Lymphoma: Difference between revisions

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{{Lymphoma}}
{{Lymphoma}}


{{CMG}}; '''Associate Editor-in-Chief:''' Ross Bonander ; {{ADG}}
{{CMG}}; {{AE}} Ross Bonander, {{ADG}}


==Overview==
==Overview==
'''Lymphoma''' is  a type of [[cancer]] that originates in [[lymphocyte]]s (a type of white blood cell in the vertebrate immune system). There are many types of lymphoma. Lymphomas are part of the broad group of diseases called [[Hematological malignancy|hematological neoplasms]]. In the 19th and 20th centuries the affliction was called [[Hodgkin's Disease]], as it was discovered by [[Thomas Hodgkin]] in 1832. Colloquially, lymphoma is broadly categorized as [[Hodgkin's lymphoma]] and [[Non-Hodgkin lymphoma|non-Hodgkin lymphoma]] (all other types of lymphoma). Scientific classification of the types of lymphoma is more detailed. Although older classifications referred to histiocytic lymphomas, these are recognized in newer classifications as of B, T or NK cell lineage. Histiocytic malignancies are rare and are classified as sarcomas.<ref name="isbn92-832-2411-6">{{cite book |author= |title=Pathology and Genetics of Haemo (World Health Organization Classification of Tumours S.) |publisher=Oxford Univ Pr |location= |year= |pages= |isbn=92-832-2411-6 |oclc= |doi=}}</ref>
'''Lymphoma''' is  a type of [[cancer]] that originates in [[lymphocyte]]s (a type of white blood cell in the vertebrate immune system). There are many types of lymphoma. Lymphomas are part of the broad group of diseases called [[Hematological malignancy|hematological neoplasms]]. It was discovered by [[Thomas Hodgkin]] in 1832 and was called [[Hodgkin's Disease]] throughout the 19th and 20th centuries. Colloquially, lymphoma is broadly categorized as [[Hodgkin's lymphoma]] or [[Non-Hodgkin lymphoma|non-Hodgkin lymphoma]] (all other types of lymphoma). Scientific classification of the types of lymphoma is more detailed. Although older classifications referred to histiocytic lymphomas, these are recognized in newer classifications as of B, T or NK cell lineage. Histiocytic malignancies are rare and are classified as sarcomas.<ref name="isbn92-832-2411-6">{{cite book |author= |title=Pathology and Genetics of Haemo (World Health Organization Classification of Tumours S.) |publisher=Oxford Univ Pr |location= |year= |pages= |isbn=92-832-2411-6 |oclc= |doi=}}</ref>


