Everything you need to know about lymphoma — from Hodgkin and Non-Hodgkin subtypes to symptoms, staging, treatment options, and life after diagnosis — explained clearly by Dr. Aditya Sarin.
This page is for informational purposes only and does not constitute medical advice, diagnosis or treatment. Every case of lymphoma is different. Please consult Dr Aditya Sarin or a qualified oncologist for evaluation, diagnosis and a treatment plan specific to your condition.
Persistent, painless swelling in the neck, underarm, or groin should never be ignored. Schedule an evaluation with Dr. Aditya Sarin today.
Lymphoma is a cancer that begins in the lymphatic system — the network of lymph nodes, vessels, and organs, including the spleen and bone marrow, that helps the body fight infection. It develops when white blood cells called lymphocytes grow and divide abnormally.
There are two main types of lymphoma. Hodgkin lymphoma is characterised by a specific abnormal cell, the Reed-Sternberg cell, and can often be cured, particularly when caught early. Non-Hodgkin lymphoma is a much larger and more diverse group of over 60 subtypes, with a prognosis that depends heavily on the specific subtype involved.
Lymphoma is not a single disease. Understanding whether it is Hodgkin or Non-Hodgkin, and which specific subtype, is essential to designing the right treatment plan. Dr. Aditya Sarin evaluates each case individually, including molecular subtyping, to determine the precise diagnosis.
Hodgkin lymphoma usually begins in lymph nodes in the neck, chest, or underarms, and tends to spread in a predictable, step-by-step pattern between adjacent lymph node groups.
Characterised by the presence of Reed-Sternberg cells under the microscope.
The most common subtype of classical Hodgkin lymphoma, particularly in young adults.
More frequently seen in older adults and those with HIV.
Lacks classic Reed-Sternberg cells and is treated somewhat differently.
Non-Hodgkin lymphoma can begin in B cells, T cells, or, rarely, natural killer cells, and is broadly grouped into indolent, slow-growing forms and aggressive, fast-growing forms.
An aggressive subtype that grows quickly but often responds well to treatment.
Generally slow-growing and sometimes managed initially with active monitoring.
Chronic lymphocytic leukaemia and small lymphocytic lymphoma are different manifestations of the same slow-growing disease.
Requires a more intensive treatment approach.
Including mycosis fungoides and anaplastic large cell lymphoma, more common in teenagers and young adults.
A fast-growing subtype that requires urgent treatment.
The most common early symptom of lymphoma is painless swelling of one or more lymph nodes, typically in the neck, underarm, or groin. Many cases are found this way before other symptoms appear.
Note: Fever, night sweats, and weight loss together are sometimes referred to by doctors as "B symptoms," and their presence can affect staging and treatment planning. Many of these symptoms overlap with common infections, so persistent or unexplained swelling should always be evaluated by a doctor.
The exact cause of lymphoma is not fully understood, but several factors are known to increase risk. Being aware of your risk profile allows for earlier and more targeted evaluation.
Hodgkin lymphoma has two peak age ranges — young adults aged 15 to 40 and adults over 55 — while Non-Hodgkin lymphoma risk generally rises with age.
HIV infection, organ transplantation, and certain inherited immune conditions significantly increase lymphoma risk.
Epstein-Barr virus, Helicobacter pylori, and certain other chronic infections are linked to specific lymphoma subtypes.
Having a first-degree relative with lymphoma modestly increases risk, though most cases occur without any family history.
Having one or more risk factors does not mean a person will develop lymphoma, and many people diagnosed have no identifiable risk factor at all.
There is no routine screening test for lymphoma in the general population, unlike mammography for breast cancer or PSA testing for prostate cancer. Early detection instead depends on recognising symptoms and prompt evaluation.
A doctor checks for swollen lymph nodes in the neck, underarm, and groin, and examines the spleen and liver for enlargement.
A complete blood count and other blood tests can reveal abnormalities that may indicate lymphoma or rule out other causes.
CT, PET, or PET-CT scans identify affected lymph node regions and help determine how far the disease has spread.
Tissue sampling from an affected lymph node is required to confirm a lymphoma diagnosis and determine the exact subtype.
A swollen lymph node does not confirm lymphoma. Infections are a far more common cause. A node that persists beyond two to three weeks, continues to grow, or feels hard and fixed warrants prompt evaluation.
