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{{Plasma cell disorder}}
{{Plasma cell disorder}}
{{CMG}};  {{AE}} {{N.F}}
{{CMG}};  {{AE}} {{N.F}}, {{Anmol}}
 


{{SK}} Plasma cell dyscrasia


==[[Plasma cell disorder overview|Overview]]==   
==[[Plasma cell disorder overview|Overview]]==   


Plasma cell disorders are a diverse type of blood disorders characterized by the presence of a monoclonal paraprotein in the [[serum]] or urine.  Monoclonal plasma cells are present in the [[bone marrow]] or, rarely, in other tissues. Plasma cell disorders include [[Monoclonal gammopathy of undetermined significance classification|monoclonal gammopathy of undetermined significance]] (MGUS)[[Multiple myeloma|, multiple myeloma]] (MM), [[lymphoplasmacytic lymphoma]]/ [[Waldenström's macroglobulinemia|Waldenstrom macroglobulinemia]]  (LPL/WM), [[Lymphoproliferative disorders|lymphoproliferative disorders,]] smoldering multiple myeloma (SMM); solitary or extramedullary plasmacytoma,  [[amyloidosis]], and [[POEMS syndrome]] ([[polyneuropathy]], [[Organomegaly|organomegaly,]] [[endocrinopathy]],, Monoclonal protein, and Skin changes). Plasma-cell disorders are characterized by proliferation of a single clone of plasma cells that produces a [[homogeneous]] monoclonal (M) protein. These disorders have been defined by the International Myeloma Working Group.1 In 2006.  
Plasma cell disorders are a diverse type of blood disorders characterized by [[proliferation]] of a single clone of [[plasma cells]] that produces a [[homogeneous]] monoclonal (M) protein. These monoclonal paraprotein are seen in the [[serum]] or urine.  Monoclonal [[plasma cells]] are present in the [[bone marrow]] or, rarely, in other tissues. Plasma cell disorders include [[Monoclonal gammopathy of undetermined significance classification|monoclonal gammopathy of undetermined significance]] (MGUS)[[Multiple myeloma|, multiple myeloma]] (MM), [[lymphoplasmacytic lymphoma]] or [[Waldenström's macroglobulinemia|Waldenstrom macroglobulinemia]]  (LPL/WM), [[Lymphoproliferative disorders|lymphoproliferative disorders,]] smoldering multiple myeloma (SMM); solitary or extramedullary plasmacytoma,  [[amyloidosis]], and [[POEMS syndrome]] ([[polyneuropathy]], [[Organomegaly|organomegaly,]] [[endocrinopathy]], monoclonal protein, and skin changes). These disorders have been defined by the International Myeloma Working Group in 2006.  


==[[Plasma cell disorder classification|Classification]]==
==[[Plasma cell disorder classification|Classification]]==
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{{family tree | | | | | | | | | | | | A01 | | | | | | | | | | | | | | A01=Plasma cell disorder}}
{{family tree | | | | | | | | | | | | A01 | | | | | | | | | | | | | | A01=Plasma cell disorder}}
{{family tree | |,|-|-|-|v|-|-|-|v|-|-|^|-|-|v|-|-|-|v|-|-|-|.| | | }}
{{family tree | |,|-|-|-|v|-|-|-|v|-|-|^|-|-|v|-|-|-|v|-|-|-|.| | | }}
{{Family tree | B01 | | B02 | | B03 | | | | B04 | | B05 | | B06 | | B01=[[Primary amyloidosis]]|B02=[[Plasma cell disorder#Malignant monoclonal gammopathies|Malignant monoclonal gammopathy]]|B03=[[Chronic lymphocytic leukemia]] |B04=[[plasma cell disorder#Heavy-chain diseases|Heavy chain diseases]]| B05=[[Cryoglobulinemia]] | B06=[[Monoclonal gammopathy of undetermined significance]] (MGUS)}}
{{Family tree | B01 | | B02 | | B03 | | | | B04 | | B05 | | B06 | | B01=[[Primary amyloidosis]]|B02=[[Plasma cell disorder#Malignant monoclonal gammopathies|Malignant monoclonal gammopathy]]|B03=[[Chronic lymphocytic leukemia]] |B04=[[plasma cell disorder#Heavy-chain diseases|Heavy chain diseases (HCD)]]| B05=[[Cryoglobulinemia]] | B06=[[Monoclonal gammopathy of undetermined significance]] (MGUS)}}
{{Family tree | | | | | |!| | | | | | | | | |!| | | | | | | |!| | | }}
{{Family tree | | | | | |!| | | | | | | | | |!| | | | | | | |!| | | }}
{{Family tree | | |,|-|-|^|-|.| | | |,|-|-|-|+|-|-|-|.| | | |!| | | }}
{{Family tree | | |,|-|-|^|-|.| | | |,|-|-|-|+|-|-|-|.| | | |!| | | }}
{{Family tree | | C01 | | | C02 | | C03 | | C04 | | C05 | | |!| | | |C01=[[Multiple myeloma]]|C02=[[Malignant lymphoproliferative disorders]]|C03=γHCD|C04=αHCD|C05=μHCD}}
{{Family tree | | C01 | | | C02 | | C03 | | C04 | | C05 | | |!| | | |C01=[[Multiple myeloma]]|C02=[[Plasma cell disorder#Malignant lymphoproliferative disorders|Malignant lymphoproliferative disorders]]|C03=[[Plasma cell disorder#γHCD|γHCD]]|C04=[[Plasma cell disorder#αHCD|αHCD]]|C05=[[Plasma cell disorder#μHCD|μHCD]]}}
{{family tree | | |!| | | | |!| | | | | | | | | | | | | | | |!| | | }}
{{family tree | | |!| | | | |!| | | | | |,|-|-|-|v|-|-|-|v|-|^|-|.|}}
{{family tree | | |!| | | | |!| | | | | |,|-|-|-|v|-|-|-|v|-|^|-|.|}}
{{family tree | | |!| | |,|-|^|-|.| | | F01 | | F02 | | F03 | | F04 | |F01= [[Benign]]<br>(IgG, IgA, IgD, IgM, and,<br>rarely, free light chains)|F02=Associated [[Neoplasm|neoplasms]]<br>or other diseases not known to<br>produce monoclonal proteins|F03=Biclonal and triclonal<br>[[Gammopathy|gammopathies]]|F04= Idiopathic<br>(Bence Jones<br>proteinuria)}}
{{family tree | | |!| | |,|-|^|-|.| | | F01 | | F02 | | F03 | | F04 | |F01= [[Benign]]<br>(IgG, IgA, IgD, IgM, and,<br>rarely, free light chains)|F02=Associated [[Neoplasm|neoplasms]]<br>or other diseases not known to<br>produce monoclonal proteins|F03=Biclonal and triclonal<br>[[Gammopathy|gammopathies]]|F04= Idiopathic<br>(Bence Jones<br>proteinuria)}}
{{family tree | | |!| | D01 | | D02 | | | | | | | | | | | | | | | | |D01=[[Waldenstrom macroglobulinemia]] | D02=[[Malignant lymphoma]]}}
{{family tree | | |!| | D01 | | D02 | | | | | | | | | | | | | | | | |D01=[[Waldenstrom macroglobulinemia]] | D02=[[Malignant lymphoma]]}}
{{family tree | | |!| | | | | | | | | | | | | | | | | | | | | | | | | | | | }}
{{family tree | | |!| | | | | | | | | | | | | | | | | | | | | | | | | | | | }}
{{family tree | |,|^|-|-|v|-|-|-|v|-|-|-|v|-|-|-|v|-|-|-|-|v|-|-|-|.| | | | }}
{{family tree | |,|^|-|-|v|-|-|-|v|-|-|-|v|-|-|-|v|-|-|-|v|-|-|-|v|-|-|-|.|}}
{{family tree | E01 | | E02 | | E03 | | E04 | | E05 | | | E06 | | E07 | | E01=Symptomatic multiple myeloma | E02=Smoldering multiple myeloma | E03=Plasma-cell leukemia|E04=Non-secretory myeloma | E05=Solitary plasmacytoma of bone | E06=Osteosclerotic myeloma | E07=[[Extramedullary plasmacytoma]]}}
{{family tree | E01 | | E02 | | E03 | | E04 | | E05 | | E06 | | E07 | | E08 | | E01=[[Plasma cell disorder#Symptomatic multiple myeloma|Symptomatic multiple myeloma]] | E02=[[Plasma cell disorder#Smoldering multiple myeloma|Smoldering multiple myeloma]] | E03=[[Plasma cell disorder#Plasma-cell leukemia|Plasma-cell leukemia]]|E04=[[Plasma cell disorder#Non-secretory myeloma|Non-secretory myeloma]] |E05=[[Plasma cell disorder#IgD myeloma|IgD myeloma]] | E06=[[Plasma cell disorder#Osteosclerotic myeloma|Osteosclerotic myeloma]] | E07=[[Plasma cell disorder#Solitary plasmacytoma of bone|Solitary plasmacytoma of bone]] |E08=[[Plasma cell disorder#Extramedullary plasmacytoma|Extramedullary plasmacytoma]]}}
{{Family tree/end}}
{{Family tree/end}}


