This study focused on 19 patients with renal lymphoma (RL) from whom 20 ini
tial (1 patient with fine-needle aspiration [FNA] specimens of masses in bo
th kidneys) and 1 repeated FNA specimen were obtained. Of the 19 patients,
10 had secondary RL, 8 primary RL, and 1 transplant RL. The FNA samples wer
e studied by smears tall cases), tissues (II), phenotyping by immunostainin
g (13) or flow cytometry (4), and gene rearrangement (3). The final diagnos
es included 1 T-cell lymphoma and 18 B-cell lymphomas. Of the 20 original s
pecimens, 14 were reported as positive for lymphoma, 3 suggestive of lympho
ma, 1 positive for transitional cell carcinoma, and 2 unsatisfactory. The f
ollow-up specimen showed reactive changes. Tissue correlation, available in
11 cases, confirmed a positive cytodiagnosis (7), provided a final diagnos
is in the cytologically inconclusive cases (3), or revised the misdiagnosis
of transitional cell carcinoma from smears (1). The phenotyping elucidated
the B vs T lineage of the lymphoma in all tested cases, confirmed the posi
tive cytodiagnosis in 10 cases, confirmed the reactive cytodiagnosis in 1 c
ase, and helped achieve a conclusive diagnosis in 2 cases suggestive of lym
phoma. Gene rearrangement studies showed light chain restriction in the 2 t
ested cases. FNA has an essential role in treatment planning for RL. Althou
gh FNA usually is diagnostically conclusive, a high index of suspicion and
awareness of atypical or misleading cytomorphologic features are important
for a correct interpretation, especially for primary RL. Ancillary testing
is essential for the diagnosis in problematic cases and lays the foundation
for the differential diagnosis.