India
Haematology · 4 min read

Hodgkin Lymphoma

Learn about Hodgkin Lymphoma, its reported features, relevant specialists, and questions to discuss at a medical consultation.

Also known as: Hodgkin Disease

Compiled from public sources
Text selected and arranged from MedlinePlus (US National Library of Medicine) health topic. It describes the condition as those sources do; it has not been rewritten for India.
01 Oct 2026
Not medically reviewed
No registered doctor has reviewed this page. Use it to decide who to see and what to ask — not to diagnose or treat.
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This is not medical advice. If symptoms are severe, sudden or getting worse, call 112 (or 108 for an ambulance) or go to the nearest emergency department.

The sources compiled here do not cover: prevention, prognosis. Ask the treating doctor about these.

What is Hodgkin lymphoma?

From: MedlinePlus, National Library of Medicine

Hodgkin lymphoma, also called Hodgkin disease, is a type of cancer that develops in the lymph system. Your lymph system is part of your immune system. It helps protect your body from infection and disease.

The lymph system is made up of tissues and organs that produce, store, and carry white blood cells. It includes your:

  • Bone marrow
  • Lymph nodes
  • Lymphatic vessels
  • Spleen
  • Thymus
  • Tonsils

Hodgkin lymphoma is one of the main types of lymphoma. The other is non-Hodgkin lymphoma. Each type starts in different types of white blood cells.

What causes Hodgkin lymphoma?

From: MedlinePlus, National Library of Medicine

The cause of Hodgkin lymphoma is unknown. But there are certain people who are at higher risk of developing it.

Who is more likely to develop Hodgkin lymphoma?

From: MedlinePlus, National Library of Medicine

Certain factors can make you more likely to develop Hodgkin lymphoma:

  • Age. Hodgkin lymphoma is most common in early adulthood (age 20-39 years) and in late adulthood (age 65 years and older).
  • Being male. The risk of adult Hodgkin lymphoma is slightly higher in males than in females.
  • Past Epstein-Barr virus (EBV) infection. Having an infection with EBV as a young child or teenager increases your risk of Hodgkin lymphoma.
  • A family history of Hodgkin lymphoma. Having a parent or sibling with Hodgkin lymphoma increases your risk of developing it.

What are the symptoms of Hodgkin lymphoma?

From: MedlinePlus, National Library of Medicine

The signs and symptoms of Hodgkin lymphoma may include:

  • Painless, swollen lymph nodes in the neck, underarm, or groin
  • Fever for no known reason
  • Drenching night sweats (very heavy sweating during sleep)
  • Weight loss for no known reason in the past 6 months
  • Itchy skin, especially after bathing or drinking alcohol
  • Fatigue

How is Hodgkin lymphoma diagnosed?

From: MedlinePlus, National Library of Medicine

To find out if you have Hodgkin lymphoma, your provider:

  • Will ask about your symptoms and medical history. This will include checking for signs of disease, such as lumps or anything else that seems unusual.
  • May order some lab tests, such as: Complete blood count Blood chemistry studies Lactate dehydrogenase (LDH) test Erythrocyte sedimentation rate (ESR) test Blood tests to rule out other medical conditions May do imaging tests such as a CT and PET (positron emission tomography) scans May do a lymph node biopsy

What are the treatments for Hodgkin lymphoma?

From: MedlinePlus, National Library of Medicine

Treatments for Hodgkin lymphoma include:

  • Chemotherapy
  • Radiation therapy
  • Targeted therapy, which uses drugs or other substances that attack specific cancer cells with less harm to normal cells
  • Cancer immunotherapy

Hodgkin lymphoma can usually be cured if it is found and treated early.

Understanding terms used in the source

These definitions explain medical words used above. A definition is not evidence that another condition is present, and it does not predict how a symptom will develop. Ask the clinician which terms apply to the actual examination or test result.

Non-Hodgkin lymphoma
A type of lymphoma characterized microscopically by the absence of multinucleated Reed-Sternberg cells.
Family history
Information about close relatives of an individual who is the proband of a study or who is being investigated with the goal of identifying a medical diagnosis. Usually, the family history includes information from three generations of relatives, including children, brothers and sisters, parents, aunts and uncles, nieces and nephews, grandparents, and cousins.
Lymphoma
A cancer originating in lymphocytes and presenting as a solid tumor of lymhpoid cells.
Fatigue
A subjective feeling of tiredness characterized by a lack of energy and motivation.

Which doctor should you see?

The suggested department for discussing Hodgkin Lymphoma is Haematology, with a haematologist as the relevant type of clinician. General physician / Family Medicine; paediatrician for children. Referral depends on symptoms.

This is an editorial referral starting point. The appropriate clinic depends on the person’s age, symptoms, previous diagnosis and local services. The first clinician can decide whether another specialty or a team is needed; a department label does not confirm the diagnosis.

How to prepare for an assessment

Bring a short timeline of the main symptoms: when they first appeared, whether they are constant or episodic, what seems to change them, and how they affect daily activities. Include previous reports, discharge summaries, current medicines and supplements, allergies, and any relevant family history. A dated record is more useful than trying to match every feature in an online article.

Ask the clinician what is already established and what remains uncertain. If a test is suggested, ask what question it answers, what its limitations are and how the result would change the next step. The information here is not an instruction to arrange every possible test. In children, bring growth, developmental and school information if it is relevant to the concern.

  • Which blood-cell, marrow, bleeding or clotting finding matters most?
  • Does the diagnosis need confirmation or a more precise subtype?
  • Which symptoms or laboratory changes should trigger earlier review?

Treatment discussions and follow-up

Where the source describes treatments, these are an overview of possible care, not a prescription for an individual. Ask which option applies to the confirmed diagnosis, what benefit is expected, what adverse effects to watch for and how progress will be assessed. Availability, approvals and local practice can differ from the country described in the source.

Before leaving the appointment, clarify the next review date, who will communicate results, and whom to contact if the situation changes. Discuss difficulties with sleep, work, school, mobility, eating or emotional wellbeing when these are relevant. Practical support may require coordination between the treating clinician and other services.

The collected references do not establish a complete prevention or long-term outlook section for this entry. Missing information should not be interpreted as proof that prevention is impossible or that a particular outcome is inevitable. Ask what is known for the exact subtype, stage and personal circumstances, and which uncertainties remain.

When to seek emergency help

Severe breathing difficulty, collapse, new stroke-like symptoms, a seizure that is prolonged or repeated without recovery, uncontrolled major bleeding, or an immediate risk of self-harm require emergency help. In India, call 112 or reach the nearest emergency department. This is a general, non-exhaustive warning list; it is not a condition-specific triage tool.

Find a doctor for Hodgkin Lymphoma

This condition is usually assessed by a haematologist. Every profile shows the doctor’s registration and what has been checked.

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Sources

Source: MedlinePlus, National Library of Medicine. Orphadata Science: Free access data from Orphanet. © INSERM 1999; July 2026 data, CC BY 4.0. This product uses the Human Phenotype Ontology (hp/releases/2026-09-01). Only sources listed for this article apply. Source material has been selected and arranged; HPO definitions are reproduced without alteration. No source organisation endorses this compilation. Köhler S et al. The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data. Nucleic Acids Research 2014;42(D1):D966–D974. doi:10.1093/nar/gkt1026.

General information, not advice about your situation. Errors can be reported through the corrections process. Reference TDI-C-1173.