Jp. Sleater et al., INTRAVASCULAR (ANGIOTROPIC) LARGE-CELL LYMPHOMA - DETERMINATION OF MONOCLONALITY BY POLYMERASE CHAIN-REACTION ON PARAFFIN-EMBEDDED TISSUES, Modern pathology, 7(5), 1994, pp. 593-598
Angiotropic lymphoma is a rare, aggressive, intravascular non-Hodgkin'
s lymphoma, usually of B-cell phenotype. Because lymphoma is often cli
nically unsuspected, the small skin or muscle biopsies typically obtai
ned for evaluation make assessment of lymphoid clonality through cell
surface markers or Southern blot hybridization analysis difficult or i
mpossible. The recent development of polymerase chain reaction methodo
logies to detect chromosomal translocations and immunoglobulin heavy c
hain gene rearrangement on paraffin-embedded tissue offers an attracti
ve alternative for ascertaining the clonality of lymphoproliferative p
rocesses. We report a case of B-cell angiotropic lymphoma in which a m
onoclonal variable diversity joining region rearrangement of the immun
oglobulin heavy chain locus was detected by polymerase chain reaction
in both ante- and postmortem, formalin-fixed, paraffin-embedded skelet
al muscle. The use of polymerase chain reaction in assessing clonality
in angiotropic lymphoma is enhanced by the general absence of a backg
round of reactive B-lymphoid cells in angiotropic lymphoma, which can
obscure the monoclonal band and/or compromise sensitivity. No amplific
ation product was obtained for t(14;18) involving the bcl-2 major brea
kpoint region. It is interesting to note that this case exhibited rare
circulating lymphoma cells and more extensive bone marrow involvement
(more than 100 tumor cells/high magnification field) than has been pr
eviously described.