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==Overview==
==Overview==
'''Acute myeloid leukemia''' ('''AML'''), also known as '''acute myelogenous leukemia''', is a [[cancer]] of the [[myeloid]] line of [[white blood cell]]s, characterized by the rapid proliferation of abnormal cells which accumulate in the [[bone marrow]] and interfere with [[haematopoiesis|the production of normal blood cells]]. Acute myeloid leukemia may be classified according to the [[French-American-British classification | French-American-British (FAB) classification]] and [[World Health Organization]] (WHO). Acute myeloid leukemia arises from [[myeloblasts]], which are hematologic white cells that are normally involved in [[hematopoiesis]]. Genetic translocations involved in the pathogenesis of acute myeloid leukemia include translocations between chromosome 8 and 21 t(8;21) and translocations between chromosome 15 and 17 t(15;17). Inversions in the chromosomal translocations in chromosome 16 inv(16) are envolved in the pathogenesis of acute myeloid leukemia. 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 syndrome|myelodysplastic]] syndromes, [[aplastic anemia]], [[myelofibrosis]] and [[paroxysmal nocturnal hemoglobinuria]]. Common complications of acute myeloid leukemia include [[infections]], [[disseminated intravascular coagulation]], [[pyoderma gangrenosum]] and [[hemorrhage]]. Symptoms of acute myeloid leukemia include [[fever]], [[fatigue (physical)|fatigue]], [[weight loss]] and [[loss of appetite]]. Common physical examination findings of acute myeloid leukemia include [[anemia]], [[fever]], [[pallor]], [[Chloroma|Leukemia cutis]], [[bruising]], [[petechia]]e, [[ecchymosis]] and [[tachycardia]]. Laboratory findings consistent with the diagnosis of acute myeloid leukemia include [[leukocytosis]], [[thrombocytopenia]], [[anemia]] and [[leucopenia]].  
'''Acute myeloid leukemia''' ('''AML'''), also known as '''acute myelogenous leukemia''', is a [[cancer]] of the [[myeloid]] line of [[white blood cell]]s, characterized by the rapid proliferation of abnormal cells which accumulate in the [[bone marrow]] and interfere with [[haematopoiesis|the production of normal blood cells]]. Acute myeloid leukemia may be classified according to the [[French-American-British classification | French-American-British (FAB) classification]] and [[World Health Organization]] (WHO). This leukemia arises from [[myeloblasts]], which are hematologic white cells that are normally involved in [[hematopoiesis]]. Genetic translocations involved in the pathogenesis of acute myeloid leukemia include translocations between chromosome 8 and 21 t(8;21) and translocations between chromosome 15 and 17 t(15;17). 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 syndrome|myelodysplastic]] syndromes, [[aplastic anemia]], [[myelofibrosis]] and [[paroxysmal nocturnal hemoglobinuria]]. Common complications of acute myeloid leukemia include [[infections]], [[disseminated intravascular coagulation]], [[pyoderma gangrenosum]] and [[hemorrhage]]. Symptoms of acute myeloid leukemia include [[fever]], [[fatigue (physical)|fatigue]], [[weight loss]] and [[loss of appetite]]. Common physical examination findings of acute myeloid leukemia include [[anemia]], [[fever]], [[pallor]], [[Chloroma|Leukemia cutis]], [[bruising]], [[petechia]]e, [[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 of acute myeloid leukemia. 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.
If a lung infection is suspected chest x-ray may be helpful in the diagnosis of acute myeloid leukemia. 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.


==Historical Perspective==
==Historical Perspective==

Revision as of 14:09, 4 September 2015

Acute myeloid leukemia Microchapters

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Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Acute myeloid leukemia from other Diseases

Epidemiology and Demographics

Risk Factors

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Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

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Chest X Ray

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]

Overview

Acute myeloid leukemia (AML), also known as acute myelogenous leukemia, 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. Acute myeloid leukemia may be classified according to the French-American-British (FAB) classification and World Health Organization (WHO). This leukemia arises from myeloblasts, which are hematologic white cells that are normally involved in hematopoiesis. Genetic translocations involved in the pathogenesis of acute myeloid leukemia include translocations between chromosome 8 and 21 t(8;21) and translocations between chromosome 15 and 17 t(15;17). 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 of acute myeloid leukemia include infections, disseminated intravascular coagulation, pyoderma gangrenosum and hemorrhage. Symptoms of acute myeloid leukemia include fever, fatigue, weight loss and loss of appetite. Common 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 of acute myeloid leukemia. 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.

Historical Perspective

Leukemia was first described in 1827 by a french physician named Alfred-Armand-Louis-Marie Velpeau. In 1900 the myeloblast was first identified in the pathogenesis of acute myeloid leukemia.

Classification

Acute myeloid leukemia may be classified according to the French-American-British (FAB) classification and World Health Organization (WHO).

Pathophysiology

Acute myeloid leukemia arises from myeloblasts, which are hematologic white cells that are normally involved in hematopoiesis. Genetic translocations involved in the pathogenesis of acute myeloid leukemia include translocations between chromosome 8 and 21 t(8;21) and translocations between chromosome 15 and 17 t(15;17). Inversions in the chromosomal translocations in chromosome 16 inv(16) are envolved in the pathogenesis of acute myeloid leukemia.

Differentiating Acute lymphoblastic leukemia from other Diseases

Acute myeloid leukemia must be differentiated from other diseases such as acute lymphoblastic leukemia, chronic myeloid leukemia, agranulocytosis, aplastic anemia and lymphoma.

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 myelodysplastic or myeloproliferative syndromes, aplastic anemia, myelofibrosis, paroxysmal nocturnal hemoglobinuria, polycythemia vera, chemical exposure and several congenital conditions such as Down syndrome, Bloom syndrome, Fanconi anemia, neurofibromatosis and congenital neutropenia.

Natural History, Complications, and Prognosis

Common complications of acute myeloid leukemia include infections, disseminated intravascular coagulation, pyoderma gangrenosum, hemorrhage and complications due to side effects of chemotherapy. Prognosis of acute myelogenous leukemia depends on cytogenetics. Cytogenetics that indicate a good prognosis include inversions in chromosome 16 inv(16), translocations between chromosome 8 and 21 t(8;21) and translocations between chromosome 15 and 17 t(15;17).

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 and leucopenia.

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.

References

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