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Pregnancy complicated by juxtaglomerular cell tumor of the kidney: A case report
BACKGROUND: Juxtaglomerular cell tumor (JGCT) of the kidney, also known as reninoma, is a rare renal tumor that typically clinically manifests as hypertension, hypokalemia, high renin, and high aldosterone. It is a cause of secondary hypertension. Pregnancy with JGCT is rarer and easily misdiagnosed...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130993/ https://www.ncbi.nlm.nih.gov/pubmed/37123308 http://dx.doi.org/10.12998/wjcc.v11.i11.2541 |
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author | Fu, Xian Deng, Gang Wang, Kai Shao, Chang Xie, Li-Ping |
author_facet | Fu, Xian Deng, Gang Wang, Kai Shao, Chang Xie, Li-Ping |
author_sort | Fu, Xian |
collection | PubMed |
description | BACKGROUND: Juxtaglomerular cell tumor (JGCT) of the kidney, also known as reninoma, is a rare renal tumor that typically clinically manifests as hypertension, hypokalemia, high renin, and high aldosterone. It is a cause of secondary hypertension. Pregnancy with JGCT is rarer and easily misdiagnosed as pregnancy-induced hypertension, thus affecting treatment. CASE SUMMARY: A 28-year-old woman presented in early pregnancy with hypertension (blood pressure of 229/159 mmHg), nausea, and occasional dizziness and headache. The patient was diagnosed with pregnancy-induced hypertension, and no relief was found after symptomatic treatment; hence, the pregnancy was terminated by artificial abortion. Her blood pressure remained high following termination of pregnancy. Blood tests suggested hypokalemia (2.997 mmol/L), blood aldosterone measured 613 ng/L, and computed tomography urography showed a tumor in the right kidney. Therefore, laparoscopic partial nephrectomy was performed. After surgery, the patient’s blood pressure returned to normal, and blood potassium, aldosterone, and renin normalized. Postoperative pathological examination revealed JGCT. After long-term follow-up, the patient became pregnant again 6 mo after surgery. No hypertension occurred during pregnancy, and the patient delivered a healthy female neonate. CONCLUSION: Patients with pregnancy complicated by JGCT are difficult to diagnose. Herein, we advise surgeons on proper handling of such situations. |
format | Online Article Text |
id | pubmed-10130993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-101309932023-04-27 Pregnancy complicated by juxtaglomerular cell tumor of the kidney: A case report Fu, Xian Deng, Gang Wang, Kai Shao, Chang Xie, Li-Ping World J Clin Cases Case Report BACKGROUND: Juxtaglomerular cell tumor (JGCT) of the kidney, also known as reninoma, is a rare renal tumor that typically clinically manifests as hypertension, hypokalemia, high renin, and high aldosterone. It is a cause of secondary hypertension. Pregnancy with JGCT is rarer and easily misdiagnosed as pregnancy-induced hypertension, thus affecting treatment. CASE SUMMARY: A 28-year-old woman presented in early pregnancy with hypertension (blood pressure of 229/159 mmHg), nausea, and occasional dizziness and headache. The patient was diagnosed with pregnancy-induced hypertension, and no relief was found after symptomatic treatment; hence, the pregnancy was terminated by artificial abortion. Her blood pressure remained high following termination of pregnancy. Blood tests suggested hypokalemia (2.997 mmol/L), blood aldosterone measured 613 ng/L, and computed tomography urography showed a tumor in the right kidney. Therefore, laparoscopic partial nephrectomy was performed. After surgery, the patient’s blood pressure returned to normal, and blood potassium, aldosterone, and renin normalized. Postoperative pathological examination revealed JGCT. After long-term follow-up, the patient became pregnant again 6 mo after surgery. No hypertension occurred during pregnancy, and the patient delivered a healthy female neonate. CONCLUSION: Patients with pregnancy complicated by JGCT are difficult to diagnose. Herein, we advise surgeons on proper handling of such situations. Baishideng Publishing Group Inc 2023-04-16 2023-04-16 /pmc/articles/PMC10130993/ /pubmed/37123308 http://dx.doi.org/10.12998/wjcc.v11.i11.2541 Text en ©The Author(s) 2023. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Case Report Fu, Xian Deng, Gang Wang, Kai Shao, Chang Xie, Li-Ping Pregnancy complicated by juxtaglomerular cell tumor of the kidney: A case report |
title | Pregnancy complicated by juxtaglomerular cell tumor of the kidney: A case report |
title_full | Pregnancy complicated by juxtaglomerular cell tumor of the kidney: A case report |
title_fullStr | Pregnancy complicated by juxtaglomerular cell tumor of the kidney: A case report |
title_full_unstemmed | Pregnancy complicated by juxtaglomerular cell tumor of the kidney: A case report |
title_short | Pregnancy complicated by juxtaglomerular cell tumor of the kidney: A case report |
title_sort | pregnancy complicated by juxtaglomerular cell tumor of the kidney: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130993/ https://www.ncbi.nlm.nih.gov/pubmed/37123308 http://dx.doi.org/10.12998/wjcc.v11.i11.2541 |
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