== [[Plasma cell disorder| Differential Diagnosis]] ==
==[[Plasma cell disorder| Differential Diagnosis]]==
{| class="wikitable"
{| class="wikitable"
|+
|+
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| style="background:#F5F5F5;" align="center" + |<10%
| style="background:#F5F5F5;" align="center" + |<10%
| style="background:#F5F5F5;" align="left" + |
| style="background:#F5F5F5;" align="left" + |
* No end-organ damage
*No end-organ damage
|-
|-
| style="background:#DCDCDC;" align="center" + |Smoldering MM
| style="background:#DCDCDC;" align="center" + |Smoldering MM
Line 74: Line 75:
| style="background:#F5F5F5;" align="center" + |10-60%
| style="background:#F5F5F5;" align="center" + |10-60%
| style="background:#F5F5F5;" align="left" + |
| style="background:#F5F5F5;" align="left" + |
* No myeloma-defining event  
*No myeloma-defining event
* No  CRAB features
*No  CRAB features
|-
|-
| style="background:#DCDCDC;" align="center" + |[[Monoclonal gammopathy of undetermined significance|Light chain MGUS]]
| style="background:#DCDCDC;" align="center" + |[[Monoclonal gammopathy of undetermined significance|Light chain MGUS]]
Line 87: Line 88:
| style="background:#F5F5F5;" align="center" + |<10%
| style="background:#F5F5F5;" align="center" + |<10%
| style="background:#F5F5F5;" align="left" + |
| style="background:#F5F5F5;" align="left" + |
* No end-organ damage
*No end-organ damage
|-
|-
| style="background:#DCDCDC;" align="center" + |[[Multiple myeloma classification|Active symptomatic Multiple myeloma]]
| style="background:#DCDCDC;" align="center" + |[[Multiple myeloma classification|Active symptomatic Multiple myeloma]]
Line 99: Line 100:
| style="background:#F5F5F5;" align="center" + |>60%
| style="background:#F5F5F5;" align="center" + |>60%
| style="background:#F5F5F5;" align="left" + |
| style="background:#F5F5F5;" align="left" + |
* ≥1 myeloma-defining event
*≥1 myeloma-defining event
* CRAB features
*CRAB features
|-
|-
| style="background:#DCDCDC;" align="center" + |[[Waldenström's macroglobulinemia|Waldenstrom macroglobulinemia]]
| style="background:#DCDCDC;" align="center" + |[[Waldenström's macroglobulinemia|Waldenstrom macroglobulinemia]]
Line 112: Line 113:
| style="background:#F5F5F5;" align="center" + |>10%
| style="background:#F5F5F5;" align="center" + |>10%
| style="background:#F5F5F5;" align="left" + |
| style="background:#F5F5F5;" align="left" + |
* Evidence of organ/tissue damage
*Evidence of organ/tissue damage
* [[Anemia]]
*[[Anemia]]
* [[Hepatosplenomegaly]]
*[[Hepatosplenomegaly]]
|-
|-
| style="background:#DCDCDC;" align="center" + |Solitary Plasmacytoma
| style="background:#DCDCDC;" align="center" + |Solitary Plasmacytoma
Line 124: Line 125:
| style="background:#F5F5F5;" align="center" + |<3mg/dl
| style="background:#F5F5F5;" align="center" + |<3mg/dl
| style="background:#F5F5F5;" align="center" + |Abnormal in 47% cases
| style="background:#F5F5F5;" align="center" + |Abnormal in 47% cases
| style="background:#F5F5F5;" align="center" + |Normal  
| style="background:#F5F5F5;" align="center" + |Normal
| style="background:#F5F5F5;" align="left" + |
| style="background:#F5F5F5;" align="left" + |
* Solitory bone lesion due to plasma cell tumor
*Solitory bone lesion due to [[plasma cell]] tumor
* Preserved levels of uninvolved immunoglobulins
*Preserved levels of uninvolved [[immunoglobulins]]
* No [[anemia]], [[hypercalcemia]] or [[renal disease]]
*No [[anemia]], [[hypercalcemia]] or [[renal disease]]
|-
|-
| style="background:#DCDCDC;" align="center" + |[[AL amyloidosis|Primary amyloidosis]]
| style="background:#DCDCDC;" align="center" + |[[AL amyloidosis|Primary amyloidosis]]
Line 137: Line 138:
| style="background:#F5F5F5;" align="center" + |−
| style="background:#F5F5F5;" align="center" + |−
| style="background:#F5F5F5;" align="center" + |<3md/dl
| style="background:#F5F5F5;" align="center" + |<3md/dl
| style="background:#F5F5F5;" align="center" + |[[Light chain|Light chains]] of [[Immunoglobulin|immunoglobulines]]  
| style="background:#F5F5F5;" align="center" + |[[Light chain|Light chains]] of [[Immunoglobulin|immunoglobulines]]
| style="background:#F5F5F5;" align="center" + |<10%
| style="background:#F5F5F5;" align="center" + |<10%
| style="background:#F5F5F5;" align="left" + |
| style="background:#F5F5F5;" align="left" + |
* No bone lesions,
*No bone lesions
* [[Nephrotic syndrome]]
*[[Nephrotic syndrome]]
* [[Restrictive cardiomyopathy]]
*[[Restrictive cardiomyopathy]]
* [[Peripheral neuropathy]]
*[[Peripheral neuropathy]]
* [[Hepatomegaly]] with elevated [[liver enzymes]]
*[[Hepatomegaly]] with elevated [[liver enzymes]]
* [[Macroglossia]]
*[[Macroglossia]]
* [[Purpura]] and an unexplained [[Hemorrhagic diathesis|bleeding diathesis]]
*[[Purpura]] and an unexplained [[Hemorrhagic diathesis|bleeding diathesis]]
|-
|-
| colspan="10" style="background:#DCDCDC;" align="left" + |
| colspan="10" style="background:#DCDCDC;" align="left" + |
Line 154: Line 155:
|}
|}


