ICD-10: C91.12
Chronic lymphocytic leukemia of B-cell type in relapse
Additional Information
Description
Chronic lymphocytic leukemia (CLL) is a type of cancer that primarily affects the blood and bone marrow, characterized by the accumulation of abnormal B-lymphocytes. The ICD-10 code C91.12 specifically refers to "Chronic lymphocytic leukemia of B-cell type in relapse." This classification is crucial for accurate diagnosis, treatment planning, and billing purposes.
Clinical Description of CLL
Overview
Chronic lymphocytic leukemia is a hematological malignancy that typically progresses slowly. It is most commonly diagnosed in older adults and is characterized by the proliferation of B-cells that do not function properly. These abnormal cells can crowd out normal blood cells, leading to various complications, including anemia, increased susceptibility to infections, and bleeding issues.
Symptoms
Patients with CLL may experience a range of symptoms, which can include:
- Fatigue and weakness
- Swollen lymph nodes (lymphadenopathy)
- Splenomegaly (enlarged spleen)
- Unexplained weight loss
- Frequent infections
- Easy bruising or bleeding
Diagnosis
Diagnosis of CLL is typically made through blood tests that reveal elevated lymphocyte counts, along with bone marrow biopsy and flow cytometry to confirm the presence of abnormal B-cells. Genetic testing may also be performed to assess prognostic factors.
Relapse in CLL
Definition of Relapse
A relapse in CLL refers to the return of the disease after a period of remission. This can occur after initial treatment, which may include chemotherapy, targeted therapy, or immunotherapy. The relapse may manifest as an increase in lymphocyte counts or the re-emergence of symptoms.
Clinical Implications
The identification of CLL in relapse (ICD-10 code C91.12) is significant for several reasons:
- Treatment Decisions: Relapsed CLL may require different therapeutic approaches, including second-line treatments or clinical trials.
- Prognosis: The prognosis for patients with relapsed CLL can vary based on factors such as the duration of the initial remission and the specific characteristics of the leukemia cells.
- Monitoring: Patients in relapse need close monitoring for disease progression and response to new treatments.
Coding and Billing Considerations
ICD-10 Code C91.12
The ICD-10 code C91.12 is used in medical records and billing to specify the diagnosis of chronic lymphocytic leukemia of B-cell type in relapse. Accurate coding is essential for:
- Insurance Reimbursement: Ensuring that healthcare providers receive appropriate compensation for the treatment of relapsed CLL.
- Data Collection: Contributing to cancer registries and databases that track the incidence and outcomes of CLL.
Related Codes
Other relevant codes in the ICD-10 classification for CLL include:
- C91.10: Chronic lymphocytic leukemia of B-cell type, not in relapse.
- C91.11: Chronic lymphocytic leukemia of B-cell type, in remission.
Conclusion
Understanding the clinical description and details associated with ICD-10 code C91.12 is vital for healthcare providers managing patients with chronic lymphocytic leukemia. Recognizing the implications of relapse not only aids in treatment planning but also ensures accurate documentation and billing practices. As research continues to evolve, new therapies and management strategies for relapsed CLL are likely to emerge, improving patient outcomes and quality of life.
Approximate Synonyms
Chronic lymphocytic leukemia (CLL) of B-cell type in relapse, designated by the ICD-10 code C91.12, is a specific classification within the broader category of lymphoid leukemias. 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 C91.12.
Alternative Names
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B-cell Chronic Lymphocytic Leukemia (B-CLL): This term emphasizes the B-cell origin of the leukemia, which is crucial for understanding its pathophysiology and treatment options.
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Relapsed Chronic Lymphocytic Leukemia: This name highlights the condition's status as a relapse, indicating that the disease has returned after a period of remission.
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Recurrent B-cell Chronic Lymphocytic Leukemia: Similar to the previous term, this emphasizes the recurrence of the disease, which is a critical aspect of patient management.
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B-cell Lymphocytic Leukemia in Relapse: This term is a more general description that still specifies the B-cell lineage and the relapse status.
