It is not associated with Henoch Schonlein purpura or thrombocytopenic purpura

It is best to go to the hospital to check if it is allergic, if it is. Be sure to find the allergen. That way you don't have to worry.

It is recommended to go to the hospital for a blood routine and urine test, and find a doctor to look at the patient's symptoms. z

Purpura is the most common clinical manifestation of a bleeding disorder, and the presence of purpura suggests the following: Vonillary purpura. It is common due to damage to the blood vessel wall or increased fragility and permeability, and is common in immunological (eg, Henoch-Schonlein purpura), infectious (eg, sepsis), vascular structural abnormalities (eg, hereditary hemorrhagic telangiectasia), and other (eg, dysproteinemia, simple or senile purpura).

Examination is unabnormal except for a possibly positive bundle arm test. Thrombocytoplasmic purpura. The most common, most of them are due to thrombocytopenia, hyperplasia, and dysfunction, and if there is purpura or blood blisters on the buccal mucosa of the mouth, it often indicates severe bleeding and should be treated aggressively.

Coagulation mechanism disorders, including coagulation factor deficiency, circulating anticoagulant substances or hyperfibrinolysis, generally speaking, bleeding caused by coagulation mechanism disorders, mainly manifested as hemarthrosis, muscle hematoma and visceral hemorrhage, less manifested **purpura, only sometimes manifested as large ecchymosis, and the examination of coagulation has obvious abnormalities, so that it can be distinguished from vascular purpura and purpura caused by platelet abnormalities. Purpura varies from one to the other.

Have you had your blood routine checked? Is it abnormal ?

Hello, this disease is an immune syndrome, is a common bleeding disorder, characterized by the presence of antiplatelet antibodies in the blood circulation, so that platelets are destroyed too much, causing purpura; In contrast, megakaryocytes in the bone marrow are normal or increased, but they are impaired during maturation and lead to a decrease in platelet production.

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.

It is necessary to go to an authoritative hematology hospital and find an authoritative expert to diagnose and treat this disease.

Idiopathic thrombocytopenic purpura is a type of bleeding disorder that is also known as autoimmune thrombocytopenic purpura because of no obvious exogenous **, but most of them are due to increased platelet destruction caused by the immune response. What is the platelet value? Have you ever done a bone piercing?

The combination of traditional Chinese medicine and Western medicine mainly uses traditional Chinese medicine to regulate**, and the effect is good. You can find out.

Thrombocytopenic purpura is a hematologic bleeding disorder, mainly due to immune-mediated excessive destruction of platelets, characterized by extensive ** mucosal and visceral hemorrhage, thrombocytopenia, impaired maturation of megakaryocytes in the bone marrow, shortened platelet survival time and the emergence of platelet membrane glycoprotein-specific autoantibodies. Thrombocytopenic purpura is clinically divided into acute type and chronic type, the acute type is more common in children, and the chronic type is more common in adults.

Not necessarily.

Recurrent **purpuraIn addition to simple purpura, thrombocytopenia, capillary lesions, and coagulation disorders should be thought of, and a comprehensive examination must be done in the hematology department.

Capillary damage: Blood leaks from the capillaries under the skin and causes purpura, most commonly Henoch-Schonlein purpura, which can be caused by taking certain drugs, foods, or inhaling certain substances. This purpura distribution is often characterized by bilateral symmetry.

Coagulation disorders: There are more than 10 kinds of coagulation factors in the human body, and any deficiency of any factor can cause bleeding.

Thrombocytopenic purpura: These people have lower than normal platelets in their blood. It is more common in idiopathic thrombocytopenic purpura paralysis, aplastic anemia (dysfunction of platelet production in the bone marrow), leukemia (the bone marrow is congested by leukemic cells, affecting platelet production), taking certain drugs, severe infection, and hypersplenism caused by splenomegaly.

**Thrombocytopenic purpura, there is no good method in Western medicine, mainly hormones and blood transfusion**, and long-term medication will also bring huge pain and health risks to patients, and traditional Chinese medicine nourishing blood and spleen decoction is based on ** syndrome differentiation treatment, avoiding forced blood replenishment, but also avoiding hormone ** harm to the body, the effect is very significant.

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