== Monoclonal gammopathies of undetermined significance (MGUS) ==
==Monoclonal gammopathies of undetermined significance (MGUS)==
* [[Monoclonal gammopathy of undetermined significance]] is a condition in which a low or non-quantifiable level of a [[monoclonal]] [[paraprotein]] is detected in the blood by means of [[protein electrophoresis]].<ref name="pmid16628189">{{cite journal |vauthors=Jego G, Bataille R, Geffroy-Luseau A, Descamps G, Pellat-Deceunynck C |title=Pathogen-associated molecular patterns are growth and survival factors for human myeloma cells through Toll-like receptors |journal=Leukemia |volume=20 |issue=6 |pages=1130–7 |date=June 2006 |pmid=16628189 |doi=10.1038/sj.leu.2404226 |url=}}</ref><ref name="pmid19181642">{{cite journal |vauthors=Dinarello CA |title=Targeting the pathogenic role of interleukin 1{beta} in the progression of smoldering/indolent myeloma to active disease |journal=Mayo Clin. Proc. |volume=84 |issue=2 |pages=105–7 |date=February 2009 |pmid=19181642 |pmc=2664579 |doi=10.4065/84.2.105 |url=}}</ref><ref name="pmid23233640">{{cite journal |vauthors=Merlini G, Palladini G |title=Differential diagnosis of monoclonal gammopathy of undetermined significance |journal=Hematology Am Soc Hematol Educ Program |volume=2012 |issue= |pages=595–603 |date=2012 |pmid=23233640 |doi=10.1182/asheducation-2012.1.595 |url=}}</ref>
*<nowiki/>In addition, some patients develop a [[polyneuropathy]]<nowiki/>or other problems related to the secreted antibody.
* MGUS is a premalignant condition and is distinct fr<nowiki/>om [[multiple myeloma]].
* Pathologically, the lesion in [[Monoclonal gammopathy of undetermined significance]] is in fact very similar to that in [[multiple myeloma]].
For more information about Monoclonal gammopathies of undetermined significance  '''[[Monoclonal gammopathies of undetermined significance |click here]]'''


== Malignant monoclonal gammopathies ==
*[[Monoclonal gammopathy of undetermined significance]] is a condition in which a low or non-quantifiable level of a [[monoclonal]] [[paraprotein]] is detected in the blood by means of [[protein electrophoresis]].<ref name="pmid16628189">{{cite journal |vauthors=Jego G, Bataille R, Geffroy-Luseau A, Descamps G, Pellat-Deceunynck C |title=Pathogen-associated molecular patterns are growth and survival factors for human myeloma cells through Toll-like receptors |journal=Leukemia |volume=20 |issue=6 |pages=1130–7 |date=June 2006 |pmid=16628189 |doi=10.1038/sj.leu.2404226 |url=}}</ref><ref name="pmid19181642">{{cite journal |vauthors=Dinarello CA |title=Targeting the pathogenic role of interleukin 1{beta} in the progression of smoldering/indolent myeloma to active disease |journal=Mayo Clin. Proc. |volume=84 |issue=2 |pages=105–7 |date=February 2009 |pmid=19181642 |pmc=2664579 |doi=10.4065/84.2.105 |url=}}</ref><ref name="pmid23233640">{{cite journal |vauthors=Merlini G, Palladini G |title=Differential diagnosis of monoclonal gammopathy of undetermined significance |journal=Hematology Am Soc Hematol Educ Program |volume=2012 |issue= |pages=595–603 |date=2012 |pmid=23233640 |doi=10.1182/asheducation-2012.1.595 |url=}}</ref>
*<nowiki/>In addition, some patients develop a [[polyneuropathy]]<nowiki/> or other problems related to the secreted antibody.
*MGUS is a premalignant condition and is distinct fr<nowiki/>om [[multiple myeloma]].
*Pathologically, the lesion in [[Monoclonal gammopathy of undetermined significance]] is in fact very similar to that in [[multiple myeloma]].


=== '''Multiple myeloma''' ===
For more information about monoclonal gammopathies of undetermined significance  '''[[Monoclonal gammopathies of undetermined significance |click here]].'''


==== Symptomatic multiple myeloma ====
==Malignant monoclonal gammopathies==
* People with [[Multiple myeloma classification|multiple myeloma]] with symptoms are categorized to have [[Multiple myeloma Classification|active multiple myeloma]] and will exibit any of the following features.<ref name="SergentanisZagouri2015">{{cite journal|last1=Sergentanis|first1=Theodoros N.|last2=Zagouri|first2=Flora|last3=Tsilimidos|first3=Gerasimos|last4=Tsagianni|first4=Anastasia|last5=Tseliou|first5=Melina|last6=Dimopoulos|first6=Meletios A.|last7=Psaltopoulou|first7=Theodora|title=Risk Factors for Multiple Myeloma: A Systematic Review of Meta-Analyses|journal=Clinical Lymphoma Myeloma and Leukemia|volume=15|issue=10|year=2015|pages=563–577.e3|issn=21522650|doi=10.1016/j.clml.2015.06.003}}</ref>
** [[M protein]] in blood or urine
** [[Bone marrow cells|Bone marrow]] [[plasma cells]] constitute more than 10% of the [[blood cells]]
** Presence of solitary [[plasmacytoma]] in bone
** ≥1 myeloma-defining event
** CRAB features ( explained above)
** Osteolytic lesions on bone x-ray


* Patients with active [[Multiple myeloma diagnostic criteria|Multiple myeloma]] usually require treatment to prevent progression of disease which can lead to death.
==='''Multiple myeloma'''===


==== Smoldering multiple myeloma ====
====Symptomatic multiple myeloma====
* It is asymptomatic type of [[Multiple myeloma classification|multiple myeloma]]<ref name="pmid27291302">{{cite journal |vauthors=Rajkumar SV |title=Multiple myeloma: 2016 update on diagnosis, risk-stratification, and management |journal=Am. J. Hematol. |volume=91 |issue=7 |pages=719–34 |date=July 2016 |pmid=27291302 |pmc=5291298 |doi=10.1002/ajh.24402 |url=}}</ref>
* Shows presence of M-spike that quantitates > 3 g/dl on [[protein electrophoresis]]


* Presence of [[Bone marrow cells|bone marrow plasma cell]] burden of > 10% but < 60%
*People with [[Multiple myeloma classification|multiple myeloma]] with symptoms are categorized to have [[Multiple myeloma Classification|active multiple myeloma]] and will exhibit any of the following features:<ref name="SergentanisZagouri2015">{{cite journal|last1=Sergentanis|first1=Theodoros N.|last2=Zagouri|first2=Flora|last3=Tsilimidos|first3=Gerasimos|last4=Tsagianni|first4=Anastasia|last5=Tseliou|first5=Melina|last6=Dimopoulos|first6=Meletios A.|last7=Psaltopoulou|first7=Theodora|title=Risk Factors for Multiple Myeloma: A Systematic Review of Meta-Analyses|journal=Clinical Lymphoma Myeloma and Leukemia|volume=15|issue=10|year=2015|pages=563–577.e3|issn=21522650|doi=10.1016/j.clml.2015.06.003}}</ref>
**[[M protein]] in blood or urine
**[[Bone marrow cells|Bone marrow]] [[plasma cells]] constitute more than 10% of the [[blood cells]]
**Presence of solitary [[plasmacytoma]] in bone
**≥ 1 myeloma-defining event
**CRAB features ( explained above)
**Osteolytic lesions on bone x-ray


* Absence of end-organ damage such as [[anemia]], [[hypercalcemia]], renal dysfunction, or [[Osseous|osseous lesions]]
*Patients with active [[multiple myeloma]] usually require treatment to prevent progression of disease which can lead to death.


* Patients with smoldering (asymptomatic) [[Multiple myeloma diagnostic criteria|Multiple myeloma]] are managed by observation and undergoing follow up tests every 3 to 6 months
====Smoldering multiple myeloma====
* There is high risk of developing [[Multiple myeloma Classification|active multiple myeloma.]]


