Is Henoch Scholastic purpura serious? 20

Purpura is a general term for the color change after mucosal bleeding, the clinical manifestations are hemorrhagic spots, purpura and ecchymosis, it has vascular purpura, thrombocytopenic purpura, coagulation mechanism disorder purpura three points, among them, henoch-Schonlein purpura belongs to a kind of vascular purpura, which begins to be purple-red, does not fade under pressure, gradually becomes lighter after healing, and turns yellow in about two weeks and subsides mainly on bed rest.

Purpura: Mostly caused by thrombocytopenia or drug allergies. The symptoms are internal bleeding such as **, mucous membranes, etc., and purple scars on **.

In Henoch-Schonlein purpura, the allergen should first be identified, and the determination of the allergen is conducive to targeting**.

For Henoch-Schonlein purpura, you can take Angelica pills. Angelica pills, which have the effect of enhancing immunity, are clinically used for various anemias, allergic purpura and other people with blood deficiency and qi weakness.

**: One is a decrease in immunity, and the other is immune dysfunction, these two reasons cause the body to be in an allergic constitution, so there are symptoms.

Henoch-Schonlein purpura, which is a self-healing disease, will only be intervened with medication if necessary, generally when there are more bleeding spots, ecchymosis, urine routine urine protein, or other clinical symptoms, such as dyspnea, etc., need to seek medical attention.

If there are only 3-4 sporadic bleeding points in both lower limbs, it means that it is not very serious, and at this time, there are two ways to regulate the body's immunity and immune function. One is self-discipline, version of the diet rules, work and rest rules, etc.; The other is to relax and not get stuck in a depressing environment; If there are still more bleeding spots, it is recommended to routine**, VC+rutin tablets, and do not use hormones as much as possible. Traditional Chinese medicine can also regulate the internal organs and alleviate them, mainly to improve the dialectical idea of allergic constitution.

If you have any unclear rights, you can click the [official**] below to get help.

For diseases caused by broken capillaries, you can go to the hematology department.

Solemn warning: Henoch-Schonlein purpura is a blood system disease, do not treat it as a ** disease, nephritis treatment!

Many patients lack sufficient awareness of Henoch-Schonlein purpura, thinking that Henoch-Schonlein purpura is just an ordinary **inflammation, which will get better after taking some medicine, injection or infusion for a period of time, and some patients mistakenly regard Henoch-Schonlein purpura as nephritis**, and at the same time fall into the embarrassing situation of "the old disease is not cured, and the new disease is added". Here, experts remind patients that Henoch-Schonlein purpura is a typical hemorrhagic hemorrhagic blood system disease, if it is not properly regulated in time, it is easy to make the disease reversed, resulting in many complications and seriously threatening the life and health of patients.

There are three main reasons why Henoch-Schonlein purpura is difficult and easy:

The course of Henoch-Schonlein purpura is generally about 2 weeks, and the prognosis is good. If left untreated, a small number of patients will develop purpuric nephritis and nephrotic syndrome. In other words, it will not cause damage to the kidneys. Hope it helps.

The most serious thing is that it will penetrate into the kidneys, and the consequences are very serious.

Hello; Henoch-Schonlein purpura is a common disease in children, which is related to parasite allergies in children, and some are also caused by drugs and food. The main symptoms are abdominal pain, purpura of the lower limbs, and it is easy to misdiagnose appendicitis. In severe cases, bloody stools may occur.

A complication of this disease is purpuric nephritis. So don't be careless!

**The most important drugs are hormones, such as prednisone, dexamethasone, etc., combined with anti-allergic drugs such as chlorpheniramine, phenagen, etc.**, and the symptomatic drugs are hyoscyamine (654-2), which is mainly to relieve the symptoms of abdominal pain.

Generally, after regular**, it can be completely relieved in 1-2 weeks, but some are easy**, and it needs to be maintained** for a period of time before it is completely cured.

