Who introduced aplastic anemia and what is the best place to watch?

The reference criteria for patients with hematology to choose a specialized hematology hospital are as follows: First of all, the hospital should have a considerable number of hematology beds and the number of permanent patients. Secondly, the reputation in the industry and the excellent team of hematology experts.

There is no doubt that excellent hematologists have a high level of academic and academic communication in the industry. Finally, the advanced facilities for clinical examination of hematology are also one of the conditions for choosing a hospital. At present, the diagnosis and diagnosis of blood diseases have a strong dependence on laboratory tests, and many blood diseases cannot make an effective diagnosis from the symptoms and signs.

In short, we should start from three aspects: the scale of the specialty, the reputation of the department and the expert team, and the guarantee of good experimental equipment. Especially in terms of blood diseases in traditional Chinese medicine, there have been mixed phenomena in blood diseases in traditional Chinese medicine in recent years, and many small hospitals are also blinding the majority of blood disease patients under the banner of blood diseases in traditional Chinese medicine. (Dr. Liu Qingchi solemnly reminds:

Hello, aplastic anemia is a group of syndromes caused by a variety of ** bone marrow dysfunction, with pancytopenia as the main manifestation. The annual incidence rate in China is about 10,000. Exactly** is not known, but the onset of aplastic is known to be related to chemical drugs, radiation, viral infection, and genetic factors.

There are three main theories of pathogenesis, namely stem cell damage, hematopoietic microenvironment defects, and immune dysfunction. Aplastic is divided into congenital and acquired, and the latter is divided into primary aplastic of unknown origin and secondary aplastic aplastic for which the cause can be identified. It is recommended to take a look at CCTV-4 "Chinese Medicine" to defeat the blood killer.

Western medicine is Tianjin Blood Disease Clinic, but Western medicine can only be temporary. If the symptoms are not cured, they will still recur after being discontinued, and the fundamental problem will not be solved. It is recommended to combine Chinese herbal medicines**.

Fundamentally**. But a good plan is important. If there is no way to do it in other hospitals.

If you come directly to Beijing, you can avoid a lot of detours.

Patients mainly present with progressively worsening anemia, infection, and hemorrhage, which can be divided into severe and non-severe according to the severity of the disease and the speed of onset.

Patients with aplastic aplastic may develop suddenly or slowly over a longer period of time.

Typical symptoms. Major aplastic anemia is characterized by acute onset, rapid progression, and severe disease. Non-severe aplastic anemia is characterized by slow onset, slow progression, and mild disease.

Anaemia. Progressive exacerbation, mainly manifested as pallor, fatigue, dizziness, palpitations, shortness of breath and other symptoms.

Infect. Most patients have a fever.

In severe cases, fever is high and difficult to control, with respiratory tract infections being the most common, often with sepsis. In non-severe patients, fever is mild, infection is easily controlled, and the duration is usually less than a week, and sepsis is rare.

Haemorrhage. Different degrees of bleeding from the mucous membranes and internal organs, mainly manifested as bleeding spots, ecchymosis, bleeding from the gums, oral mucosa and nose.

The bleeding in non-severe patients is mainly based on the ** mucosa, which is easy to control, and severe patients may also have visceral bleeding such as hematemesis, blood in the stool, blood in the urine, fundus bleeding, and even intracranial hemorrhage.

When chronic aplastic anemia occurs, the onset is usually slow, and patients can have anemia as the main manifestation, and the symptoms of infection and bleeding are generally mild. A decrease in trilineage cells can also be seen in the blood picture, but the standard of trilineage cell decline does not meet the criteria for severe aplasia. For example, reticulocytes can be reduced, but usually greater than 1%, and the absolute value is greater than 15 to 10 to the ninth power per liter.

There may also be a marked decrease in the number of white blood cells, a decrease in the proportion of neutrobulated nuclear granulocytes, and a decrease in absolute values, but usually greater than the ninth power per liter. The platelet count is also lower than normal, usually around 50 to 60 times ten to the ninth power per liter, and generally greater than 20 to 10 to the ninth power per liter. In other words, in the case of chronic aplastic anemia, the blood picture can be reduced in three lineages, but it cannot meet the diagnostic criteria for severe aplastic anemia, and chronic aplastic anemia can be diagnosed.

Yes, you can cooperate with the doctor for bone marrow transplantation, you can also carry out drugs, you should strengthen exercise, actively deal with the disease, not negatively, maintain a positive attitude, which is conducive to the recovery of the disease.

Yes. This disease can be **, you can also take some drugs in normal times, and then you should also eat more fresh vegetables and fruits, pay attention to the balanced combination of diet, pay attention to nutritional supplements, and you can also use traditional Chinese medicine to **.

Yes, it can be done using the method of immunization, and it is possible in mild cases.

It can be treated, whether it is ** or not, depends on the actual situation of the patient, including physical condition, age, severity of the disease, ** plan selection and so on.

Different situations have different methods, chronic aplastic disease, combined traditional Chinese and Western medicine diagnosis and treatment; Acute aplasia, if critical, may be considered for bone marrow transplantation, although there are some risks.

Bone marrow needs to be replaced, and the right bone marrow must be found to be able to be paired with the patient's bone marrow, and then the surgery will be performed, and there will be a period of rejection after the surgery.

Aplastic anemia is conditioned under the doctor's correct plan, and the doctor's plan can better promote the health of the body. Generally, iron supplementation is the main method.

I have a relative's daughter who suffered from regenerative anemia when she was about 10 years old, and was finally cured with home remedies, and drank it in a soup made of beef bones.

As long as it is diagnosed with "aplastic anemia", taking Chinese herbal medicine for 3 courses can be stable** (1 month per course of treatment).

Aplastic anemia predisposing factors:

1. Biological factors, with viral infection as the main manifestation, mostly hepatitis virus, hepatitis virus can lead to abnormal performance of bone marrow hematopoietic stem cells, from the perspective of embryogenesis, liver and bone marrow both belong to the monocyte-macrophage system, this inhibitory factor and liver-bone marrow may have a cross-effect.

2. Other functional failure factors, such as chronic renal failure, anemia, immune dysregulation, and genetic factors that have not been carried out for a long time, can cause aplasia, and some paroxysmal nocturnal hemoglobinuria can also be transformed into aplasia. There is no satisfactory explanation for the pathogenesis, but it is generally summarized as the interaction of seeds (hematopoietic stem cells), soil (hematopoietic microenvironment), and insects (immune abnormalities).

3. Chemical factors, regular exposure to chemical drugs will induce aplastic anemia.

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.