==== Plasma-cell leukemia ====
*It is asymptomatic type of [[Multiple myeloma classification|multiple myeloma]].<ref name="pmid27291302">{{cite journal |vauthors=Rajkumar SV |title=Multiple myeloma: 2016 update on diagnosis, risk-stratification, and management |journal=Am. J. Hematol. |volume=91 |issue=7 |pages=719–34 |date=July 2016 |pmid=27291302 |pmc=5291298 |doi=10.1002/ajh.24402 |url=}}</ref>
* Charecterized by large number of [[plasma cells]] circulating in the blood<ref name="Rajkumar2016" />
*Shows presence of M-spike that quantitates > 3 g/dl on [[protein electrophoresis]].
* Rare condition, can develop in to most aggressive form of [[Multiple myeloma Classification|multiple myeloma]].
* Treatment options for [[plasma cell leukemia]] is [[chemotherapy]] or [[Hematopoietic stem cell transplantation|stem cell transplant]].


==== Non-secretory myeloma ====
*Presence of [[Bone marrow cells|bone marrow plasma cell]] burden of > 10% but < 60%.
* Type of [[Multiple myeloma classification|multiple myeloma]] with less amount of [[M protein|M proteins]] secretion in [[blood]] or urine.<ref name="Rajkumar2016" />
* M protein is not detected by [[serum protein electrophoresis]]
* [[Bone marrow]] exibit [[Myeloma|myeloma cells]].
* Osteolytic bone lesions are seen on xrays.


==== IgD myeloma ====
*Absence of end-organ damage such as [[anemia]], [[hypercalcemia]], [[Renal dysfunction|renal dysfunction,]] or [[Osseous|osseous lesions]].
* IgD type constitues 2% of [[Multiple myeloma Classification|multiple myeloma]]<ref name="Rajkumar2016" />
* IgD [[Multiple myeloma classification|multiple myeloma]] has similar signs and symptoms as other types of [[Multiple myeloma classification|multiple myeloma]].


* IgD myeloma mostly affect people of younger age.
*Patients with smoldering (asymptomatic) [[multiple myeloma]] are managed by observation and undergoing follow up tests every 3 to 6 months.
*There is high risk of developing active [[multiple myeloma]].


==== Osteosclerotic myeloma ====
====Plasma-cell leukemia====
* It is a rare disorder affecting multiple systems of the body<ref name="Rajkumar2016">{{cite journal|last1=Rajkumar|first1=S. Vincent|title=Multiple myeloma: 2016 update on diagnosis, risk-stratification, and management|journal=American Journal of Hematology|volume=91|issue=7|year=2016|pages=719–734|issn=03618609|doi=10.1002/ajh.24402}}</ref>


* It is called POEMS syndrome: [[polyneuropathy]], [[Organomegaly|organomegaly,]] [[endocrinopathy]], monoclonal protein, skin changes
*Characterized by large number of [[plasma cells]] circulating in the blood.<ref name="Rajkumar2016" />
* Treatment option for osteoclastic myeloma include:
*Rare condition, can develop in to most aggressive form of [[Multiple myeloma Classification|multiple myeloma]].
** [[Chemotherapy]]
*Can occur as a secondary type in a patient with multiple myeloma.
** [[Radiation therapy]]
*Treatment options for [[plasma cell leukemia]] is [[chemotherapy]] or [[Hematopoietic stem cell transplantation|stem cell transplant]].
** [[Hematopoietic stem cell transplantation|Stem cell transplant]]


==== Solitary plasmacytoma of bone ====
====Non-secretory myeloma====
* [[Plasmacytoma]] is collection of abnormal [[plasma cells]] forming a singl e tumor.<ref name="CaersPaiva2018">{{cite journal|last1=Caers|first1=J.|last2=Paiva|first2=B.|last3=Zamagni|first3=E.|last4=Leleu|first4=X.|last5=Bladé|first5=J.|last6=Kristinsson|first6=S. Y.|last7=Touzeau|first7=C.|last8=Abildgaard|first8=N.|last9=Terpos|first9=E.|last10=Heusschen|first10=R.|last11=Ocio|first11=E.|last12=Delforge|first12=M.|last13=Sezer|first13=O.|last14=Beksac|first14=M.|last15=Ludwig|first15=H.|last16=Merlini|first16=G.|last17=Moreau|first17=P.|last18=Zweegman|first18=S.|last19=Engelhardt|first19=M.|last20=Rosiñol|first20=L.|title=Diagnosis, treatment, and response assessment in solitary plasmacytoma: updated recommendations from a European Expert Panel|journal=Journal of Hematology & Oncology|volume=11|issue=1|year=2018|issn=1756-8722|doi=10.1186/s13045-017-0549-1}}</ref>
* [[Plasmacytoma|Solitary plasmacytoma]] is occurence of single bone [[tumor]] made up of myeloma cells.
* Xray shows an osteolytic lesion at the site of the [[Tumor|tumor.]]
* [[Bone marrow]] plasma population remains less than 10%
* One third of patients with solitary [[plasmacytoma]] will develop [[Multiple myeloma classification|multiple myeloma]].


==== Extramedullary plasmacytoma ====
*Type of [[Multiple myeloma classification|multiple myeloma]] with less amount of [[M protein|M proteins]] secretion in [[blood]] or urine.<ref name="Rajkumar2016" />
* It is develped outside the bone marrow in soft tissues of the body<ref name="Rajkumar2016" />
*M protein is not detected by [[serum protein electrophoresis]].
* Most commonly seen in throat,[[paranasal sinuses]], [[nasal cavity]], [[larynx]], [[Gastrointestinal tract|GI tract,]] [[breast]] and [[brain]].
*[[Bone marrow]] exibit [[Myeloma|myeloma cells]].
* Diagnosis is confirmed by [[biopsy]] of the [[Tumor|tumor.]]
*Osteolytic bone lesions are seen on X-ray.
* X-rays and  [[bone marrow]] [[biopsy]] is normal.
* Treatment is done with either [[radiation therapy]] or surgery.
For more information about Multiple myeloma '''[[Multiple myeloma |click here]]'''


=== Malignant lymphoproliferative disorders ===
====IgD myeloma====
==== Waldenstrom macroglobulinemia ====
* [[Waldenström's macroglobulinemia|Waldenstrom macroglobulinemia]] is a cancer involving  [[lymphocytes]].<ref name="pmid22773606">{{cite journal |vauthors=Braggio E, Philipsborn C, Novak A, Hodge L, Ansell S, Fonseca R |title=Molecular pathogenesis of Waldenstrom's macroglobulinemia |journal=Haematologica |volume=97 |issue=9 |pages=1281–90 |date=September 2012 |pmid=22773606 |pmc=3436227 |doi=10.3324/haematol.2012.068478 |url=}}</ref>
* The main attributing [[antibody]] is [[IgM]].
* It is a type of [[lymphoproliferative disease]],
* It shares clinical characteristics with the indolent [[Non-Hodgkin lymphoma|non-Hodgkin lymphomas]].
* [[Waldenström's macroglobulinemia|Waldenstrom macroglobulinemia]] represents 1% of all hematological cancers
* Common causes of [[Waldenström's macroglobulinemia]] include [[genetic]], environmental, and [[autoimmune]] factors.
* Common [[risk factors]] in the development of [[Waldenström's macroglobulinemia]] are [[Monoclonal gammopathy of undetermined significance]].
For more information about Waldenström's macroglobulinemia  '''[[Waldenström's macroglobulinemia |click here]]'''


