Hodgkin lymphoma

Other names: Hodgkin's lymphoma, Hodgkin's disease[1]
Micrograph showing Hodgkin lymphoma (Field stain)
Specialty| Hematology and oncology
Symptoms| Fever, night sweats, weight loss, non-painful enlarged lymph nodes[2]
Risk factors| Epstein–Barr virus, family history, HIV/AIDS[2][3]
Diagnostic method| Lymph node biopsy[2]
Treatment| Chemotherapy, radiation therapy, stem cell transplant[4]
Prognosis| Five-year survival rate 86% (USA)[5]
Frequency| 574,000 (affected during 2015)[6]
Deaths| 23,900 (2015)[7]

Hodgkin lymphoma (HL) is a type of lymphoma in which cancer originates from a specific type of white blood cells called lymphocytes.[8] Symptoms may include fever, night sweats, and weight loss.[2] Often there will be non-painful enlarged lymph nodes in the neck, under the arm, or in the groin.[2] Those affected may feel tired or be itchy.[2]

There are two major types of Hodgkin lymphoma: classical 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][9] Other risk factors include a family history of the condition and having HIV/AIDS.[2][3] Diagnosis is by finding Hodgkin cells such as multinucleated Reed–Sternberg cells (RS cells) in lymph nodes.[2] The virus-positive cases are classified as a form of the Epstein-Barr virus-associated lymphoproliferative diseases.[10]

Hodgkin lymphoma may be treated with chemotherapy, radiation therapy, and stem cell transplant.[4] The choice of treatment often depends on how advanced the cancer has become and whether or not it has favorable features.[4] In early disease, a cure is often possible.[11] The percentage of people who survive five years in the United States is 86%.[5] For those under the age of 20, rates of survival are 97%.[12] Radiation and some chemotherapy drugs, however, increase the risk of other cancers, heart disease, or lung disease over the subsequent decades.[11]

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] The most common age of diagnosis is between 20 and 40 years old.[5] It was named after the English physician Thomas Hodgkin, who first described the condition in 1832.[11][13]

## Contents

* 1 Signs and symptoms
* 2 Diagnosis
* 2.1 Types
* 2.1.1 Classical
* 2.1.2 Nodular lymphocyte predominant
* 2.2 Staging
* 2.3 Pathology
* 3 Management
* 3.1 Side effects
* 4 Prognosis
* 5 Epidemiology
* 5.1 Canada
* 5.2 UK
* 5.3 United States
* 6 History
* 7 Notable cases
* 8 References
* 9 Further reading
* 10 External links

## Signs and symptoms[edit | edit source]

People with Hodgkin lymphoma may present with the following 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 and shoulders (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]
* Itchy skin[15]
* Night sweats.[15]
* Unexplained weight loss of at least 10% of the person's total body mass in six months or less.[15]
* Low-grade fever.[15]
* Fatigue (lassitude).[15]
* Systemic symptoms such as fever, night sweats, and weight loss are known as B symptoms; thus, presence of these indicate that the person's stage is, for example, 2B instead of 2A.[15]
* Splenomegaly: enlargement of the spleen is often present in people with Hodgkin lymphoma. The enlargement, however, 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 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.[citation needed]
* Cyclical fever: people may also present with a cyclical high-grade fever known as the Pel–Ebstein fever,[18] or more simply "P-E fever". However, there is debate as to whether the P-E fever truly exists.[19]
* Nephrotic syndrome can occur in individuals with Hodgkin lymphoma and is most commonly caused by minimal change disease.[20]

## Diagnosis[edit | edit source]

Hodgkin lymphoma must be distinguished from non-cancerous 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 to assess safety for chemotherapy. 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.

* Hodgkin lymphoma (gross pathology)

* Hodgkin lymphoma

* Hodgkin lymphoma- hilum overlay sign

### Types[edit | edit source]

There are two main types of Hodgkin lymphoma: classical Hodgkin lymphoma and nodular lymphocyte predominant Hodgkin lymphoma. The prevalence of classical Hodgkin lymphoma and nodular lymphocyte Hodgkin lymphoma are approximately 90% and 10%, respectively.[21][22]

#### Classical[edit | edit source]

Classical 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)).

