Cargando…

Collecting duct carcinoma with retroperitoneal mass as initial presentation: a rare case report

BACKGROUND: Collecting duct carcinoma (CDC) is a rare renal tumor, originating from the distal collecting duct. CDC rarely presents as a primary tumor outside the renal system. CASE PRESENTATION: In this study, we report a rare case of collecting duct carcinoma, with an initial presentation of retro...

Descripción completa

Detalles Bibliográficos
Autores principales: Ye, Rupei, Liao, Yehui, Xia, Tian, Zhang, Xinfeng, Lu, Qiyi, Xiao, Xiuli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373255/
https://www.ncbi.nlm.nih.gov/pubmed/37495956
http://dx.doi.org/10.1186/s12894-023-01295-6
_version_ 1785078527460114432
author Ye, Rupei
Liao, Yehui
Xia, Tian
Zhang, Xinfeng
Lu, Qiyi
Xiao, Xiuli
author_facet Ye, Rupei
Liao, Yehui
Xia, Tian
Zhang, Xinfeng
Lu, Qiyi
Xiao, Xiuli
author_sort Ye, Rupei
collection PubMed
description BACKGROUND: Collecting duct carcinoma (CDC) is a rare renal tumor, originating from the distal collecting duct. CDC rarely presents as a primary tumor outside the renal system. CASE PRESENTATION: In this study, we report a rare case of collecting duct carcinoma, with an initial presentation of retroperitoneal lymph node metastasis, and no identifiable primary renal tumor on CT, at the time of diagnosis. The patient was a 64-year-old man presenting with lower back pain. Preoperative CT showed a round, soft tissue mass, measuring 6.7 × 4.4 × 3.3 cm, in the left retroperitoneum with no exact occupying lesion in the left kidney. Clinically, ectopic pheochromocytoma was considered to be a differential diagnosis, and tumor resection was performed. Postoperative pathological results demonstrated that the mass was a fused lymph node, and the tumor cells were destroying the structure. The final diagnosis was lymph node metastatic collecting duct carcinoma, by histology and immunohistochemistry. No further treatment was performed as no space occupying lesion was found in the kidney. Three months later, CT was reexamined, and a mass of 3.6 cm in diameter, was found in the lower left kidney, along with multiple soft tissue masses, in the left renal hilum. Considering recurrence or metastasis, the patient was recommended to undergo surgical treatment, but the patient refused. Four months later, CT was re-examined. The tumor had rapidly progressed but the patient refused treatment again. As per the author’s press release (eleven months after the first discovery), the patient is still alive. CONCLUSION: CDC is a rare malignant renal carcinoma, with a high chance of rapid progress, regional lymph nodes involvement and metastasis. It presents diagnostic challenges to clinicians and pathologists, particularly, in the absence of radiographically detectable intrarenal lesions. Definite diagnosis is based on pathological examination combined with immunohistochemical staining.
format Online
Article
Text
id pubmed-10373255
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-103732552023-07-28 Collecting duct carcinoma with retroperitoneal mass as initial presentation: a rare case report Ye, Rupei Liao, Yehui Xia, Tian Zhang, Xinfeng Lu, Qiyi Xiao, Xiuli BMC Urol Case Report BACKGROUND: Collecting duct carcinoma (CDC) is a rare renal tumor, originating from the distal collecting duct. CDC rarely presents as a primary tumor outside the renal system. CASE PRESENTATION: In this study, we report a rare case of collecting duct carcinoma, with an initial presentation of retroperitoneal lymph node metastasis, and no identifiable primary renal tumor on CT, at the time of diagnosis. The patient was a 64-year-old man presenting with lower back pain. Preoperative CT showed a round, soft tissue mass, measuring 6.7 × 4.4 × 3.3 cm, in the left retroperitoneum with no exact occupying lesion in the left kidney. Clinically, ectopic pheochromocytoma was considered to be a differential diagnosis, and tumor resection was performed. Postoperative pathological results demonstrated that the mass was a fused lymph node, and the tumor cells were destroying the structure. The final diagnosis was lymph node metastatic collecting duct carcinoma, by histology and immunohistochemistry. No further treatment was performed as no space occupying lesion was found in the kidney. Three months later, CT was reexamined, and a mass of 3.6 cm in diameter, was found in the lower left kidney, along with multiple soft tissue masses, in the left renal hilum. Considering recurrence or metastasis, the patient was recommended to undergo surgical treatment, but the patient refused. Four months later, CT was re-examined. The tumor had rapidly progressed but the patient refused treatment again. As per the author’s press release (eleven months after the first discovery), the patient is still alive. CONCLUSION: CDC is a rare malignant renal carcinoma, with a high chance of rapid progress, regional lymph nodes involvement and metastasis. It presents diagnostic challenges to clinicians and pathologists, particularly, in the absence of radiographically detectable intrarenal lesions. Definite diagnosis is based on pathological examination combined with immunohistochemical staining. BioMed Central 2023-07-26 /pmc/articles/PMC10373255/ /pubmed/37495956 http://dx.doi.org/10.1186/s12894-023-01295-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Ye, Rupei
Liao, Yehui
Xia, Tian
Zhang, Xinfeng
Lu, Qiyi
Xiao, Xiuli
Collecting duct carcinoma with retroperitoneal mass as initial presentation: a rare case report
title Collecting duct carcinoma with retroperitoneal mass as initial presentation: a rare case report
title_full Collecting duct carcinoma with retroperitoneal mass as initial presentation: a rare case report
title_fullStr Collecting duct carcinoma with retroperitoneal mass as initial presentation: a rare case report
title_full_unstemmed Collecting duct carcinoma with retroperitoneal mass as initial presentation: a rare case report
title_short Collecting duct carcinoma with retroperitoneal mass as initial presentation: a rare case report
title_sort collecting duct carcinoma with retroperitoneal mass as initial presentation: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373255/
https://www.ncbi.nlm.nih.gov/pubmed/37495956
http://dx.doi.org/10.1186/s12894-023-01295-6
work_keys_str_mv AT yerupei collectingductcarcinomawithretroperitonealmassasinitialpresentationararecasereport
AT liaoyehui collectingductcarcinomawithretroperitonealmassasinitialpresentationararecasereport
AT xiatian collectingductcarcinomawithretroperitonealmassasinitialpresentationararecasereport
AT zhangxinfeng collectingductcarcinomawithretroperitonealmassasinitialpresentationararecasereport
AT luqiyi collectingductcarcinomawithretroperitonealmassasinitialpresentationararecasereport
AT xiaoxiuli collectingductcarcinomawithretroperitonealmassasinitialpresentationararecasereport