==== Malignant lymphoma ====
*IgD type constitues 2% of [[Multiple myeloma Classification|multiple myeloma]].<ref name="Rajkumar2016" />
* Type of [[cancer]] that originates in [[Lymphocyte|lymphocytes]]<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>
*IgD [[Multiple myeloma classification|multiple myeloma]] has similar signs and symptoms as other types of [[Multiple myeloma classification|multiple myeloma]].
* Also called [[Hematological malignancy|hematological neoplasms]].
* Main types are Hodgkin lymphoma and Non-Hodgkin lymphoma
For more information about lymphoma '''[[lymphoma |click here]]'''


=== Chronic lymphocytic leukemia ===
*IgD myeloma mostly affect people of younger age.
* [[Chronic lymphocytic leukemia]] arises from pre-follicular center [[B cell|B cells]], normally involved in [[Immunoglobulin|immunoglobulins]] production.<ref name="Hallek2015">{{cite journal|last1=Hallek|first1=Michael|title=Chronic lymphocytic leukemia: 2015 Update on diagnosis, risk stratification, and treatment|journal=American Journal of Hematology|volume=90|issue=5|year=2015|pages=446–460|issn=03618609|doi=10.1002/ajh.23979}}</ref>
* Development of [[chronic lymphocytic leukemia]] is the result of multiple [[Genetic mutation|genetic mutations]] that promote both [[malignant]] leukemic proliferation and [[apoptotic]] resistance of mature [[B cells]].
* [[Chronic lymphocytic leukemia]] must be differentiated from [[hairy cell leukaemia]], prolymphocytic leukaemia, [[follicular lymphoma]], and [[mantle cell lymphoma]].
* Prognosis is generally good, and the 5-year survival rate of patients with [[chronic lymphocytic leukemia]] is approximately 81.7%.
* The mainstay of therapy for symptomatic [[chronic lymphocytic leukemia]] patients is immunochemotherapy.
For more information about chronic lymphocytic leukemia '''[[ chronic lymphocytic leukemia|click here]]'''


== Heavy-chain diseases ==
====Osteosclerotic myeloma====
* Heavy chain diseases are [[Neoplasias|plasma cell neoplasias]], featuring overproduction of [[Immunoglobulin|immunoglobulin heavy chains]].<ref name="MunshiCabot2008">{{cite journal|last1=Munshi|first1=Nikhil C.|last2=Cabot|first2=Richard C.|last3=Harris|first3=Nancy Lee|last4=Shepard|first4=Jo-Anne O.|last5=Rosenberg|first5=Eric S.|last6=Cort|first6=Alice M.|last7=Ebeling|first7=Sally H.|last8=Peters|first8=Christine C.|last9=Digumarthy|first9=Subba|last10=Rahemtullah|first10=Aliyah|title=Case 13-2008|journal=New England Journal of Medicine|volume=358|issue=17|year=2008|pages=1838–1848|issn=0028-4793|doi=10.1056/NEJMcpc0800959}}</ref>


=== γHCD ===
*It is a rare disorder affecting multiple systems of the body.<ref name="Rajkumar2016">{{cite journal|last1=Rajkumar|first1=S. Vincent|title=Multiple myeloma: 2016 update on diagnosis, risk-stratification, and management|journal=American Journal of Hematology|volume=91|issue=7|year=2016|pages=719–734|issn=03618609|doi=10.1002/ajh.24402}}</ref>
* Gamma chain or IgG heavy chain disease


** Primarily seen in elderly men but can occur in children.
*It is called POEMS syndrome: [[polyneuropathy]], [[Organomegaly|organomegaly,]] [[endocrinopathy]], monoclonal protein, skin changes.
** High levels of IgG with reduction of normal [[immunoglobulin]] level
*Treatment option for osteoclastic myeloma include:
** [[Lymphadenopathy|Lymphadenopath]]<nowiki/>y, [[hepatosplenomegaly]] and recurrent infections are common features
**[[Chemotherapy]]
** [[Vincristine]], [[Corticosteroid|corticosteroids]] and [[radiation therapy]] may produce [[Remission (medicine)|remission]].
**[[Radiation therapy]]
**[[Hematopoietic stem cell transplantation|Stem cell transplant]]


=== αHCD ===
====Solitary plasmacytoma of bone====
* Alpha chain or IgA heavy chain


** Appears between age 10-30 as an [[immune]] response to a [[microorganism]]
*[[Plasmacytoma]] is collection of abnormal [[plasma cells]] forming a single tumor.<ref name="CaersPaiva2018">{{cite journal|last1=Caers|first1=J.|last2=Paiva|first2=B.|last3=Zamagni|first3=E.|last4=Leleu|first4=X.|last5=Bladé|first5=J.|last6=Kristinsson|first6=S. Y.|last7=Touzeau|first7=C.|last8=Abildgaard|first8=N.|last9=Terpos|first9=E.|last10=Heusschen|first10=R.|last11=Ocio|first11=E.|last12=Delforge|first12=M.|last13=Sezer|first13=O.|last14=Beksac|first14=M.|last15=Ludwig|first15=H.|last16=Merlini|first16=G.|last17=Moreau|first17=P.|last18=Zweegman|first18=S.|last19=Engelhardt|first19=M.|last20=Rosiñol|first20=L.|title=Diagnosis, treatment, and response assessment in solitary plasmacytoma: updated recommendations from a European Expert Panel|journal=Journal of Hematology & Oncology|volume=11|issue=1|year=2018|issn=1756-8722|doi=10.1186/s13045-017-0549-1}}</ref>
** Patients present with diffuse abdominal [[lymphoma]] and [[malabsorption]].
*[[Plasmacytoma|Solitary plasmacytoma]] is occurrence of single bone [[tumor]] made up of myeloma cells.
** Course is variable, some patients die in 1-2 yrs, others go in to [[Remission (medicine)|remission]] lasting for many years.
*X-ray shows an osteolytic lesion at the site of the [[Tumor|tumor.]]
** [[Serum protein electrophoresis]] detect increased α & β fraction.
*[[Bone marrow]] plasma population remains less than 10%.
** Treatment is [[Corticosteroid|corticosteroids]], [[cytotoxic drugs]] and broadspectrum antibiotics
*One third of patients with solitary [[plasmacytoma]] will develop [[Multiple myeloma classification|multiple myeloma]].


=== μHCD ===
====Extramedullary plasmacytoma====
* MU chain or IGM heavy chain disease


** Mainly affects individuals > 50 yrs
*It is developed outside the [[bone marrow]] in soft tissues of the body<ref name="Rajkumar2016" />
** [[Spleen]], [[liver]] and abdominal [[lymph nodes]] involvement is more common than peripheral [[lymphadenopathy]]
*Most commonly seen in throat, [[paranasal sinuses]], [[nasal cavity]], [[larynx]], [[Gastrointestinal tract|GI tract,]] [[breast]], and [[brain]].
** [[Serum]] [[protein electrophoresis]] exibit [[hypogammaglobulinemia]].
*Diagnosis is confirmed by [[biopsy]] of the [[Tumor|tumor.]]
** Vacuolated [[Plasma cell|plasma cells]] are pathognomic on [[bone marrow]] exam.
*X-rays and [[bone marrow]] [[biopsy]] is normal.
** Treatment consists of [[Alkylating agent|alkylating agents]] and [[Corticosteroid|corticosteroids]].
*Treatment is done with either [[radiation therapy]] or surgery.