== Classification ==
== Classification ==
{{family tree/start}}
{{family tree/start}}
{{family tree | | | | | | | | | | | | | | | A01 | | | | | | | | | | | | |A01=Lymphoma }}
{{family tree | | | | | | | | | | | | | A01 | | | | | | | | | | | | |A01=Lymphoma }}
{{family tree | | | | | | | | | | | | | | | |!| | | | | | | | | | | | | |}}
{{family tree | | | | | | | | | | | | | |!| | | | | | | | | | | | | |}}
{{family tree | | | | | | | | |,|-|-|-|-|-|-|^|-|-|-|-|-|-|.| | | |}}
{{family tree | | | | | | |,|-|-|-|-|-|-|^|-|-|-|-|-|-|.| | | |}}
{{family tree | | | | | | | | B01 | | | | | | | | | | | | B02 | | | |B01=Non-Hodgkin lymphoma|B02= Hodgkin's Lymphoma}}
{{family tree | | | | | | B01 | | | | | | | | | | | | B02 | | | |B01=[[Non-Hodgkin lymphoma]]|B02= [[Hodgkin's Lymphoma]]}}
{{family tree | | | | | | | | |!| | | | | | | | | | | | | |!| | | | |}}
{{family tree | | | | | | |!| | |,|-|-|-|v|-|-|-|v|-|-|^|v|-|-|-|v|-|-|-|.|}}
{{family tree | | | | | | |,|-|^|-|-|-|-|-|-|-|-|.| | | | C01 | | | | | | |C01=Classical<br> Nodular sclerosis<br> Lymphocyte rich <br> Mixed cellularity <br> Lymphocyte depleted <br> Nodular lymphocyte}}
{{family tree | | | | | | |!| | E01 | | E02 | | E03 | | E04 | | E05 | | E06|E01=Classical|E02=Nodular sclerosis|E03=Lymphocyte rich|E04=Mixed cellularity|E05=Lymphocyte depleted|E06=Nodular lymphocyte}}
{{family tree | | | | | | C01 | | | | | | | | | C02 | | | | | | | | | | | | | | | | | |C01=B-cell Lymphoma|C02=T cell Lymphoma }}
{{family tree | | | | | | |!| | | | | | | | | | | | | | | | | | |}}
{{family tree | | | | | | |!| | | | | | | | | | |!| | | | | | | |}}
{{family tree | | | | | | |)|-|-|-|-|-|-|-|-|-|.| | | | | | | | | | | | | }}
{{family tree | | |,|-|-|-|^|-|-|-|.| | | | |,|-|^|-|-|-|-|-|.| | | |}}
{{family tree | | | | | | C01 | | | | | | | | C02 | | | | | | | | | | | | | | | | | |C01=B-cell Lymphoma|C02=T cell Lymphoma }}
{{family tree | | | | | | |!| | | | | | | | | |!| | | | | | | |}}
{{family tree | | |,|-|-|-|^|-|-|-|.| | | | |,|^|-|-|-|-|-|-|.| | | |}}
{{family tree | | D01 | | | | | | D02 | | | D03 | | | | | | D04 | | | | |D01=Precursor B cell |D02=Peripheral B cell| D03=Precursor B cell |D04=Peripheral B cell}}  
{{family tree | | D01 | | | | | | D02 | | | D03 | | | | | | D04 | | | | |D01=Precursor B cell |D02=Peripheral B cell| D03=Precursor B cell |D04=Peripheral B cell}}  
{{family tree | | |!| | | | | | | |!| | | | |!| | | | | | | |!| | | }}
{{family tree | | |!| | | | | | | |!| | | | |!| | | | | | | |!| | | }}
{{family tree | | C01 | | | | | | C02 | | | C03 | | | | | | C04 | | | |C01=Acute Lymphobalstic lymphoma|C02=Small Lymphocytic lymphoma (SLL)<br> Chronic lymphocytic leukemia<br>Mantle cell lymphoma<br> Follicular Lymphoma<br> Marginal zone lymphoma <br> Diffuse large B cell lymphoma <br> Burkitt lymphoma| C03= Acute Lymphobalstic lymphoma|C04=Anaplastic large cell T lymphoma<br>Peripheral T cell lymphoma<br> Mycosis fungoidis}}
{{family tree | | C01 | | | | | | C02 | | | C03 | | | | | | C04 | | | |C01=[[Acute Lymphobalstic lymphoma]]|C02=Small Lymphocytic lymphoma (SLL)<br> [[Chronic lymphocytic leukemia]]<br>[[Mantle cell lymphoma]]<br> Follicular Lymphoma<br> Marginal zone lymphoma <br> Diffuse large B cell lymphoma <br> [[Burkitt lymphoma]]| C03= [[Acute Lymphobalstic lymphoma]]|C04=Anaplastic large cell T lymphoma<br>Peripheral T cell lymphoma<br> Mycosis fungoidies}}
{{family tree/end}}
{{family tree/end}}


