Diffuse large B-cell lymphoma
(Redirected from Primary cutaneous large B-cell lymphoma)
Diffuse Large B-Cell Lymphoma[edit | edit source]
Diffuse Large B-Cell Lymphoma[edit | edit source]
Diffuse large B-cell lymphoma (DLBCL) is a type of B-cell non-Hodgkin lymphoma, which is a cancer of the immune system. It is known for being aggressive, or fast-growing, and is the most common type of non-Hodgkin lymphoma. DLBCL typically manifests as rapidly enlarging tumors in the lymph nodes, spleen, liver, bone marrow, or other organs.
Symptoms[edit | edit source]
Common symptoms of DLBCL include:
- Fever
- Night sweats
- Weight loss
- Enlarged lymph nodes
- Fatigue
- Loss of appetite
Subtypes of DLBCL[edit | edit source]
DLBCL can be classified into several subtypes based on genetic, molecular, and clinical features, including:
- Germinal Center B-cell-like (GCB)
- Activated B-cell-like (ABC)
- Primary Mediastinal B-cell lymphoma
- Others, as identified through advanced molecular and genetic testing
Diagnosis[edit | edit source]
Diagnosing DLBCL involves:
- Physical examination, particularly of the lymph nodes
- Laboratory tests including complete blood count (CBC) and lactate dehydrogenase (LDH) levels
- Imaging studies such as CT scans and PET scans
- Biopsy of the lymph node or other affected tissues
Treatment[edit | edit source]
Treatment for DLBCL generally includes:
- Chemotherapy, often combined with the monoclonal antibody Rituximab
- In some cases, Radiation therapy may be used
- Advanced cases may require bone marrow or stem cell transplantation
Prognosis[edit | edit source]
The prognosis for DLBCL varies based on factors such as:
- Age and overall health of the patient
- Stage of the lymphoma at diagnosis
- Response to initial treatment
- Specific subtype of DLBCL
Ongoing Research[edit | edit source]
Research into DLBCL is focused on:
- Developing targeted therapies
- Improving the effectiveness of current treatments
- Understanding the genetic and molecular basis of the disease
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