Hodgkin lymphoma (HL) is a type of lymphoma in which cancer originates from a specific type of white blood cell called lymphocytes, where multinucleated Reed–Sternberg cells (RS cells) are present in the patient's lymph nodes.[2][8] The condition was named after the English physician Thomas Hodgkin, who first described it in 1832.[9][10] Symptoms may include fever, night sweats, and weight loss.[2] Often, nonpainful enlarged lymph nodes occur in the neck, under the arm, or in the groin.[2] Persons affected may feel tired or be itchy.[2]

Hodgkin lymphoma
Other namesHodgkin's lymphoma, Hodgkin's disease[1]
Micrograph showing Hodgkin lymphoma (Field stain)
SpecialtyHematology and oncology
SymptomsFever, night sweats, weight loss, nonpainful enlarged lymph nodes[2]
Risk factorsEpstein–Barr virus, family history, HIV/AIDS[2][3]
Diagnostic methodLymph node biopsy[2]
TreatmentChemotherapy, radiation therapy, stem-cell transplant,[4] immunotherapy
PrognosisFive-year survival rate 88% (US)[5]
Frequency574,000 (affected during 2015)[6]
Deaths23,900 (2015)[7]
Named afterThomas Hodgkin

The two major types of Hodgkin lymphoma are classic Hodgkin lymphoma and nodular lymphocyte-predominant Hodgkin lymphoma.[5] About half of cases of Hodgkin lymphoma are due to Epstein–Barr virus (EBV) and these are generally the classic form.[3][11] Other risk factors include a family history of the condition and having HIV/AIDS.[2][3] Diagnosis is conducted by confirming the presence of cancer and identifying RS cells in lymph node biopsies.[2] The virus-positive cases are classified as a form of the Epstein–Barr virus-associated lymphoproliferative diseases.[12]

Hodgkin lymphoma may be treated with chemotherapy, radiation therapy, and stem-cell transplantation.[4] The choice of treatment often depends on how advanced the cancer has become and whether or not it has favorable features.[4] If the disease is detected early, a cure is often possible.[9] In the United States, 88% of people diagnosed with Hodgkin lymphoma survive for five years or longer.[5] For those under the age of 20, rates of survival are 97%.[13] Radiation and some chemotherapy drugs, however, increase the risk of other cancers, heart disease, or lung disease over the subsequent decades.[9]

In 2015, about 574,000 people globally had Hodgkin lymphoma, and 23,900 (4.2%) died.[6][7] In the United States, 0.2% of people are affected at some point in their life.[5] Most people are diagnosed with the disease between the ages of 20 and 40.[5]

Signs and symptoms


People with Hodgkin lymphoma may present with these symptoms:

  • Lymphadenopathy: The most common symptom of Hodgkin is the painless enlargement of one or more lymph nodes.[14] The nodes may also feel rubbery and swollen when examined. The nodes of the neck, armpits and groin (cervical and supraclavicular) are most frequently involved (80–90% of the time, on average).[14] The lymph nodes of the chest are often affected, and these may be noticed on a chest radiograph.[14]
  • Systemic symptoms: About one-third of people with Hodgkin disease may also present with systemic symptoms, including:[15]
  • Splenomegaly: Enlargement of the spleen is often present in people with Hodgkin lymphoma. The enlargement is seldom massive, and the size of the spleen may fluctuate during the course of treatment.[14]
  • Hepatomegaly: Enlargement of the liver, due to liver involvement, is infrequent in people with Hodgkin lymphoma.[14]
  • Hepatosplenomegaly: The enlargement of both the liver and spleen can be caused by the same disease.
  • Pain following alcohol consumption: Classically, involved nodes are painful after alcohol consumption, though this phenomenon is very uncommon,[16] occurring in only two to three percent of people with Hodgkin lymphoma,[17] thus having a low sensitivity. On the other hand, its positive predictive value is high enough for it to be regarded as a pathognomonic sign of Hodgkin lymphoma.[17] The pain typically has an onset within minutes after ingesting alcohol, and is usually felt as coming from the vicinity where there is an involved lymph node.[17] The pain has been described as either sharp and stabbing or dull and aching.[17]
  • Back pain: Nonspecific back pain (pain that cannot be localised or its cause determined by examination or scanning techniques) has been reported in some cases of Hodgkin lymphoma. The lower back is most often affected.[18]
  • Cyclical fever: People may also present with a cyclical high-grade fever known as the Pel–Ebstein fever,[19] or more simply "P-E fever". However, there is debate as to whether the P-E fever truly exists.[20]
  • Nephrotic syndrome can occur in individuals with Hodgkin lymphoma and is most commonly caused by minimal change disease.[21]
  • May present with airway obstruction, pleural/pericardial effusion, hepatocellular dysfunction, or bone-marrow infiltration.



Hodgkin lymphoma must be distinguished from noncancerous causes of lymph node swelling (such as various infections) and from other types of cancer. Definitive diagnosis is by lymph node biopsy (usually excisional biopsy with microscopic examination). Blood tests are also performed to assess function of major organs and safety for chemotherapy.[22] Positron emission tomography (PET) is used to detect small deposits that do not show on CT scanning. PET scans are also useful in functional imaging (by using a radiolabeled glucose to image tissues of high metabolism). In some cases, a gallium scan may be used instead of a PET scan.[23]



The two main types of Hodgkin lymphoma are classic Hodgkin lymphoma and nodular lymphocyte-predominant Hodgkin lymphoma. The prevalence of classic Hodgkin lymphoma and nodular-lymphocyte Hodgkin lymphoma are about 90 and 10%, respectively.[24][25] The morphology, phenotype, molecular features, and, therefore, the clinical behaviour and presentation of the two types differ.[26]



Classic Hodgkin lymphoma (excluding nodular lymphocyte predominant Hodgkin lymphoma) can be subclassified into four pathologic subtypes based upon Reed–Sternberg cell morphology and the composition of the reactive cell infiltrate seen in the lymph node biopsy specimen (the cell composition around the Reed–Sternberg cell(s)). Presence of EBV in Reed-Sternberg cells is most commonly found in the subtypes lymphocyte depleted HL (>70%) and mixed cellularity HL (70%), whilst being less prevalent in lymphocyte-rich HL (40%) and relatively uncommon by comparison in nodular sclerosing HL.[27][28]

Name Description ICD-10 ICD-O
Nodular sclerosing HL Is the most common subtype and is composed of large tumor nodules showing scattered lacunar classic RS cells set in a background of reactive lymphocytes, eosinophils and plasma cells with varying degrees of collagen fibrosis/sclerosis. C81.1 M9663/3
Mixed-cellularity subtype Is a common subtype and is composed of numerous classic RS cells admixed with numerous inflammatory cells including lymphocytes, histiocytes, eosinophils, and plasma cells without sclerosis. This type is most often associated with Epstein-Barr virus infection and may be confused with the early, so-called 'cellular' phase of the nodular sclerosing subtype. This type of Hodgkin lymphoma is most commonly seen in immunocompromised people. C81.2 M9652/3.
Lymphocyte-rich Is a rare subtype, show many features which may cause diagnostic confusion with nodular lymphocyte predominant B-cell non-Hodgkin lymphoma (B-NHL). This form also has the most favorable prognosis. C81.0 M9651/3
Lymphocyte depleted Is a rare subtype, composed of large numbers of often pleomorphic RS cells with only few reactive lymphocytes which may easily be confused with diffuse large cell lymphoma. Many cases previously classified within this category would now be reclassified under anaplastic large cell lymphoma.[29] C81.3 M9653/3
Unspecified C81.9 M9650/3
Lymph node biopsy showing Hodgkin lymphoma, mixed-cellularity type
CT image of a 46-year-old person with Hodgkin lymphoma, image at neck height. On the left side of the person's neck enlarged lymph nodes are visible (marked in red).

