ICD-10: C92.0
Acute myeloblastic leukemia
Clinical Information
Inclusion Terms
- Acute myeloblastic leukemia 1/ETO
- Acute myeloblastic leukemia M0
- Acute myeloblastic leukemia M2
- Acute myeloblastic leukemia, minimal differentiation
- Refractory anemia with excess blasts in transformation [RAEB T]
- Acute myeloblastic leukemia (with maturation)
- Acute myeloblastic leukemia (without a FAB classification) NOS
- Acute myeloblastic leukemia M1
- Acute myeloblastic leukemia with t(8;21)
Additional Information
Description
Acute myeloblastic leukemia (AML), classified under ICD-10 code C92.0, is a type of cancer that affects the blood and bone marrow. This condition is characterized by the rapid proliferation of myeloblasts, which are immature white blood cells. Below is a detailed overview of the clinical description, characteristics, and implications of this diagnosis.
Clinical Description of Acute Myeloblastic Leukemia (AML)
Definition and Classification
Acute myeloblastic leukemia is a hematological malignancy that arises from the myeloid lineage of blood cells. It is classified as an acute leukemia due to the rapid onset and progression of the disease. The term "myeloblastic" refers to the presence of myeloblasts in the bone marrow and peripheral blood, which are precursors to mature granulocytes, monocytes, and erythrocytes[4][5].
Pathophysiology
In AML, genetic mutations lead to the uncontrolled growth of myeloblasts, which crowd out normal blood cells in the bone marrow. This results in a deficiency of healthy red blood cells, white blood cells, and platelets, leading to symptoms such as anemia, increased susceptibility to infections, and bleeding disorders. The exact cause of these mutations can vary, with some cases linked to environmental factors, previous chemotherapy, or genetic predispositions[5][6].
Symptoms
Patients with acute myeloblastic leukemia may present with a variety of symptoms, including:
- Fatigue and weakness: Due to anemia from a lack of red blood cells.
- Frequent infections: Resulting from neutropenia (low white blood cell count).
- Easy bruising or bleeding: Caused by thrombocytopenia (low platelet count).
- Fever: Often due to infections or the disease itself.
- Bone pain: As the bone marrow becomes overcrowded with myeloblasts[6][7].
Diagnosis
The diagnosis of AML typically involves:
- Blood tests: To check for abnormal levels of blood cells.
- Bone marrow biopsy: To confirm the presence of myeloblasts and assess the extent of the disease.
- Cytogenetic analysis: To identify specific genetic abnormalities that can influence treatment and prognosis[5][6].
Treatment
Treatment for acute myeloblastic leukemia usually involves:
- Chemotherapy: The primary treatment modality, aimed at inducing remission by killing cancerous cells.
- Targeted therapy: For specific genetic mutations, such as FLT3 inhibitors.
- Stem cell transplant: May be considered for eligible patients, especially those with high-risk features or relapsed disease[6][7].
Prognosis
The prognosis for patients with AML can vary significantly based on several factors, including age, overall health, specific genetic mutations, and response to initial treatment. Generally, younger patients and those with favorable genetic profiles tend to have better outcomes[5][6].
Conclusion
ICD-10 code C92.0 encapsulates the complexities of acute myeloblastic leukemia, a serious and aggressive form of leukemia. Understanding its clinical features, diagnostic criteria, and treatment options is crucial for healthcare providers in managing this condition effectively. Early diagnosis and appropriate treatment are essential for improving patient outcomes and survival rates in those affected by this challenging disease.
Clinical Information
Acute Myeloblastic Leukemia (AML), classified under ICD-10 code C92.0, is a type of cancer that affects the blood and bone marrow. It is characterized by the rapid proliferation of myeloblasts, a type of immature white blood cell. Understanding the clinical presentation, signs, symptoms, and patient characteristics associated with this condition is crucial for timely diagnosis and treatment.
Clinical Presentation
Signs and Symptoms
Patients with Acute Myeloblastic Leukemia often present with a variety of symptoms that can be broadly categorized into hematological, systemic, and specific signs:
-
Hematological Symptoms:
- Anemia: Patients frequently experience fatigue, weakness, and pallor due to a decrease in red blood cells.
- Thrombocytopenia: Low platelet counts can lead to easy bruising, bleeding gums, and petechiae (small red or purple spots on the skin).