== Cryoglobulinemia ==
For more information about [[multiple myeloma]], '''[[Multiple myeloma |click here]].'''
* [[Cryoglobulinemia]] is the presence of high amount of heavy [[Globulin|globulins]] (e.g. [[IgM]]) in the [[bloodstream]] which thicken on exposure to cold.<ref name="pmid16026843">{{cite journal| author=Scotto G, Cibelli DC, Saracino A, Prato R, Palumbo E, Fazio V et al.| title=Cryoglobulinemia in subjects with HCV infection alone, HIV infection and HCV/HIV coinfection. | journal=J Infect | year= 2006 | volume= 52 | issue= 4 | pages= 294-9 | pmid=16026843 | doi=10.1016/j.jinf.2005.05.025 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16026843  }} </ref><ref name="pmid29558353">{{cite journal| author=Suszek D, Majdan M| title=[Cryoglobulins and cryoglobulinemic vasculitis]. | journal=Wiad Lek | year= 2018 | volume= 71 | issue= 1 pt 1 | pages= 59-63 | pmid=29558353 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=29558353  }} </ref><ref name="pmid27034078">{{cite journal| author=Blank N, Lorenz HM| title=[Cryoglobulinemic vasculitis]. | journal=Z Rheumatol | year= 2016 | volume= 75 | issue= 3 | pages= 303-15 | pmid=27034078 | doi=10.1007/s00393-016-0076-4 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27034078  }} </ref><ref name="pmid10787003">{{cite journal| author=Ramos-Casals M, Trejo O, García-Carrasco M, Cervera R, Font J| title=Mixed cryoglobulinemia: new concepts. | journal=Lupus | year= 2000 | volume= 9 | issue= 2 | pages= 83-91 | pmid=10787003 | doi=10.1191/096120300678828127 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10787003  }} </ref>
* Cryoglobulins are circulating [[immunoglobulins]] or [[Protein|proteins]] that become insoluble at less than 4 degrees Celsius.
* [[Cryoglobulinemia]] can lead to a medium-sized vessel [[vasculitis]] due to vascular deposition of circulating [[immune complexes]].
* This leads to the triad of palpable [[purpura]], [[Arthralgia|arthralgias]] and [[peripheral neuropathy]]
* Common causes of[[Cryoglobulinemia]] are primarily [[hematologic]], [[Oncology|oncologic]], and [[rheumatic]]
For more information on Cryoglobulinemia [[Cryoglobulinemia| click here]]


== AL Primary amyloidosis ==
===Malignant lymphoproliferative disorders===
* The "AL" refers to [[amyloid]] [[light chain]].<ref name="pmid15198347">{{cite journal |author=Gertz MA |title=The classification and typing of amyloid deposits |journal=Am. J. Clin. Pathol. |volume=121 |issue=6 |pages=787–9 |year=2004 |month=June |pmid=15198347 |doi=10.1309/TR4L-GLVR-JKAM-V5QT |url=http://ajcp.metapress.com/openurl.asp?genre=article&issn=0002-9173&volume=121&issue=6&spage=787}}</ref><ref name="urlAmyloidosis Causes, Diagnosis, Symptoms, and Treatment on MedicineNet.com">{{cite web |url=http://www.medicinenet.com/amyloidosis/article.htm |title=Amyloidosis Causes, Diagnosis, Symptoms, and Treatment on MedicineNet.com |format= |work= |accessdate=}}</ref>
====Waldenstrom macroglobulinemia====


** [[AL amyloidosis]] is the most common form of systemic [[amyloidosis]] in the US.
*[[Waldenström's macroglobulinemia|Waldenstrom macroglobulinemia]] is a cancer involving [[lymphocytes]].<ref name="pmid22773606">{{cite journal |vauthors=Braggio E, Philipsborn C, Novak A, Hodge L, Ansell S, Fonseca R |title=Molecular pathogenesis of Waldenstrom's macroglobulinemia |journal=Haematologica |volume=97 |issue=9 |pages=1281–90 |date=September 2012 |pmid=22773606 |pmc=3436227 |doi=10.3324/haematol.2012.068478 |url=}}</ref>
** Occurs in 5 to 15% of people with [[multiple myeloma]].
*The main attributing [[antibody]] is [[IgM]].
** Treatment can involve application of [[chemotherapy]] similar to that used in [[Multiple myeloma Classification|multiple myeloma]]
*It is a type of [[lymphoproliferative disease]].
For more information on amyloidosis [[ amyloidosis | click here]]
*It shares clinical characteristics with the indolent [[Non-Hodgkin lymphoma|non-Hodgkin lymphomas]].
*[[Waldenström's macroglobulinemia|Waldenstrom macroglobulinemia]] represents 1% of all hematological cancers.
*Common causes of [[Waldenström's macroglobulinemia]] include [[genetic]], environmental, and [[autoimmune]] factors.
*Common [[risk factors]] in the development of [[Waldenström's macroglobulinemia]] are [[monoclonal gammopathies of undetermined significance]].
 
For more information about [[Waldenström's macroglobulinemia]], '''[[Waldenström's macroglobulinemia |click here]].'''
 
====Malignant lymphoma====
 
*Type of [[cancer]] that originates in [[Lymphocyte|lymphocytes]].<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>
*Also called [[Hematological malignancy|hematological neoplasms]].
*Primary types include [[Hodgkin lymphoma]] and [[non-Hodgkin lymphoma]].
 
For more information about [[malignant lymphoma]], '''[[lymphoma |click here]].'''
 
===Chronic lymphocytic leukemia===
 
*[[Chronic lymphocytic leukemia]] arises from pre-follicular center [[B cell|B cells]], normally involved in [[Immunoglobulin|immunoglobulins]] production.<ref name="Hallek2015">{{cite journal|last1=Hallek|first1=Michael|title=Chronic lymphocytic leukemia: 2015 Update on diagnosis, risk stratification, and treatment|journal=American Journal of Hematology|volume=90|issue=5|year=2015|pages=446–460|issn=03618609|doi=10.1002/ajh.23979}}</ref>
*Development of [[chronic lymphocytic leukemia]] is the result of multiple [[Genetic mutation|genetic mutations]] that promote both [[malignant]] leukemic proliferation and [[apoptotic]] resistance of mature [[B cells]].
*[[Chronic lymphocytic leukemia]] must be differentiated from [[hairy cell leukaemia]], prolymphocytic leukaemia, [[follicular lymphoma]], and [[mantle cell lymphoma]].
*[[Prognosis]] is generally good, and the 5-year survival rate of patients with [[chronic lymphocytic leukemia]] is approximately 81.7%.
*The mainstay of therapy for [[symptomatic]] [[chronic lymphocytic leukemia]] patients is immunochemotherapy.
 
For more information about [[chronic lymphocytic leukemia]], '''[[ chronic lymphocytic leukemia|click here]]'''
 
==Heavy-chain diseases (HCD)==
 
*Heavy chain diseases are [[plasma cell]] [[neoplasia]] featuring overproduction of [[Immunoglobulin|immunoglobulin heavy chains]].<ref name="MunshiCabot2008">{{cite journal|last1=Munshi|first1=Nikhil C.|last2=Cabot|first2=Richard C.|last3=Harris|first3=Nancy Lee|last4=Shepard|first4=Jo-Anne O.|last5=Rosenberg|first5=Eric S.|last6=Cort|first6=Alice M.|last7=Ebeling|first7=Sally H.|last8=Peters|first8=Christine C.|last9=Digumarthy|first9=Subba|last10=Rahemtullah|first10=Aliyah|title=Case 13-2008|journal=New England Journal of Medicine|volume=358|issue=17|year=2008|pages=1838–1848|issn=0028-4793|doi=10.1056/NEJMcpc0800959}}</ref>
 
===γHCD===
 
*Also known as gamma chain or IgG heavy chain disease.
**Primarily seen in elderly men but can occur in children.
**High levels of IgG with reduction of normal [[immunoglobulin]] level.
**[[Lymphadenopathy|Lymphadenopath]]<nowiki/>y, [[hepatosplenomegaly]], and recurrent infections are common features.
**[[Vincristine]], [[Corticosteroid|corticosteroids]] and [[radiation therapy]] may produce [[Remission (medicine)|remission]].
 