For the other forms, although the traditional B-cell markers (such as CD20) are not expressed on all cells,[29] Reed–Sternberg cells are usually of B cell origin.[30][31] Although Hodgkin's is now frequently grouped with other B-cell malignancies, some T-cell markers (such as CD2 and CD4) are occasionally expressed.[32] However, this may be an artifact of the ambiguity inherent in the diagnosis.

Hodgkin cells produce interleukin-21 (IL-21), which was once thought to be exclusive to T-cells. This feature may explain the behavior of classic Hodgkin lymphoma, including clusters of other immune cells gathered around HL cells (infiltrate) in cultures.[33]

Nodular lymphocyte predominant


Nodular lymphocyte predominant Hodgkin lymphoma (NLPHL) is another subtype of Hodgkin lymphoma distinct from classic Hodgkin lymphoma and is characterized by the presence of popcorn cells which express CD20.[25][34] Due to these differences, among others, NLPHL is often treated differently from classic Hodgkin lymphoma, including using rituximab in combination with AVBD chemotherapy, though individual cases vary and clinical trials are ongoing.[25]



The staging is the same for both Hodgkin and non-Hodgkin lymphomas.

After Hodgkin lymphoma is diagnosed, a person will be staged: that is, they will undergo a series of tests and procedures that will determine what areas of the body are affected. These procedures may include documentation of their histology, a physical examination, blood tests, chest X-ray radiographs, computed tomography (CT)/positron emission tomography (PET)/magnetic resonance imaging (MRI) scans of the chest, abdomen and pelvis, and usually a bone marrow biopsy. PET scan is now used instead of the gallium scan for staging. On the PET scan, sites involved with lymphoma light up very brightly enabling accurate and reproducible imaging.[35] In the past, a lymphangiogram or surgical laparotomy (which involves opening the abdominal cavity and visually inspecting for tumors) were performed. Lymphangiograms or laparotomies are very rarely performed, having been supplanted by improvements in imaging with the CT scan and PET scan.[18]

On the basis of this staging, the person will be classified according to a staging classification (the Ann Arbor staging classification scheme is a common one):[36]

  • Stage I is involvement of a single lymph node region (I) (mostly the cervical region) or single extralymphatic site (Ie);
  • Stage II is involvement of two or more lymph node regions on the same side of the diaphragm (II) or of one lymph node region and a contiguous extralymphatic site (IIe);
  • Stage III is involvement of lymph node regions on both sides of the diaphragm, which may include the spleen (IIIs) or limited contiguous extralymphatic organ or site (IIIe, IIIes);
  • Stage IV is disseminated involvement of one or more extralymphatic organs.

The absence of systemic symptoms is signified by adding "A" to the stage; the presence of systemic symptoms is signified by adding "B" to the stage. For localised extranodal extension from mass of nodes that does not advance the stage, subscript "E" is added. Splenic involvement is signified by adding "S" to the stage. The inclusion of "bulky disease" is signified by "X".[37]





Affected lymph nodes (most often, laterocervical lymph nodes) are enlarged, but their shape is preserved because the capsule is not invaded. Usually, the cut surface is white-grey and uniform; in some histological subtypes (e.g. nodular sclerosis) a nodular aspect may appear.[38]

A fibrin ring granuloma may be seen.


Micrograph of a classic Reed–Sternberg cell
Micrograph showing a "popcorn cell", the Reed–Sternberg cell variant seen in nodular lymphocyte predominant Hodgkin lymphoma. H&E stain

Microscopic examination of the lymph node biopsy reveals complete or partial effacement of the lymph node architecture by scattered large malignant cells known as Reed-Sternberg cells (RSC) (typical and variants) admixed within a reactive cell infiltrate composed of variable proportions of lymphocytes, histiocytes, eosinophils, and plasma cells. The Reed–Sternberg cells are identified as large often bi-nucleated cells with prominent nucleoli and an unusual CD45−, CD30+, CD15+/− immunophenotype. In approximately 50% of cases, the Reed–Sternberg cells are infected by the Epstein–Barr virus.[39]

Characteristics of classic Reed–Sternberg cells include large size (20–50 micrometres), abundant, amphophilic, finely granular/homogeneous cytoplasm; two mirror-image nuclei (owl eyes) each with an eosinophilic nucleolus and a thick nuclear membrane (chromatin is distributed close to the nuclear membrane). Almost all of these cells have an increased copy number of chromosome 9p/9p24.1.[40]


  • Hodgkin cell (atypical mononuclear RSC) is a variant of RS cell, which has the same characteristics but is mononucleated.[41]
  • Lacunar RSC is large, with a single hyperlobulated nucleus, multiple, small nucleoli and eosinophilic cytoplasm which is retracted around the nucleus, creating an empty space ("lacunae").
  • Pleomorphic RSC has multiple irregular nuclei.
  • "Popcorn" RSC (lympho-histiocytic variant) is a small cell, with a very lobulated nucleus, small nucleoli.
  • "Mummy" RSC has a compact nucleus with no nucleolus and basophilic cytoplasm.

Hodgkin lymphoma can be sub-classified by histological type. The cell histology in Hodgkin lymphoma is not as important as it is in non-Hodgkin lymphoma: the treatment and prognosis in classic Hodgkin lymphoma usually depends on the stage of disease rather than the histotype.[42]



The current approach for treatment aims to reduce the acute and long-term toxicities associated with Hodgkin lymphoma (e.g. cardiac damage and secondary cancers) and increase overall survival.[43]

People with early stage disease (IA or IIA) can be treated effectively with radiation therapy or chemotherapy. The choice of treatment depends on the age, sex, bulk and the histological subtype of the disease.[42] Adding localised radiation therapy after the chemotherapy regimen may provide a longer progression-free survival compared with chemotherapy treatment alone.[44] People with later disease (III, IVA, or IVB) are treated with combination chemotherapy alone. People of any stage with a large mass in the chest are usually treated with combined chemotherapy and radiation therapy.[45]

The original treatment for Hodgkin's was MOPP. The abbreviation stands for the four drugs Mustargen (also known as chlormethine), Oncovin (also known as vincristine), Prednisone and Procarbazine (also known as Matulane). The treatment is usually administered in four week cycles, often for six cycles. MSD and VCR are administered intravenously, while procarbazine and prednisone are pills taken orally. MOPP was the first combination chemotherapy brought in that achieved a high success rate. It was developed at the National Cancer Institute in the 1960s by a team that included Vincent DeVita Jr.

Although no longer the most effective combination, MOPP is still used after relapse or where the person has certain allergies or lung or heart problems which prevents the use of another regimen.

