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__NOTOC__
{{Burkitt's lymphoma}}
{{Burkitt's lymphoma}}
{{CMG}}
{{CMG}}; {{AE}} {{AS}}
==Overview==
==Overview==
'''Burkitt's lymphoma''' (or "Burkitt's tumor", or "Malignant lymphoma, Burkitt's type") is a cancer of the lymphatic system (in particular, B lymphocytes). It is associated with the [[Epstein-Barr virus]], also the cause of [[mononucleosis]] as well as other cancers. It is named after [[Denis Parsons Burkitt]], a [[surgery|surgeon]] who first described the disease in 1956 while working in equatorial Africa.
'''Burkitt's lymphoma''' ("Burkitt's tumor", or "Malignant lymphoma, Burkitt's type") is a cancer of the lymphatic system (in particular, B lymphocytes). Burkitt's lymphoma was first described by [[Denis Parsons Burkitt]], a [[surgeon]], in 1958 while working in equatorial Africa. Burkitt's lymphoma may be classified according to [[WHO]] classification into 3 clinical variants: endemic Burkitt's lymphoma, sporadic Burkitt's lymphoma, and immunodeficiency-associated Burkitt's lymphoma. Gene involved in the pathogenesis of Burkitt's lymphoma includes ''[[c-myc]]''. On gross pathology, ulceration and discharge are characteristic findings of Burkitt's lymphoma. On microscopic histopathological analysis, "starry sky" appearance is characteristic finding of Burkitt's lymphoma. There are no established causes for Burkitt's lymphoma. Burkitt's lymphoma must be differentiated from other diseases  such as [[Hodgkin's lymphoma]], [[diffuse large B cell lymphoma]], [[follicular lymphoma]], [[Mucosa-Associated Lymphatic Tissue lymphoma]] (MALT), [[small cell lymphocytic lymphoma]], and [[mantle cell lymphoma]] (MCL). Burkitt's lymphoma is a common disease that tends to affect children or young adults. Males are more commonly affected with Burkitt's lymphoma than females. Burkitt's lymphoma usually affects individuals of the African race. Common risk factors in the development of Burkitt's lymphoma may be [[HIV]]/[[AIDS]] and post-transplant immunosuppression. According to the the U.S. Preventive Service Task Force (USPSTF), there is insufficient evidence to recommend routine screening for Burkitt's lymphoma. The prognosis varies with the age, children have the most favorable prognosis. Burkitt's lymphoma in children is associated with a 5 year survival rate of 90%. The presence of metastasis in [[bone marrow]] or [[CNS]] is associated with a particularly poor prognosis among patients with Burkitt's lymphoma. According to the Murphy staging system, there are four stages of Burkitt's lymphoma based on the number of nodes and extra nodal involvement. Laboratory tests for Burkitt's lymphoma include [[complete blood count]] (CBC), blood chemistry studies, immuno histochemistry, [[HIV]] blood test, flow cytometric analysis, and [[cytogenetics]]. Chest and knee x ray may be helpful in the diagnosis of Burkitt's lymphoma. [[CT]] and [[MRI]] may be helpful in the diagnosis of Burkitt's lymphoma. [[Lymph node]] or extra nodal tissue [[biopsy]] is diagnostic of Burkitt's lymphoma. [[PET]] and [[bone scan]] may be helpful in the diagnosis of Burkitt's lymphoma. Other diagnostic studies for the diagnosis of Burkitt's lymphoma include [[bone marrow biopsy]] and spinal fluid examination. The predominant therapy for Burkitt's lymphoma is [[chemotherapy]]. Adjunctive [[immunotherapy]] and [[stem cell transplantation]] may be required. Surgical intervention is not recommended for the management of Burkitt's lymphoma.
 
==Historical Perspective==
Children affected with the disease often also had chronic [[malaria]] which is believed to have reduced resistance to the Epstein-Barr virus and allowed it to take hold. This is known as classical African or endemic Burkitt's lymphoma. Disease characteristics include large tumors in the facial or abdominal regions.
Burkitt's lymphoma was first described by [[Denis Parsons Burkitt]], a [[surgeon]], in 1958 while working in equatorial Africa.
 