Name | Description | ICD-10 | ICD-O

|
|
|

Nodular sclerosing HL | Is the most common subtype and is composed of large tumor nodules showing scattered lacunar classical 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 nodular sclerosing Chl . 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.[23] | 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,[23] Reed–Sternberg cells are usually of B cell origin.[24][25] Although Hodgkin's is now frequently grouped with other B-cell malignancies, some T-cell markers (such as CD2 and CD4) are occasionally expressed.[26] 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 classical Hodgkin lymphoma, including clusters of other immune cells gathered around HL cells (infiltrate) in cultures.[27]

#### Nodular lymphocyte predominant[edit | edit source]

Nodular lymphocyte predominant Hodgkin lymphoma (NLPHL) is another subtype of Hodgkin lymphoma distinct from Classical Hodgkin lymphoma and is characterized by the presence of popcorn cells which express CD20.[22][28] Due to these differences, among others, NLPHL is often treated differently from Classical Hodgkin lymphoma, including using Rituximab in combination with AVBD chemotherapy, though individual cases vary and clinical trials are ongoing.[22]

### Staging[edit | edit source]

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. Positron emission tomography (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.[29] 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.

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):

* 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".

* Stage 1 Hodgkin lymphoma

* Stage 2 Hodgkin lymphoma

* Stage 3 Hodgkin lymphoma

* Stage 4 Hodgkin lymphoma

### Pathology[edit | edit source]

Macroscopy

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.

A fibrin ring granuloma may be seen.

Microscopy
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.[30]

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.[31]

Variants:

* Hodgkin cell (atypical mononuclear RSC) is a variant of RS cell, which has the same characteristics, but is mononucleated.
* 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.

## Management[edit | edit source]

People with early stage disease (IA or IIA) are effectively treated with radiation therapy or chemotherapy. The choice of treatment depends on the age, sex, bulk and the histological subtype of the disease.[citation needed] Adding localised radiation therapy after the chemotherapy regimen may provide a longer progression-free survival compared with chemotherapy treatment alone.[32] 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.[citation needed]

MOPP | ABVD | Stanford V | BEACOPP

|
|
|

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;[33] however, this study has been heavily criticized due to its incorrect administration of radiotherapy, diverging from the original Stanford V protocol.[34] | 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).[35]
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.[36]

Although increased age is an adverse risk factor for Hodgkin lymphoma, in general elderly people without major comorbidities are sufficiently fit to tolerate standard therapy, and have a treatment outcome comparable to that of younger people. However, the disease is a different entity in older people and different considerations enter into treatment decisions.[37]

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.[38] 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.[39]

### Side effects[edit | edit source]

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.

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.[40]

## Prognosis[edit | edit source]

Treatment of Hodgkin's disease has been improving over the past few decades. Recent trials that have made use of new types of chemotherapy have indicated higher survival rates than have previously been seen. In one recent European trial, the 5-year survival rate for those people with a favorable prognosis (FFP) was 98%, while that for people with worse outlooks was at least 85%.[41]

In 1998, an international effort[42] 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 5 years was directly related to the number of factors present in a person. The 5-year FFP for people with zero factors is 84%. Each additional factor lowers the 5-year FFP rate by 7%, such that the 5-year FFP for a person with 5 or more factors is 42%.

The adverse prognostic factors identified in the international study are:

* Age ≥ 45 years
* Stage IV disease
* Hemoglobin < 10.5 g/dl
* Lymphocyte count < 600/µl or < 8%
* Male
* Albumin < 4.0 g/dl
* White blood count ≥ 15,000/µl

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.)

More recently, use of positron emission tomography (PET) early after commencing chemotherapy has demonstrated to have powerful prognostic ability.[43] 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,[43] 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 power exceeds conventional factors discussed above. Several trials are underway to see if PET-based risk adapted response can be used to improve a persons outcomes by changing chemotherapy early in people who are not responding.