== Differentiating Lymphoma From Other Diseases ==
== Differentiating Lymphoma From Other Diseases ==
{| class="wikitable"
{| class="wikitable"
!Differentiating diagnosis of Lymphoma  
! rowspan="2" style="background:#4479BA; color: #FFFFFF;" align="center" + |Differentiating diagnosis of Lymphoma  
! colspan="5" |Symptoms
! colspan="5" style="background:#4479BA; color: #FFFFFF;" align="center" + |Symptoms
! colspan="3" |Signs
! colspan="3" style="background:#4479BA; color: #FFFFFF;" align="center" + |Signs
!Diagnosis
! style="background:#4479BA; color: #FFFFFF;" align="center" + |Diagnosis
!Additional Findings
! rowspan="2" style="background:#4479BA; color: #FFFFFF;" align="center" + |Additional Findings
|-
|-
|
! style="background:#4479BA; color: #FFFFFF;" align="center" + |Fever
|Fever
! style="background:#4479BA; color: #FFFFFF;" align="center" + |Rash
|Rash
! style="background:#4479BA; color: #FFFFFF;" align="center" + |Diarrhea
|Diarrhea
! style="background:#4479BA; color: #FFFFFF;" align="center" + |Abdominal pain
|Abdominal pain
! style="background:#4479BA; color: #FFFFFF;" align="center" + |Weight loss
|Weight loss
! style="background:#4479BA; color: #FFFFFF;" align="center" + |Painful lymphadenopathy
|Painful lymphadenopathy
! style="background:#4479BA; color: #FFFFFF;" align="center" + |Hepatosplenomegaly
|Hepatosplenomegaly
! style="background:#4479BA; color: #FFFFFF;" align="center" + |Arthritis
|Arthritis
! style="background:#4479BA; color: #FFFFFF;" align="center" + |Lab Findings
|Lab Findings
|-
|
| style="background:#DCDCDC;" align="center" + |[[Lymphoma]]
| +
|–
|–
| +
| +
|–
| +
|–
|Increase [[ESR]], increased [[LDH]]
|[[Night sweats]], constant fatigue
|-
|-
|[[Brucellosis]]
| style="background:#DCDCDC;" align="center" + |[[Brucellosis]]
|
| +
|
| +
|
|
|
| +
|
| +
|
| +
|
| +
|
| +
|[[Lymphocytosis|Relative lymphocytosis]]
|[[Lymphocytosis|Relative lymphocytosis]]
|[[Night sweats]], often with characteristic smell, likened to wet hay
|[[Night sweats]], often with characteristic smell, likened to wet hay
|-
|-
|[[Typhoid fever]]
| style="background:#DCDCDC;" align="center" + |[[Typhoid fever]]
|
| +
|
| +
|
|
|
| +
|
|
|
|
|
| +
|
| +
|Decreased [[hemoglobin]]
|Decreased [[hemoglobin]]
|Incremental increase in temperature initially and than sustained [[fever]] as high as 40°C (104°F)
|Incremental increase in temperature initially and than sustained [[fever]] as high as 40°C (104°F)
|-
|-
|[[Malaria]]
| style="background:#DCDCDC;" align="center" + |[[Malaria]]
|
| +
|
|
|
| +
|
| +
|
|
|
|
|
| +
|
| +
|Microcytosis,
|Microcytosis,
elevated [[LDH]]
elevated [[LDH]]
|"Tertian" fever: paroxysms occur every second day
|"Tertian" fever: paroxysms occur every second day
|-
|-
|[[Tuberculosis]]
| style="background:#DCDCDC;" align="center" + |[[Tuberculosis]]
|
| +
|
| +
|
|
|
| +
|
| +
|
| +
|
|
|
| +
|Mild normocytic [[anemia]], [[hyponatremia]], and
|Mild normocytic [[anemia]], [[hyponatremia]], and
[[hypercalcemia]]
[[hypercalcemia]]
|[[Night sweats]], constant fatigue
|[[Night sweats]], constant fatigue
|-
|-
|[[Lymphoma]]
| style="background:#DCDCDC;" align="center" + |[[Mumps]]
|✔
| +
|✘
|
|✘
|
|✔
|
|✔
|
|✘
| +
|✔
|
|✘
|
|Increase [[ESR]], increased [[LDH]]
|[[Night sweats]], constant fatigue
|-
|[[Mumps]]
|
|
|
|
|
|
|
|
|[[Lymphocytosis|Relative lymphocytosis]], serum [[amylase]]<nowiki/>elevated
|[[Lymphocytosis|Relative lymphocytosis]], serum [[amylase]]<nowiki/>elevated
|[[Parotid gland|Parotid]]<nowiki/>swelling/tenderness
|[[Parotid gland|Parotid]]<nowiki/>swelling/tenderness
|-
|-
|[[Rheumatoid arthritis]]
| style="background:#DCDCDC;" align="center" + |[[Rheumatoid arthritis]]
|
|
|
| +
|
|
|
|
|
|
|
|
|
|
|
| +
|[[ESR]] and [[CRP]] elevated, positive [[rheumatoid factor]]
|[[ESR]] and [[CRP]] elevated, positive [[rheumatoid factor]]
|Morning stiffness
|Morning stiffness
|-
|-
|[[SLE]]
| style="background:#DCDCDC;" align="center" + |[[SLE]]
|
|
|
| +
|
|
|
| +
|
| +
|
|
|
|
|
| +
|[[ESR]] and [[CRP]] elevated, positive [[ANA]]
|[[ESR]] and [[CRP]] elevated, positive [[ANA]]
|[[Fatigue]]
|[[Fatigue]]
|-
|-
|[[Human Immunodeficiency Virus|HIV]]
| style="background:#DCDCDC;" align="center" + |[[Human Immunodeficiency Virus|HIV]]
|
|
|
|
|
|
|
| +
|
| +
|
| +
|
|
|
| +
|
|Leukopenia
|Constant fatigue
|Constant fatigue
|}
|}


