ReviewThe Kaohsiung journal of medical sciences2012
Lymphoepithelioma-like carcinoma of ureter-a rare case report and review of the literature.
Review in The Kaohsiung journal of medical sciences, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 13 citations in OpenAlex.
- Right-sided ureteral hemangiosarcoma in a paraplegic dog.BMC veterinary research · 2024Article
- Article
- Analysis of genetic profiling, pathomics signature, and prognostic features of primary lymphoepithelioma-like carcinoma of the renal pelvis.Molecular oncology · 2022Article
- Eight-year follow-up of locally advanced lymphoepithelioma-like carcinoma at upper urinary tract: A case report.World journal of clinical cases · 2020Article
- Rare primary lymphoepithelioma-like carcinoma of the renal pelvis.World journal of clinical cases · 2020Review
- Lymphoepithelioma-like carcinoma of the upper urinary tract: A systematic review of case reports.World journal of clinical cases · 2020Article
- Lymphoepithelioma-like carcinoma of the upper urinary tract.Virchows Archiv : an international journal of pathology · 2017Article
- Lymphoepithelioma-like carcinoma of the bladder: a case report.Journal of medical case reports · 2014Article
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Authors and funding
7 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Lymphoepithelioma-like carcinoma (LELC) is best known to occur in the nasopharynx. When LELC occurs in the urinary tract, this extremely rare neoplasm most commonly affects the bladder but has also been reported in the renal pelvis, ureter, prostate [1], and urethra [2]. We present a case of LELC arising in the right proximal ureter of a 64-year-old male patient with hydronephrosis and nausea. Computed tomography demonstrated right ureter tumor. On biopsy, the patient was diagnosed with infiltrating urothelial carcinoma. An operation consisting of right nephroureterectomy and bladder cuff removal was carried out. The pathologic examination showed pure subtype of LELC, pT3N0. Unlike lymphoepithelioma in the nasopharynx, immunohistochemical analysis of this urinary LELC was negative for the Epstein-Barr virus. No disease progression was noted at 6 months' follow-up. Only eight previous cases of LELC involving the ureter have been reported, and a review of the available literature and a summary of ureter cases are presented here. This is the first report of a ureteral LELC case and third urothelial LELC cases [3] in Taiwan.
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