Pure red aplastic anemia How many people worldwide get this disease

In pure red blood cell aplastic anemia, you should eat more foods that strengthen the spleen and kidney, such as yam, yam, barley, white lentils, etc., all of which have the above curative effects. In addition, patients also need to avoid physical exertion in daily life and not exercise excessively, otherwise the body's oxygen consumption will increase, which will lead to the appearance of anemia and then the adverse reactions of the body. If you need to consult about aplastic conditions or medication guidance, you can click [Official**] below for help.

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 400-0387-185.

Aplastic anemia is a very complex condition that is divided into acute and chronic aplastic disorders based on presentation. In the acute attack stage, the main manifestations of the patient are bleeding and infection, and the course of the disease develops rapidly, without **, which will lead to lesions in multiple organs. <

People who are prone to aplastic anemia:

1. Premature babies. If the mother herself has severe anemia, then the premature baby has a very high chance of developing aplastic anemia due to the imperfect development of various organs.

2. Patients with chronic diseases. When patients develop chronic liver and kidney disease, these can lead to endocrine dysfunction, which can lead to abnormalities in hematopoietic stem cells, which can eventually lead to aplastic anemia.

3. The elderly. With the growth of age, the elderly continue to decline in various organs, especially the decline of bone marrow hematopoietic function is the most obvious, coupled with poor diet and insufficient blood production factors, it is easy to develop aplastic anemia.

4. Women during pregnancy. Women have a strong physical consumption capacity after pregnancy, coupled with physiological changes, the increase in iron consumption in the body, and aplastic anemia is prone to occur. <>

Pathogenesis: 1. Bone marrow hematopoietic stem cells are damaged or reduced, which is equivalent to the inferior seeds used by farmers to grow crops, resulting in insufficient blood cell production;

2. The defect of the bone marrow hematopoietic microenvironment is equivalent to the infertile soil of farmers planting crops, which also affects the production of blood cells;

3. The immune system is disordered, and there is an increase in inhibitory lymphocytes, which is equivalent to the production of insect pests in crops, which aggravates the production of hematopoietic cells.

These three mechanisms lead to the simultaneous reduction of hematopoietic red blood cells, white blood cells, and platelets, which makes the patient's condition more serious, the difficulty increases, and many patients have poor results. <>

Decoration workers, people who use chloramphenicol, this kind of person may get this disease, the main reason is that this disease develops very quickly, and the process is more complicated, so it is difficult.

Babies who may be born prematurely and do not take proper nutritional measures after birth may cause anemia and should seek help from a doctor.

Some babies born early, as well as patients with some chronic diseases, some older people and women during childbirth, are prone to anemia, because their physical consumption capacity will become slow, and the organs are either incomplete or mentally declining, so it is not good**.

People who eat irregularly, are picky eaters, and lack of exercise are prone to this disease. Because there is currently no good way to treat this disease, it can only be alleviated through recuperation in life.

Leukemia is because once the best time for this disease is missed, there is no way to change it, because blood cells cannot make blood, so it is difficult.

For example, people who lack nutrients, and people who usually don't pay attention to their diet, eat very singlely, the probability of this disease is relatively low, and it is already at an advanced stage after it is discovered.

For example, people who often eat irregularly, as well as people with poor physical fitness, and then people with congenital anemia are also included, because this disease is a chronic disease, and there is no particularly good way.

First of all, aplastic anemia is caused by various physical and chemical factors, biological factors and immune factors, and its incidence is related to two peak age periods, which are 5 to 25 years old and 60 years old. Aplastic anemia is diagnosed with a combination of clinical manifestations, blood count, and bone marrow to determine the progression of the disease. It can mainly occur with hemoglobin less than 100 grams per liter, platelets less than 5*109 per liter, and neutrophil count less than per liter.

It is not difficult to diagnose aplastic anemia with these three points.

For this part of the patient, the bone marrow can have multi-site hypoplasia, two or more bone marrow puncture sites hypoplasia, and the hematopoietic cells of the three lineages are significantly reduced, so the drugs for this type of disease are differentiated from leukemia pH and myelodysplastic syndrome.

