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Idiopathic thrombocytopenic purpura, also known as primary or immune thrombocytopenic purpura, is characterized by peripheral blood thrombocytopenia and bone marrow megakaryocyte maturation disorders, and the clinical manifestations are:
1. Acute type, common in children, no gender difference, mostly 2-6 years old, often with a history of viral infection in the upper respiratory tract or other parts 1-3 weeks before the onset of the disease; Sudden onset. There may be stomach cold, fever, sudden occurrence of widespread and severe bleeding, manifested as a large number of petechiae and flaky ecchymosis, varying in size, unevenly distributed in the lower limbs, not high and **.
2.The chronic type, mostly 20-40, is 3-4 times more common in women than in men, with a slow onset and no obvious cause before the onset of the disease. With **, mucosal bleeding is more common, and it has the characteristics of reverse action, mainly manifested as **petechiae, ecchymosis, nosebleeds, and gingival bleeding.
Oral and tongue mucosal blood blisters, women often have menorrhagia as the main manifestation, the severity of the symptoms is related to the number of platelets, severe cases can occur visceral bleeding, Western medicine ** program, hormones, C globulin [immunoglobulin], immunosuppressants, transfusion of component platelets, spleen cutting, all over the country is the same, generally can play a certain role in alleviating the condition, but can not achieve the root cause, and the long-term use of hormones and immunosuppressants is very important to the body, with the reduction or discontinuation of the drug, Platelets will still fall; C-ball can only be maintained for about a week to half a month, and some patients are only effective for a few days, and platelets will still decline when the drug is stopped; Multiple transfusions of component platelets are not recommended as they allow platelets to produce antibodies on their own, which accelerates the destruction of platelets.
It is recommended that the patient's condition be combined with the fundamental conditioning of Chinese herbal medicine, and the use of traditional Chinese medicine DBT immunity**, which can completely ** the disease, no longer recurring, and will not be contagious.
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The main symptoms of thrombocytopenia are: first, bleeding from the nose, mouth, gums and other parts; blood spots on the body; The slightest touch can cause bruising on the body; **Prolonged bleeding in the presence of trauma; There is blood in the stool (usually caused by internal bleeding), accompanied by abdominal pain and headache; Long-term bleeding will inevitably lead to dull yellow, malaise, etc. The most common and typical symptoms of thrombocytopenia are purpura, bleeding gums, and thrombocytopenia.
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Hello; A general term for purpura** and color changes after mucosal hemorrhage. The clinical manifestations are hemorrhagic spots, purpura and ecchymosis, which are generally not high above the skin surface, and can only be slightly raised in the case of Henoch-Schonlein purpura, which is purple-red at first, and does not fade under pressure, and then gradually becomes lighter, and then turns yellow and fades in about two weeks.
Henoch-Schonlein purpura can lead to Henoch-Schonlein purpura nephritis if not timely, and may be life-threatening if not timely.
Platelets mainly play hemostatic coagulation function, low platelets will have the possibility of spontaneous bleeding, mild is subcutaneous bleeding, that is, **purpura, or gum bleeding, nosebleed, serious visceral bleeding or intracranial hemorrhage, is life-threatening. The root cause of this disease is the defect of the body's immune mechanism, and the onset of the immune system is caused by the imbalance of the immune system, which is also known as immune thrombocytopenia in medicine. >>>More
The Department of Hematology of Ping'an Hospital Affiliated to Hebei Medical University is a national key clinical specialty of the Ministry of Health, with strong expert skills and rich clinical experience. If you need help from a hematologist or want to know more, you can consult with a hematologist for free** or call us at 400-0387-121.
In the course of diagnosis, it should be distinguished from aplastic anemia, acute leukemia, Henoch-Schonlein purpura, Wiskortt-Aldrich syndrome, Evans syndrome, thrombotic thrombocytopenic purpura, secondary thrombocytopenic purpura. According to the specific clinical symptoms, find out the best in order to treat the symptoms, otherwise the condition will be delayed. >>>More
Idiopathic thrombocytopenic purpura is the most common bleeding disorder in children, characterized by spontaneous bleeding, and most children have a history of viral infection about 3 weeks before the onset of the disease. >>>More
The number of normal platelets in the blood is 300,000 cubic millimeters, which can be reduced to 45,000 when sick, and when the number of platelets drops to 20,000, patients may have gastrointestinal bleeding, intracranial hemorrhage, hematuria, etc., which is life-threatening. The typical symptoms of thrombocytopenia are bleeding, in the early stage of the disease, there will be pinprick red spots, and then it will develop into lumpy thrombocytopenic purpura, purpura varies in size, small as soybean grains, large can reach the size of the palm. The location of thrombocytopenic purpura is generally in the most relaxed parts of the body, such as the neck, around the eyes, lower limbs, etc., and is accompanied by swelling and pain, and in severe cases, purple spots will appear in the oral mucosa. >>>More