Currently, the ABVD chemotherapy regimen is the standard treatment of Hodgkin's disease in the US. The abbreviation stands for the four drugs Adriamycin, bleomycin, vinblastine, and dacarbazine. Developed in Italy in the 1970s, the ABVD treatment typically takes between six and eight months, although longer treatments may be required. The newer Stanford V regimen is typically only half as long as the ABVD but involves a more intensive chemotherapy schedule and incorporates radiation therapy. In a randomised controlled study in Italy, Stanford V was inferior to ABVD;[46] however, this study has been heavily criticized due to its incorrect administration of radiotherapy, diverging from the original Stanford V protocol.[47] BEACOPP is a form of treatment for stages > II mainly used in Europe. The cure rate with the BEACOPP esc. regimen is approximately 10–15% higher than with standard ABVD in advanced stages. This was shown in a paper in The New England Journal of Medicine (Diehl et al.), but US physicians still favor ABVD, maybe because some physicians think that BEACOPP induces more secondary leukemia. However, this seems negligible compared to the higher cure rates. BEACOPP is more expensive because of the requirement for concurrent treatment with GCSF to increase production of white blood cells. Currently, the German Hodgkin Study Group tests 8 cycles (8x) BEACOPP esc vs. 6x BEACOPP esc vs. 8x BEACOPP-14 baseline (HD15-trial).[48]
Chlormethine Doxorubicin Doxorubicin Doxorubicin
Oncovin Bleomycin Bleomycin Bleomycin
Prednisone Vinblastine Vinblastine, Vincristine Vincristine
Procarbazine Dacarbazine Chlormethine Cyclophosphamide, Procarbazine
Etoposide Etoposide
Prednisone Prednisone

The common non-Hodgkin treatment, rituximab (which is a monoclonal antibody against CD20) is not routinely used to treat Hodgkin lymphoma due to the lack of CD20 surface antigens in most cases. The use of rituximab in Hodgkin lymphoma, including the lymphocyte predominant subtype has been recently reviewed.[49] The evidence is very uncertain about the effect of Nivolumab for patients with a Hodgkin's lymphoma e.g. on the overall survival.[50]

Increased age is an adverse risk factor for Hodgkin lymphoma, but in general elderly people (≥ 60 years of age) without major comorbidities are sufficiently fit to tolerate therapy with curative intent. Despite this, treatment outcome in the elderly patient is not comparable to that of younger people and the disease is a different entity in older people where different considerations enter into treatment decisions.[51][52]

Recently, two novel targeted drugs have been developed for relapsing and refractory HL patients; Brentuximab vedotin, a CD30 antibody conjugated with a cytotoxic component MMAE,[53] and the checkpoint inhibitors, Nivolumab and Pembrolizumab.[54][55][56][57] This has been an important step in the treatment for the few, but still existing refractory patients.

For Hodgkin lymphomas, radiation oncologists typically use external beam radiation therapy (sometimes shortened to EBRT or XRT). Radiation oncologists deliver external beam radiation therapy to the lymphoma from a machine called a linear accelerator which produces high energy X-rays and electrons. People usually describe treatments as painless and similar to getting an X-ray. Treatments last less than 30 minutes each.

For lymphomas, there are a few different ways radiation oncologists target the cancer cells. Involved site radiation is when the radiation oncologists give radiation only to those parts of the person's body known to have the cancer.[58] Very often, this is combined with chemotherapy. Radiation therapy directed above the diaphragm to the neck, chest or underarms is called mantle field radiation. Radiation to below the diaphragm to the abdomen, spleen or pelvis is called inverted-Y field radiation. Total nodal irradiation is when the therapist gives radiation to all the lymph nodes in the body to destroy cells that may have spread.[59]

Adverse effects


The high cure rates and long survival of many people with Hodgkin lymphoma has led to a high concern with late adverse effects of treatment, including cardiovascular disease and second malignancies such as acute leukemias, lymphomas, and solid tumors within the radiation therapy field. Most people with early-stage disease are now treated with abbreviated chemotherapy and involved site radiation therapy rather than with radiation therapy alone. Clinical research strategies are exploring reduction of the duration of chemotherapy and dose and volume of radiation therapy in an attempt to reduce late morbidity and mortality of treatment while maintaining high cure rates. Hospitals are also treating those who respond quickly to chemotherapy with no radiation.[60]

In childhood cases of Hodgkin lymphoma, long-term endocrine adverse effects are a major concern, mainly gonadal dysfunction and growth retardation. Gonadal dysfunction seems to be the most severe endocrine long-term effect, especially after treatment with alkylating agents or pelvic radiotherapy.[61]

It is possible that patients undergoing a chemotherapy need a platelet transfusion.[62][63] If a stem cell transplantation is necessary for the treatment of a relapse, graft-versus-host diseases might occur.[64]

Supportive treatment


Adding physical exercises to the standard treatment for adult patients with haematological malignancies like Hodgkin lymphoma may result in little to no difference in the mortality, the quality of life and the physical functioning. These exercises may result in a slight reduction in depression. Furthermore, aerobic physical exercises probably reduce fatigue. The evidence is very uncertain about the effect on anxiety and serious adverse events.[65] 



Treatment of Hodgkin's disease has been improving over the past few decades. Recent[when?] trials that have made use of new types of chemotherapy have indicated higher survival rates than have previously been seen. In a 2007 European trial, the five-year survival rate for those people with a favorable prognosis (FFP) was 98%, while that for people with worse outlooks was at least 85%.[66]

In 1998, an international effort[67] identified seven prognostic factors that accurately predict the success rate of conventional treatment in people with locally extensive or advanced-stage Hodgkin lymphoma. Freedom from progression (FFP) at five years was directly related to the number of factors present in a person. The five-year FFP for people with zero factors is 84%. Each additional factor lowers the five-year FFP rate by 7%, such that the five-year FFP for a person with five or more factors is 42%.[68]

The adverse prognostic factors identified in the international study are:

Other studies have reported the following to be the most important adverse prognostic factors: mixed-cellularity or lymphocyte-depleted histologies, male sex, large number of involved nodal sites, advanced stage, age of 40 years or more, the presence of B symptoms, high erythrocyte sedimentation rate, and bulky disease (widening of the mediastinum by more than one third, or the presence of a nodal mass measuring more than 10 cm in any dimension.)[69]

More recently, the use of positron emission tomography (PET) early after commencing chemotherapy has demonstrated to have powerful prognostic ability.[70] This enables assessment of an individual's response to chemotherapy as the PET activity switches off rapidly in people who are responding. In this study,[70] after two cycles of ABVD chemotherapy, 83% of people were free of disease at 3 years if they had a negative PET versus only 28% in those with positive PET scans. This prognostic method improves on FFP estimates based on the seven conventional factors. Several trials are underway to see if PET-based risk adapted response can be used to improve a person's outcomes by changing chemotherapy early in people who are not responding.

The evidence is very uncertain about the effect of negative (= good prognosis) or positive (= bad prognosis) interim PET scan results for patients with a Hodgkin's lymphoma on the progression-free survival. Negative interim PET scan results may result in an increase in progression-free survival compared if the adjusted result was measured. Negative interim PET scan results probably result in a large increase in the overall survival compared to those with a positive interim PET scan result,[43]


Age-standardized death from lymphomas and multiple myeloma per 100,000 inhabitants in 2004[71]
  no data
  less than 1.8
  more than 19.8

Unlike some other lymphomas, whose number of new cases per year increases with age, Hodgkin lymphoma has a bimodal curve for the number of cases; that is, it occurs most frequently in two separate age groups, the first being young adulthood (age 15–35) and the second being in those over 55 years old although these peaks may vary slightly with nationality.[72] Overall, it is more common in males, except for the nodular sclerosis variant, which is slightly more common in females. The annual number of cases of Hodgkin lymphoma is 2.7 per 100,000 per persons per year, and the disease accounts for slightly less than 1% of all cancers worldwide.[73]

In 2010, globally it resulted in about 18,000 deaths down from 19,000 in 1990.[1] In 2012, there were an estimated 65,950 cases and 25,469 deaths from Hodgkin lymphoma worldwide, with 28,852 and 37,098 cases occurring in developed and developing countries, respectively.[74] However, the age-standardized rates were higher in developed regions, with the greatest rates in the Americas (1.5 per 100,000), East Mediterranean Region (1.5 per 100,000), and Europe (2.0 per 100,000).[74] The East Mediterranean Region also has the highest age-standardized mortality rate of 1.0 per 100,000, which is mainly attributed to lifestyle and environmental risk factors associated with transitional economies such as smoking, obesity, physical inactivity, and reproductive behaviors, as well as availability of diagnostic practices and awareness of the disease.[74]

The number of cases of Hodgkin lymphoma is increased in people with HIV infection.[75] In contrast to many other lymphomas associated with HIV infection it occurs most commonly in people with higher CD4 T cell counts.



