CASE REPORT
Year : 2017 | Volume
: 31 | Issue : 1 | Page : 52--55
Collecting duct carcinoma: Sarcomatoid variant - A rare entity
Leena Konjengbam, Thingujam Bipin Singh
Department of Pathology, Babina Diagnostics, Imphal, Manipur, India
Correspondence Address:
Leena Konjengbam
Department of Pathology, Babina Diagnostics, Soibam Leikai, Porompat, Imphal, Manipur
India
Collecting duct carcinoma (CDC) is an extremely rare subtype of renal epithelial neoplasm arising from the distal segment of the collecting ducts of Bellini in the renal medulla. It accounts for <1% of all renal cell carcinoma cases. It has been reported to have a tendency toward early dissemination. This aggressive malignancy is difficult to be diagnosed despite its characteristic histological and immunohistochemical findings. We report a case of a CDC with sarcomatoid differentiation in a 64-year-old female who presented with a right renal mass and underwent right radical nephrectomy.
How to cite this article:
Konjengbam L, Singh TB. Collecting duct carcinoma: Sarcomatoid variant - A rare entity.J Med Soc 2017;31:52-55
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How to cite this URL:
Konjengbam L, Singh TB. Collecting duct carcinoma: Sarcomatoid variant - A rare entity. J Med Soc [serial online] 2017 [cited 2023 Jun 9 ];31:52-55
Available from: https://www.jmedsoc.org/article.asp?issn=0972-4958;year=2017;volume=31;issue=1;spage=52;epage=55;aulast=Konjengbam;type=0 |
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