglobulins. But since some immunoglobulins exhibit an alpha or beta electrophoretic mobility, that usage is in decline.
Platelet Count - The number of PLATELETS per unit volume in a sample of venous BLOOD.
Blood Transfusion - The introduction of whole blood or blood component directly into the blood stream. (Dorland, 27th ed)
