We report a case of clinically aggressive reticulum cell sarcoma with mixed
follicular dendritic cell (FDC) and fibroblastic reticular cell (FRC) feat
ures. Histologically, the tumor was confined to lymph nodes occurring as a
multifocal epitheliold and spindle cell proliferation with appreciable mito
tic rate and numerous admixed non-neoplastic B-cells. Ultrastructural exami
nation revealed elongated cells with prominent nucleoli, interdigitating ce
ll processes and frequent desmosomes. These features are typical of FDC sar
coma. However, immunohistochemical stains showed no expression of antigens
characteristic of FDCs, including CD21, CD23 and CD35. Cytogenetic characte
rization of this tumor, by conventional G-banding and multicolor spectral k
aryotyping, revealed multiple clonal chromosomal aberrations, including del
(X)(p11.4) and add (21) (p11.2). Gene expression analysis by cDNA microarra
y of RNA obtained from short-term tumor cultures revealed high-level expres
sion of a set of genes (including PDGF receptor-alpha and -beta, certain me
talloproteinases, and CD105) that were also highly expressed in cultures of
nodal FRC cultured from non-neoplastic lymph nodes. We propose that this t
umor represents a nodal sarcoma with intermediate differentiation between F
DCs and FRCs. This case adds to the diversity of tumors that may arise from
lymph node stroma and supports a possible relationship between the FDC and
FRC lineages.