Hodgkin lymphoma accounts for 0.6% of all male cancer cases, and 0.4% of all female cancer cases in Canada. In 2017, approximately 990 Canadians will be diagnosed with Hodgkin lymphoma, and 140 will die of the disease.[76]

Hodgkin lymphoma accounts for less than 1% of all cancer cases and deaths in the UK. Around 1,800 people were diagnosed with the disease in 2011, and around 330 people died in 2012.[77]

United States


In 2016, there were 8,389 new cases and 1,000 mortalities attributed to Hodgkin lymphoma, a decrease from the 8,625 new cases and 1,120 mortalities in 2015.[78] As of January 1, 2016, the 5-year limited duration prevalence of Hodgkin lymphoma was 37,513 representing 0.71% of all diagnosed cancers in the U.S.[78]


Photograph of Hodgkin's disease from a 1938 medical textbook

Hodgkin lymphoma was first described in an 1832 report by Thomas Hodgkin, although Hodgkin noted that perhaps an earlier reference to the condition was provided by Marcello Malpighi in 1666.[79][10] While occupied as museum curator at Guy's Hospital, London, Hodgkin studied seven people with painless lymph node enlargement. Of the seven cases, two were under the care of Richard Bright, one was of Thomas Addison, and one was of Robert Carswell.[79] Carswell's report of the seventh case was accompanied by numerous illustrations that aided early descriptions of the disease.[80]

Hodgkin's report on the seven cases, entitled "On some morbid appearances of the absorbent glands and spleen", was presented to the Medical and Chirurgical Society of London in January 1832 and was subsequently published in the society's journal, Medical-Chirurgical Society Transactions.[79] Hodgkin's paper went largely unnoticed, however, even though Bright highlighted it in an 1838 publication.[79] Indeed, Hodgkin himself did not view his contribution as particularly significant.[81]

In 1856, Samuel Wilks independently reported on a series of patients with the same disease that Hodgkin had previously described.[81] Wilks, a successor to Hodgkin at Guy's Hospital, was unaware of Hodgkin's prior work on the subject. Bright informed Wilks of Hodgkin's contribution and in 1865, Wilks published a second paper, entitled "Cases of enlargement of the lymphatic glands and spleen", in which he named the illness "Hodgkin's disease" in honor of his predecessor.[81]

Theodor Langhans and WS Greenfield first described the microscopic characteristics of Hodgkin lymphoma in 1872 and 1878, respectively.[79] In 1898 and 1902, respectively, Carl Sternberg and Dorothy Reed independently described the cytogenetic features of the malignant cells of Hodgkin lymphoma, now called Reed–Sternberg cells.[79]

Tissue specimens from Hodgkin's seven cases were preserved at Guy's Hospital. Nearly 100 years after Hodgkin's initial publication, histopathologic reexamination confirmed Hodgkin lymphoma in only three of seven of these people.[81] The remaining cases included non-Hodgkin lymphoma, tuberculosis, and syphilis.[81]

Hodgkin lymphoma was one of the first cancers to be treated successfully with radiation therapy and, later, it was one of the first to be treated by combination chemotherapy.

