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2008 ICD-9-CM Volume 1 Diagnosis Codes Home > Diseases Of The Blood And Blood-Forming Organs 280-289 > ICD-9-CM Diagnosis 287 Purpura and other hemorrhagic conditions 287 is a non-specific code that cannot be used to specify a diagnosis ICD-9-CM Diagnosis 287.0 Allergic purpura A form of nonthrombocytopenic purpura due to a hypersensitivity vasculitis associated with a variety of clinical symptoms including urticaria and erythema, arthropathy and arthritis, gastrointestinal symptoms, and renal involvement. Heterogeneous group of disorders characterized by a vasculitic syndrome presumed to be associated with a hypersensitivity reaction following exposure to an antigen such as an infectious agent, a drug, or other foreign or endogenous substance (Wilson et al, Harrison's Principles of Internal Medicine, 12th ed, p1459). 287.0 is a specific code that can be used to specify a diagnosis 287.0 contains 36 index entries ICD-9-CM Diagnosis 287.1 Qualitative platelet defects A congenital bleeding disorder with prolonged bleeding time, absence of aggregation of platelets in response to most agents, especially ADP, and impaired or absent clot retraction. Platelet membranes are deficient in or have a defect in the glycoprotein IIb-IIIa complex (PLATELET GLYCOPROTEIN GPIIB-IIIA COMPLEX). A familial coagulation disorder characterized by a prolonged bleeding time, unusually large platelets, and impaired prothrombin consumption. Disorders caused by abnormalities in platelet count or function. 287.1 is a specific code that can be used to specify a diagnosis 287.1 contains 16 index entries ICD-9-CM Diagnosis 287.2 Other nonthrombocytopenic purpuras Purplish or brownish red discoloration, easily visible through the epidermis, caused by hemorrhage into the tissues. 287.2 is a specific code that can be used to specify a diagnosis 287.2 contains 22 index entries ICD-9-CM Diagnosis 287.3 Primary thrombocytopenia 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. 287.3 is a non-specific code that cannot be used to specify a diagnosis ICD-9-CM Diagnosis 287.30 Primary thrombocytopenia, unspecified 287.30 is a specific code that can be used to specify a diagnosis 287.30 contains 10 index entries ICD-9-CM Diagnosis 287.31 Immune thrombocyopenic purpura 287.31 is a specific code that can be used to specify a diagnosis 287.31 contains 7 index entries ICD-9-CM Diagnosis 287.32 Evans' syndrome 287.32 is a specific code that can be used to specify a diagnosis 287.32 contains 3 index entries ICD-9-CM Diagnosis 287.33 Congenital and hereditary thrombocytopenic purpura 287.33 is a specific code that can be used to specify a diagnosis 287.33 contains 6 index entries ICD-9-CM Diagnosis 287.39 Other primary thrombocytopenia 287.39 is a specific code that can be used to specify a diagnosis 287.39 contains 17 index entries ICD-9-CM Diagnosis 287.4 Secondary thrombocytopenia 287.4 is a specific code that can be used to specify a diagnosis 287.4 contains 7 index entries ICD-9-CM Diagnosis 287.5 Thrombocytopenia unspecified A condition in which there is an abnormally small number of platelets in the circulating blood. A decrease in the number of blood platelets. A decrease in the number of platelets in the blood that may result in easy bruising and excessive bleeding from wounds or bleeding in mucous membranes and other tissues. 287.5 is a specific code that can be used to specify a diagnosis 287.5 contains 7 index entries ICD-9-CM Diagnosis 287.8 Other specified hemorrhagic conditions Group of hemorrhagic disorders in which the von Willebrand factor (Factor VIII-related antigen) is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion. The susceptibility of CAPILLARIES, under conditions of increased stress, to leakage. 287.8 is a specific code that can be used to specify a diagnosis 287.8 contains 12 index entries ICD-9-CM Diagnosis 287.9 Unspecified hemorrhagic conditions Spontaneous or near spontaneous bleeding caused by a defect in clotting mechanisms (BLOOD COAGULATION DISORDERS) or another abnormality causing a structural flaw in the blood vessels (VASCULAR HEMOSTATIC DISORDERS). 287.9 is a specific code that can be used to specify a diagnosis 287.9 contains 7 index entries