Why is the aplastic so terrible, and how to treat the apocalypse?

With the development of modern medicine, aplastic is no longer an incurable disease, as long as you maintain a good attitude, adhere to a positive, healthy and regular life, and do not increase psychological pressure on yourself, you can make your life longer. It's not scary to have another astacle, it's scary to have the confidence to overcome it and defeat it. If you have a condition that you don't understand and need to be consulted, you can directly click on the [Consultation Appointment Application Form].

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It's terrible to be sick, it costs money, it takes time. The body is still not good.

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.

If the plate count is consistently low, it can easily induce fatal bleeding symptoms. So it's terrible.

Most people are controlled by hormones, but long-term use of hormones will slowly develop drug resistance, so many people use eltrombopag, but also shout that it is too expensive to live, and many people use Bangladeshi moxa, which can solve this problem to a large extent.

Deficit Answer]: c

Answer: c) Aplastic is a disease characterized by hematopoietic stem cell damage, bone marrow hematopoietic failure, and peripheral blood pancytopenia, so the bone marrow transplantation of normal bone marrow stem cells to the patient, especially the transplantation of the same bone marrow with the same HLA of identical twins is the most ideal**, which can not only supply hematopoietic stem cells** disease, but also will not cause serious complications such as graft-versus-host disease, while the other four ** are not ideal.

Hello Judge!

Aplastic and leukemia are both blood disorders, and aplastic refers to primary bone marrow hematopoietic failure syndrome,** unknown. The main manifestations are low bone marrow hematopoietic function, pancytopenia and anemia, hemorrhage, and infection.

Leukemia is a round and malignant disease of hematopoietic tissue, also known as "blood cancer". It is characterized by the unrestricted proliferation of a large number of non-nucleated cells in the bone cavity and other hematopoietic tissues, and enters the peripheral blood, which obviously adsorbs the core of normal blood cells, and many factors such as mineral radioactivity of food, poisoning (benzene, etc.) or drug mutation, genetic predisposition, etc. may be pathogenic cofactors. Depending on the degree of immaturity of the leukemia cells and the natural history of the leukemia.

Patients are advised to undergo bone marrow aspirates and biopsies, and provide detailed information and results to help and guide patients.

Aplastic anemia is a common type of blood rot fluid disease, referred to as aplastic aplasia. With the development of modern medicine, aplastic is no longer a disease that is not cured, as long as you maintain a good attitude, adhere to a positive, healthy and regular life, and do not increase psychological pressure on yourself, you can make your life longer. If you need to consult aplastic disease or drug guidance, you can poke [Official**] below for help.

What is the condition of the patient now, chronic aplasia.

In the presence of infection.

or in the case of bleeding, it will be transformed into.

Heavy re-ascalation. It is more common to be infected. After more than 3,000 clinical studies, Botong has shown that blood cell regeneration**.

This 1 comprehensive healing.

Aplastic anemia. Methods of 1 to 9 months to be effective, the average months to be effective, hemoglobin to rise to more than 10 grams of liters takes 1 2 months, an average of 6 months. This method is effective quickly, the effective force is more than 90%, and the mitigation rate is more than 60%, which is a new development of the treatment method of aplastic anemia in recent years, and there are more and more of them.

Aplastic anemia.

The patient is treated with blood cell regeneration**.

Is it a heavy or non-heavy abrasion, and how is it at the moment. If it is a chronic aplasia, it is recommended that Chinese medicine dominate**, you can take compound soap alum pills, symptomatic Chinese herbal medicine, etc.

It consists of two parts: support** and disease-specific goals**. The goal of support is to prevent complications related to cytopenias; The goal is to replace and replace extremely reduced and damaged hematopoietic stem cells, such as allogeneic hematopoietic stem cell transplantation or immunosuppression**. Hematopoietic stem cell transplantation should be preferred for patients aged 30 years with severe aplastic anemia without specific contraindications and with HLA-matched sibling donors, and intensive immunosuppression ** is preferred for major aplastic anemia without HLA-matched sibling donors at age 40 years.

For non-severe aplastic disorders, androgens and cyclosporine** may be used.

If the hormone is ineffective, you have to use eltrombopag, I have been taking Bangladesh eltrombopag for more than ten years, and the number of plates is normal.

At present, the best plan for chronic aplastic disease is the combination of Western medicine, and it is recommended to provide detailed analysis of the disease, blood routine, bone puncture and medication, and help improve the analysis.