Aims: Follicular dendritic cell tumours are very rare neoplasms that often
occur in lymph nodes. We report here a case in the colon, a hitherto unrepo
rted site, in a 37-year-old female. The differentiation from gastrointestin
al stromal tumour is emphasized.
Methods and results: The tumour was tan, elastic and solid with surface ulc
eration. Microscopically, it was composed of oval to spindle tumour cells w
ith syncytial cytoplasm arranged in fascicular and whorled patterns. There
were many infiltrating lymphocytes. The histological appearance resembled g
astrointestinal stromal tumour, thymoma or meningioma, Distinct from the st
romal tumour, the lymph node was also involved by the tumour. Immunohistoch
emically, the tumour cells were positive for CD21, CD35 and CD68, but negat
ive for cytokeratin, CD34, smooth muscle actin, desmin, S100 protein, epith
elial membrane antigen, leukocyte common antigen, HMB-45 and c-kit. In-situ
hybridization study was negative for Epstein-Barr virus RNA sequences. Ult
rastructurally, the tumour cells possessed cytoplasmic processes joined by
desmosomes.
Conclusions: This entity should be considered in the list of differential d
iagnoses for gastrointestinal stromal tumour. The lymph node metastasis and
immunohistochemical features are of value for identification of this rare
neoplasm,