Find information on thousands of medical conditions and prescription drugs.

Acute myelogenous leukemia

Acute myelogenous leukemia (AML), also known as acute myeloid leukemia, is a cancer of the myeloid line of blood cells. The median age of patients with AML is 70; it is rare among children. more...

Home
Diseases
A
Aagenaes syndrome
Aarskog Ose Pande syndrome
Aarskog syndrome
Aase Smith syndrome
Aase syndrome
ABCD syndrome
Abdallat Davis Farrage...
Abdominal aortic aneurysm
Abdominal cystic...
Abdominal defects
Ablutophobia
Absence of Gluteal muscle
Acalvaria
Acanthocheilonemiasis
Acanthocytosis
Acarophobia
Acatalasemia
Accessory pancreas
Achalasia
Achard syndrome
Achard-Thiers syndrome
Acheiropodia
Achondrogenesis
Achondrogenesis type 1A
Achondrogenesis type 1B
Achondroplasia
Achondroplastic dwarfism
Achromatopsia
Acid maltase deficiency
Ackerman syndrome
Acne
Acne rosacea
Acoustic neuroma
Acquired ichthyosis
Acquired syphilis
Acrofacial dysostosis,...
Acromegaly
Acrophobia
Acrospiroma
Actinomycosis
Activated protein C...
Acute febrile...
Acute intermittent porphyria
Acute lymphoblastic leukemia
Acute lymphocytic leukemia
Acute mountain sickness
Acute myelocytic leukemia
Acute myelogenous leukemia
Acute necrotizing...
Acute promyelocytic leukemia
Acute renal failure
Acute respiratory...
Acute tubular necrosis
Adams Nance syndrome
Adams-Oliver syndrome
Addison's disease
Adducted thumb syndrome...
Adenoid cystic carcinoma
Adenoma
Adenomyosis
Adenosine deaminase...
Adenosine monophosphate...
Adie syndrome
Adrenal incidentaloma
Adrenal insufficiency
Adrenocortical carcinoma
Adrenogenital syndrome
Adrenoleukodystrophy
Aerophobia
Agoraphobia
Agrizoophobia
Agyrophobia
Aicardi syndrome
Aichmophobia
AIDS
AIDS Dementia Complex
Ainhum
Albinism
Albright's hereditary...
Albuminurophobia
Alcaptonuria
Alcohol fetopathy
Alcoholic hepatitis
Alcoholic liver cirrhosis
Alektorophobia
Alexander disease
Alien hand syndrome
Alkaptonuria
Alliumphobia
Alopecia
Alopecia areata
Alopecia totalis
Alopecia universalis
Alpers disease
Alpha 1-antitrypsin...
Alpha-mannosidosis
Alport syndrome
Alternating hemiplegia
Alzheimer's disease
Amaurosis
Amblyopia
Ambras syndrome
Amelogenesis imperfecta
Amenorrhea
American trypanosomiasis
Amoebiasis
Amyloidosis
Amyotrophic lateral...
Anaphylaxis
Androgen insensitivity...
Anemia
Anemia, Diamond-Blackfan
Anemia, Pernicious
Anemia, Sideroblastic
Anemophobia
Anencephaly
Aneurysm
Aneurysm
Aneurysm of sinus of...
Angelman syndrome
Anguillulosis
Aniridia
Anisakiasis
Ankylosing spondylitis
Ankylostomiasis
Annular pancreas
Anorchidism
Anorexia nervosa
Anosmia
Anotia
Anthophobia
Anthrax disease
Antiphospholipid syndrome
Antisocial personality...
Antithrombin deficiency,...
Anton's syndrome
Aortic aneurysm
Aortic coarctation
Aortic dissection
Aortic valve stenosis
Apert syndrome
Aphthous stomatitis
Apiphobia
Aplastic anemia
Appendicitis
Apraxia
Arachnoiditis
Argininosuccinate...
Argininosuccinic aciduria
Argyria
Arnold-Chiari malformation
Arrhythmogenic right...
Arteriovenous malformation
Arteritis
Arthritis
Arthritis, Juvenile
Arthrogryposis
Arthrogryposis multiplex...
Asbestosis
Ascariasis
Aseptic meningitis
Asherman's syndrome
Aspartylglycosaminuria
Aspergillosis
Asphyxia neonatorum
Asthenia
Asthenia
Asthenophobia
Asthma
Astrocytoma
Ataxia telangiectasia
Atelectasis
Atelosteogenesis, type II
Atherosclerosis
Athetosis
Atopic Dermatitis
Atrial septal defect
Atrioventricular septal...
Atrophy
Attention Deficit...
Autoimmune hepatitis
Autoimmune...
Automysophobia
Autonomic dysfunction
Familial Alzheimer disease
Senescence
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
Medicines