CNS lymphoma must be differentiated from other causes of seizures, headache, and fever in immunocompromised patients such as disseminated tuberculosis and disseminated aspergelosis.
CNS lymphoma must be differentiated from other causes of seizures, headache, and fever in immunocompromised patients such as disseminated tuberculosis and disseminated aspergillosis.
{| class="wikitable"
{| class="wikitable"
! style="background:#4479BA; color: #FFFFFF;" align="center" + |Disease
! style="background:#4479BA; color: #FFFFFF;" align="center" + |Disease
Line 166: Line 166:
! style="background:#4479BA; color: #FFFFFF;" align="center" + |Differentiating tests
! style="background:#4479BA; color: #FFFFFF;" align="center" + |Differentiating tests
|-
|-
|[[Lymphoma|CNS lymphoma]]<ref name="pmid20212226">{{cite journal |vauthors=Gerstner ER, Batchelor TT |title=Primary central nervous system lymphoma |journal=Arch. Neurol. |volume=67 |issue=3 |pages=291–7 |year=2010 |pmid=20212226 |doi=10.1001/archneurol.2010.3 |url=}}</ref>
| style="background:#DCDCDC;" align="center" + |[[Lymphoma|CNS lymphoma]]<ref name="pmid20212226">{{cite journal |vauthors=Gerstner ER, Batchelor TT |title=Primary central nervous system lymphoma |journal=Arch. Neurol. |volume=67 |issue=3 |pages=291–7 |year=2010 |pmid=20212226 |doi=10.1001/archneurol.2010.3 |url=}}</ref>
|
|
* Patient is [[immunocompetent]]
* Patient is [[immunocompetent]]
Line 174: Line 174:
*Single solitary ring enhancing [[lesion]] on [[CT]] or [[MRI]]
*Single solitary ring enhancing [[lesion]] on [[CT]] or [[MRI]]
|-
|-
|[[Disseminated tuberculosis]]<ref name="pmid21740673">{{cite journal |vauthors=von Reyn CF, Kimambo S, Mtei L, Arbeit RD, Maro I, Bakari M, Matee M, Lahey T, Adams LV, Black W, Mackenzie T, Lyimo J, Tvaroha S, Waddell R, Kreiswirth B, Horsburgh CR, Pallangyo K |title=Disseminated tuberculosis in human immunodeficiency virus infection: ineffective immunity, polyclonal disease and high mortality |journal=Int. J. Tuberc. Lung Dis. |volume=15 |issue=8 |pages=1087–92 |year=2011 |pmid=21740673 |doi=10.5588/ijtld.10.0517 |url=}}</ref>
| style="background:#DCDCDC;" align="center" + |[[Disseminated tuberculosis]]<ref name="pmid21740673">{{cite journal |vauthors=von Reyn CF, Kimambo S, Mtei L, Arbeit RD, Maro I, Bakari M, Matee M, Lahey T, Adams LV, Black W, Mackenzie T, Lyimo J, Tvaroha S, Waddell R, Kreiswirth B, Horsburgh CR, Pallangyo K |title=Disseminated tuberculosis in human immunodeficiency virus infection: ineffective immunity, polyclonal disease and high mortality |journal=Int. J. Tuberc. Lung Dis. |volume=15 |issue=8 |pages=1087–92 |year=2011 |pmid=21740673 |doi=10.5588/ijtld.10.0517 |url=}}</ref>
|
|
* Prior history of residence in an [[Endemic (epidemiology)|endemic]] area
* Prior history of residence in an [[Endemic (epidemiology)|endemic]] area
Line 185: Line 185:
* CXR shows [[Cavitation|cavitations]]
* CXR shows [[Cavitation|cavitations]]
|-
|-
|[[Aspergillosis]]<ref name="pmid10194462">{{cite journal |vauthors=Latgé JP |title=Aspergillus fumigatus and aspergillosis |journal=Clin. Microbiol. Rev. |volume=12 |issue=2 |pages=310–50 |year=1999 |pmid=10194462 |pmc=88920 |doi= |url=}}</ref>
| style="background:#DCDCDC;" align="center" + |[[Aspergillosis]]<ref name="pmid10194462">{{cite journal |vauthors=Latgé JP |title=Aspergillus fumigatus and aspergillosis |journal=Clin. Microbiol. Rev. |volume=12 |issue=2 |pages=310–50 |year=1999 |pmid=10194462 |pmc=88920 |doi= |url=}}</ref>
|
|
* [[Pulmonary]] [[lesions]] in addition to [[CNS]] [[lesions]]
* [[Pulmonary]] [[lesions]] in addition to [[CNS]] [[lesions]]
Line 192: Line 192:
*[[CSF]] fungal culture, [[galactomannan]]
*[[CSF]] fungal culture, [[galactomannan]]
|-
|-