==Classification==
The sporadic type of Burkitt's lymphoma (also known as "non-African") is another form of [[non-Hodgkin lymphoma]] found outside of Africa in which cancer cells have a similar appearance to the cancer cells of classical African or endemic Burkitt's lymphoma. Again it is believed that impaired immunity provides an opening for development of the Epstein-Barr virus. Examination of chromosomes from these tumor cells often shows translocation of the [[myc]] and [[Immunoglobulin|Ig]] genes (t: 8;14).
Burkitt's lymphoma may be classified according to [[WHO]] classification into 3 clinical variants: endemic Burkitt's lymphoma, sporadic Burkitt's lymphoma, and immunodeficiency-associated Burkitt's lymphoma.
==Pathophysiology==
The ''[[c-myc]]'' gene involved in the pathogenesis of Burkitt's lymphoma. On gross pathology, ulceration and discharge are characteristic findings of Burkitt's lymphoma. On microscopic histopathological analysis, "starry sky" appearance is a characteristic finding of Burkitt's lymphoma.
==Causes==
There are no established causes for Burkitt's lymphoma.
==Differential diagnosis==
Burkitt's lymphoma must be differentiated from other diseases  such as [[Hodgkin's lymphoma]], [[diffuse large B cell lymphoma]], [[follicular lymphoma]], [[Mucosa-Associated Lymphatic Tissue lymphoma]] (MALT), [[small cell lymphocytic lymphoma]], and [[mantle cell lymphoma]] (MCL).
==Epidemiology and Demographics==
Burkitt's lymphoma is a common disease that tends to affect children or young adults. Males are more commonly affected with Burkitt's lymphoma than females. Burkitt's lymphoma usually affects individuals of the African race.
==Risk Factors==
Common risk factors in the development of Burkitt's lymphoma may be [[HIV]]/[[AIDS]] and post-transplant immunosuppression.
==Screening==
According to the the U.S. Preventive Service Task Force (USPSTF), there is insufficient evidence to recommend routine screening for Burkitt's lymphoma.
==Prognosis==
The prognosis varies with the age, children have the most favorable prognosis. Burkitt's lymphoma in children is associated with a 5 year survival rate of 90%. The presence of metastasis in [[bone marrow]] or [[CNS]] is associated with a particularly poor prognosis among patients with Burkitt's lymphoma.
==Diagnosis==
===Staging===
According to the Murphy staging system, there are four stages of Burkitt's lymphoma based on the number of nodes and extra nodal involvement.
===Laboratory Findings===
Laboratory tests for Burkitt's lymphoma include [[complete blood count]] (CBC), blood chemistry studies, immuno histochemistry, [[HIV]] blood test, flow cytometric analysis, and [[cytogenetics]].
===X Ray Findings===
Chest and knee x ray may be helpful in the diagnosis of Burkitt's lymphoma.
===CT===
Chest, abdomen, and pelvis [[CT]] scan may be helpful in the diagnosis of Burkitt's lymphoma.
===MRI===
[[MRI]] may be helpful in the diagnosis of Burkitt's lymphoma.
===Biopsy===
[[Lymph node]] or extra nodal tissue [[biopsy]] is diagnostic of Burkitt's lymphoma.
===Other Imaging Studies===
[[PET]] and [[bone scan]] may be helpful in the diagnosis of Burkitt's lymphoma.
===Other diagnostic studies===
Other diagnostic studies for the diagnosis of Burkitt's lymphoma include [[bone marrow biopsy]] and spinal fluid examination.
==Treatment==
===Medical Therapy===
The predominant therapy for Burkitt's lymphoma is [[chemotherapy]]. Adjunctive [[immunotherapy]] and [[stem cell transplantation]] may be required.
===Surgery===
Surgical intervention is not recommended for the management of Burkitt's lymphoma.


==References==
==References==
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{{Hematological malignancy histology}}


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[[es:Linfoma de Burkitt]]
[[it:Linfoma di Burkitt]]
[[pl:Chłoniak Burkitta]]
[[pt:Linfoma de Burkitt]]
[[ru:Лимфома Беркитта]]
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[[Category:Hematology]]
[[Category:Hematology]]
[[Category:Types of cancer]]
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[[Category:Up-To-Date]]
[[Category:Oncology]]
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[[Category:Medicine]]
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[[Category:Immunology]]

Latest revision as of 02:38, 6 November 2017

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sowminya Arikapudi, M.B,B.S. [2]