Myeloid leukemias are characterized as "acute" or "chronic" based on how quickly they progress if not treated. Chronic myelogenous leukemia (CML) is often without symptoms and can remain dormant for years before transforming into a blast crisis, which is markedly similar to AML.

Pathophysiology

Specific chromosomal abnormalities are seen in patients with some forms of AML. These chromosomal abnormalities tend to disrupt genes that encode for transcription factors needed for myeloid stem cells to differentiate into specific blood components. Without differentiation occurring, these myeloid precursor cells fill the bone marrow and spill out into the blood. The overpopulation of the bone marrow with myeloid precursors also results in supression of normal marrow stem cells, giving rise to the symptoms of anemia (lack of red blood cells), thrombocytopenia (lack of platelets), and neutropenia (lack of neutrophils).

Subtypes

World Health Organization (WHO) classification

The World Health Organization (WHO) classification of acute myeloid leukemia (AML) attempts to be more applicable and produce more meaningful prognostic information then the older French-American-British (FAB) criteria, described below.

The WHO criteria are:

  • AML with characteristic genetic abnormalities, which includes AML with translocations between chromosome 8 and 21 , inversions in chromosome 16 and acute promyelocytic leukemia (APL). Patients with AML in this category generally have a high rate of remission and a better prognosis compared to other types of AML.
  • AML with multilineage dysplasia. This category includes patients who have had prior myelodysplastic syndrome (MDS) or a myeloproliferative diseases (MPD) that transforms into AML. This category of AML occurs primarily in elderly patients
  • AML and MDS, therapy related. This category includes patients who have had prior chemotherapy and/or radiation and subsequently develop AML or MDS.
  • AML not otherwise categorized. Includes subtypes of AML that do not fall into the above categories.
  • Acute leukemias of ambiguous lineage. Acute leukemias of ambiguous lineage (also known as mixed phenotype acute leukemia) occur when the leukemic cells can not be classified as either myeloid or lymphoid cells or where both types of cells are present.

French-American-British (FAB) classification

The older French-American-British (FAB) classification system divided AML into 8 subtypes, M0 through to M7 based on the type of cell from which the leukemia developed and degree of maturity. This is done by examining the appearance of the malignant cells under light microscopy or cytogenetically by characterization of the underlying chromosomal abnormality. Each subtype is characterised by a particular pattern of chromosomal translocations and have varying prognoses and responses to therapy. Although the WHO classification is more useful, the FAB system is still in use.

Read more at Wikipedia.org


[List your site here Free!]


Acute Interstitial Pneumonitis Occurring After Consolidation Chemotherapy With High Dose Cytarabine For Acute Myelogenous Leukemia - Abstract
From CHEST, 10/1/99 by Poh Hock Leng

Introduction: Acute interstitial pneumonitis is an uncommon complication of cytarabine. We report a case of acute interstitial pneumonitis caused by cytarabine with good response to steroid therapy.

