Peripheral T-cell lymphomas are uncommon, accounting for only 10% to 15% of
all non-Hodgkin lymphomas and their classification has been controversial.
We report a case of peripheral T-cell lymphoma with angiocentric growth pa
ttern which presented as a paratesticular tumoral nodule in a 47-year-old-m
an. Formalin-fixed paraffin-embedded samples from the paratesticular tumor
and non-infiltrated adjacent tissue were submitted to histological, immunoh
istochemical, polymerase chain reaction (PCR)-based and in situ hybridizati
on analysis. Histopathologically, there was a lymphomatous infiltrate in th
e paratesticular soft tissue, composed of a variable mixture of medium-size
d to large cells with large cytoplasm and irregular-shaped nuclei, together
with blood vessel destruction, necrosis and karyorrhexis. Immunohistochemi
cal study revealed a high p53 expression in neoplastic cells that showed T
cytotoxic immunophenotype, failing to express the natural killer (NK)-cell
antigen CD56. A monoclonal rearrangement of the T-cell receptor (TCR) gamma
gene by a PCR technique was demonstrated. Type-A Epstein-Barr Virus (EBV)
DNA was detected by PCR-based analysis. A combined in situ hybridization an
d immunohistochemical study revealed that most cells labeled positive for E
BV RNA showed immunostaining with the CD45RO antibody. Based on the above r
esults, the case reported was classified as extranodal peripheral T-cell ly
mphoma with cytotoxic phenotype and EBV associated. The present case does n
ot fit neatly into any of the specific types of peripheral T-cell lymphomas
of the REAL classification, so a diagnosis of peripheral T-cell lymphoma u
nspecified was made.