Notable cases



  1. ^ a b Lozano R, Naghavi M, Foreman K, Lim S, Shibuya K, Aboyans V, et al. (December 2012). "Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010". Lancet. 380 (9859): 2095–128. doi:10.1016/S0140-6736(12)61728-0. hdl:10536/DRO/DU:30050819. OCLC 23245604. PMC 10790329. PMID 23245604. S2CID 1541253.
  2. ^ a b c d e f g h i "Adult Hodgkin Lymphoma Treatment (PDQ) – Patient Version". NCI. August 3, 2016. Archived from the original on 28 July 2016. Retrieved 12 August 2016.
  3. ^ a b c World Cancer Report 2014. World Health Organization. 2014. Chapter 2.4. ISBN 978-928320429-9.
  4. ^ a b c "Adult Hodgkin Lymphoma Treatment (PDQ) – Patient Version". NCI. August 3, 2016. Archived from the original on 28 July 2016. Retrieved 13 August 2016.
  5. ^ a b c d e "SEER Stat Fact Sheets: Hodgkin Lymphoma". NCI. April 2016. Archived from the original on 17 October 2012. Retrieved 13 August 2016.
  6. ^ a b Vos T, Allen C, Arora M, Barber RM, Bhutta ZA, Brown A, Carter A, Casey DC, Charlson FJ, Chen AZ, Coggeshall M, Cornaby L, Dandona L, Dicker DJ, Dilegge T, Erskine HE, Ferrari AJ, Fitzmaurice C, Fleming T, Forouzanfar MH, Fullman N, Gething PW, Goldberg EM, Graetz N, Haagsma JA, Hay SI, Johnson CO, Kassebaum NJ, Kawashima T, Kemmer L (October 2016). "Global, regional, and national incidence, prevalence, and years lived with disability for 310 diseases and injuries, 1990–2015: a systematic analysis for the Global Burden of Disease Study 2015". Lancet. 388 (10053): 1545–1602. doi:10.1016/S0140-6736(16)31678-6. PMC 5055577. PMID 27733282.
  7. ^ a b Wang H, Naghavi M, Allen C, Barber RM, Bhutta ZA, Carter A, Casey DC, Charlson FJ, Chen AZ, Coates MM, Coggeshall M, Dandona L, Dicker DJ, Erskine HE, Ferrari AJ, Fitzmaurice C, Foreman K, Forouzanfar MH, Fraser MS, Fullman N, Gething PW, Goldberg EM, Graetz N, Haagsma JA, Hay SI, Huynh C, Johnson CO, Kassebaum NJ, Kinfu Y, Kulikoff XR (October 2016). "Global, regional, and national life expectancy, all-cause mortality, and cause-specific mortality for 249 causes of death, 1980–2015: a systematic analysis for the Global Burden of Disease Study 2015". Lancet. 388 (10053): 1459–1544. doi:10.1016/s0140-6736(16)31012-1. PMC 5388903. PMID 27733281.
  8. ^ Bower M, Waxman J (2011). Lecture Notes: Oncology (2nd ed.). Wiley. p. 195. ISBN 978-1-118-29300-3. Archived from the original on 2017-09-10.
  9. ^ a b c Armitage JO (August 2010). "Early-stage Hodgkin's lymphoma". The New England Journal of Medicine. 363 (7): 653–662. doi:10.1056/NEJMra1003733. PMID 20818856.
  10. ^ a b Hodgkin T (1832). "On some morbid experiences of the absorbent glands and spleen". Med Chir Trans. 17: 69–97.
  11. ^ Grewal R, Irimie A, Naidoo N, Mohamed N, Petrushev B, Chetty M, Tomuleasa C, Abayomi EA (March 2018). "Hodgkin's lymphoma and its association with EBV and HIV infection". Critical Reviews in Clinical Laboratory Sciences. 55 (2): 102–114. doi:10.1080/10408363.2017.1422692. PMID 29316828. S2CID 46790198.
  12. ^ Rezk SA, Zhao X, Weiss LM (September 2018). "Epstein-Barr virus (EBV)-associated lymphoid proliferations, a 2018 update". Human Pathology. 79: 18–41. doi:10.1016/j.humpath.2018.05.020. PMID 29885408. S2CID 47010934.
  13. ^ Ward E, DeSantis C, Robbins A, Kohler B, Jemal A (2014). "Childhood and adolescent cancer statistics, 2014". CA: A Cancer Journal for Clinicians. 64 (2): 83–103. doi:10.3322/caac.21219. PMID 24488779.
  14. ^ a b c d e Ansell SM (November 2015). "Hodgkin Lymphoma: Diagnosis and Treatment". Mayo Clinic Proceedings. 90 (11): 1574–83. doi:10.1016/j.mayocp.2015.07.005. PMID 26541251.
  15. ^ a b c d e f g Portlock CS (July 2008). "Hodgkin Lymphoma". Merck Manual Professional. Archived from the original on June 28, 2009. Retrieved June 18, 2009.
  16. ^ Bobrove AM (June 1983). "Alcohol-related pain and Hodgkin's disease". The Western Journal of Medicine. 138 (6): 874–5. PMC 1010854. PMID 6613116.
  17. ^ a b c d Page 242 Archived 2015-09-20 at the Wayback Machine in: John Kearsley (1998). Cancer: A Comprehensive Clinical Guide. Taylor & Francis. ISBN 978-90-5702-215-9.
  18. ^ a b "Hodgkin Lymphoma". The Lecturio Medical Concept Library. Retrieved 25 July 2021.
  19. ^ Hodgon DC, Gospodarowicz MK (2007). "Clinical Evaluation and Staging of Hodgkin Lymphoma". In Hoppe RT, Mauch PT, Armitage JO, Diehl V, Weiss LM (eds.). Hodgkin's disease (2nd ed.). Lippincott Williams & Wilkins. pp. 123–132. ISBN 978-0-7817-6422-3.
  20. ^ Hilson AJ (July 1995). "Pel-Ebstein fever". The New England Journal of Medicine. 333 (1): 66–7. doi:10.1056/NEJM199507063330118. PMID 7777006.
  21. ^ Audard V, Zhang SY, Copie-Bergman C, Rucker-Martin C, Ory V, Candelier M, Baia M, Lang P, Pawlak A, Sahali D (May 2010). "Occurrence of minimal change nephrotic syndrome in classic Hodgkin lymphoma is closely related to the induction of c-mip in Hodgkin-Reed Sternberg cells and podocytes". Blood. 115 (18): 3756–62. doi:10.1182/blood-2009-11-251132. PMC 2890576. PMID 20200355.
  22. ^ "Hodgkin Lymphoma Diagnosis | Tests for Hodgkin Lymphoma". www.cancer.org. Retrieved 2022-11-09.
  23. ^ Lennon AM, Buchanan AH, Kinde I, Warren A, Honushefsky A, Cohain AT, Ledbetter DH, Sanfilippo F, Sheridan K, Rosica D, Adonizio CS, Hwang HJ, Lahouel K, Cohen JD, Douville C (2020-07-03). "Feasibility of blood testing combined with PET-CT to screen for cancer and guide intervention". Science. 369 (6499): eabb9601. doi:10.1126/science.abb9601. PMC 7509949. PMID 32345712.
  24. ^ McKay P, Fielding P, Gallop-Evans E, Hall GW, Lambert J, Leach M, Marafioti T, McNamara C (January 2016). "Guidelines for the investigation and management of nodular lymphocyte predominant Hodgkin lymphoma". British Journal of Haematology. 172 (1): 32–43. doi:10.1111/bjh.13842. PMID 26538004.
  25. ^ a b c Swerdlow SH (2017-09-18). WHO classification of tumours of haematopoietic and lymphoid tissues (Revised 4th ed.). Lyon: International Agency for Research on Cancer, World Health Organization. ISBN 978-92-832-4494-3. OCLC 1011064243.
  26. ^ Re D, Thomas RK, Behringer K, Diehl V (2005-06-15). "From Hodgkin disease to Hodgkin lymphoma: biologic insights and therapeutic potential". Blood. 105 (12): 4553–60. doi:10.1182/blood-2004-12-4750. PMID 15728122. S2CID 8192701.
  27. ^ Gobbi PG, Ferreri AJ, Ponzoni M, Levis A (February 2013). "Hodgkin lymphoma". Critical Reviews in Oncology/Hematology. 85 (2): 216–237. doi:10.1016/j.critrevonc.2012.07.002. PMID 22867814. S2CID 27274760.