Staging describes how far the lymphoma has spread and directly shapes the treatment approach. Both Hodgkin and Non-Hodgkin lymphoma are staged using the Lugano classification, an updated version of the older Ann Arbour system, which assesses which lymph node regions are involved and whether the disease has spread to organs outside the lymph system. This staging guidance is current as of 2026.
Source: American Cancer Society, Non-Hodgkin Lymphoma Stages.
Survival statistics are population averages. They describe outcomes across large groups of patients and do not predict what will happen to any individual patient.
Source: Real-World Outcomes of Hodgkin Lymphoma: A Multi-Centric Registry From India, and Diffuse Large B-Cell Lymphoma, Experience from a Tertiary Care Hospital in Eastern India, Indian Journal of Haematology and Blood Transfusion.
Unlike several other cancers, Indian Hodgkin lymphoma outcomes from specialist centres are broadly comparable to those in the developed world, reflecting how well this cancer responds to standard treatment when patients can access it.
Treatment is tailored to the specific lymphoma type and subtype, stage, and the patient's overall health. Dr. Aditya Sarin develops a comprehensive, personalised treatment plan for every patient.
Combination regimens such as ABVD for Hodgkin lymphoma or R-CHOP for Non-Hodgkin lymphoma remain a backbone of treatment for most subtypes.
Targeted radiation to affected lymph node regions, often combined with chemotherapy for early-stage disease.
Checkpoint inhibitors that help the immune system recognise and attack lymphoma cells, now approved for both newly diagnosed and relapsed Hodgkin lymphoma.
Antibody-drug conjugates and other agents that act on specific proteins found on lymphoma cells, with fewer effects on healthy tissue.
A patient's own T-cells are engineered to recognise and destroy lymphoma cells, used for certain relapsed or refractory Non-Hodgkin lymphomas.
Lab-made antibodies that bring a patient's T-cells into direct contact with lymphoma cells, an increasingly important option for relapsed disease.
Used for relapsed or high-risk lymphoma, allowing higher-dose chemotherapy followed by restoration of healthy blood-forming cells.
For some slow-growing, indolent Non-Hodgkin lymphomas, regular monitoring without immediate treatment is an appropriate first approach.
Lymphoma treatment has changed meaningfully in the past year, particularly with the expansion of immunotherapy, bispecific antibodies, and CAR-T cell therapy into new patient groups. As of 2026, notable developments include the following.
On March 20, 2026, the FDA approved nivolumab in combination with doxorubicin, vinblastine, and dacarbazine (AVD chemotherapy) for adult and pediatric patients aged 12 and older with previously untreated Stage III or IV classical Hodgkin lymphoma. In the supporting Phase 3 trial, the nivolumab combination showed superior progression-free survival compared with the prior standard regimen.
On November 18, 2025, the FDA approved epcoritamab-bysp in combination with lenalidomide and rituximab for relapsed or refractory follicular lymphoma, as well as traditional approval as monotherapy after two or more prior lines of therapy.
Source: Oncology Nursing Society — Bispecific Antibody approvals update.
On February 19, 2026, the FDA expanded the label for axicabtagene ciloleucel (Yescarta), a CAR-T cell therapy, to include patients with relapsed or refractory primary central nervous system lymphoma, a rare and aggressive form of Non-Hodgkin lymphoma.
A lymphoma diagnosis affects not just physical health but emotional well-being and quality of life. Comprehensive support — from managing treatment side effects to emotional care — is an integral part of treatment at every stage.
Practical strategies and, where needed, medical support to manage treatment-related fatigue, nausea, and other side effects.
Professional emotional support and peer groups for patients and families navigating diagnosis and treatment.
Personalised dietary guidance to support the immune system and maintain strength through chemotherapy or immunotherapy.
ESMO Board Certified · Harvard Trained · Sir Ganga Ram Hospital, New Delhi
ESMO Board-certified oncologist with advanced training in precision oncology and cancer genomics from Harvard Medical School.
Access to the latest immunotherapy, targeted therapy, and personalised treatment protocols tailored to your specific lymphoma subtype.
Personalised treatment plans, emotional counselling, and end-to-end support for patients and their families.
High-quality oncology care with insurance assistance, flexible appointment options, and both in-person and remote consultations.
Don't wait for symptoms — schedule your evaluation today. If you've noticed persistent swelling, unexplained fever or fatigue, or simply want expert guidance on your lymph health, speak with Dr. Aditya Sarin — a trusted lymphoma specialist in New Delhi.
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