Hematopoietic stem cells are dysfunctional or the hematopoietic microenvironment does not provide effective hematopoietic factors due to the decrease in hematopoietic function, which is a benign disease. Hematopoietic aplastic anemia is a bone marrow failure disease with low hematopoietic function, so there will be severe leukopenia and anemia thrombocytopenia.

Aplastic anemia, referred to as aplasia, is a group of bone marrow hematopoietic failure syndromes caused by a variety of **, characterized by decreased bone marrow hematopoietic cell proliferation and peripheral blood pancytopenia, with anemia, bleeding and infection as the main clinical manifestations. Exactly** is not known, but the onset of aplastic may be related to chemical drugs, radiation, viral infections, and genetic factors. Aplastic disease is mainly seen in young adults, and there are two peaks in the incidence period, namely the age group of 15 to 25 years old and the elderly group over 60 years old.

The incidence is slightly higher in males than in females. According to the severity of bone marrow failure and the progression of the clinical course, it is divided into severe and non-major aplastic and acute and chronic aplasia.

Aplastic anemia is a common disease in hematology, which is mainly related to the following factors, the first may be related to family inheritance, the second may be related to gene mutations, the third may be related to the regular use of certain drugs, and the fourth may be related to exposure to certain rays or radiation. Patients with regenerative anemia generally present with a trilineage decrease, that is, a decrease in white blood cells, hemoglobin, and platelets.

Aplastic anemia is a primary bone marrow hematopoietic failure syndrome, and the main mechanism of the disease is immune abnormalities. Cyclosporine is an immunological drug, and the course of treatment is generally longer than one year, and the dose cannot be adjusted and reduced at will. After taking the drug, it once improved, and now the platelets have dropped to 50, I don't know whether there is bleeding, whether the red blood cells, white blood cells have decreased, if the single platelet is reduced, it should be rechecked again, and if necessary, the hospital should be admitted to find the cause.

Aplastic anemia is a bone marrow failure disease, which is manifested as a bone marrow hematopoietic disorder, mainly including a decrease in whole blood cells and peripheral blood. If there is dizziness, palpitation, fever, purpura, etc., the blood routine should be checked, and when the blood routine shows that the blood of all three lines is reduced, the problem of aplastic anemia should be considered. Trilineary anemia refers to a possible decrease in white blood cells, red blood cells, and platelets, and typical aplastic anemia refers to a decrease in blood trilineage.

If you have aplastic anemia, you should seek medical attention as soon as possible to avoid serious consequences.

Aplastic anemia is a refractory hematologic disease. Characterized by bone marrow hematopoietic failure. The clinical manifestations are pancytopenia, anemia, bleeding, infection and other symptoms.

Aplastic anemia is divided into major and non-major aplasia. Severe aplastic aplastic disease has an acute onset, severe disease, rapid progression, severe anemia, bleeding, infection and other symptoms, and bone marrow aspirate and bone marrow biopsy are generally required to confirm the diagnosis. Patients with severe aplastic disease may require a bone marrow transplant**, and immunosuppressants may be used**.

Aplastic anemia, a problem with the hematopoietic function of the bone marrow, has been found to be autoimmune-related. If the disease is confirmed, the bone marrow hematopoiesis, such as hematopoietic area and hematopoietic quality, should be confirmed by examination. For patients with mild aplastic anemia, there is a slight decrease in white blood cells, hemoglobin, and platelets, and some patients can present with acute severe aplastic anemia as the disease progresses, and the bone marrow can be completely exhausted in 1-2 weeks, and platelets, red blood cells, and white blood cells cannot be produced.

Chronic aplastic anemia requires oral immunological preparations, such as cyclosporine A, and acute severe aplastic anemia requires strong immune preparations, such as ATG, ALG immunoglobulin**, and some patients even require hematopoietic stem cell transplantation**.

According to your description, there are two main types of aplastic anemia: support and disease-specific goals, and the goal of support is to prevent complications related to cytopenias. In terms of target, for severe aplastic anemia and non-severe aplastic anemia, the main focus is cyclosporine combined with androgens.