  28. ^ Gandhi MK, Tellam JT, Khanna R (May 2004). "Epstein-Barr virus-associated Hodgkin's lymphoma: Review". British Journal of Haematology. 125 (3): 267–281. doi:10.1111/j.1365-2141.2004.04902.x. PMID 15086409. S2CID 2355660.
  29. ^ a b "HMDS: Hodgkin's Lymphoma". Archived from the original on March 4, 2009. Retrieved February 1, 2009.
  30. ^ Küppers R, Schwering I, Bräuninger A, Rajewsky K, Hansmann ML (2002). "Biology of Hodgkin's lymphoma". Annals of Oncology. 13 (Suppl 1): 11–8. doi:10.1093/annonc/13.S1.11. PMID 12078890.
  31. ^ Bräuninger A, Schmitz R, Bechtel D, Renné C, Hansmann ML, Küppers R (April 2006). "Molecular biology of Hodgkin's and Reed/Sternberg cells in Hodgkin's lymphoma". International Journal of Cancer. 118 (8): 1853–61. doi:10.1002/ijc.21716. PMID 16385563.
  32. ^ Tzankov A, Bourgau C, Kaiser A, Zimpfer A, Maurer R, Pileri SA, Went P, Dirnhofer S (December 2005). "Rare expression of T-cell markers in classic Hodgkin's lymphoma". Modern Pathology. 18 (12): 1542–9. doi:10.1038/modpathol.3800473. PMID 16056244. S2CID 22493125.
  33. ^ Lamprecht B, Kreher S, Anagnostopoulos I, Jöhrens K, Monteleone G, Jundt F, Stein H, Janz M, Dörken B, Mathas S (October 2008). "Aberrant expression of the Th2 cytokine IL-21 in Hodgkin lymphoma cells regulates STAT3 signaling and attracts Treg cells via regulation of MIP-3alpha". Blood. 112 (8): 3339–47. doi:10.1182/blood-2008-01-134783. PMID 18684866.
  34. ^ Ansell S (2015). "Hodgkin Lymphoma: Diagnosis and Treatment". Mayo Clinic Proceedings. 90 (11): 1574–1583. doi:10.1016/j.mayocp.2015.07.005. PMID 26541251.
  35. ^ Hofman MS, Smeeton NC, Rankin SC, Nunan T, O'Doherty MJ (October 2009). "Observer variation in interpreting 18F-FDG PET/CT findings for lymphoma staging". Journal of Nuclear Medicine. 50 (10): 1594–7. doi:10.2967/jnumed.109.064121. PMID 19759113. S2CID 11505564.
  36. ^ ((PDQ Pediatric Treatment Editorial Board (2022-04-08). "Table 4. Ann Arbor Staging Classification for Hodgkin Lymphomaa". PDQ Cancer Information Summaries [Internet]. NBK65726.
  37. ^ Sapkota S, Shaikh H (2022), "Non-Hodgkin Lymphoma", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 32644754, retrieved 2022-11-09
  38. ^ Baba AI, Câtoi C (2007). TUMORS OF HEMATOPOIETIC AND LYMPHOID TISSUES. The Publishing House of the Romanian Academy.
  39. ^ Vockerodt M, Cader FZ, Shannon-Lowe C, Murray P (December 2014). "Epstein-Barr virus and the origin of Hodgkin lymphoma". Chinese Journal of Cancer. 33 (12): 591–7. PMC 4308654. PMID 25418190.
  40. ^ Wienand K, Chapuy B, Stewart C, Dunford AJ, Wu D, Kim J, Kamburov A, Wood TR, Cader FZ, Ducar MD, Thorner AR, Nag A, Heubeck AT, Buonopane MJ, Redd RA, Bojarczuk K, Lawton LN, Armand P, Rodig SJ, Fromm JR, Getz G, Shipp MA (December 2019). "Genomic analyses of flow-sorted Hodgkin Reed-Sternberg cells reveal complementary mechanisms of immune evasion". Blood Advances. 3 (23): 4065–4080. doi:10.1182/bloodadvances.2019001012. PMC 6963251. PMID 31816062.
  41. ^ Aggarwal P, Limaiem F (2022), "Reed Sternberg Cells", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 31194473, retrieved 2022-11-09
  42. ^ a b "Hodgkin lymphoma". NHS. 23 October 2017. Retrieved 25 July 2021.
  43. ^ a b Aldin A, Umlauff L, Estcourt LJ, Collins G, Moons KG, Engert A, Kobe C, von Tresckow B, Haque M, Foroutan F, Kreuzberger N, Trivella M, Skoetz N, et al. (Cochrane Haematology Group) (January 2020). "Interim PET-results for prognosis in adults with Hodgkin lymphoma: a systematic review and meta-analysis of prognostic factor studies". The Cochrane Database of Systematic Reviews. 1 (8): CD012643. doi:10.1002/14651858.CD012643.pub3. PMC 6984446. PMID 31930780.
  44. ^ Blank O, von Tresckow B, Monsef I, Specht L, Engert A, Skoetz N (April 2017). "Chemotherapy alone versus chemotherapy plus radiotherapy for adults with early stage Hodgkin lymphoma". The Cochrane Database of Systematic Reviews. 2017 (4): CD007110. doi:10.1002/14651858.CD007110.pub3. PMC 6478261. PMID 28447341.
  45. ^ Perri F, Della Vittoria Scarpati G, Buonerba C, Di Lorenzo G, Longo F, Muto P, Schiavone C, Sandomenico F, Caponigro F (2013-05-10). "Combined chemo-radiotherapy in locally advanced nasopharyngeal carcinomas". World Journal of Clinical Oncology. 4 (2): 47–51. doi:10.5306/wjco.v4.i2.47. PMC 3659263. PMID 23696962.
  46. ^ Gobbi PG, Levis A, Chisesi T, Broglia C, Vitolo U, Stelitano C, Pavone V, Cavanna L, Santini G, Merli F, Liberati M, Baldini L, Deliliers GL, Angelucci E, Bordonaro R, Federico M (December 2005). "ABVD versus modified stanford V versus MOPPEBVCAD with optional and limited radiotherapy in intermediate- and advanced-stage Hodgkin's lymphoma: final results of a multicenter randomized trial by the Intergruppo Italiano Linfomi". Journal of Clinical Oncology. 23 (36): 9198–207. doi:10.1200/JCO.2005.02.907. PMID 16172458. S2CID 24367707.
  47. ^ Edwards-Bennett SM, Jacks LM, Moskowitz CH, Wu EJ, Zhang Z, Noy A, Portlock CS, Straus DJ, Zelenetz AD, Yahalom J (March 2010). "Stanford V program for locally extensive and advanced Hodgkin lymphoma: the Memorial Sloan-Kettering Cancer Center experience". Annals of Oncology. 21 (3): 574–581. doi:10.1093/annonc/mdp337. PMID 19759185.
  48. ^ "Home | German Hodgkin Study Group". Ghsg.org. Archived from the original on 2011-08-17. Retrieved 2012-08-26.
  49. ^ Saini KS, Azim HA, Cocorocchio E, Vanazzi A, Saini ML, Raviele PR, Pruneri G, Peccatori FA (August 2011). "Rituximab in Hodgkin lymphoma: is the target always a hit?". Cancer Treatment Reviews. 37 (5): 385–90. doi:10.1016/j.ctrv.2010.11.005. PMID 21183282.
  50. ^ Ekstrand BC, Lucas JB, Horwitz SM, Fan Z, Breslin S, Hoppe RT, Natkunam Y, Bartlett NL, Horning SJ (2003-06-01). "Rituximab in lymphocyte-predominant Hodgkin disease: results of a phase 2 trial". Blood. 101 (11): 4285–4289. doi:10.1182/blood-2002-08-2644. PMID 12586628. S2CID 16108474.
  51. ^ Borchmann S, Engert A, Böll B (September 2018). "Hodgkin lymphoma in elderly patients". Curr Opin Oncol. 30 (5): 308–316. doi:10.1097/CCO.0000000000000464. PMID 29994901.
  52. ^ Klimm B, Diehl V, Engert A (July 2007). "Hodgkin's lymphoma in the elderly: a different disease in patients over 60". Oncology. 21 (8): 982–90, discussion 990, 996, 998 passim. PMID 17715698. Archived from the original on 2009-05-12.
  53. ^ Townsend W, Linch D (September 2012). "Hodgkin's lymphoma in adults". The Lancet. 380 (9844): 836–847. doi:10.1016/S0140-6736(12)60035-X. PMID 22835602. S2CID 15815020.