Related Terms
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Chronic Lymphocytic Leukemia (CLL): The broader category under which C91.12 falls, encompassing all forms of CLL, not just those in relapse.
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Minimal Residual Disease (MRD): This term refers to the small number of cancer cells that may remain in a patient after treatment, which can lead to relapse. Monitoring MRD is crucial in managing CLL.
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Lymphoid Leukemia: A general term that includes various types of leukemia originating from lymphoid cells, including CLL.
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B-cell Neoplasm: This term encompasses a range of malignancies arising from B-cells, including CLL, and can be relevant in discussions of related conditions.
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ICD-10 Code C91.10: This code refers to chronic lymphocytic leukemia of B-cell type without mention of relapse, providing a direct comparison to C91.12.
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ICD-10 Code C91.11: This code designates chronic lymphocytic leukemia of B-cell type in remission, further illustrating the spectrum of CLL classifications.
Understanding these alternative names and related terms is essential for healthcare professionals involved in the diagnosis, treatment, and coding of chronic lymphocytic leukemia, particularly in the context of relapsed cases. Accurate terminology ensures effective communication among medical teams and aids in the appropriate management of patients.
Clinical Information
Chronic lymphocytic leukemia (CLL) is a type of cancer that primarily affects the blood and bone marrow, characterized by the accumulation of abnormal B-lymphocytes. The ICD-10 code C91.12 specifically refers to "Chronic lymphocytic leukemia of B-cell type in relapse." Understanding the clinical presentation, signs, symptoms, and patient characteristics associated with this condition is crucial for effective diagnosis and management.
Clinical Presentation
Definition and Overview
Chronic lymphocytic leukemia is a hematological malignancy that typically progresses slowly. The "B-cell type" indicates that the leukemia originates from B-lymphocytes, which are a type of white blood cell involved in the immune response. When CLL is described as being in relapse, it means that the disease has returned after a period of remission, indicating a need for renewed treatment and monitoring.
Signs and Symptoms
Patients with CLL in relapse may exhibit a variety of signs and symptoms, which can vary in severity. Common manifestations include:
- Lymphadenopathy: Swelling of lymph nodes, particularly in the neck, armpits, or groin, is often one of the first signs of CLL. In relapse, lymph nodes may become enlarged again.
- Splenomegaly: Enlargement of the spleen can occur, leading to discomfort or a feeling of fullness in the abdomen.
- Fatigue: Persistent tiredness is a common complaint, often due to anemia or the body's response to the cancer.
- Weight Loss: Unintentional weight loss may occur, often linked to the increased metabolic demands of the cancer.
- Night Sweats: Patients may experience excessive sweating during the night, which can disrupt sleep.
- Fever: Low-grade fevers may be present, often as a response to infection or the disease itself.
- Increased Infections: Due to compromised immune function, patients may experience recurrent infections, which can be more frequent during relapse.
Patient Characteristics
Certain characteristics are commonly observed in patients diagnosed with CLL, particularly those experiencing a relapse:
- Age: CLL predominantly affects older adults, with the median age at diagnosis being around 70 years. Relapse may occur in this demographic, although younger patients can also be affected.
- Gender: Males are more frequently diagnosed with CLL than females, with a ratio of approximately 2:1.
- Genetic Factors: Some patients may have specific genetic mutations or chromosomal abnormalities that can influence the course of the disease and the likelihood of relapse.
- Previous Treatment History: Patients who have undergone treatment for CLL, such as chemotherapy or targeted therapies, may have varying responses, with some experiencing a relapse sooner than others.
Conclusion
Chronic lymphocytic leukemia of B-cell type in relapse presents a complex clinical picture characterized by a range of symptoms and signs, including lymphadenopathy, splenomegaly, fatigue, and increased susceptibility to infections. Understanding these clinical features, along with patient demographics and treatment history, is essential for healthcare providers to tailor appropriate management strategies for individuals facing this challenging condition. Regular monitoring and timely intervention are critical in managing relapsed CLL effectively.
