Saj. Loyson et al., MANTLE CELL LYMPHOMA - A MORPHOLOGICAL, IMMUNOHISTOCHEMICAL AND MOLECULAR-GENETIC STUDY, Pathology research and practice, 192(8), 1996, pp. 781-789
In order to identify helpful markers in the classification of mantle c
ell lymphoma, a morphological, immunohistochemical and molecular genet
ic analysis of 41 cases of NHL, originally referred to us as CC, ILL o
r LDL, was performed. We revised these lymphomas using the strict morp
hological criteria described in the updated Kiel classification and th
e more recently described criteria for MCL. The term MCL was used to d
esignate the small lymphocytic B-cell NHL, previously referred to as C
C or ILL/IDL. This revision yielded 20 MCL, 8 CLL, 3 Cb/Cc, 1 CB, 6 JC
and 3 MALT lymphomas. The presence of scattered histiocytes was seen
in 90% of MCL and 5% of the other cases. No other morphological parame
ter besides the used criteria, differentiated between MCL and similar
small lymphocytic B cell lymphomas. Helpful immunohistochemical marker
s to distinguish MCL from similar small lymphocytic lymphomas were CD5
+, CD10 -, CD23 - and Alkaline Phosphatase +. Large fields of dendrit
ic reticulum cells, often in a loose and disrupted arrangement were se
en in 82% of MCL and in 19% of the other lymphomas. Analysis with Sout
hern blotting showed a rearrangement in the BCL-1 locus in 12/20 cases
of MCL but not in the other 21 lymphomas. Although very specific for
MCL, Southern blotting to detect BCL-1 rearrangements is, due to the l
arge number of probes necessary, not of great help in daily practice f
or routine diagnostic purposes. We conclude that using strict morpholo
gical criteria, the diagnosis MCL can be made reliably and that immuno
phenotyping is helpful in supporting the diagnosis.