  54. ^ Ansell SM (July 2014). "Hodgkin lymphoma: 2014 update on diagnosis, risk-stratification, and management: Hodgkin lymphoma". American Journal of Hematology. 89 (7): 771–779. doi:10.1002/ajh.23750. PMID 24953862. S2CID 43857382.
  55. ^ Küppers R, Engert A, Hansmann ML (2012-10-01). "Hodgkin lymphoma". Journal of Clinical Investigation. 122 (10): 3439–3447. doi:10.1172/jci61245. PMC 3534167. PMID 23023715.
  56. ^ Eichenauer D, Engert A, André M, Federico M, Illidge T, Hutchings M, Ladetto M (September 2014). "Hodgkin's lymphoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up". Annals of Oncology. 25: iii70–5. doi:10.1093/annonc/mdu181. hdl:2318/1612165. PMID 25185243.
  57. ^ Bradley AM, Devine M, DeRemer D (2013-04-01). "Brentuximab vedotin: An anti-CD30 antibody–drug conjugate". American Journal of Health-System Pharmacy. 70 (7): 589–597. doi:10.2146/ajhp110608. PMID 23515511.
  58. ^ Specht L, Yahalom J, Illidge T, Berthelsen AK, Constine LS, Eich HT, Girinsky T, Hoppe RT, Mauch P, Mikhaeel NG, Ng A (July 2014). "Modern radiation therapy for Hodgkin lymphoma: field and dose guidelines from the international lymphoma radiation oncology group (ILROG)". International Journal of Radiation Oncology, Biology, Physics. 89 (4): 854–62. doi:10.1016/j.ijrobp.2013.05.005. PMID 23790512.
  59. ^ "RTanswers.com". RTanswers.com. 2010-12-03. Archived from the original on 2012-09-09. Retrieved 2012-08-26.
  60. ^ Moding EJ, Kastan MB, Kirsch DG (2013). "Strategies for optimizing the response of cancer and normal tissues to radiation". Nature Reviews. Drug Discovery. 12 (7): 526–542. doi:10.1038/nrd4003. PMC 3906736. PMID 23812271.
  61. ^ van Dorp W, van Beek RD, Laven JS, Pieters R, de Muinck Keizer-Schrama SM, van den Heuvel-Eibrink MM (2011). "Long-term endocrine side effects of childhood Hodgkin's lymphoma treatment: a review". Human Reproduction Update. 18 (1): 12–28. doi:10.1093/humupd/dmr038. PMID 21896559.
  62. ^ Estcourt L, Stanworth S, Doree C, Hopewell S, Murphy MF, Tinmouth A, Heddle N, et al. (Cochrane Haematological Malignancies Group) (May 2012). "Prophylactic platelet transfusion for prevention of bleeding in patients with haematological disorders after chemotherapy and stem cell transplantation". The Cochrane Database of Systematic Reviews (5): CD004269. doi:10.1002/14651858.CD004269.pub3. PMID 22592695.
  63. ^ Estcourt LJ, Stanworth SJ, Doree C, Hopewell S, Trivella M, Murphy MF, et al. (Cochrane Haematological Malignancies Group) (November 2015). "Comparison of different platelet count thresholds to guide administration of prophylactic platelet transfusion for preventing bleeding in people with haematological disorders after myelosuppressive chemotherapy or stem cell transplantation". The Cochrane Database of Systematic Reviews. 2015 (11): CD010983. doi:10.1002/14651858.CD010983.pub2. PMC 4717525. PMID 26576687.
  64. ^ Fisher SA, Cutler A, Doree C, Brunskill SJ, Stanworth SJ, Navarrete C, Girdlestone J, et al. (Cochrane Haematological Malignancies Group) (January 2019). "Mesenchymal stromal cells as treatment or prophylaxis for acute or chronic graft-versus-host disease in haematopoietic stem cell transplant (HSCT) recipients with a haematological condition". The Cochrane Database of Systematic Reviews. 1 (1): CD009768. doi:10.1002/14651858.CD009768.pub2. PMC 6353308. PMID 30697701.
  65. ^ Knips L, Bergenthal N, Streckmann F, Monsef I, Elter T, Skoetz N, et al. (Cochrane Haematological Malignancies Group) (January 2019). "Aerobic physical exercise for adult patients with haematological malignancies". The Cochrane Database of Systematic Reviews. 1 (1): CD009075. doi:10.1002/14651858.CD009075.pub3. PMC 6354325. PMID 30702150.
  66. ^ Fermé C, Eghbali H, Meerwaldt JH, Rieux C, Bosq J, Berger F, Girinsky T, Brice P, van't Veer MB, Walewski JA, Lederlin P, Tirelli U, Carde P, Van den Neste E, Gyan E, Monconduit M, Diviné M, Raemaekers JM, Salles G, Noordijk EM, Creemers GJ, Gabarre J, Hagenbeek A, Reman O, Blanc M, Thomas J, Vié B, Kluin-Nelemans JC, Viseu F, Baars JW, Poortmans P, Lugtenburg PJ, Carrie C, Jaubert J, Henry-Amar M (November 2007). "Chemotherapy plus involved-field radiation in early-stage Hodgkin's disease". The New England Journal of Medicine. 357 (19): 1916–27. doi:10.1056/NEJMoa064601. PMID 17989384. S2CID 11153555.
  67. ^ Hasenclever D, Diehl V (November 1998). "A prognostic score for advanced Hodgkin's disease. International Prognostic Factors Project on Advanced Hodgkin's Disease". The New England Journal of Medicine. 339 (21): 1506–14. doi:10.1056/NEJM199811193392104. PMID 9819449.
  68. ^ Wang Q, Qin Y, Kang SY, He XH, Liu P, Yang S, Zhou SY, Zhang CG, Gui L, Yang JL, Sun Y, Shi YK (2016-12-05). "Decreased Prognostic Value of International Prognostic Score in Chinese Advanced Hodgkin Lymphoma Patients Treated in the Contemporary Era". Chinese Medical Journal. 129 (23): 2780–5. doi:10.4103/0366-6999.194661. PMC 5146782. PMID 27900988.
  69. ^ Ali S, Basit A, Kazmi AS, Sidhu A, Badar F, Hameed A (2016). "Chemotherapy alone or combined chemotherapy and involved field radiotherapy in favorable risk early-stage classical Hodgkin lymphoma-a 10 years experience". Pakistan Journal of Medical Sciences. 32 (6): 1408–13. doi:10.12669/pjms.326.11080. PMC 5216291. PMID 28083035.
  70. ^ a b Biggi A, Gallamini A, Chauvie S, Hutchings M, Kostakoglu L, Gregianin M, Meignan M, Malkowski B, Hofman MS, Barrington SF (May 2013). "International validation study for interim PET in ABVD-treated, advanced-stage hodgkin lymphoma: interpretation criteria and concordance rate among reviewers". Journal of Nuclear Medicine. 54 (5): 683–90. doi:10.2967/jnumed.112.110890. PMID 23516309. S2CID 9959867.
  71. ^ "WHO Disease and injury country estimates". World Health Organisation. 2009. Archived from the original on 2009-11-11. Retrieved Nov 11, 2009.
  72. ^ Mauch P, Armitage J, Diehl V, Hoppe R, Weiss L (1999). Hodgkin's Disease. Lippincott Williams & Wilkins. pp. 62–64. ISBN 978-0-7817-1502-7.
  73. ^ "SEER Stat Fact Sheets: Leukemia". NCI Surveillance, Epidemiology, and End Results Program. Archived from the original on 17 October 2012. Retrieved 18 August 2014.
  74. ^ a b c Salati M, Cesaretti M, Macchia M, Mistiri ME, Federico M (2014-06-29). "Epidemiological Overview of Hodgkin Lymphoma across the Mediterranean Basin". Mediterranean Journal of Hematology and Infectious Diseases. 6 (1): e2014048. doi:10.4084/mjhid.2014.048. PMC 4103499. PMID 25045456.