|[[Cryptococcosis]]
| style="background:#DCDCDC;" align="center" + |[[Cryptococcosis]]
|
|
*Symptoms include [[cough]], [[chest pain]], and [[hemoptysis]]
*Symptoms include [[cough]], [[chest pain]], and [[hemoptysis]]
Line 199: Line 199:
*[[CSF]] fungal culture
*[[CSF]] fungal culture
|-
|-
|[[Chagas disease]]<ref name="pmid20399979">{{cite journal |vauthors=Rassi A, Rassi A, Marin-Neto JA |title=Chagas disease |journal=Lancet |volume=375 |issue=9723 |pages=1388–402 |year=2010 |pmid=20399979 |doi=10.1016/S0140-6736(10)60061-X |url=}}</ref>
| style="background:#DCDCDC;" align="center" + |[[Chagas disease]]<ref name="pmid20399979">{{cite journal |vauthors=Rassi A, Rassi A, Marin-Neto JA |title=Chagas disease |journal=Lancet |volume=375 |issue=9723 |pages=1388–402 |year=2010 |pmid=20399979 |doi=10.1016/S0140-6736(10)60061-X |url=}}</ref>
|
|
*History of residence in Central or  South America
*History of residence in Central or  South America
Line 209: Line 209:
*[[Trypanosoma cruzi]] in [[blood]], [[Tissue (biology)|tissue]], or [[CSF]], [[PCR]] of [[Tissue (biology)|tissue]] or [[body fluids]], and [[Serological testing|serologic tests]]
*[[Trypanosoma cruzi]] in [[blood]], [[Tissue (biology)|tissue]], or [[CSF]], [[PCR]] of [[Tissue (biology)|tissue]] or [[body fluids]], and [[Serological testing|serologic tests]]
|-
|-
|[[Cytomegalovirus infection|CMV infection]]<ref name="pmid11215290">{{cite journal |vauthors=Emery VC |title=Investigation of CMV disease in immunocompromised patients |journal=J. Clin. Pathol. |volume=54 |issue=2 |pages=84–8 |year=2001 |pmid=11215290 |pmc=1731357 |doi= |url=}}</ref>
| style="background:#DCDCDC;" align="center" + |[[Cytomegalovirus infection|CMV infection]]<ref name="pmid11215290">{{cite journal |vauthors=Emery VC |title=Investigation of CMV disease in immunocompromised patients |journal=J. Clin. Pathol. |volume=54 |issue=2 |pages=84–8 |year=2001 |pmid=11215290 |pmc=1731357 |doi= |url=}}</ref>
|
|
*Most common [[CNS]] [[opportunistic infection]] in [[AIDS]] patients
*Most common [[CNS]] [[opportunistic infection]] in [[AIDS]] patients
Line 219: Line 219:
*[[Brain biopsy]] with + [[staining]] for [[CMV]] or evidence of owl's eyes is also diagnostic, but it is rarely performed because of the location of [[brain]] lesions
*[[Brain biopsy]] with + [[staining]] for [[CMV]] or evidence of owl's eyes is also diagnostic, but it is rarely performed because of the location of [[brain]] lesions
|-
|-
|[[HSV|HSV infection]]<ref name="pmid1919640">{{cite journal |vauthors=Bustamante CI, Wade JC |title=Herpes simplex virus infection in the immunocompromised cancer patient |journal=J. Clin. Oncol. |volume=9 |issue=10 |pages=1903–15 |year=1991 |pmid=1919640 |doi=10.1200/JCO.1991.9.10.1903 |url=}}</ref>
| style="background:#DCDCDC;" align="center" + |[[HSV|HSV infection]]<ref name="pmid1919640">{{cite journal |vauthors=Bustamante CI, Wade JC |title=Herpes simplex virus infection in the immunocompromised cancer patient |journal=J. Clin. Oncol. |volume=9 |issue=10 |pages=1903–15 |year=1991 |pmid=1919640 |doi=10.1200/JCO.1991.9.10.1903 |url=}}</ref>
|
|
*[[Seizures]], [[headache]], [[confusion]] and/or [[urinary retention]] can be seen in [[disseminated disease]], which usually affects only the [[immunocompromised]] or acute [[infections]]
*[[Seizures]], [[headache]], [[confusion]] and/or [[urinary retention]] can be seen in [[disseminated disease]], which usually affects only the [[immunocompromised]] or acute [[infections]]
Line 228: Line 228:
*[[PCR]] of [[CSF]] with detectable [[virus]] is diagnostic
*[[PCR]] of [[CSF]] with detectable [[virus]] is diagnostic
|-
|-