## Epidemiology[edit | edit source]

Age-standardized death from lymphomas and multiple myeloma per 100,000 inhabitants in 2004[44]

no data

less than 1.8

1.8–3.6

3.6–5.4

5.4–7.2

7.2–9

9–10.8

10.8–12.6

12.6–14.4

14.4–16.2

16.2–18

18–19.8

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.[45] 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.[46]

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.[47] 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).[47] 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.[47]

The number of cases of Hodgkin lymphoma is increased in people with HIV infection.[48] In contrast to many other lymphomas associated with HIV infection it occurs most commonly in people with higher CD4 T cell counts.

### Canada[edit | edit source]

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.[49]

### UK[edit | edit source]

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.[50]

### United States[edit | edit source]

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.[51] 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.[51]

## History[edit | edit source]

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 the earliest reference to the condition was provided by Marcello Malpighi in 1666.[52][13] 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.[52] Carswell's report of this seventh person was accompanied by numerous illustrations that aided early descriptions of the disease.[53]

Hodgkin's report on these seven people, 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.[52] Hodgkin's paper went largely unnoticed, however, even despite Bright highlighting it in an 1838 publication.[52] Indeed, Hodgkin himself did not view his contribution as particularly significant.[54]

In 1856, Samuel Wilks independently reported on a series of people with the same disease that Hodgkin had previously described.[54] Wilks, a successor to Hodgkin at Guy's Hospital, was unaware of Hodgkin's prior work on the subject. Bright made Wilks aware 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 called the disease "Hodgkin's disease" in honor of his predecessor.[54]

Theodor Langhans and WS Greenfield first described the microscopic characteristics of Hodgkin lymphoma in 1872 and 1878, respectively.[52] 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.[52]

Tissue specimens from Hodgkin seven people remained at Guy's Hospital for a number of years. Nearly 100 years after Hodgkin's initial publication, histopathologic reexamination confirmed Hodgkin lymphoma in only three of seven of these people.[54] The remaining cases included non-Hodgkin lymphoma, tuberculosis, and syphilis.[54]

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

## Notable cases[edit | edit source]

* Paul Allen, co-founder of Microsoft was diagnosed with Hodgkin lymphoma in 1982. He later died from non-Hodgkin lymphoma on October 15, 2018.[55]
* Eric Berry, All-Pro strong safety for the Kansas City Chiefs of the National Football League, diagnosed in 2014.[56]
* Howard Carter, Egyptologist and discoverer of the Tomb of Tutankhamun, died in 1939 from Hodgkin's disease.[57][58]
* Starchild Abraham Cherrix, a teenager whose refusal to undergo further conventional treatment after relapsing in 2006 resulted in a court battle and a change to Virginia laws about medical neglect.[59]
* James Conner, running back and 2014 ACC Player of the Year for the Pittsburgh Steelers.[60]
* Michael Cuccione, a Canadian child actor was diagnosed in 1994 at age 9.[61]
* Victoria Duval, American tennis player was diagnosed in 2014.[62]
* Gerald Finzi, British composer was diagnosed in 1951 and died in 1956.[63]
* Delta Goodrem, Australian singer, songwriter, and actress. Delta was diagnosed in July 2003 at the age of 18.[64]
* Jiří Grossmann, Czechoslovak theatre actor, poet, and composer [65]
* Michael C. Hall (born February 1, 1971), American actor, best known for his lead role as Dexter Morgan, in Showtime's crime series Dexter. In 2010, aged 38, Hall announced he was undergoing treatment for Hodgkin lymphoma; within two years, the disease was in full remission.[66]
* Richard Harris, Irish actor who portrayed Albus Dumbledore in the first two Harry Potter movies, diagnosed in 2002, and died on October 25, 2002.[67]
* Daniel Hauser, whose mother fled with him in 2009 in order to prevent him from undergoing chemotherapy.[68]
* Tessa James, Australian actress, was diagnosed in 2014.[69]
* Mario Lemieux, Hall of Fame NHL player, co-owner of the Pittsburgh Penguins and founder of the Mario Lemieux Foundation, diagnosed in 1993.[70]
* Dinu Lipatti (1917–1950), Romanian classical pianist and composer. Diagnosed in 1947, received cortisone treatment in 1949; died from a burst abscess on his one lung.[71]
* Nikola Pokrivač, Croatian soccer international was diagnosed in 2015.[72]
* Anthony Rizzo, MLB All-Star first baseman for the Chicago Cubs, diagnosed in May 2008 while signed as a minor league player for the Boston Red Sox.[73]
* Flip Saunders, head coach of the NBA team Minnesota Timberwolves, announced in August 2015 that he was diagnosed with Hodgkin's disease. He later died of the disease in October 2015.[74]
* Brandon Tartikoff, American television executive, diagnosed around 1974, died in 1997.[75]
* Ethan Zohn, American professional soccer player and a winner of the Survivor reality television series. Zohn was diagnosed twice (in 2009 and 2011).[76]

