Clear Cell Adenocarcinoma of the Renal Pelvis in a Male Patient
Carcinoma of the renal pelvis is an uncommon renal neoplasm. Clear cell adenocarcinoma in the urinary tract is rare and has a histomorphology resembling that of the female genital tract. We herein present a case of clear cell adenocarcinoma of the renal pelvis, which is the first example in a male p...
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2013-01-01
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Series: | Case Reports in Pathology |
Online Access: | http://dx.doi.org/10.1155/2013/494912 |
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doaj-3fecebbee36b44219eea76dd97304ae82020-11-24T22:03:17ZengHindawi LimitedCase Reports in Pathology2090-67812090-679X2013-01-01201310.1155/2013/494912494912Clear Cell Adenocarcinoma of the Renal Pelvis in a Male PatientSarawut Kongkarnka0Pruit Kitirattakarn1Hironori Katayama2Surapan Khunamornpong3Department of Pathology, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, ThailandDepartment of Surgery, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, ThailandDepartment of Pathology, Nippon Medical School, Tama-Nagayama Hospital, Tokyo 206-8512, JapanDepartment of Pathology, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, ThailandCarcinoma of the renal pelvis is an uncommon renal neoplasm. Clear cell adenocarcinoma in the urinary tract is rare and has a histomorphology resembling that of the female genital tract. We herein present a case of clear cell adenocarcinoma of the renal pelvis, which is the first example in a male patient to our knowledge. A 54-year-old man presented with right flank pain. The tumor was associated with renal stones and hydronephrosis and invaded into the peripelvic fat tissue with regional lymph node metastasis. The patient died of metastatic disease six months postoperatively. Histologically, the tumor showed complex papillary architecture lined with clear and hobnail cells. Clear cell adenocarcinoma of the renal pelvis may pose a diagnostic challenge on histological grounds, particularly in the distinction from renal cell carcinoma. The immunohistochemical stains could help confirm the diagnosis. Due to its rarity, an effective treatment regimen remains to be determined.http://dx.doi.org/10.1155/2013/494912 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sarawut Kongkarnka Pruit Kitirattakarn Hironori Katayama Surapan Khunamornpong |
spellingShingle |
Sarawut Kongkarnka Pruit Kitirattakarn Hironori Katayama Surapan Khunamornpong Clear Cell Adenocarcinoma of the Renal Pelvis in a Male Patient Case Reports in Pathology |
author_facet |
Sarawut Kongkarnka Pruit Kitirattakarn Hironori Katayama Surapan Khunamornpong |
author_sort |
Sarawut Kongkarnka |
title |
Clear Cell Adenocarcinoma of the Renal Pelvis in a Male Patient |
title_short |
Clear Cell Adenocarcinoma of the Renal Pelvis in a Male Patient |
title_full |
Clear Cell Adenocarcinoma of the Renal Pelvis in a Male Patient |
title_fullStr |
Clear Cell Adenocarcinoma of the Renal Pelvis in a Male Patient |
title_full_unstemmed |
Clear Cell Adenocarcinoma of the Renal Pelvis in a Male Patient |
title_sort |
clear cell adenocarcinoma of the renal pelvis in a male patient |
publisher |
Hindawi Limited |
series |
Case Reports in Pathology |
issn |
2090-6781 2090-679X |
publishDate |
2013-01-01 |
description |
Carcinoma of the renal pelvis is an uncommon renal neoplasm. Clear cell adenocarcinoma in the urinary tract is rare and has a histomorphology resembling that of the female genital tract. We herein present a case of clear cell adenocarcinoma of the renal pelvis, which is the first example in a male patient to our knowledge. A 54-year-old man presented with right flank pain. The tumor was associated with renal stones and hydronephrosis and invaded into the peripelvic fat tissue with regional lymph node metastasis. The patient died of metastatic disease six months postoperatively. Histologically, the tumor showed complex papillary architecture lined with clear and hobnail cells. Clear cell adenocarcinoma of the renal pelvis may pose a diagnostic challenge on histological grounds, particularly in the distinction from renal cell carcinoma. The immunohistochemical stains could help confirm the diagnosis. Due to its rarity, an effective treatment regimen remains to be determined. |
url |
http://dx.doi.org/10.1155/2013/494912 |
work_keys_str_mv |
AT sarawutkongkarnka clearcelladenocarcinomaoftherenalpelvisinamalepatient AT pruitkitirattakarn clearcelladenocarcinomaoftherenalpelvisinamalepatient AT hironorikatayama clearcelladenocarcinomaoftherenalpelvisinamalepatient AT surapankhunamornpong clearcelladenocarcinomaoftherenalpelvisinamalepatient |
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