| Literature DB >> 24565683 |
Mahmoud Abbas1, Mario W Kramer2, Tilmann Spieker3, Thomas R W Herrman2, Axel S Merseburger2, Klaus-Michael Müller3, Marcus A Kuczyk2, Jan U Becker4, Hans-Heinrich Kreipe4.
Abstract
Primary epithelial tumor of the renal pelvis is rare and only 100 cases are reported in the literature [1]. Histological examination of the tumor showed glands, cysts, and papillae lined by pseudostratified columnar epithelium with hyperchromatic nuclei. Scattered signet ring-type cells were also seen floating in large pools of extracellular mucin. Sections from the ureter showed a component of adenocarcinoma in situ. No invasive tumor was identified in ureteric tissue. One case was reported with carcinoma in situ of the ureter (2). Immunohistochemically: The tumor showed positivity for CK7, CK20, CK8/18, GATA-3, MSH-2, MSH-6, MLH-1, Ber-EP4, and S-100-P with focal positivity for CDX-2, weak positivity for PMS-2 and negativity in TTF-1 and Her-2. Molecular pathological analysis revealed microsatellite stability and without mutation in K-ras-gene. Thus, a diagnosis of mucinous adenocarcinoma of the renal pelvis with in situ adenocarcinoma of the ureter was made.Entities:
Keywords: Adenocarcinoma; Carcinoma in situ; Renal pevis; Ureter
Mesh:
Year: 2014 PMID: 24565683 DOI: 10.1016/j.jnci.2013.11.002
Source DB: PubMed Journal: J Egypt Natl Canc Inst ISSN: 1110-0362