## References[edit | edit source]

1. ↑ 1.0 1.1 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. PMID 23245604.
2. ↑ 2.0 2.1 2.2 2.3 2.4 2.5 2.6 2.7 "Adult Hodgkin Lymphoma Treatment (PDQ®)–Patient Version". NCI. August 3, 2016. Archived from the original on 28 July 2016. Retrieved 12 August 2016.
3. ↑ 3.0 3.1 3.2 World Cancer Report 2014. World Health Organization. 2014. pp. Chapter 2.4. ISBN 978-928320429-9.
4. ↑ 4.0 4.1 4.2 "Adult Hodgkin Lymphoma Treatment (PDQ®)–Patient Version". NCI. August 3, 2016. Archived from the original on 28 July 2016. Retrieved 13 August 2016.
5. ↑ 5.0 5.1 5.2 5.3 5.4 "SEER Stat Fact Sheets: Hodgkin Lymphoma". NCI. April 2016. Archived from the original on 17 October 2012. Retrieved 13 August 2016.
6. ↑ 6.0 6.1 GBD 2015 Disease Injury Incidence Prevalence Collaborators (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. ↑ 7.0 7.1 GBD 2015 Mortality Causes of Death Collaborators (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, Mark; Waxman, Jonathan (2011). Lecture Notes: Oncology (2 ed.). John Wiley & Sons. p. 195\. ISBN 978-1118293003. Archived from the original on 2017-09-10.
9. ↑ Grewal, Ravnit; Irimie, Alexandra; Naidoo, Nasheen; Mohamed, Nooroudien; Petrushev, Bobe; Chetty, Manogari; Tomuleasa, Ciprian; Abayomi, Emmanuel-Akinola (2018-01-09). "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. ISSN 1040-8363. PMID 29316828.
10. ↑ 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.
11. ↑ 11.0 11.1 11.2 Armitage JO (August 2010). "Early-stage Hodgkin's lymphoma". The New England Journal of Medicine. 363 (7): 653–62. doi:10.1056/NEJMra1003733. PMID 20818856.
12. ↑ Ward E, DeSantis C, Robbins A, Kohler B, Jemal A (2014). "Childhood and adolescent cancer statistics, 2014". Ca. 64 (2): 83–103. doi:10.3322/caac.21219. PMID 24488779.
13. ↑ 13.0 13.1 Hodgkin T (1832). "On some morbid experiences of the absorbent glands and spleen". Med Chir Trans. 17: 69–97.
14. ↑ 14.0 14.1 14.2 14.3 14.4 Ansell, Stephen M. (November 2015). "Hodgkin Lymphoma: Diagnosis and Treatment". Mayo Clinic Proceedings. 90 (11): 1574–1583. doi:10.1016/j.mayocp.2015.07.005. PMID 26541251.
15. ↑ 15.0 15.1 15.2 15.3 15.4 15.5 15.6 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. ↑ 17.0 17.1 17.2 17.3 Page 242 Archived 2015-09-20 at the Wayback Machine in: John Kearsley (1998). Cancer: A Comprehensive Clinical Guide. Washington, DC: Taylor & Francis. ISBN 978-90-5702-215-9.
18. ↑ 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.
19. ↑ Hilson AJ (July 1995). "Pel-Ebstein fever". The New England Journal of Medicine. 333 (1): 66–7. doi:10.1056/NEJM199507063330118. PMID 7777006.
20. ↑ Audard V, Zhang SY, Copie-Bergman C, Rucker-Martin C, Ory V, Candelier M, et al. (May 2010). "Occurrence of minimal change nephrotic syndrome in classical 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.
21. ↑ McKay, Pamela; Fielding, Patrick; Gallop-Evans, Eve; Hall, Georgina W.; Lambert, Jonathan; Leach, Mike; Marafioti, Teresa; McNamara, Christopher; the British Committee for Standards in Haematology (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.
