Aplastic anemia and myelodysplastic syndromes

The patient's condition needs to be grasped quickly, this disease has the possibility of transforming leukemia, combined with Chinese herbal medicine, the prognosis can be achieved clinically, but a good program is very important.

MDS is a malignant clonal disease, but a small fraction, after or not, can survive for a long time. Aplastic is a benign disease, and although it is life-threatening in severe cases, the overall prognosis is good.

Of course, there are cures, Chinese medicine is recommended**. This requires seeing the patient's laboratory results and understanding the patient's condition before formulating a ** plan.

This is because each patient has different symptoms due to their different constitutions and living environments. Therefore, it is necessary to formulate a plan according to the different symptoms of different patients and their own conditions, and adjust the taste of medicine.

Answer]: A test point: the clinical significance of the vertical dissection of the myeloproliferative process.

Analysis] Myelohyperplasia is extremely active, reflecting the hyperpoietic function of the bone marrow, which is common in various acute leukemias, chronic myeloid leukemias, etc.; Bone marrow hyperplasia is obviously active, reflecting the vigorous hematopoietic function of bone marrow, which is common in iron deficiency anemia, megaloblastic anemia, lycophilic fibrous anemia, ITP, etc.; Bone marrow hyperplasia is active, reflecting that the hematopoietic function of bone marrow is basically normal, and it is common in normal bone marrow images, multiple myeloma, etc.; Decreased bone marrow hyperplasia, reflecting decreased bone marrow hematopoietic function, commonly seen in hypoproliferative leukemia, PNH, etc.; Extremely low bone marrow hyperplasia, reflecting bone marrow hematopoietic failure, seen in aplastic anemia, after chemotherapy, etc.

Answer]: eAcute aplastic aplastic is severe reduction of myeloproliferasia in multiple sites, and there is a significant decrease in trilineage hematopoietic cells, especially megakaryocytes and erythroblasts; Non-hematopoietic cytosis, especially lymphocytosis. In the chronic form, bone marrow images from different sites are very inconsistent, ranging from dysplasia to hyperplasia, but at least one site is malhyperplasia; If the hyperplasia is good, the proportion of late erythroblasts (charcoal nuclei) often increases, and its nuclei are irregularly lobulated, showing deenucleation disorders, but megakaryocytes are significantly reduced.

Answer: Sedan Ant] :d

The bone marrow of aplastic crisis is like a closed beam burial: most of the slag is active, but some are reduced, especially the red blood cell line is inhibited, the proportion of granulosus red is increased, and the appearance of large primitive red blood cells in the peripheral part of the smear is a prominent feature of the disease, and the cell body is round or oval.

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.

Aplastic is the reduction of the three lineages in the blood routine, the reduction of the bone marrow image of the three lineages, the bone marrow image of the hypoproliferative bone marrow, if there is a clone PNH positive index, PNH disease should be considered, not aplasia, pay attention to the distinction.

The specific cause is the decline of bone marrow hematopoietic function, and then leads to a blood disease, **There are two kinds, generally congenital and one is acquired. There are many agenogens, such as viral infection, chemical drugs, genetic mutations and so on.

Aplastic anemia is a blood disorder caused by a variety of causes, most likely due to congenital genetic factors or acquired factors.