Diagnostic Criteria
Chronic lymphocytic leukemia (CLL) is a type of cancer that affects the blood and bone marrow, characterized by the accumulation of abnormal B-lymphocytes. The ICD-10 code C91.12 specifically refers to "Chronic lymphocytic leukemia of B-cell type in relapse." Diagnosing CLL, particularly in the context of relapse, involves a combination of clinical evaluation, laboratory tests, and imaging studies. Below are the key criteria used for diagnosis:
Clinical Criteria
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Symptoms: Patients may present with various symptoms, including:
- Fatigue
- Unexplained weight loss
- Night sweats
- Fever
- Swollen lymph nodes (lymphadenopathy)
- Splenomegaly (enlarged spleen) or hepatomegaly (enlarged liver) [1]. -
Physical Examination: A thorough physical examination is essential to assess for lymphadenopathy, splenomegaly, and other signs of systemic illness.
Laboratory Tests
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Complete Blood Count (CBC): A CBC is crucial for evaluating blood cell counts. In CLL, there is typically:
- Elevated white blood cell count (WBC), often with a predominance of lymphocytes.
- Anemia (low red blood cell count) and thrombocytopenia (low platelet count) may also be present [2]. -
Flow Cytometry: This test is used to analyze the characteristics of the lymphocytes. In CLL, the abnormal B-cells typically express specific surface markers, such as:
- CD5
- CD19
- CD23
- Weak expression of immunoglobulin [3]. -
Bone Marrow Biopsy: A bone marrow biopsy may be performed to assess the infiltration of leukemic cells in the bone marrow. In cases of relapse, the percentage of leukemic cells may increase compared to previous evaluations [4].
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Cytogenetic Analysis: This involves examining the chromosomes of the leukemic cells to identify specific genetic abnormalities, such as deletions or mutations that can influence prognosis and treatment decisions [5].
Imaging Studies
- Ultrasound or CT Scans: Imaging studies may be utilized to evaluate the extent of lymphadenopathy or splenomegaly, helping to assess disease progression or relapse [6].
Diagnosis of Relapse
The diagnosis of relapse in CLL is typically based on:
- A significant increase in the number of circulating leukemic cells compared to previous assessments.
- The re-emergence of symptoms that were previously controlled or absent during remission.
- Changes in laboratory findings indicating disease progression, such as worsening anemia or thrombocytopenia [7].
Conclusion
The diagnosis of Chronic lymphocytic leukemia of B-cell type in relapse (ICD-10 code C91.12) is a multifaceted process that requires careful clinical evaluation, laboratory testing, and imaging studies. Understanding these criteria is essential for healthcare providers to accurately diagnose and manage patients with CLL, particularly when assessing for relapse. Continuous monitoring and follow-up are crucial for effective management and treatment planning.
Treatment Guidelines
Chronic lymphocytic leukemia (CLL) of B-cell type, particularly in relapse, is a complex condition that requires a nuanced approach to treatment. The International Classification of Diseases (ICD-10) code C91.12 specifically refers to this type of leukemia, which is characterized by the accumulation of functionally incompetent B lymphocytes in the blood, bone marrow, and lymphoid tissues. Here, we will explore the standard treatment approaches for managing relapsed CLL.
Overview of Chronic Lymphocytic Leukemia
Chronic lymphocytic leukemia is a hematological malignancy that primarily affects older adults. It is marked by a slow progression and can often be asymptomatic in its early stages. However, once the disease relapses, it can lead to more severe symptoms and complications, necessitating a change in treatment strategy.
Standard Treatment Approaches
1. Targeted Therapies
Targeted therapies have revolutionized the treatment of relapsed CLL. These therapies focus on specific molecular targets associated with cancer cells, leading to more effective and less toxic treatment options. Key agents include:
- Bruton’s Tyrosine Kinase (BTK) Inhibitors:
- Ibrutinib is a first-line BTK inhibitor that has shown significant efficacy in relapsed CLL. It works by blocking signals that promote the survival and proliferation of malignant B cells[1].