Overview

Burkitt's lymphoma ("Burkitt's tumor", or "Malignant lymphoma, Burkitt's type") is a cancer of the lymphatic system (in particular, B lymphocytes). Burkitt's lymphoma was first described by Denis Parsons Burkitt, a surgeon, in 1958 while working in equatorial Africa. Burkitt's lymphoma may be classified according to WHO classification into 3 clinical variants: endemic Burkitt's lymphoma, sporadic Burkitt's lymphoma, and immunodeficiency-associated Burkitt's lymphoma. Gene involved in the pathogenesis of Burkitt's lymphoma includes c-myc. On gross pathology, ulceration and discharge are characteristic findings of Burkitt's lymphoma. On microscopic histopathological analysis, "starry sky" appearance is characteristic finding of Burkitt's lymphoma. There are no established causes for Burkitt's lymphoma. Burkitt's lymphoma must be differentiated from other diseases such as Hodgkin's lymphoma, diffuse large B cell lymphoma, follicular lymphoma, Mucosa-Associated Lymphatic Tissue lymphoma (MALT), small cell lymphocytic lymphoma, and mantle cell lymphoma (MCL). Burkitt's lymphoma is a common disease that tends to affect children or young adults. Males are more commonly affected with Burkitt's lymphoma than females. Burkitt's lymphoma usually affects individuals of the African race. Common risk factors in the development of Burkitt's lymphoma may be HIV/AIDS and post-transplant immunosuppression. According to the the U.S. Preventive Service Task Force (USPSTF), there is insufficient evidence to recommend routine screening for Burkitt's lymphoma. The prognosis varies with the age, children have the most favorable prognosis. Burkitt's lymphoma in children is associated with a 5 year survival rate of 90%. The presence of metastasis in bone marrow or CNS is associated with a particularly poor prognosis among patients with Burkitt's lymphoma. According to the Murphy staging system, there are four stages of Burkitt's lymphoma based on the number of nodes and extra nodal involvement. Laboratory tests for Burkitt's lymphoma include complete blood count (CBC), blood chemistry studies, immuno histochemistry, HIV blood test, flow cytometric analysis, and cytogenetics. Chest and knee x ray may be helpful in the diagnosis of Burkitt's lymphoma. CT and MRI may be helpful in the diagnosis of Burkitt's lymphoma. Lymph node or extra nodal tissue biopsy is diagnostic of Burkitt's lymphoma. PET and bone scan may be helpful in the diagnosis of Burkitt's lymphoma. Other diagnostic studies for the diagnosis of Burkitt's lymphoma include bone marrow biopsy and spinal fluid examination. The predominant therapy for Burkitt's lymphoma is chemotherapy. Adjunctive immunotherapy and stem cell transplantation may be required. Surgical intervention is not recommended for the management of Burkitt's lymphoma.

Historical Perspective

Burkitt's lymphoma was first described by Denis Parsons Burkitt, a surgeon, in 1958 while working in equatorial Africa.

Classification

Burkitt's lymphoma may be classified according to WHO classification into 3 clinical variants: endemic Burkitt's lymphoma, sporadic Burkitt's lymphoma, and immunodeficiency-associated Burkitt's lymphoma.

Pathophysiology

The c-myc gene involved in the pathogenesis of Burkitt's lymphoma. On gross pathology, ulceration and discharge are characteristic findings of Burkitt's lymphoma. On microscopic histopathological analysis, "starry sky" appearance is a characteristic finding of Burkitt's lymphoma.

Causes

There are no established causes for Burkitt's lymphoma.

Differential diagnosis

Burkitt's lymphoma must be differentiated from other diseases such as Hodgkin's lymphoma, diffuse large B cell lymphoma, follicular lymphoma, Mucosa-Associated Lymphatic Tissue lymphoma (MALT), small cell lymphocytic lymphoma, and mantle cell lymphoma (MCL).

Epidemiology and Demographics

Burkitt's lymphoma is a common disease that tends to affect children or young adults. Males are more commonly affected with Burkitt's lymphoma than females. Burkitt's lymphoma usually affects individuals of the African race.

Risk Factors

Common risk factors in the development of Burkitt's lymphoma may be HIV/AIDS and post-transplant immunosuppression.

Screening

According to the the U.S. Preventive Service Task Force (USPSTF), there is insufficient evidence to recommend routine screening for Burkitt's lymphoma.

Prognosis

The prognosis varies with the age, children have the most favorable prognosis. Burkitt's lymphoma in children is associated with a 5 year survival rate of 90%. The presence of metastasis in bone marrow or CNS is associated with a particularly poor prognosis among patients with Burkitt's lymphoma.

Diagnosis

Staging

According to the Murphy staging system, there are four stages of Burkitt's lymphoma based on the number of nodes and extra nodal involvement.

Laboratory Findings

Laboratory tests for Burkitt's lymphoma include complete blood count (CBC), blood chemistry studies, immuno histochemistry, HIV blood test, flow cytometric analysis, and cytogenetics.

X Ray Findings

Chest and knee x ray may be helpful in the diagnosis of Burkitt's lymphoma.

CT

Chest, abdomen, and pelvis CT scan may be helpful in the diagnosis of Burkitt's lymphoma.

MRI

MRI may be helpful in the diagnosis of Burkitt's lymphoma.

Biopsy

Lymph node or extra nodal tissue biopsy is diagnostic of Burkitt's lymphoma.

Other Imaging Studies

PET and bone scan may be helpful in the diagnosis of Burkitt's lymphoma.

Other diagnostic studies

Other diagnostic studies for the diagnosis of Burkitt's lymphoma include bone marrow biopsy and spinal fluid examination.

Treatment

Medical Therapy

The predominant therapy for Burkitt's lymphoma is chemotherapy. Adjunctive immunotherapy and stem cell transplantation may be required.

Surgery

Surgical intervention is not recommended for the management of Burkitt's lymphoma.

References

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