22. ↑ 22.0 22.1 22.2 WHO classification of tumours of haematopoietic and lymphoid tissues. Swerdlow, Steven H.,, World Health Organization,, International Agency for Research on Cancer (Revised 4th ed.). Lyon. 2017-09-18. ISBN 978-92-832-4494-3. OCLC 1011064243.`{{cite book}}`: CS1 maint: others (link)
23. ↑ 23.0 23.1 "HMDS: Hodgkin's Lymphoma". Archived from the original on March 4, 2009. Retrieved February 1, 2009.
24. ↑ 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. Archived from the original on 2012-07-11. Retrieved 2020-08-04.
25. ↑ 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.
26. ↑ Tzankov A, Bourgau C, Kaiser A, Zimpfer A, Maurer R, Pileri SA, et al. (December 2005). "Rare expression of T-cell markers in classical Hodgkin's lymphoma". Modern Pathology. 18 (12): 1542–9. doi:10.1038/modpathol.3800473. PMID 16056244.
27. ↑ Lamprecht B, Kreher S, Anagnostopoulos I, Jöhrens K, Monteleone G, Jundt F, et al. (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.
28. ↑ Ansell S (2015). "Hodgkin Lymphoma: Diagnosis and Treatment". Mayo Clinic Proceedings. 90 (11): 1574–1583. doi:10.1016/j,mayocp.2015.07.005.
29. ↑ 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.
30. ↑ 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. doi:10.5732/cjc.014.10193. PMC 4308654. PMID 25418190.
31. ↑ 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 (2019). "Genomic analyses of flow-sorted Hodgkin Reed-Sternberg cells reveal complementary mechanisms of immune evasion". Blood Adv. 3 (23): 4065–4080. doi:10.1182/bloodadvances.2019001012.
32. ↑ 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. 4: CD007110. doi:10.1002/14651858.CD007110.pub3. PMC 6478261. PMID 28447341.
33. ↑ Gobbi PG, Levis A, Chisesi T, Broglia C, Vitolo U, Stelitano C, et al. (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. Archived from the original on 2021-08-29. Retrieved 2020-08-04.
34. ↑ Edwards-Bennett SM, Jacks LM, Moskowitz CH, Wu EJ, Zhang Z, Noy A, et al. (March 2010). "Stanford V program for locally extensive and advanced Hodgkin lymphoma: the Memorial Sloan-Kettering Cancer Center experience". Annals of Oncology. 21 (3): 574–81. doi:10.1093/annonc/mdp337. PMID 19759185.
35. ↑ "Home | German Hodgkin Study Group". Ghsg.org. Archived from the original on 2011-08-17. Retrieved 2012-08-26.
36. ↑ Saini KS, Azim HA, Cocorocchio E, Vanazzi A, Saini ML, Raviele PR, et al. (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.
37. ↑ 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.
38. ↑ Specht L, Yahalom J, Illidge T, Berthelsen AK, Constine LS, Eich HT, et al. (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.
39. ↑ "RTanswers.com". RTanswers.com. 2010-12-03. Archived from the original on 2012-09-09. Retrieved 2012-08-26.
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42. ↑ 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.
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44. ↑ "WHO Disease and injury country estimates". World Health Organisation. 2009. Archived from the original on 2009-11-11. Retrieved Nov 11, 2009.
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## Further reading[edit | edit source]