|[[Chickenpox|Varicella Zoster infection]]<ref name="pmid15864101">{{cite journal |vauthors=Hambleton S |title=Chickenpox |journal=Curr. Opin. Infect. Dis. |volume=18 |issue=3 |pages=235–40 |year=2005 |pmid=15864101 |doi= |url=}}</ref>
| style="background:#DCDCDC;" align="center" + |[[Chickenpox|Varicella Zoster infection]]<ref name="pmid15864101">{{cite journal |vauthors=Hambleton S |title=Chickenpox |journal=Curr. Opin. Infect. Dis. |volume=18 |issue=3 |pages=235–40 |year=2005 |pmid=15864101 |doi= |url=}}</ref>
|
|
*Multifocal involvement has subacute course, usually only in [[immunosuppressed]], with [[headache]], [[fever]], focal deficits, and [[seizures]].  
*Multifocal involvement has subacute course, usually only in [[immunosuppressed]], with [[headache]], [[fever]], focal deficits, and [[seizures]].  
Line 237: Line 237:
*[[PCR]] of [[CSF]] with detectable [[virus]] is diagnostic
*[[PCR]] of [[CSF]] with detectable [[virus]] is diagnostic
|-
|-
|[[Brain abscess]]<ref name="pmid24174804">{{cite journal |vauthors=Alvis Miranda H, Castellar-Leones SM, Elzain MA, Moscote-Salazar LR |title=Brain abscess: Current management |journal=J Neurosci Rural Pract |volume=4 |issue=Suppl 1 |pages=S67–81 |year=2013 |pmid=24174804 |pmc=3808066 |doi=10.4103/0976-3147.116472 |url=}}</ref><ref name="pmid25360205">{{cite journal |vauthors=Patel K, Clifford DB |title=Bacterial brain abscess |journal=Neurohospitalist |volume=4 |issue=4 |pages=196–204 |year=2014 |pmid=25360205 |pmc=4212419 |doi=10.1177/1941874414540684 |url=}}</ref>
| style="background:#DCDCDC;" align="center" + |[[Brain abscess]]<ref name="pmid24174804">{{cite journal |vauthors=Alvis Miranda H, Castellar-Leones SM, Elzain MA, Moscote-Salazar LR |title=Brain abscess: Current management |journal=J Neurosci Rural Pract |volume=4 |issue=Suppl 1 |pages=S67–81 |year=2013 |pmid=24174804 |pmc=3808066 |doi=10.4103/0976-3147.116472 |url=}}</ref><ref name="pmid25360205">{{cite journal |vauthors=Patel K, Clifford DB |title=Bacterial brain abscess |journal=Neurohospitalist |volume=4 |issue=4 |pages=196–204 |year=2014 |pmid=25360205 |pmc=4212419 |doi=10.1177/1941874414540684 |url=}}</ref>
|
|
*Associated with [[sinusitis]] (abutting the sinuses) or with [[bacteremia]]
*Associated with [[sinusitis]] (abutting the sinuses) or with [[bacteremia]]
Line 244: Line 244:
*[[CSF]] culture or culture of [[brain abscess]]
*[[CSF]] culture or culture of [[brain abscess]]
|-
|-
|[[Progressive multifocal leukoencephalopathy]]<ref name="pmid20298966">{{cite journal |vauthors=Tan CS, Koralnik IJ |title=Progressive multifocal leukoencephalopathy and other disorders caused by JC virus: clinical features and pathogenesis |journal=Lancet Neurol |volume=9 |issue=4 |pages=425–37 |year=2010 |pmid=20298966 |pmc=2880524 |doi=10.1016/S1474-4422(10)70040-5 |url=}}</ref>
| style="background:#DCDCDC;" align="center" + |[[Progressive multifocal leukoencephalopathy]]<ref name="pmid20298966">{{cite journal |vauthors=Tan CS, Koralnik IJ |title=Progressive multifocal leukoencephalopathy and other disorders caused by JC virus: clinical features and pathogenesis |journal=Lancet Neurol |volume=9 |issue=4 |pages=425–37 |year=2010 |pmid=20298966 |pmc=2880524 |doi=10.1016/S1474-4422(10)70040-5 |url=}}</ref>
|
|
*Symptoms are often more insidious in onset and progress over months. Symptoms include progressive [[weakness]], poor [[coordination]], with gradual slowing of [[mental]] function. Only seen in the [[immunosuppressed]]. Rarely associated with [[fever]] or other systemic symptoms
*Symptoms are often more insidious in onset and progress over months. Symptoms include progressive [[weakness]], poor [[coordination]], with gradual slowing of [[mental]] function. Only seen in the [[immunosuppressed]]. Rarely associated with [[fever]] or other systemic symptoms