===αHCD===
 
*Also known as alpha chain or IgA heavy chain.
**Appears between age 10-30 as an [[immune]] response to a [[microorganism]].
**Patients present with diffuse abdominal [[lymphoma]] and [[malabsorption]].
**Course is variable, some patients die in 1-2 yrs, others go in to [[Remission (medicine)|remission]] lasting for many years.
**[[Serum protein electrophoresis]] detect increased α & β fraction.
**Treatment is [[Corticosteroid|corticosteroids]], [[cytotoxic drugs]] and broadspectrum antibiotics
 
===μHCD===
 
*Also known as mu chain or IGM heavy chain disease.
**Mainly affects individuals > 50 yrs.
**[[Spleen]], [[liver]] and abdominal [[lymph nodes]] involvement is more common than peripheral [[lymphadenopathy]].
**[[Serum]] [[protein electrophoresis]] exibit [[hypogammaglobulinemia]].
**Vacuolated [[Plasma cell|plasma cells]] are pathognomic on [[bone marrow]] exam.
**Treatment consists of [[Alkylating agent|alkylating agents]] and [[Corticosteroid|corticosteroids]].
 
==Cryoglobulinemia==
 
*[[Cryoglobulinemia]] is the presence of high amount of heavy [[Globulin|globulins]] (e.g. [[IgM]]) in the [[bloodstream]] which thicken on exposure to cold.<ref name="pmid16026843">{{cite journal| author=Scotto G, Cibelli DC, Saracino A, Prato R, Palumbo E, Fazio V et al.| title=Cryoglobulinemia in subjects with HCV infection alone, HIV infection and HCV/HIV coinfection. | journal=J Infect | year= 2006 | volume= 52 | issue= 4 | pages= 294-9 | pmid=16026843 | doi=10.1016/j.jinf.2005.05.025 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16026843  }} </ref><ref name="pmid29558353">{{cite journal| author=Suszek D, Majdan M| title=[Cryoglobulins and cryoglobulinemic vasculitis]. | journal=Wiad Lek | year= 2018 | volume= 71 | issue= 1 pt 1 | pages= 59-63 | pmid=29558353 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=29558353  }} </ref><ref name="pmid27034078">{{cite journal| author=Blank N, Lorenz HM| title=[Cryoglobulinemic vasculitis]. | journal=Z Rheumatol | year= 2016 | volume= 75 | issue= 3 | pages= 303-15 | pmid=27034078 | doi=10.1007/s00393-016-0076-4 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27034078  }} </ref><ref name="pmid10787003">{{cite journal| author=Ramos-Casals M, Trejo O, García-Carrasco M, Cervera R, Font J| title=Mixed cryoglobulinemia: new concepts. | journal=Lupus | year= 2000 | volume= 9 | issue= 2 | pages= 83-91 | pmid=10787003 | doi=10.1191/096120300678828127 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10787003  }} </ref>
*Cryoglobulins are circulating [[immunoglobulins]] or [[Protein|proteins]] that become insoluble at less than 4 degrees celsius.
*[[Cryoglobulinemia]] can lead to a medium-sized vessel [[vasculitis]] due to vascular deposition of circulating [[immune complexes]].
*This leads to the triad of palpable [[purpura]], [[Arthralgia|arthralgias]] and [[peripheral neuropathy]].
*Common causes of [[Cryoglobulinemia CT|cryoglobulinemia]] are primarily [[hematologic]], [[Oncology|oncologic]], and [[rheumatic]]
 
For more information on [[cryoglobulinemia]], [[Cryoglobulinaemia|'''click here''']].
 
==Primary amyloidosis==
 
*The "AL" refers to [[amyloid]] [[light chain]].<ref name="pmid15198347">{{cite journal |author=Gertz MA |title=The classification and typing of amyloid deposits |journal=Am. J. Clin. Pathol. |volume=121 |issue=6 |pages=787–9 |year=2004 |month=June |pmid=15198347 |doi=10.1309/TR4L-GLVR-JKAM-V5QT |url=http://ajcp.metapress.com/openurl.asp?genre=article&issn=0002-9173&volume=121&issue=6&spage=787}}</ref><ref name="urlAmyloidosis Causes, Diagnosis, Symptoms, and Treatment on MedicineNet.com">{{cite web |url=http://www.medicinenet.com/amyloidosis/article.htm |title=Amyloidosis Causes, Diagnosis, Symptoms, and Treatment on MedicineNet.com |format= |work= |accessdate=}}</ref>
**[[AL amyloidosis]] is the most common form of systemic [[amyloidosis]] in the US.
**Occurs in 5 to 15% of people with [[multiple myeloma]].
**Treatment can involve application of [[chemotherapy]] similar to that used in [[Multiple myeloma Classification|multiple myeloma]]
 
For more information on primary amyloidosis, '''[[Primary amyloidosis|click here]].'''


==References==
==References==
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[[Category:Medicine]]
[[Category:Hematology]]
[[Category:Oncology]]

Latest revision as of 11:52, 19 July 2022


Plasma cell disorders

Overview

Classification

Monoclonal gammopathy of undetermined significance (MGUS)
Malignant monoclonal gammopathies
Multiple myeloma
Malignant lymphoproliferative disorders
Chronic lymphocytic leukemia
Heavy-chain diseases
Cryoglobulinemia
Primary amyloidosis

Differentiating Plasma Cell Disorder

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

Synonyms and keywords: Plasma cell dyscrasia

Overview

Plasma cell disorders are a diverse type of blood disorders characterized by proliferation of a single clone of plasma cells that produces a homogeneous monoclonal (M) protein. These monoclonal paraprotein are seen in the serum or urine. Monoclonal plasma cells are present in the bone marrow or, rarely, in other tissues. Plasma cell disorders include monoclonal gammopathy of undetermined significance (MGUS), multiple myeloma (MM), lymphoplasmacytic lymphoma or Waldenstrom macroglobulinemia (LPL/WM), lymphoproliferative disorders, smoldering multiple myeloma (SMM); solitary or extramedullary plasmacytoma, amyloidosis, and POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes). These disorders have been defined by the International Myeloma Working Group in 2006.

Classification

 
 
 
 
 
 
 
 
 
 
 
Plasma cell disorder
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Primary amyloidosis
 
Malignant monoclonal gammopathy
 
Chronic lymphocytic leukemia
 
 
 
Heavy chain diseases (HCD)
 
Cryoglobulinemia
 
Monoclonal gammopathy of undetermined significance (MGUS)
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Multiple myeloma
 
 
Malignant lymphoproliferative disorders
 
γHCD
 
αHCD
 
μHCD
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Benign
(IgG, IgA, IgD, IgM, and,
rarely, free light chains)
 
Associated neoplasms
or other diseases not known to
produce monoclonal proteins
 
Biclonal and triclonal
gammopathies
 
Idiopathic
(Bence Jones
proteinuria)
 
 
 
 
 
 
 
 
 
 
 
 
Waldenstrom macroglobulinemia
 
Malignant lymphoma
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Symptomatic multiple myeloma
 
Smoldering multiple myeloma
 
Plasma-cell leukemia
 
Non-secretory myeloma
 
IgD myeloma
 
Osteosclerotic myeloma
 
Solitary plasmacytoma of bone
 
Extramedullary plasmacytoma
 

Differential Diagnosis

Disease IgM IgG IgA IgE IgD Monoclonal Ig level SFLC Bone marrow plasma cells Other criteria
IgM MGUS + < 3gm/dl N/A <10%
  • No end-organ damage
Non igM MGUS + + < 3gm/dl N/A <10%
  • No end-organ damage
Smoldering MM + + > 3gm/dl N/A 10-60%
  • No myeloma-defining event
  • No CRAB features
Light chain MGUS <500 mg/24 hrs (urine) Free kappa or lambda light chain
Abnormal ratio (<0.26 or >1.65)
Increase in involved light chain concentration
<10%
  • No end-organ damage
Active symptomatic Multiple myeloma + + + + >3gm/dl >100 >60%
  • ≥1 myeloma-defining event
  • CRAB features
Waldenstrom macroglobulinemia + Variable N/A >10%
Solitary Plasmacytoma + <3mg/dl Abnormal in 47% cases Normal
Primary amyloidosis <3md/dl Light chains of immunoglobulines <10%
  • Myeloma defining events: >60% clonal plasma cells on B.M exam; serum involved: uninvolved FLC ratio >100; >1 focal lesion on MRI >5mm
  • CRAB features: elevated calcium >11mg/dl, renal insufficiency, anemia Hb <10 g/dL , bone disease ≥1 lytic lesions on skeletal radiography, CT, or PET-CT , SFLC: serum free light chains, kappa and lambda immunoglobulin light chains.
  • The normal κ:λ ratio is 0.26 to 1.65 (17,18). A κ:λ ratio of <0.26 strongly suggests the presence of a of plasma cells that are producing clonal λ free light chains. Ratio >1.65 suggests production of clonal κ free light chains.

