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Immune thrombocytopenic purpura in Adult
Other Resources UpToDate PubMed

Immune thrombocytopenic purpura in Adult

Contributors: Edward Li PhD, Eric Ingerowski MD, FAAP, Susan Burgin MD
Other Resources UpToDate PubMed

Synopsis

Immune thrombocytopenic purpura (ITP), also known as idiopathic thrombocytopenic purpura, is an acquired autoimmune disease characterized by an isolated decrease in platelet counts in the absence of bone marrow abnormalities and other identifiable causes of low platelet counts. ITP patients have circulating antibodies directed against platelet surface proteins that lead to platelet destruction, primarily by the reticuloendothelial system of the spleen. Signs and symptoms vary according to the patient's platelet levels. Patients with platelet counts between 30 000 and 50 000 usually present with easy bruising. Patients with platelet counts between 10 000 to 20 000 can have significant petechiae, purpura, or ecchymoses on the skin and mucosal surfaces. Female patients may experience menorrhagia. In cases of extremely low platelet counts, severe fatal bleeding complications, including intracranial hemorrhage and gastrointestinal bleeds, can occur.

The pathogenesis of ITP is not completely understood but is generally attributed to the autoimmune production of antibodies against platelet surface antigens, in particular to glycoprotein (GP) IIb/IIIa. Antibody-coated platelets have reduced lifespans due to increased clearance by the reticuloendothelial system.

The trigger for ITP is not well established and seems to have both genetic and environmental contributions. Although usually idiopathic, ITP can be triggered by viral infections (eg, HIV, cytomegalovirus [CMV], hepatitis C virus [HCV], varicella zoster virus [VZV]), systemic autoimmune diseases (eg, systemic lupus erythematosus), and lymphoproliferative disorders. It is important to exclude other causes of thrombocytopenia that have similar clinical presentations as ITP but significantly different management strategies. Secondary thrombocytopenia may be drug-induced, alcohol-related, or caused by chronic liver disease with associated hypersplenism.

ITP may be classified as acute or chronic, based on the duration of disease. The acute form lasts less than 6 months and is generally more common in children, in whom it tends to be a self-limiting disease. The chronic form lasts longer than 6 months, is more commonly seen in adults, and often requires medical treatment. ITP has been estimated to have a prevalence of 8 in 100 000 in children and 12 in 100 000 in adults, due to the often chronic nature of the disease in adults. While ITP has been reported to have a higher incidence in young women, the incidence is the same between men and women later in life. ITP in children is clinically distinct from ITP in adults.

Codes

ICD10CM:
D69.3 – Immune thrombocytopenic purpura

SNOMEDCT:
32273002 – Idiopathic thrombocytopenic purpura

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Therapy

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Drug Reaction Data

Below is a list of drugs with literature evidence indicating an adverse association with this diagnosis. The list is continually updated through ongoing research and new medication approvals. Click on Citations to sort by number of citations or click on Medication to sort the medications alphabetically.

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References

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Last Reviewed:07/23/2020
Last Updated:07/31/2020
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Immune thrombocytopenic purpura in Adult
Immune thrombocytopenic purpura : Easy bruising, Ecchymosis, Gingival bleeding, PLT decreased
Clinical image of Immune thrombocytopenic purpura
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