Latest revision as of 21:06, 9 January 2019

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Lymphoma
Lymph node: Malignant Lymphoma Large Cell Type: Gross natural color excellent view of cut mesentery showing massively enlarged mesenteric nodes with focal hemorrhages case diagnosed several years ago as reticulum cell sarcoma excellent demonstration of nodes with lymphoma.
Image courtesy of Professor Peter Anderson DVM PhD and published with permission © PEIR, University of Alabama at Birmingham, Department of Pathology

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

Overview

Lymphoma is a type of cancer that originates in lymphocytes (a type of white blood cell in the vertebrate immune system). There are many types of lymphoma. Lymphomas are part of the broad group of diseases called hematological neoplasms. It was discovered by Thomas Hodgkin in 1832 and was called Hodgkin's Disease throughout the 19th and 20th centuries. Colloquially, lymphoma is broadly categorized as Hodgkin's lymphoma or non-Hodgkin lymphoma (all other types of lymphoma). Scientific classification of the types of lymphoma is more detailed. Although older classifications referred to histiocytic lymphomas, these are recognized in newer classifications as of B, T or NK cell lineage. Histiocytic malignancies are rare and are classified as sarcomas.[1]

Classification

 
 
 
 
 
 
 
 
 
 
 
 
Lymphoma
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Non-Hodgkin lymphoma
 
 
 
 
 
 
 
 
 
 
 
Hodgkin's Lymphoma
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Classical
 
Nodular sclerosis
 
Lymphocyte rich
 
Mixed cellularity
 
Lymphocyte depleted
 
Nodular lymphocyte
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
B-cell Lymphoma
 
 
 
 
 
 
 
T cell Lymphoma
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Precursor B cell
 
 
 
 
 
Peripheral B cell
 
 
Precursor B cell
 
 
 
 
 
Peripheral B cell
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Acute Lymphobalstic lymphoma
 
 
 
 
 
Small Lymphocytic lymphoma (SLL)
Chronic lymphocytic leukemia
Mantle cell lymphoma
Follicular Lymphoma
Marginal zone lymphoma
Diffuse large B cell lymphoma
Burkitt lymphoma
 
 
Acute Lymphobalstic lymphoma
 
 
 
 
 
Anaplastic large cell T lymphoma
Peripheral T cell lymphoma
Mycosis fungoidies
 
 
 