After getting better, it is recommended to do a deworming**, and the anti-troubles will stop again**take it badly! Liquid sensitizers.

Hope mine helps you!

1.Have allergies or have more certain allergens. 2.

There are the following clinical manifestations: (1) Prodromal symptoms: 1-3 weeks before the onset of purpura, symptoms such as low-grade fever, upper respiratory tract infection and general malaise.

2) Typical ** purpura and corresponding skin lesions. (3) During the course of the disease, there may be abdominal pain or joint or kidney involvement. 3.

Platelet count, platelet function and coagulation time were normal, and capillary fragility test was positive. 4.Histological examination:

A homogeneous allergic vasculitis may be seen in the affected area** or tissue, with a large number of leukocyte infiltrates in the retrocapillary venules, fibrous necrosis and red blood cell exudation, active necrosis of the vessel wall, and epithelial cell proliferation. 5.Other diseases caused by vasculitis, cryoglobulin syndrome, benign hyperglobulin purpura, annular telangiectasia purpura, pigmented purpura lichenoid dermatitis, etc.

Specifically, you can also go to the China Medical Service Network to have a look, which will have more detailed answers.

Hello, most patients with Henoch-Schonlein purpura have prodromal symptoms such as general malaise, low-grade fever, fatigue and upper respiratory tract infection 1-2 weeks before the onset of the disease, followed by typical clinical manifestations. According to its different symptoms and signs, it can be divided into the following types:

Simplex: The most common type. The main manifestation is **purpura.

Purpura varies in size and can coalesce into patches to form ecchymosis. Purpura is mainly confined to the limbs, especially the lower limbs and buttocks, and rarely occurs on the trunk, which can be accompanied by **edema and urticaria at the same time, and gradually subsides after 7-14 days.

Abdominal type: In addition to **purpura, a series of gastrointestinal symptoms and signs (about 2 3 patients occur) are affected due to the involvement of the mucosa of the digestive tract and the capillaries of the peritoneal visceral layer, such as: nausea, vomiting, hematemesis, diarrhea, mucus stool, blood in the stool, etc.

Among them, abdominal pain is the most common, often paroxysmal colic, mostly located in the periumbilical, lower abdomen or whole abdomen, and the onset can be misdiagnosed as a surgical acute abdomen due to abdominal muscle tension and obvious tenderness, and hyperintestinal sounds. In young children, intussusception can be caused by intestinal wall edema and increased peristalsis. Abdominal symptoms and signs often appear at the same time as **purpura, and occasionally occur before purpura.

Articular type: In addition to ** purpura, joint swelling, pain, tenderness and dysfunction occur due to the involvement of blood vessels in the joint (about 1 2 patients have joint symptoms), which mostly occur in large joints such as knees, ankles, wrists, elbows, etc., and the joint swelling is generally mild, migratory, and reversed, and heals after a few days, leaving no joint deformity.

Renal type: the most severe, occurring in up to 12% to 40% of patients. In addition to **purpura, hematuria, proteinuria, and casturia occur due to glomerular capillary inflammation.

Renal symptoms may occur at any stage of the disease, but are more than a week after purpura. It is generally believed that the earlier the urine changes, the more severe the nephritis, and a small number of cases have evolved into chronic nephritis (hematuria, proteinuria, edema, hypertension), nephrotic syndrome (urine protein, hypoplasma albuminemia <30g l, edema, elevated blood lipids), and even renal failure, and these kidney damage caused by Henoch-Schonlein purpura is called Henoch-Schonlein purpura nephritis.

Mixed type: In addition to **purpura, two or more types of the other three types exist.

Others: In addition to the above common types, a small number of patients with this disease can also have optic nerve atrophy, iritis, retinal hemorrhage and edema, and symptoms and signs related to the central nervous system due to lesions involving the eyes, brain and meningeal blood vessels. You need to go to an authoritative hospital for treatment, and there is generally no problem with the diagnosis.