  75. ^ Biggar RJ, Jaffe ES, Goedert JJ, Chaturvedi A, Pfeiffer R, Engels EA (December 2006). "Hodgkin lymphoma and immunodeficiency in persons with HIV/AIDS". Blood. 108 (12): 3786–91. doi:10.1182/blood-2006-05-024109. PMC 1895473. PMID 16917006.
  76. ^ "Canadian Cancer Statistics". www.cancer.ca. Archived from the original on 2018-01-25. Retrieved 2018-02-08.
  77. ^ "Hodgkin lymphoma statistics". Cancer Research UK. Archived from the original on 17 October 2014. Retrieved 27 October 2014.
  78. ^ a b "Lymphoma | CDC". www.cdc.gov. 2019-01-16. Retrieved 2019-11-25.
  79. ^ a b c d e f Hellman S (2007). "Brief Consideration of Thomas Hodgkin and His Times". In Hoppe RT, Mauch PT, Armitage JO, Diehl V, Weiss LM (eds.). Hodgkin Lymphoma (2nd ed.). Philadelphia: Wolters Kluwer Health/Lippincott Williams & Wilkins. pp. 3–6. ISBN 978-0-7817-6422-3.
  80. ^ Dawson PJ (December 1999). "The original illustrations of Hodgkin's disease". Annals of Diagnostic Pathology. 3 (6): 386–93. doi:10.1016/S1092-9134(99)80018-5. PMID 10594291.
  81. ^ a b c d e Geller SA (August 1984). "Comments on the anniversary of the description of Hodgkin's disease". Journal of the National Medical Association. 76 (8): 815–7. PMC 2609834. PMID 6381744.
  82. ^ "Microsoft co-founder Paul Allen diagnosed with cancer". CNN. Retrieved 2017-12-23.
  83. ^ "Eric Berry has Hodgkin's lymphoma". ESPN. 2014-12-08. Archived from the original on 2015-03-08.
  84. ^ "Bournemouth midfielder David Brooks diagnosed with cancer". Sky Sports. 13 October 2021. Retrieved 13 October 2021.
  85. ^ "Dale Carnagie at Biography.com". 6 February 2024. Retrieved 6 February 2024.
  86. ^ "Dale Carnagie page: strategies for influence". 6 February 2024. Retrieved 8 February 2024.
  87. ^ Stovall J, Johnson K (6 February 2024). Book: Words that Shaped our World, ref to Dale Carnagie+death. Sound Wisdom. ISBN 978-1-64095-416-8. Retrieved 8 February 2024.
  88. ^ James TG (2012) [2001]. Howard Carter: The Path to Tutankhamun. Tauris Parke Paperbacks. pp. 454–5. ISBN 978-1-84511-258-5. Archived from the original on 2017-09-10.
  89. ^ James T (2004). "Carter, Howard (1874–1939)". Oxford Dictionary of National Biography (online ed.). Oxford University Press. doi:10.1093/ref:odnb/32312. (Subscription or UK public library membership required.)
  90. ^ "Teen, court reach agreement over cancer care". NBC News. Associated Press. September 5, 2006. Retrieved June 18, 2009.
  91. ^ "James Conner Announces Cancer Diagnosis". Archived from the original on 2016-09-12. Retrieved 2016-09-29.
  92. ^ "Childhood Cancer Research Program—Michael Cuccione Foundation". www.childhoodcancerresearch.org. Archived from the original on 2016-08-18. Retrieved 2016-07-22.
  93. ^ Michael Cuccione
  94. ^ "Victoria Duval battling cancer". 2014-07-04. Archived from the original on 2016-01-12.
  95. ^ "Gerald Finzi biography". Retrieved 27 November 2017.
  96. ^ Ásta Sigrún Magnúsdóttir (16 October 2015). "Vá, hvað get ég gert meira?". Dagblaðið Vísir (in Icelandic). pp. 30–31. Retrieved 23 April 2021.
  97. ^ Gunnar Birgisson (11 October 2020). "Ótrúleg endurkoma eftir röð áfalla". RÚV (in Icelandic). Retrieved 23 April 2021.
  98. ^ "Delta Goodrem Hospitalized With Cancer". Billboard. 2003-07-14.
  99. ^ vlogbrothers (19 May 2023). "So, I've got cancer". YouTube. Retrieved 19 May 2023.
  100. ^ vlogbrothers (25 August 2023), Remission, retrieved 2023-08-26
  101. ^ Skálová, Johana. Nevyjasněná úmrtí V. 1st Ed. Praha: The World Circle Foundation, 2000. ISBN 80-902731-7-3.
  102. ^ Huver S (2010-07-23). "Cancer-Free Michael C. Hall Back to Work on Dexter—Health, Dexter, Michael C. Hall". People. Archived from the original on 2015-02-08. Retrieved 2015-03-04.
  103. ^ "Lionhearted—Death, Richard Harris". People. Archived from the original on 2015-02-04. Retrieved 2015-03-04.
  104. ^ "Minnesota: Evaluation Ordered for a 13-Year-Old With Cancer". The New York Times. Associated Press. May 16, 2009. Archived from the original on May 31, 2015. Retrieved June 18, 2009.
  105. ^ "Tessa James reveals she is in remission". Yahoo! News Australia. Archived from the original on 2015-12-22. Retrieved 2015-12-16.
  106. ^ "Comedian Sean Kent laughs off hecklers, cancer to stay on road". Columbia Daily Tribune. Retrieved 19 May 2023.
  107. ^ a b Chandler R (28 November 2007). "Funnyman Sean Kent winning fight vs. cancer". www.tahoedailytribune.com. Retrieved 19 May 2023.
  108. ^ "Mario Lemieux Foundation". Archived from the original on 3 April 2013. Retrieved 11 April 2013.
  109. ^ Mark Ainley (2002). "Dinu Lipatti: Prince of Pianists". markainley.com. Archived from the original on 22 October 2015. Retrieved 30 August 2015.
  110. ^ "Cancer fight gives Lisowski new angle on life". Daily Telegraph. Archived from the original on April 30, 2013.
  111. ^ Mamta Mohandas
  112. ^ Laura Winters (2002). "FILM; An Italian Satirist Takes a Very Serious Turn". The New York Times. Retrieved 6 September 2020.
  113. ^ "Denver health care activist speaking at Democratic convention". Denver Post. 2020-08-18.
  114. ^ "Nikola Pokrivač: Nema predaje, sve ću podnijeti za ženu i kćer" (in Croatian). 8 June 2017. Retrieved 10 September 2015.[permanent dead link]
  115. ^ "Emma: Anthony Rizzo's Indelible Impact". CBS Chicago. 8 May 2014. Archived from the original on 14 September 2015. Retrieved 30 August 2015.
  116. ^ "'04 Red Sox hero Roberts treated for lymphoma". ESPN.com. 2010-05-03. Retrieved 2020-10-28.
  117. ^ Chasnoff B (May 13, 2018). "Chip Roy's plan to get Washington out of the way includes going there himself". San Antonio Express-News. ExpressNews.com. Retrieved September 18, 2020.
  118. ^ |"Minnesota Timberwolves Say Head Coach Flip Saunders Has Died". abc.go.com. Archived from the original on 2015-10-26. Retrieved 2015-10-25.
  119. ^ "Specter diagnosed with Hodgkin's disease". CNN. 16 February 2005. Retrieved 31 August 2021.
  120. ^ Carter B (1997-08-28). "Brandon Tartikoff, Former NBC Executive Who Transformed TV in the 80's, Dies at 48". The New York Times.
  121. ^ "Portuguese midfielder Bernardo Tengarrinha diagnosed with linfoma de Hodgkin". Abola. 30 October 2021. Retrieved 30 October 2021.
  122. ^ "Ethan Zohn is a survivor in more ways than one". Chicago Tribune. 18 June 2014. Archived from the original on 2016-03-17. Retrieved 2016-03-26.
  123. ^ Thompson A (17 Feb 2023). "Richard Holliday completes cancer treatment". Post Wrestling. Retrieved 23 May 2023.
  124. ^ Czaplewski R (2023-09-30). "Home". www.rickczaplewski.com. Retrieved 2024-01-18.

Further reading