Aplastic anemia is a group of bone marrow hematopoietic failure syndromes caused by a variety of **, characterized by decreased bone marrow hematopoietic cell proliferation and peripheral blood pancytopenia, with anemia, hemorrhage and infection as the main clinical manifestations. The exact cause of aplastic aplastic is unknown, and the onset of aplastic may be related to chemical drugs, radiation, viral infections, and genetic factors.

Aplastic anemia refers to the inhibition of the hematopoietic function of the bone marrow, resulting in decreased bone marrow hematopoiesis, resulting in intractable anemia or intractable thrombocytopenia in the child's peripheral blood. It is divided into acute aplastic anemia and chronic, and it is necessary to do bone puncture and bone marrow imaging analysis to identify whether it is acute or chronic.

There are two kinds of aplastic anemia, one is acute aplastic anemia, the other is chronic aplastic anemia, aplastic anemia eats immune preparations such as cyclosporine, etc., many patients can survive for a long time, and even a small number can not affect life expectancy, of course, aplastic anemia is sometimes through bone marrow transplantation, and a very small number of patients are able to do so.

Pediatric aplastic anemia is in remission in most patients after active treatment. Normally, if the hemoglobin concentration is less than 60g L, the patient can be transfused with red blood cells when there are obvious clinical symptoms, platelets can be transfused when the patient has obvious bleeding, and bacterial culture is required when there is infection and fever, and then the appropriate antibiotic is selected according to the culture results**.

Aplastic hyperhaemosaemia (referred to as aplastic aplasia) is a group of syndromes caused by a variety of causes of total red bone marrow volume reduction, hematopoietic failure, and pancytopenia.

The aplastic is a problem with blood regeneration, go to a big hospital in the top three**, the current medical technology is so high, it can be fully healed, you have to be confident, I wish you an early **!

Integrative medicine until the condition is stable. It may take a few months, or even half a year. Then, depending on your condition, your doctor will recommend that you stop taking western medications.

Pure Chinese medicine conditioning**. Consolidate for a while. **After not easy**.

If you want to use traditional Chinese medicine for conditioning, you can learn about traditional Chinese medicine Yuan**.

Hematopoietic dysfunction and inability to form reticulocytes.

Correct answer: B

Analysis: Aplastic anemia bone marrow hyperplasia is inhibited, and trilineage hematopoietic cell proliferation is reduced.

There is a stable period, and it is not easy to be thorough.

You have to go to the hospital, and you have to consult with the doctor who treats you.

Aplastic anemia, as the name suggests, we just know that the obstacle is a kind of anemia, the body has symptoms of anemia, and the hematopoietic substance has been blocked, which is the most popular way to say this obstructive anemia, for this disease, its course of treatment is relatively long, but it is not completely impossible, it needs to be actively carried out, go to the hospital for a detailed examination.

Aplastic anemia (

Aplasia), hematopoietic function.

The main manifestations of failure are:

Pancytopenia.

Hemoglobin, leukocytes, and platelets). Ecchymosis and bleeding gums are common.

Epistaxis. Poor resistance is susceptible to infection, fatigue, and palpitations. In layman's terms, it is the blood system.

of disease (AA or aplasia).

To alleviate symptoms, patients often need red blood cell transfusions, usually once every 1 to 2 weeks. Other commonly used methods are as follows:

1.Corticosteroids.

The drug of choice is corticosteroids, which may cause remission in some patients. For example, with prednisone, 40-60 mg daily; Androgenic steroids are also effective in some patients. **It must be sustained for a longer period of time, e.g. from a few months to half a year.

2.Immunosuppressant.

Antithymocyte globulin (ATG), cyclosporine A (CSA), and intravenous gamma globulin are described in Aplastic Disease**.

3.Thymectomy.

Surgical excision is done when enlargement of the thymus gland is found. The purpose of resection is to accurately diagnose malignant changes and to promote bone marrow hematopoiesis. Fifty-six cases of pure red aplasia were reported, of which 25 were thymectomy and 16 were ineffective.

In addition, 5 cases of thymus X-ray irradiation were ineffective. If there is no thymic enlargement and no thymoma, resection is ineffective.

4.Plasmapheresis.

Removal of immunosuppressants from plasma.

5.Erythropoietin.

The effect on the disease is not ideal.

6.Splenectomy.

About 14% of patients respond.