Difference between revisions of "Burkitt lymphoma"

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313 bytes added ,  17:34, 12 May 2018
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a few minor points
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==General==
==General==
*Extremely high proliferative rate & rate of [[apoptosis]].
*Extremely high proliferative rate & rate of [[apoptosis]]
*Rare in adults -- 1-2% of adult lymphomas.<ref name=omim113970>{{OMIM|113970}}</ref>
*Rare in adults -- 1-2% of adult lymphomas.<ref name=omim113970>{{OMIM|113970}}</ref>
*Relatively common in children -- 30-50% of childhood lymphomas.<ref name=omim113970>{{OMIM|113970}}</ref>
*Relatively common in children -- 30-50% of childhood lymphomas.<ref name=omim113970>{{OMIM|113970}}</ref>
*Although aggressive untreated, the high mitotic activity makes it relatively chemosensitive and complete remissions of 75-90% are described


===Pathophysiology===
===Pathophysiology===
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#*Found in Africa.
#*Found in Africa.
#*EBV ([[Epstein-Barr virus]]) associated.<ref name=pmid12610094/>
#*EBV ([[Epstein-Barr virus]]) associated.<ref name=pmid12610094/>
#Non-endemic:
#Non-endemic/sporadic:
#*Typical of the BL seen in the western world; EBV negative.
#*Typical of the BL seen in the western world; EBV negative.
#Immunodeficiency associated:
#Immunodeficiency associated:
#*Associated with [[HIV]] infection.
#*Associated with [[HIV]] infection.
#*Post-transplantation immunosuppression


==Microscopic==
==Microscopic==
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**Small nucleoli.
**Small nucleoli.
**Relatively abundant cytoplasm.
**Relatively abundant cytoplasm.
**Brisk mitotic rate.
**Brisk mitotic rate (near 100%).


DDx:
DDx:
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Others:
Others:
*BCL2 -ve.
*BCL2 -ve (may show weak BCL2


==Molecular pathology==
==Molecular pathology==
*t(8;14) (q24;q32) [[translocation]].<ref name=pmid12610094/>
*Isolated CMYC-IGH [[translocation]] - t(8;14) (q24;q32).<ref name=pmid12610094/>
*Several other variants -- involve MYC rearrangement.<ref name=pmid12610094/><ref name=omim113970>{{OMIM|113970}}</ref>
*Several other variants -- involve MYC rearrangement with other partners.<ref name=pmid12610094/><ref name=omim113970>{{OMIM|113970}}</ref>
*Should not have CCND1, BCL6 or BCL2 translocations


Note:
Note:
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