- Leukopenia: A reduction in white blood cells increases susceptibility to infections, which may manifest as recurrent fevers or infections. -
Systemic Symptoms:
- Fever: Often due to infections or the disease itself.
- Weight Loss: Unintentional weight loss can occur as the disease progresses.
- Night Sweats: Patients may experience excessive sweating during the night. -
Specific Signs:
- Splenomegaly: Enlargement of the spleen may be noted during physical examination.
- Hepatomegaly: Liver enlargement can also occur.
- Lymphadenopathy: Swelling of lymph nodes may be present, although it is less common in AML compared to other leukemias.
Patient Characteristics
Acute Myeloblastic Leukemia can affect individuals of various ages, but certain characteristics are more prevalent in specific demographics:
- Age: AML is more common in older adults, with the median age of diagnosis being around 68 years. However, it can also occur in younger individuals, including children and adolescents.
- Gender: There is a slight male predominance in the incidence of AML.
- Risk Factors: Certain factors may increase the risk of developing AML, including:
- Previous chemotherapy or radiation therapy for other cancers.
- Exposure to certain chemicals, such as benzene.
- Genetic predispositions, including conditions like Down syndrome or other inherited blood disorders.
Conclusion
Acute Myeloblastic Leukemia (ICD-10 code C92.0) presents with a range of clinical symptoms primarily related to hematological deficiencies, systemic effects, and specific physical signs. Recognizing these symptoms is vital for healthcare providers to facilitate early diagnosis and initiate appropriate treatment. Understanding patient characteristics, including age, gender, and risk factors, can further aid in identifying at-risk populations and tailoring management strategies effectively. Early intervention can significantly improve outcomes for patients diagnosed with this aggressive form of leukemia.
Approximate Synonyms
Acute myeloblastic leukemia (AML), classified under ICD-10 code C92.0, is a type of cancer that affects the blood and bone marrow. It is characterized by the rapid proliferation of myeloblasts, a type of immature white blood cell. Understanding the alternative names and related terms for this condition can enhance clarity in medical documentation and communication. Below are some of the key alternative names and related terms associated with ICD-10 code C92.0.
Alternative Names for Acute Myeloblastic Leukemia
- Acute Myeloid Leukemia (AML): This is the most commonly used term and encompasses various subtypes, including those with maturation and those without.
- Acute Myelogenous Leukemia: This term is often used interchangeably with acute myeloid leukemia and emphasizes the myeloid lineage of the leukemic cells.
- Acute Myeloblastic Leukemia: Specifically refers to the presence of myeloblasts in the blood and bone marrow, which is a hallmark of this disease.
- Acute Non-Lymphocytic Leukemia (ANLL): This term is less commonly used today but historically referred to all acute leukemias that are not of lymphoid origin, including AML.
Related Terms and Subtypes
- Acute Myeloid Leukemia with Maturation: This subtype of AML indicates that the myeloblasts are maturing into more differentiated cells, which can affect prognosis and treatment strategies[4].
- Acute Myeloid Leukemia, Not Otherwise Specified (NOS): This classification is used when the specific subtype of AML cannot be determined[7].
- Secondary Acute Myeloid Leukemia: This term refers to AML that develops as a consequence of previous hematological disorders, such as myelodysplastic syndromes[6].
- Acute Myeloblastic Leukemia, Not Having Achieved Remission: This designation is used for cases where the disease has not responded to treatment and remains active[13].
Clinical Context
Acute myeloblastic leukemia is a serious condition that requires prompt diagnosis and treatment. The terminology used can vary based on clinical context, and understanding these terms is crucial for healthcare professionals involved in the diagnosis, treatment, and coding of this disease. Accurate coding is essential for effective communication among healthcare providers and for proper billing and insurance purposes.
Conclusion
In summary, ICD-10 code C92.0 for acute myeloblastic leukemia is associated with several alternative names and related terms that reflect its clinical characteristics and subtypes. Familiarity with these terms can aid in better understanding and managing this complex disease, ensuring that patients receive appropriate care and treatment.
Diagnostic Criteria
Acute myeloblastic leukemia (AML), classified under ICD-10 code C92.0, is a type of cancer that affects the blood and bone marrow. The diagnosis of AML involves a combination of clinical evaluation, laboratory tests, and specific criteria established by medical guidelines. Below is a detailed overview of the criteria used for diagnosing acute myeloblastic leukemia.