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Acalabrutinib is another BTK inhibitor that offers a similar mechanism with potentially fewer side effects[2].
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BCL-2 Inhibitors:
- Venetoclax is a BCL-2 inhibitor that induces apoptosis in CLL cells. It is often used in combination with other agents, such as rituximab, to enhance its effectiveness[3].
2. Monoclonal Antibodies
Monoclonal antibodies are designed to target specific antigens on cancer cells. In the context of relapsed CLL, the following are commonly used:
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Rituximab: This anti-CD20 monoclonal antibody is frequently used in combination with chemotherapy or targeted therapies. It helps to deplete B cells and can be effective in relapsed cases[4].
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Obinutuzumab: Another anti-CD20 monoclonal antibody, obinutuzumab, is often used in combination with venetoclax for patients with relapsed CLL, showing improved outcomes compared to traditional therapies[5].
3. Chemotherapy
While targeted therapies have become more prominent, chemotherapy remains a viable option, especially in certain patient populations. Common regimens include:
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Fludarabine, Cyclophosphamide, and Rituximab (FCR): This combination is often used for younger patients with good performance status and can be effective in relapsed cases[6].
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Bendamustine and Rituximab: This regimen is another option for patients who have relapsed after previous treatments, particularly for those who may not tolerate more intensive chemotherapy[7].
4. Stem Cell Transplantation
For some patients, particularly those with high-risk features or who have relapsed multiple times, allogeneic stem cell transplantation may be considered. This approach can offer a potential cure but comes with significant risks and is typically reserved for younger patients or those with aggressive disease[8].
Conclusion
The management of relapsed chronic lymphocytic leukemia of B-cell type (ICD-10 code C91.12) has evolved significantly with the advent of targeted therapies and monoclonal antibodies. Treatment decisions are often individualized based on patient characteristics, prior treatment history, and specific disease features. Ongoing clinical trials continue to explore new combinations and novel agents, promising further advancements in the treatment landscape for CLL. As always, a multidisciplinary approach involving hematologists, oncologists, and supportive care teams is essential for optimizing patient outcomes.
References
Related Information
Description
- Chronic lymphocytic leukemia (CLL) type cancer
- Affects blood and bone marrow
- Accumulation of abnormal B-lymphocytes
- Slow progression typical in CLL
- Most commonly diagnosed in older adults
- Symptoms include fatigue, weakness, swollen lymph nodes
- Diagnosis made through blood tests and bone marrow biopsy
- Relapse occurs after initial treatment with chemotherapy or targeted therapy
- Second-line treatments or clinical trials may be required
Approximate Synonyms
- B-cell Chronic Lymphocytic Leukemia
- Relapsed Chronic Lymphocytic Leukemia
- Recurrent B-cell Chronic Lymphocytic Leukemia
- B-cell Lymphocytic Leukemia in Relapse
- Chronic Lymphocytic Leukemia
- Minimal Residual Disease
- Lymphoid Leukemia
- B-cell Neoplasm
Clinical Information
Diagnostic Criteria
- Elevated white blood cell count
- Predominance of lymphocytes in CBC
- Anemia and thrombocytopenia
- CD5, CD19, CD23 expression
- Weak immunoglobulin expression
- Bone marrow infiltration by leukemic cells
- Cytogenetic abnormalities such as deletions or mutations
- Increase in circulating leukemic cells
- Re-emergence of symptoms during remission
- Disease progression indicated by worsening anemia/thrombocytopenia
Treatment Guidelines
- Targeted therapies with BTK inhibitors
- Ibrutinib for relapsed CLL patients
- Acalabrutinib offers similar efficacy with fewer side effects
- Venetoclax induces apoptosis in CLL cells
- Rituximab depletes B cells and can be effective
- Obinutuzumab improves outcomes in combination with venetoclax
- FCR regimen for younger patients with good performance status
- Bendamustine and rituximab for patients with relapsed disease
- Allogeneic stem cell transplantation for high-risk patients
Related Diseases
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