Differentiating Lymphoma From Other Diseases

Differentiating diagnosis of Lymphoma Symptoms Signs Diagnosis Additional Findings
Fever Rash Diarrhea Abdominal pain Weight loss Painful lymphadenopathy Hepatosplenomegaly Arthritis Lab Findings
Lymphoma + + + + Increase ESR, increased LDH Night sweats, constant fatigue
Brucellosis + + + + + + + Relative lymphocytosis Night sweats, often with characteristic smell, likened to wet hay
Typhoid fever + + + + + Decreased hemoglobin Incremental increase in temperature initially and than sustained fever as high as 40°C (104°F)
Malaria + + + + + Microcytosis,

elevated LDH

"Tertian" fever: paroxysms occur every second day
Tuberculosis + + + + + + Mild normocytic anemiahyponatremia, and

hypercalcemia

Night sweats, constant fatigue
Mumps + + Relative lymphocytosis, serum amylaseelevated Parotidswelling/tenderness
Rheumatoid arthritis + + ESR and CRP elevated, positive rheumatoid factor Morning stiffness
SLE + + + + ESR and CRP elevated, positive ANA Fatigue
HIV + + + + Leukopenia Constant fatigue

CNS lymphoma must be differentiated from other causes of seizures, headache, and fever in immunocompromised patients such as disseminated tuberculosis and disseminated aspergillosis.

Disease Differentiating signs and symptoms Differentiating tests
CNS lymphoma[2]
Disseminated tuberculosis[3]
Aspergillosis[4]
Cryptococcosis
Chagas disease[5]
CMV infection[6]
HSV infection[7]
Varicella Zoster infection[8]
Brain abscess[9][10]
Progressive multifocal leukoencephalopathy[11]
  • Symptoms are often more insidious in onset and progress over months. Symptoms include progressive weakness, poor coordination, with gradual slowing of mental function. Only seen in the immunosuppressed. Rarely associated with fever or other systemic symptoms

Epidemiology and Demographics

  • According to the U.S. National Institutes of Health, lymphomas account for about five percent of all cases of cancer in the United States.
  • Hodgkin's lymphoma in particular accounts for less than one percent of all cases of cancer in the United States

References

  1. Pathology and Genetics of Haemo (World Health Organization Classification of Tumours S.). Oxford Univ Pr. ISBN 92-832-2411-6.
  2. Gerstner ER, Batchelor TT (2010). "Primary central nervous system lymphoma". Arch. Neurol. 67 (3): 291–7. doi:10.1001/archneurol.2010.3. PMID 20212226.
  3. von Reyn CF, Kimambo S, Mtei L, Arbeit RD, Maro I, Bakari M, Matee M, Lahey T, Adams LV, Black W, Mackenzie T, Lyimo J, Tvaroha S, Waddell R, Kreiswirth B, Horsburgh CR, Pallangyo K (2011). "Disseminated tuberculosis in human immunodeficiency virus infection: ineffective immunity, polyclonal disease and high mortality". Int. J. Tuberc. Lung Dis. 15 (8): 1087–92. doi:10.5588/ijtld.10.0517. PMID 21740673.
  4. Latgé JP (1999). "Aspergillus fumigatus and aspergillosis". Clin. Microbiol. Rev. 12 (2): 310–50. PMC 88920. PMID 10194462.
  5. Rassi A, Rassi A, Marin-Neto JA (2010). "Chagas disease". Lancet. 375 (9723): 1388–402. doi:10.1016/S0140-6736(10)60061-X. PMID 20399979.
  6. Emery VC (2001). "Investigation of CMV disease in immunocompromised patients". J. Clin. Pathol. 54 (2): 84–8. PMC 1731357. PMID 11215290.
  7. Bustamante CI, Wade JC (1991). "Herpes simplex virus infection in the immunocompromised cancer patient". J. Clin. Oncol. 9 (10): 1903–15. doi:10.1200/JCO.1991.9.10.1903. PMID 1919640.
  8. Hambleton S (2005). "Chickenpox". Curr. Opin. Infect. Dis. 18 (3): 235–40. PMID 15864101.
  9. Alvis Miranda H, Castellar-Leones SM, Elzain MA, Moscote-Salazar LR (2013). "Brain abscess: Current management". J Neurosci Rural Pract. 4 (Suppl 1): S67–81. doi:10.4103/0976-3147.116472. PMC 3808066. PMID 24174804.
  10. Patel K, Clifford DB (2014). "Bacterial brain abscess". Neurohospitalist. 4 (4): 196–204. doi:10.1177/1941874414540684. PMC 4212419. PMID 25360205.
  11. Tan CS, Koralnik IJ (2010). "Progressive multifocal leukoencephalopathy and other disorders caused by JC virus: clinical features and pathogenesis". Lancet Neurol. 9 (4): 425–37. doi:10.1016/S1474-4422(10)70040-5. PMC 2880524. PMID 20298966.


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