Monoclonal gammopathies of undetermined significance (MGUS)

For more information about monoclonal gammopathies of undetermined significance click here.

Malignant monoclonal gammopathies

Multiple myeloma

Symptomatic multiple myeloma

  • Patients with active multiple myeloma usually require treatment to prevent progression of disease which can lead to death.

Smoldering multiple myeloma

  • Patients with smoldering (asymptomatic) multiple myeloma are managed by observation and undergoing follow up tests every 3 to 6 months.
  • There is high risk of developing active multiple myeloma.

Plasma-cell leukemia

Non-secretory myeloma

IgD myeloma

  • IgD myeloma mostly affect people of younger age.

Osteosclerotic myeloma

  • It is a rare disorder affecting multiple systems of the body.[6]

Solitary plasmacytoma of bone

Extramedullary plasmacytoma

For more information about multiple myeloma, click here.

Malignant lymphoproliferative disorders

Waldenstrom macroglobulinemia

For more information about Waldenström's macroglobulinemia, click here.

Malignant lymphoma

For more information about malignant lymphoma, click here.

Chronic lymphocytic leukemia

For more information about chronic lymphocytic leukemia, click here

Heavy-chain diseases (HCD)

γHCD

αHCD

μHCD

Cryoglobulinemia

For more information on cryoglobulinemia, click here.

Primary amyloidosis

For more information on primary amyloidosis, click here.

References

  1. Jego G, Bataille R, Geffroy-Luseau A, Descamps G, Pellat-Deceunynck C (June 2006). "Pathogen-associated molecular patterns are growth and survival factors for human myeloma cells through Toll-like receptors". Leukemia. 20 (6): 1130–7. doi:10.1038/sj.leu.2404226. PMID 16628189.
  2. Dinarello CA (February 2009). "Targeting the pathogenic role of interleukin 1{beta} in the progression of smoldering/indolent myeloma to active disease". Mayo Clin. Proc. 84 (2): 105–7. doi:10.4065/84.2.105. PMC 2664579. PMID 19181642.
  3. Merlini G, Palladini G (2012). "Differential diagnosis of monoclonal gammopathy of undetermined significance". Hematology Am Soc Hematol Educ Program. 2012: 595–603. doi:10.1182/asheducation-2012.1.595. PMID 23233640.
  4. Sergentanis, Theodoros N.; Zagouri, Flora; Tsilimidos, Gerasimos; Tsagianni, Anastasia; Tseliou, Melina; Dimopoulos, Meletios A.; Psaltopoulou, Theodora (2015). "Risk Factors for Multiple Myeloma: A Systematic Review of Meta-Analyses". Clinical Lymphoma Myeloma and Leukemia. 15 (10): 563–577.e3. doi:10.1016/j.clml.2015.06.003. ISSN 2152-2650.
  5. Rajkumar SV (July 2016). "Multiple myeloma: 2016 update on diagnosis, risk-stratification, and management". Am. J. Hematol. 91 (7): 719–34. doi:10.1002/ajh.24402. PMC 5291298. PMID 27291302.
  6. 6.0 6.1 6.2 6.3 6.4 Rajkumar, S. Vincent (2016). "Multiple myeloma: 2016 update on diagnosis, risk-stratification, and management". American Journal of Hematology. 91 (7): 719–734. doi:10.1002/ajh.24402. ISSN 0361-8609.
  7. Caers, J.; Paiva, B.; Zamagni, E.; Leleu, X.; Bladé, J.; Kristinsson, S. Y.; Touzeau, C.; Abildgaard, N.; Terpos, E.; Heusschen, R.; Ocio, E.; Delforge, M.; Sezer, O.; Beksac, M.; Ludwig, H.; Merlini, G.; Moreau, P.; Zweegman, S.; Engelhardt, M.; Rosiñol, L. (2018). "Diagnosis, treatment, and response assessment in solitary plasmacytoma: updated recommendations from a European Expert Panel". Journal of Hematology & Oncology. 11 (1). doi:10.1186/s13045-017-0549-1. ISSN 1756-8722.
  8. Braggio E, Philipsborn C, Novak A, Hodge L, Ansell S, Fonseca R (September 2012). "Molecular pathogenesis of Waldenstrom's macroglobulinemia". Haematologica. 97 (9): 1281–90. doi:10.3324/haematol.2012.068478. PMC 3436227. PMID 22773606.
  9. Pathology and Genetics of Haemo (World Health Organization Classification of Tumours S.). Oxford Univ Pr. ISBN 92-832-2411-6.
  10. Hallek, Michael (2015). "Chronic lymphocytic leukemia: 2015 Update on diagnosis, risk stratification, and treatment". American Journal of Hematology. 90 (5): 446–460. doi:10.1002/ajh.23979. ISSN 0361-8609.
  11. Munshi, Nikhil C.; Cabot, Richard C.; Harris, Nancy Lee; Shepard, Jo-Anne O.; Rosenberg, Eric S.; Cort, Alice M.; Ebeling, Sally H.; Peters, Christine C.; Digumarthy, Subba; Rahemtullah, Aliyah (2008). "Case 13-2008". New England Journal of Medicine. 358 (17): 1838–1848. doi:10.1056/NEJMcpc0800959. ISSN 0028-4793.
  12. Scotto G, Cibelli DC, Saracino A, Prato R, Palumbo E, Fazio V; et al. (2006). "Cryoglobulinemia in subjects with HCV infection alone, HIV infection and HCV/HIV coinfection". J Infect. 52 (4): 294–9. doi:10.1016/j.jinf.2005.05.025. PMID 16026843.
  13. Suszek D, Majdan M (2018). "[Cryoglobulins and cryoglobulinemic vasculitis]". Wiad Lek. 71 (1 pt 1): 59–63. PMID 29558353.
  14. Blank N, Lorenz HM (2016). "[Cryoglobulinemic vasculitis]". Z Rheumatol. 75 (3): 303–15. doi:10.1007/s00393-016-0076-4. PMID 27034078.
  15. Ramos-Casals M, Trejo O, García-Carrasco M, Cervera R, Font J (2000). "Mixed cryoglobulinemia: new concepts". Lupus. 9 (2): 83–91. doi:10.1191/096120300678828127. PMID 10787003.
  16. Gertz MA (2004). "The classification and typing of amyloid deposits". Am. J. Clin. Pathol. 121 (6): 787–9. doi:10.1309/TR4L-GLVR-JKAM-V5QT. PMID 15198347. Unknown parameter |month= ignored (help)
  17. "Amyloidosis Causes, Diagnosis, Symptoms, and Treatment on MedicineNet.com".

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