- Section 1 Patients and their treatment
- Section 2 Background to medicine
- Section 3 Cell biology
- Section 4 Immunological mechanisms
- Section 5 Principles of clinical oncology
- Section 6 Old age medicine
- Section 7 Pain and palliative care
- Section 8 Infectious diseases
- Section 9 Sexually transmitted diseases
- Section 10 Environmental medicine, occupational medicine, and poisoning
- Section 11 Nutrition
- Section 12 Metabolic disorders
- Section 13 Endocrine disorders
- Section 14 Medical disorders in pregnancy
- Section 15 Gastroenterological disorders
- Section 16 Cardiovascular disorders
- Section 17 Critical care medicine
- Section 18 Respiratory disorders
- Section 19 Rheumatological disorders
- Section 20 Disorders of the skeleton
- Section 21 Disorders of the kidney and urinary tract
- Section 22 Haematological disorders
- 22.1 Introduction to haematology
- 22.2 Haematopoiesis
- 22.3 Myeloid disease
- 22.4 Lymphoid disease
- 22.4.1 Introduction to lymphopoiesis
- 22.4.2 Acute lymphoblastic leukaemia
- 22.4.3 Hodgkin lymphoma
- 22.4.4 Non-Hodgkin lymphoma
- 22.4.5 Chronic lymphocytic leukaemia
- 22.4.6 Plasma cell myeloma and related monoclonal gammopathies
- 22.5 Bone marrow failure
- 22.6 Erythroid disorders
- 22.7 Haemostasis
- 22.8 Transfusion and transplantation
- Section 23 Disorders of the skin
- Section 24 Neurological disorders
- Section 25 Disorders of the eye
- Section 26 Psychiatric and drug-related disorders
- Section 27 Forensic medicine
- Section 28 Sport and exercise medicine
- Section 29 Biochemistry in medicine
- Section 30 Acute medicine
Hodgkin lymphoma
- Chapter:
- Hodgkin lymphoma
- Author(s):
Vijaya Raj Bhatt
, and James O. Armitage
- DOI:
- 10.1093/med/9780198746690.003.0524
Hodgkin’s lymphoma is derived from a profoundly defective B cell, with the pathobiology, histology, and clinical features being both characteristic and distinct from non-Hodgkin’s lymphomas. Its cause is unknown. Incidence is about 3 per 100 000 per year in Western countries with a bimodal age distribution meaning that it is one of the commoner lymphomas of young people. Most cases are highly responsive to combination chemotherapy, with many patients being cured of their disease. Patients with Hodgkin’s lymphoma may present with lymphadenopathy, a mediastinal (or other) mass, and systemic symptoms including weight loss, fever, and night sweats (B-symptoms). Workup requires staging with positron emission tomography (PET)-CT imaging, and biopsy. Classical Hodgkin’s lymphoma is defined by the presence of the binucleate Reed–Sternberg cell in an appropriate inflammatory histological context. These cells have a characteristic immunohistochemical phenotype, showing CD15 and CD30 positivity, but being immunonegative for classical B-cell markers such as CD20. Additional histological subtypes have been defined, with the most clinically significant being lymphocyte-predominant Hodgkin’s lymphoma. Patients with localized disease may be treated with chemotherapy with or without radiotherapy. Those with more advanced-stage disease require combination chemotherapy, with radiotherapy to sites of initial bulk disease. While relapse is uncommon in patients with early-stage disease, some 20% of patients with advanced-stage disease may need ‘salvage’ chemotherapy regimens for relapsed disease, when the aim is to attain PET negativity before embarking on high-dose therapy with stem cell rescue. Since many patients have a good outcome, it is essential to minimize the long-term sequelae of treatment. Risk stratification is a major focus of clinical trials in this area to determine optimal treatment strategies.
Access to the complete content on Oxford Medicine Online requires a subscription or purchase. Public users are able to search the site and view the abstracts for each book and chapter without a subscription.
Please subscribe or login to access full text content.
If you have purchased a print title that contains an access token, please see the token for information about how to register your code.
For questions on access or troubleshooting, please check our FAQs, and if you can't find the answer there, please contact us.
- Section 1 Patients and their treatment
- Section 2 Background to medicine
- Section 3 Cell biology
- Section 4 Immunological mechanisms
- Section 5 Principles of clinical oncology
- Section 6 Old age medicine
- Section 7 Pain and palliative care
- Section 8 Infectious diseases
- Section 9 Sexually transmitted diseases
- Section 10 Environmental medicine, occupational medicine, and poisoning
- Section 11 Nutrition
- Section 12 Metabolic disorders
- Section 13 Endocrine disorders
- Section 14 Medical disorders in pregnancy
- Section 15 Gastroenterological disorders
- Section 16 Cardiovascular disorders
- Section 17 Critical care medicine
- Section 18 Respiratory disorders
- Section 19 Rheumatological disorders
- Section 20 Disorders of the skeleton
- Section 21 Disorders of the kidney and urinary tract
- Section 22 Haematological disorders
- 22.1 Introduction to haematology
- 22.2 Haematopoiesis
- 22.3 Myeloid disease
- 22.4 Lymphoid disease
- 22.4.1 Introduction to lymphopoiesis
- 22.4.2 Acute lymphoblastic leukaemia
- 22.4.3 Hodgkin lymphoma
- 22.4.4 Non-Hodgkin lymphoma
- 22.4.5 Chronic lymphocytic leukaemia
- 22.4.6 Plasma cell myeloma and related monoclonal gammopathies
- 22.5 Bone marrow failure
- 22.6 Erythroid disorders
- 22.7 Haemostasis
- 22.8 Transfusion and transplantation
- Section 23 Disorders of the skin
- Section 24 Neurological disorders
- Section 25 Disorders of the eye
- Section 26 Psychiatric and drug-related disorders
- Section 27 Forensic medicine
- Section 28 Sport and exercise medicine
- Section 29 Biochemistry in medicine
- Section 30 Acute medicine