Keywords
bladder - carcinoma - lymphoepithelioma - urothelial
Introduction
Lymphoepithelioma depicts an undifferentiated carcinoma of the nasopharynx characterized
microscopically by the predominance of lymphoid aggregates in the background. Carcinomas
with similar histological features arising outside the nasopharynx are known as LELC,
which have been reported in various organs such as the thymus, cervix, and salivary
glands.[1] Involvement of urinary bladder was first reported by Zukerberg et al in 1991 with
a reported incidence between 0.4% and 1.3% of all bladder carcinomas.[2] It has been categorized into three subgroups: pure (100% lymphoepithelioma component),
predominant (between 50% and 100%), and focal (< 50%).[3] Owing to the scarcity of the case in the English literature, we hereby present a
case of pure LELC bladder and discuss important differential diagnosis, various treatment
modalities, and prognosis of this rare tumor.
Case Report
A 63-year-old male patient presented with a complaint of painless gross hematuria.
He had no prior personal/family medical history of this complaint. There were no notable
findings in blood tests and chest radiography. Urine cytology results were negative.
A CECT abdomen was performed that revealed a tumor arising from the left anterolateral
wall of the urinary bladder projecting into its lumen with a small exophytic component
reaching beyond the serosal surface on the inferior aspect ([Fig. 1]). TURBT revealed urothelial carcinoma. Radical cystoprostatectomy was performed.
Pathological findings revealed extensively infiltrative tumor cells with pleomorphic
nuclei and prominent nucleoli, interspersed with numerous lymphocytes, eosinophils,
and mast cells and invading the muscle and reaching close to the serosa and perivesical
fat ([Figs. 2] and [3]). Perineural invasion was also noted. The final pathological diagnosis was urothelial
carcinoma, high grade, lymphoepithelial variant, pT3a. Tumor cells were positive for
CK7 and negative for CK20, p63, and GATA3 ([Fig. 4]). An adjuvant chemotherapy was initiated and cancer recurrence was not apparent
at usual follow-up as determined by CT scan.
Fig. 1 A CECT abdomen revealing a tumor arising from the left anterolateral wall of the
urinary bladder, projecting into its lumen with a small exophytic component reaching
beyond the serosal surface on the inferior aspect.
Fig. 2 Microphotograph showing epithelial tumor cells mixed with lymphoid cells (H&E, ×100).
Fig. 3 Undifferentiated tumor cells with syncytial appearance invading the muscles. Lymphoid
cells are also seen (H&E, ×400).
Fig. 4 Immunohistochemistry showing intense cytoplasmic and membrane positivity of CK7 in
tumor cells (Immunohistochemistry, CK7, ×400).
Discussion
According to 2016 WHO classification, LELC is a rare variant of urothelial carcinoma
with a reported incidence between 0.4% and 1.3% of all bladder carcinomas.[4] The majority of patients present in late adulthood and are at stage T2–T3 at diagnosis.[4] Histological features of LELC closely resemble nasopharyngeal lymphoepithelioma,
with the tumor growing in the nests, sheets, or cords of large undifferentiated malignant
epithelial cells in the background of dense inflammatory infiltrate comprising mainly
lymphocytes, plasma cells, and a few eosinophils and neutrophils.[1] Amin et al categorized LELC of the urinary bladder into three subgroups based on
lymphoepithelioma component: pure (100%), predominant (> 50%), and focal (< 50%).
These subgroups significantly determine the prognosis as disease-free survival is
higher in pure and predominant LELCB than in mixed type.[3] Pure LELCB must be differentiated from lymphoma or reactive inflammatory lesion,
small cell carcinoma, poorly differentiated urothelial carcinoma with lymphoid cell
infiltration.[5] Immunohistochemistry for cytokeratin and lymphoid markers can help in eliminating
the possibility of lymphoma.[1] Reactive inflammatory lesion can be excluded using immunohistochemistry. In the
present case, the tumor cells revealed positivity for CK7 and negativity for CK20,
p63, and GATA3 markers confirming the urothelial origin of the tumor. Due to the paucity
of the cases described, there are currently no standard treatment protocols for LELCB.
Some reports described pure and predominant LELCB as being more sensitive to chemotherapy
than conventional urothelial carcinoma;[4] this provides a potential to salvage bladder function. Focal LELCB is best managed
by multifocal therapies including radical cystectomy, EBRT, and adjuvant systemic
chemotherapy owing to its more aggressive nature.[6] Our case underwent radical cystoprostatectomy with chemotherapy and was free of
disease 8 months after the surgery.
Conclusion
LELCB is a rare tumor that occurs in older males. No standard management protocols
have been established. On account of this, reporting of this variant would add to
the caveat in literature and help clinicians to devise appropriate treatment protocols.
