| Promyelocyte | |
|---|---|
 Promyelocyte frombone marrow examination | |
| Details | |
| Precursor | Myeloblast |
| Gives rise to | Myelocyte |
| Location | Bone marrow |
| Identifiers | |
| TH | H2.00.04.3.04003 |
| Anatomical terms of microanatomy | |
Apromyelocyte (orprogranulocyte) is agranulocyte precursor, developing from themyeloblast and developing into themyelocyte. Promyelocytes measure 12–20 microns in diameter. Thenucleus of a promyelocyte is approximately the same size as a myeloblast but theircytoplasm is much more abundant.[1] They also have less prominentnucleoli than myeloblasts and theirchromatin is more coarse and clumped.[1] The cytoplasm is basophilic and contains primary red/purple granules.[2]
The differentiation of promyelocytes fromhematopoietic stem cells is regulated by various growth factors,cytokines, and transcription factors, that ensure the balanced production of white blood cells for proper immune function.[3] Promyelocytes play a critical role inhematopoiesis by serving as an intermediate in the differentiation pathway leading to maturegranulocytes (Hematopoiesis image below). This process involves a series of steps, including proliferation, differentiation, and maturation.[4]
The function of promyelocytes are closely linked to their differentiation into mature granulocytes, which includeneutrophils,eosinophils, andbasophils.[citation needed] These functions are essential for innate immunity and host defense mechanisms, includingphagocytosis,inflammation, and immune surveillance.
Abnormalities in promyelocyte development or function can have significant clinical implications, leading to varioushematologic disorders. Some of the notable conditions associated with promyelocytes includeacute promyeloytic leukemia,myelodysplastic syndromes and infections/inflammatory conditions.[5]
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Acute Promyelocytic Leukemia (APL) is a subtype ofAcute Myeloid Leukemia, known for its accumulation of abnormal, course, densely granulated promyelocytes in the bone marrow.[6] The excessive proliferation of promyelocytes, attributing at least 30% of the myeloid cells in the bone marrow, result in a depletion of blood cells, including white blood cells, red blood cells, and platelets.[7][8] This variation is also called 'hypergranual' APL, as hypergranual promyelocytes are characterized by the denseazurophilic granule concentrations in the cytoplasm.[citation needed] APL is often associated with a specificchromosomal translocation involving theretinoic acid receptor alpha (RARα) gene on chromosome 17 and the promyelocytic leukemia gene on chromosome 15.[9]
In a less common variation of APL, called hypogranual APL, patients present withleukocytosis in addition to the excessive abnormal promyelocyte concentration. The cells in hypogranual APL have an irregular nucleus with finer granulation than the typical hypergranual APL.[10]
Treatment of APL involves a three phase regiment: induction phase, consolidation phase, and maintenance phase. The induction phase serves to put APL inremission by reducing the number of leukemic cells and lasts approximately two months. This involves the use of all trans-retinoic acid (ATRA) in combination with arsenic trioxide (ATO),chemotherapy, or chemotherapy plus ATO. The consolidation phase is intended to keep the patient in remission and destroy any remaining leukemic cells. This phase lasts several months and involves the use of ATRA plus ATO, ATRA plus chemotherapy, or chemotherapy alone. The last stage, the maintenance stage, uses a lower dosage of drugs to decrease the risk of patient relapse, and lasts approximately a year.[11]
Myelodysplastic Syndromes (MDS) are a group of disorders characterized by ineffective hematopoiesis or dysplasia changes in some myeloid lineages of the bone marrow. Abnormalities in promyelocyte maturation may contribute to pathogenesis of MDS and its associated complications.[5] These associated complications may includeanemia, recurrent infections, excessive bleeding and an increased risk of cancer of the bone marrow/blood cells (leukemia).[12] Treatment of MDS is used to slow the disease, and involves blood transfusions, medications, and bone marrow transplants. There is currently no cure for MDS.
The assessment of promyelocytes and their derivatives is an essential component of the diagnosis of various hematologic disorders. Laboratory test commonly used to evaluate promyelocyte abnormalities includecomplete blood count (CBC), morphologic evaluation ofperipheral blood smears,flow cytometry, andcytogenetic analysis, including bone marrow biopsies with aspirate.[13]
Promyelocytes are essential players in the body's immune system, serving as precursors to mature granulocytes involved in host defense and inflammatory responses. Understanding the characteristics, functions, and clinical significance of promyeloctes is crucial for the diagnosis, management, and treatment of various hematologic disorders.
![Bone marrow smear from a patient with acute promyelocytic leukemia, showing characteristic abnormal promyelocytes.[14]](/mt/?noimg=&dark=on&url=https%3a%2f%2fen.wikipedia.org%2fwiki%2fFile%3aCytology_of_acute_promyelocytic_leukemia%2c_annotated.png)
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