Clinical Presentation
Symptoms
Patients with acute myeloblastic leukemia often present with a range of symptoms that may include:
- Fatigue and weakness: Due to anemia from reduced red blood cell production.
- Frequent infections: Resulting from neutropenia (low white blood cell count).
- Easy bruising or bleeding: Caused by thrombocytopenia (low platelet count).
- Bone pain: Often due to the infiltration of leukemic cells in the bone marrow.
- Fever: May occur due to infections or the disease itself.
Physical Examination
During a physical examination, clinicians may observe:
- Pallor: Indicative of anemia.
- Petechiae or ecchymosis: Signs of bleeding disorders.
- Splenomegaly or hepatomegaly: Enlargement of the spleen or liver due to leukemic infiltration.
Laboratory Tests
Complete Blood Count (CBC)
A CBC is essential for evaluating blood cell levels. In AML, findings may include:
- Elevated white blood cell count: Often with a predominance of myeloblasts.
- Low red blood cell count: Indicating anemia.
- Low platelet count: Suggesting thrombocytopenia.
Bone Marrow Biopsy
A definitive diagnosis of acute myeloblastic leukemia typically requires a bone marrow biopsy, which assesses:
- Cellularity: Increased cellularity with a high percentage of myeloblasts (≥20% of total nucleated cells).
- Morphology: Identification of myeloblasts and their characteristics, such as size, nuclear features, and cytoplasmic granules.
Cytogenetic and Molecular Studies
Cytogenetic analysis is crucial for identifying specific chromosomal abnormalities associated with AML, such as:
- Translocations: For example, t(15;17) in acute promyelocytic leukemia (APL), a subtype of AML.
- Mutations: Testing for mutations in genes like FLT3, NPM1, and CEBPA can provide prognostic information and guide treatment.
Immunophenotyping
Flow cytometry is used to analyze the surface markers on the cells, helping to confirm the diagnosis by identifying myeloid lineage markers (e.g., CD13, CD33) and excluding other types of leukemia.
Diagnostic Criteria Summary
The diagnosis of acute myeloblastic leukemia (ICD-10 code C92.0) is based on the following criteria:
1. Clinical symptoms: Presence of symptoms such as fatigue, infections, and bleeding.
2. Laboratory findings: CBC showing elevated white blood cells, low red blood cells, and low platelets.
3. Bone marrow examination: ≥20% myeloblasts in the bone marrow.
4. Cytogenetic and molecular analysis: Identification of specific chromosomal abnormalities or mutations.
5. Immunophenotyping: Confirmation of myeloid lineage through flow cytometry.
Conclusion
Diagnosing acute myeloblastic leukemia involves a comprehensive approach that integrates clinical evaluation, laboratory tests, and specialized studies. The combination of these criteria ensures accurate diagnosis and helps in formulating an effective treatment plan tailored to the patient's specific condition. Early diagnosis and intervention are crucial for improving outcomes in patients with AML.
Treatment Guidelines
Acute myeloblastic leukemia (AML), classified under ICD-10 code C92.0, is a type of cancer that affects the blood and bone marrow, characterized by the rapid proliferation of myeloblasts. The treatment of AML is complex and typically involves a combination of chemotherapy, targeted therapy, and sometimes stem cell transplantation. Below is a detailed overview of the standard treatment approaches for this condition.
Overview of Acute Myeloblastic Leukemia
Acute myeloblastic leukemia is a heterogeneous disease, meaning it can present in various forms and may respond differently to treatments. The prognosis and treatment strategies can vary significantly based on factors such as the patient's age, overall health, genetic mutations, and specific subtypes of AML.
Standard Treatment Approaches
1. Chemotherapy
Chemotherapy remains the cornerstone of treatment for AML. The standard regimen typically consists of two phases:
- Induction Therapy: The goal is to achieve remission by eliminating the majority of leukemic cells. Commonly used drugs include:
- Cytarabine (Ara-C)
- Anthracyclines (e.g., Daunorubicin or Idarubicin)
This phase usually lasts about 7 days and is followed by a period of recovery.
