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・ Idiopathic hypersomnia
・ Idiopathic hypoglycemia
・ Idiopathic infantile arterial calcification
・ Idiopathic interstitial pneumonia
・ Idiopathic intracranial hypertension
・ Idiopathic orbital inflammatory disease
・ Idiopathic osteosclerosis
・ Idiopathic pneumonia syndrome
・ Idiopathic postprandial syndrome
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・ Idiopathic pulmonary haemosiderosis
・ Idiopathic pure sudomotor failure
・ Idiopathic sclerosing mesenteritis
・ Idiopathic scrotal calcinosis
・ Idiopathic short stature
Idiopathic thrombocytopenic purpura
・ Idiopathy
・ Idiophantis
・ Idiophantis acanthopa
・ Idiophantis anisosticta
・ Idiophantis callicarpa
・ Idiophantis carpotoma
・ Idiophantis chalcura
・ Idiophantis chiridota
・ Idiophantis croconota
・ Idiophantis discura
・ Idiophantis disparata
・ Idiophantis eugeniae
・ Idiophantis habrias
・ Idiophantis hemiphaea


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Idiopathic thrombocytopenic purpura : ウィキペディア英語版
Idiopathic thrombocytopenic purpura

Idiopathic thrombocytopenic purpura (ITP), also known as primary immune thrombocytopenia, primary immune thrombocytopenic purpura or autoimmune thrombocytopenic purpura, is defined as isolated low platelet count (thrombocytopenia) with normal bone marrow and the absence of other causes of thrombocytopenia. It causes a characteristic purpuric rash and an increased tendency to bleed. Two distinct clinical syndromes manifest as an acute condition in children and a chronic condition in adults. The acute form often follows an infection and has a spontaneous resolution within 2 months. Chronic idiopathic thrombocytopenic purpura persists longer than 6 months with a specific cause being unknown.
ITP is an autoimmune disease with antibodies detectable against several platelet surface antigens.
ITP is diagnosed by a low platelet count in a complete blood count (a common blood test). However, since the diagnosis depends on the exclusion of other causes of a low platelet count, additional investigations (such as a bone marrow biopsy) may be necessary in some cases.
In mild cases, only careful observation may be required but very low counts or significant bleeding may prompt treatment with corticosteroids, intravenous immunoglobulin, anti-D immunoglobulin, or immunosuppressive drugs. ''Refractory ITP'' (not responsive to conventional treatment) may require splenectomy, the surgical removal of the spleen. Platelet transfusions may be used in severe bleeding together with a very low count. Sometimes the body may compensate by making abnormally large platelets.
==Signs and symptoms==
Signs include the spontaneous formation of bruises (purpura) and petechiae (tiny bruises), especially on the extremities, bleeding from the nostrils and/or gums, and menorrhagia (excessive menstrual bleeding), any of which may occur if the platelet count is below 20,000 per μl. A very low count (<10,000 per μl) may result in the spontaneous formation of hematomas (blood masses) in the mouth or on other mucous membranes. Bleeding time from minor lacerations or abrasions is usually prolonged.
Serious and possibly fatal complications due to extremely low counts (<5,000 per μl) include subarachnoid or intracerebral hemorrhage (bleeding inside the skull or brain), lower gastrointestinal bleeding or other internal bleeding. An ITP patient with an extremely low count is vulnerable to internal bleeding caused by blunt abdominal trauma, as might be experienced in a motor vehicle crash. These complications are not likely when the platelet count is above 20,000 per μl.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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