Case Presentation: A 50 year old woman was admitted for neutropenic fever 2 weeks after receiving high dose cytarabine at 5.6 grams (3 g/m. sq.) every 12 hours for 3 days for her second consolidation chemotherapy for acute myelogenous leukemia (AML). She had fever and a dry nonproductive cough on admission. She was diagnosed with AML in Dec 1998 and had induction chemotherapy with 95 mg. of daunorubicin and 200 mg. of cytarabine every 24 hours for 3 days. The first consolidation chemotherapy was in Feb. 1999 with high dose cytarabine at 5.6 grams (3 g/m. sq.) every 12 hours for 3 days. On exam, her temperature was 103 [degrees] F, blood pressure 128/84, pulse rate 86/min, respiratory rate 14/min and oxygen saturation was 94% on room air. The lungs were clear to auscultation. Chest X ray was clear. The white blood cell count (WBC) was 300 cells/uL. She was given levofloxacin and gentamicin for empiric antibiotic coverage, blood and platelet transfusions. Four days after admission the WBC rose to 7400 cells/uL., with 58% neutrophils, 6% lymphocytes, 33% monocytes and 1% eosinophils. Her dyspnea and cough worsened and oxygen saturation dropped to 86% on room air. A repeat CXR showed new interstitial infiltrates. A high resolution CAT scan of the chest showed diffuse ground glass infiltrates in both lung fields. Bacterial cultures from the bronchoalveolar lavage were unremarkable. Pneumocystis carinii, fungi, Legionella and acid fast bacilli were not detected in the bronchoalveolar lavage. Fungal and viral cultures were negative. A transbronchial lung biopsy showed intense inflammatory interstitial cellular infiltrates and the presence of reactive type 2 pneumocytes, indicative of a drug-induced reaction. In some areas, the inflammatory cellular reaction extended into the alveolar space. She was started on 3 mg/kg/day of methylprednisolone for drug-induced acute interstitial pneumonitis. Within 72 hours her symptoms improved remarkably and she was weaned off the oxygen. The steroids were tapered over 4 weeks. A repeat CT chest showed resolution of the ground glass infiltrates.

Discussion: The observations in this case suggest that high dose cytarabine can lead to a drug-induced acute interstitial pneumonitis, in the absence of infection and use of other chemotherapeutic agents. This is in contrast to noncardiogenic pulmonary edema, which is a known complication of cytarabine as reported in several studies. The histology seen in this patient differs from previous reports in that there is primarily a cellular inflammatory interstitial process, with extension of the inflammation into the alveoli in some areas. Additionally, a dramatic response to steroids and the fact that her symptoms worsened as her WBC count began to rise imply an immunologic lung injury. It is speculative whether this process is a harbinger of further lung injury that may eventually manifest as noncardiogenic pulmonary edema.

Conclusion: Acute interstitial pneumonitis can occur as a complication of cytarabine and this condition is highly responsive to steroid therapy.

References

[1] Haupt et al. Noncardiogenic pulmonary edema complicating cytosine arabinoside therapy of leukemia. The American Journal of Medicine 1981; 70:256-261

[2] Andersson et al. Fatal pulmonary failure complicating high dose cytosine arabinoside therapy in acute leukemia. Cancer 1990; 65:1079-1084

[3] Jehn et al. Noncardiogenic pulmonary edema complicating intermediate and high dose Ara-C for relapsed acute leukemia. Medical Oncology and Tumour Pharmacology 1988; Vol 5. 1.41-47

[4] Motomura et al. Interstitial pneumonia induced by combination therapy with low dose cytarabine and granulocyte colony-stimulating factor. American Journal of Hematology (letter) 1995; 49(4):364

Poh Hock Leng, MD, B. Murillo, MD, A. Fraire, MD--University of Massachusetts, Worcester, Massachusetts, USA

COPYRIGHT 1999 American College of Chest Physicians
COPYRIGHT 2000 Gale Group

Return to Acute myelogenous leukemia
Home Contact Resources Exchange Links ebay