* Charlotte DeCroes Jacobs. Henry Kaplan and the Story of Hodgkin's Disease (Stanford University Press; 2010) 456 pages; combines a biography of the American radiation oncologist (1918–84) with a history of the lymphatic cancer whose treatment he helped to transform.

## External links[edit | edit source]

* Hodgkin lymphoma at Curlie
* Hodgkin Disease Archived 2009-02-21 at the Wayback Machine at American Cancer Society
* Hodgkin Lymphoma at the American National Cancer Institute

Classification|

* ICD-10: C81
* ICD-9-CM: 201
* ICD-O: 9650/3-9667/3
* MeSH: D006689
* DiseasesDB: 5973

|

External resources|

* MedlinePlus: 000580
* eMedicine: med/1022

* v
* t
* e

Leukaemias, lymphomas and related disease

| B cell
(lymphoma,
leukemia)
(most CD19

* CD20)

| By
development/
marker|

| TdT+|

* ALL (Precursor B acute lymphoblastic leukemia/lymphoma)

|

CD5+|

* naive B cell (CLL/SLL)
* mantle zone (Mantle cell)

CD22+|

* Prolymphocytic
* CD11c+ (Hairy cell leukemia)

CD79a+|

* germinal center/follicular B cell (Follicular
* Burkitt's
* GCB DLBCL
* Primary cutaneous follicle center lymphoma)

* marginal zone/marginal zone B-cell (Splenic marginal zone
* MALT
* Nodal marginal zone
* Primary cutaneous marginal zone lymphoma)

RS (CD15+, CD30+)|

* Classic Hodgkin lymphoma (Nodular sclerosis)
* CD20+ (Nodular lymphocyte predominant Hodgkin lymphoma)

PCDs/PP
(CD38+/CD138+)|

* see immunoproliferative immunoglobulin disorders

By infection|

* KSHV (Primary effusion)
* EBV
* Lymphomatoid granulomatosis
* Post-transplant lymphoproliferative disorder
* Classic Hodgkin lymphoma
* Burkitt's lymphoma
* HCV
* Splenic marginal zone lymphoma
* HIV (AIDS-related lymphoma)
* Helicobacter pylori (MALT lymphoma)

Cutaneous|

* Diffuse large B-cell lymphoma
* Intravascular large B-cell lymphoma
* Primary cutaneous marginal zone lymphoma
* Primary cutaneous immunocytoma
* Plasmacytoma
* Plasmacytosis
* Primary cutaneous follicle center lymphoma

T/NK|

| T cell
(lymphoma,
leukemia)
(most CD3

* CD4
* CD8)

| By
development/
marker|

* TdT+: ALL (Precursor T acute lymphoblastic leukemia/lymphoma)

* prolymphocyte (Prolymphocytic)

* CD30+ (Anaplastic large-cell lymphoma
* Lymphomatoid papulosis type A)

|

Cutaneous|

| MF+variants|

* indolent: Mycosis fungoides
* Pagetoid reticulosis
* Granulomatous slack skin

aggressive: Sézary disease

* Adult T-cell leukemia/lymphoma

|

Non-MF|

* CD30-: Non-mycosis fungoides CD30− cutaneous large T-cell lymphoma
* Pleomorphic T-cell lymphoma
* Lymphomatoid papulosis type B

* CD30+: CD30+ cutaneous T-cell lymphoma
* Secondary cutaneous CD30+ large-cell lymphoma
* Lymphomatoid papulosis type A

Other
peripheral|

* Hepatosplenic
* Angioimmunoblastic
* Enteropathy-associated T-cell lymphoma
* Peripheral T-cell lymphoma not otherwise specified (Lennert lymphoma)
* Subcutaneous T-cell lymphoma

By infection|

* HTLV-1 (Adult T-cell leukemia/lymphoma)

NK cell/
(most CD56)|

* Aggressive NK-cell leukemia
* Blastic NK cell lymphoma

T or NK|

* EBV (Extranodal NK-T-cell lymphoma/Angiocentric lymphoma)
* Large granular lymphocytic leukemia

Lymphoid+
myeloid|

* Acute biphenotypic leukaemia

Lymphocytosis|

* Lymphoproliferative disorders (X-linked lymphoproliferative disease
* Autoimmune lymphoproliferative syndrome)
* Leukemoid reaction
* Diffuse infiltrative lymphocytosis syndrome

Cutaneous lymphoid hyperplasia|

* Cutaneous lymphoid hyperplasia
* with bandlike and perivascular patterns
* with nodular pattern
* Jessner lymphocytic infiltrate of the skin

General|

* Hematological malignancy
* leukemia
* Lymphoproliferative disorders
* Lymphoid leukemias

*[v]: View this template
*[t]: Discuss this template
*[e]: Edit this template