- Consolidation Therapy: After achieving remission, consolidation therapy aims to eliminate any remaining leukemic cells and prevent relapse. This may involve:
- High-dose cytarabine
- Additional courses of chemotherapy
2. Targeted Therapy
Recent advancements in the understanding of AML have led to the development of targeted therapies that focus on specific genetic mutations or abnormalities. Some notable examples include:
- Midostaurin: Used for patients with FLT3 mutations.
- Idhifa (Enasidenib): For patients with IDH2 mutations.
- Venclexta (Venetoclax): Often combined with other agents for older patients or those unfit for intensive chemotherapy.
These therapies can be used in conjunction with traditional chemotherapy or as standalone treatments, depending on the patient's specific genetic profile.
3. Stem Cell Transplantation
For patients with high-risk AML or those who do not achieve remission after initial chemotherapy, hematopoietic stem cell transplantation (HSCT) may be considered. This procedure involves:
- Allogeneic Transplantation: Using stem cells from a donor, which can provide a new immune system capable of fighting residual leukemia.
- Autologous Transplantation: Using the patient’s own stem cells, although this is less common in AML due to the risk of residual disease.
4. Supportive Care
Supportive care is crucial throughout the treatment process to manage side effects and complications. This includes:
- Blood Transfusions: To manage anemia and thrombocytopenia.
- Antibiotics: To prevent or treat infections, especially during periods of neutropenia (low white blood cell count).
- Growth Factors: Such as G-CSF (Granulocyte Colony-Stimulating Factor) to stimulate the production of white blood cells.
5. Clinical Trials
Patients with AML are often encouraged to consider participation in clinical trials, which may provide access to new therapies and treatment strategies that are not yet widely available. These trials can be particularly beneficial for those with relapsed or refractory disease.
Conclusion
The treatment of acute myeloblastic leukemia (ICD-10 code C92.0) is multifaceted, involving a combination of chemotherapy, targeted therapies, and potentially stem cell transplantation. The choice of treatment is highly individualized, taking into account the specific characteristics of the leukemia and the patient's overall health. Ongoing research and clinical trials continue to evolve the landscape of AML treatment, offering hope for improved outcomes in this challenging disease. For patients and caregivers, understanding these treatment options is essential for making informed decisions about care.
Related Information
Description
- Rapid proliferation of immature white blood cells
- Uncontrolled growth of myeloblasts crowds out normal cells
- Deficiency of healthy red, white, and platelet cells
- Symptoms include anemia, infections, and bleeding disorders
- Fatigue, weakness, frequent infections, easy bruising, fever, bone pain
Clinical Information
- AML a type of cancer affecting blood
- Rapid proliferation of immature white cells
- Anemia causes fatigue, weakness, and pallor
- Thrombocytopenia leads to easy bruising, bleeding
- Leukopenia increases susceptibility to infections
- Fever often due to infections or disease itself
- Weight loss occurs as disease progresses
- Splenomegaly enlargement of spleen is noted
- Hepatomegaly liver enlargement can occur
- Lymphadenopathy swelling of lymph nodes may present
- AML more common in older adults 68 years median age
- Male predominance in incidence of AML
Approximate Synonyms
- Acute Myeloid Leukemia
- Acute Myelogenous Leukemia
- Acute Non-Lymphocytic Leukemia (ANLL)
- Acute Myeloblastic Leukemia with Maturation
- Secondary Acute Myeloid Leukemia
Diagnostic Criteria
- Clinical symptoms present
- Elevated white blood cell count
- Low red blood cell count present
- Bone marrow shows ≥20% myeloblasts
- Specific chromosomal abnormalities identified
- Mutations in genes like FLT3, NPM1, CEBPA
- Myeloid lineage confirmed through flow cytometry
Treatment Guidelines
- Chemotherapy with cytarabine and anthracyclines
- Targeted therapy with midostaurin for FLT3 mutations
- Use of idhifa for IDH2 mutations
- Venclexta for older patients or those unfit
- Stem cell transplantation for high-risk AML
- Allogeneic transplantation using donor stem cells
- Blood transfusions to manage anemia and thrombocytopenia
- Antibiotics to prevent infections during neutropenia
- Growth factors to stimulate white blood cell production
Coding Guidelines
Excludes 1
- acute exacerbation of chronic myeloid leukemia (C92.10)
- refractory anemia with excess of blasts not in transformation (D46.2-)
Subcategories
Related Diseases
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