Acute myeloid leukemia overview: Difference between revisions
Shyam Patel (talk | contribs) No edit summary |
Shyam Patel (talk | contribs) |
||
| Line 38: | Line 38: | ||
==Natural History, Complications, and Prognosis== | ==Natural History, Complications, and Prognosis== | ||
The natural history of acute myeloid leukemia involves the commencement of symptoms including fatigue, bleeding, and infection. Some patients will also present with disseminated intravascular coagulation in which bleeding and thrombosis occurs simultaneously. Complications of acute myeloid leukemia include infection, hemorrhage, venous thromboembolism, and therapy-related complications. The prognosis of acute myeloid leukemia is largely based upon on the European LeukemiaNet (ELN) classification system. | |||
==Diagnosis== | ==Diagnosis== | ||
Revision as of 06:43, 1 November 2018
| https://https://www.youtube.com/watch?v=itkRVTqfPsE%7C350}} |
|
Acute myeloid leukemia Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Acute myeloid leukemia overview On the Web |
|
American Roentgen Ray Society Images of Acute myeloid leukemia overview |
|
Risk calculators and risk factors for Acute myeloid leukemia overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2] Carlos A Lopez, M.D. [3] Shyam Patel [4]
Overview
Acute myeloid leukemia (AML) is a cancer of the myeloid line of white blood cells characterized by the rapid proliferation of abnormal cells which accumulate in the bone marrow and interfere with the production of normal blood cells. This leukemia arises from myeloblasts, which are hematologic white cells that are normally involved in hematopoiesis. Acute myeloid leukemia may be classified according to the French-American-British (FAB) classification and World Health Organization (WHO). Acute myeloid leukemia must be differentiated from other diseases such as acute lymphoblastic leukemia, chronic myeloid leukemia, agranulocytosis, aplastic anemia and lymphoma. In 2015, the incidence of acute myeloid leukemia was approximately 6.5 per 100,000 individuals with a case-fatality rate of approximately 50% in the United States. The incidence of acute myeloid leukemia increases with age. Common risk factors in the development of acute myeloid leukemia are myelodysplastic syndromes, aplastic anemia, myelofibrosis and paroxysmal nocturnal hemoglobinuria. Common complications include infections, disseminated intravascular coagulation, and hemorrhage. Symptoms of acute myeloid leukemia include fever, fatigue, weight loss and loss of appetite. Physical examination findings of acute myeloid leukemia include anemia, fever, pallor, Leukemia cutis, bruising, petechiae, ecchymosis and tachycardia. Laboratory findings consistent with the diagnosis of acute myeloid leukemia include leukocytosis, thrombocytopenia, anemia and leucopenia. If a lung infection is suspected chest x-ray may be helpful in the diagnosis. The mainstay therapy is chemotherapy and usually includes a combination of daunorubicin, cytarabine and etoposide or mitoxantrone and anabolic steroids. Supportive care includes intravenous nutrition, antimicrobial therapy, and replacement of blood products.
Historical Perspective
In the 17th and 18th centuries, scientists first described blood cells, which are the malignant cells in acute myeloid leukemia. In the 19th century, the first case of acute leukemia was described. In the 20th century, chemotherapy was introduced for the treatment of acute leukemia. The 21st century witnessed advancements in the understanding of disease biology, and targeted therapies for acute myeloid leukemia were introduced to the market.
Classification
There are 3 classifications systems for acute myeloid leukemia. These include the French-American-British (FAB) classification, the World Health Organization (WHO) classification, and the European LeukemiaNet (ELN) classification. The original classification was the French-American-British (FAB) classification, and the most recent classification was the 2017 European LeukemiaNet (ELN) classification.
Pathophysiology
Normal hematopoiesis involves the production of blood cells, and this normal physiologic process is dysregulated in acute myeloid leukemia. The pathophysiology of acute myeloid leukemia involves multiple mechanisms, including altered signal transduction and autonomous proliferation, differentiation blockade, evasion of apoptosis, and self-renewal. The pathophysiology of acute promyelocytic leukemia specifically involves a fusion protein that results from a translocation between chromosomes 15 and 17.
Causes
The causes of acute myeloid leukemia are broad and include benzene, radiation, alkylating agents, topoisomerase II inhibitors, and specific gene mutations. Each of these risk factors carries a defined probability of progression to acute myeloid leukemia. Overall, most cases of acute myeloid leukemia are sporadic rather than inherited.
Differentiating Acute Myeloid Leukemia from Other Diseases
The differential diagnosis of acute myeloid leukemia includes a variety of other hematologic malignancies, specifically acute promyelocytic leukemia (APL), acute lymphoblastic leukemia (ALL), chronic myeloid leukemia (CML), and chronic lymphocytic leukemia (CLL). Each of these conditions has distinct causes and therapies. There is some overlap between the causes and laboratory abnormalities amongst these diseases.
Epidemiology and Demographics
In 2015, the incidence of acute myeloid leukemia was approximately 6.5 per 100,000 individuals with a case-fatality rate of approximately 50% in the United States. The incidence of acute myeloid leukemia increases with age; the median age at diagnosis is 63 years. Males are more commonly affected with acute myeloid leukemia than women. The male to female ratio is approximately 1.3 to 1.
Risk Factors
Common risk factors in the development of acute myeloid leukemia are advanced age, benzene exposure, prior myelodysplastic syndrome, germline mutations, and other conditions like aplastic anemia.
Screening
There are currently no guidelines for screening for acute myeloid leukemia. Monitoring of the complete blood count is done routinely.
Natural History, Complications, and Prognosis
The natural history of acute myeloid leukemia involves the commencement of symptoms including fatigue, bleeding, and infection. Some patients will also present with disseminated intravascular coagulation in which bleeding and thrombosis occurs simultaneously. Complications of acute myeloid leukemia include infection, hemorrhage, venous thromboembolism, and therapy-related complications. The prognosis of acute myeloid leukemia is largely based upon on the European LeukemiaNet (ELN) classification system.
Diagnosis
History and Symptoms
Symptoms of acute myeloid leukemia include fever, fatigue, weight loss and loss of appetite.
Physical Examination
Common physical examination findings of acute myeloid leukemia include anemia, fever, pallor, Leukemia cutis, bruising, petechiae, ecchymosis and tachycardia.
Laboratory Findings
Laboratory findings consistent with the diagnosis of acute myeloid leukemia include leukocytosis, thrombocytopenia, anemia, leucopenia and peripheral blood smear.
Chest X Ray
If a lung infection is suspected chest x-ray may be helpful in the diagnosis of acute myeloid leukemia.
CT
CT scan may be helpful in the diagnosis of acute myeloid leukemia.
Other Diagnostic Studies
Other diagnostic studies for acute myeloid leukemia include cytochemistry, flow cytometry, immunohistochemistry, PCR and biopsy.
Medical Therapy
The mainstay therapy from acute myeloid leukemia is chemotherapy and usually includes a combination of daunorubicin, cytarabine and etoposide or mitoxantrone and anabolic steroids. Supportive care includes intravenous nutrition, antimicrobial therapy, and replacement of blood products.
Surgery
Surgery is not the first-line treatment option for patients with acute myeloid leukemia, it is used to place a venous access device as a port through which chemotherapy can be delivered.
References