从间歇性膝关节疼痛到终末期肾脏疾病:一个11岁女孩双侧肾脏发育不良的不典型表现。

IF 0.5 Q4 PEDIATRICS
Case Reports in Pediatrics Pub Date : 2025-09-01 eCollection Date: 2025-01-01 DOI:10.1155/crpe/8856638
Kristie Kim, Carlos Araya, Ryan Brogan
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引用次数: 0

摘要

我们描述了一个11岁女孩的临床表现和评估,没有报告过去的病史,她的初级保健医生看到间歇性膝盖疼痛。门诊x光检查显示有佝偻病,需要进一步的血液检查。该患者因化验结果异常被紧急转至急诊科,随后发现为终末期肾病伴严重贫血、代谢性酸中毒和明显的电解质异常。尽管有这些异常,但她的血流动力学稳定,精神状态正常,她的体格检查仅与左膝疼痛有关。我们咨询了肾脏病学,她被送进儿科重症监护病房(PICU)进行电解质补充和紧急血液透析。本病例表现为继发于双侧肾脏发育不良的终末期肾脏疾病的非典型良性表现。它强调承认患有以前未发现的先天性肾病的儿童所面临的挑战,并强调需要在高风险人群,包括受健康社会决定因素影响的人群中及早发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
From Intermittent Knee Pain to End-Stage Kidney Disease: An Atypical Presentation of Bilateral Kidney Dysplasia in an 11-Year-Old Girl.

We describe the clinical presentation and evaluation of an 11-year-old girl with no reported past medical history, seen by her primary care physician for intermittent knee pain. Outpatient X-rays revealed findings concerning for rickets, prompting further evaluation with blood work. The patient was urgently referred to the emergency department due to abnormal laboratory results and was subsequently found to be in end-stage kidney disease with severe anemia, metabolic acidosis, and significant electrolyte abnormalities. Despite these abnormalities, she was hemodynamically stable with appropriate mentation, and her physical exam was only pertinent for left knee pain. Nephrology was consulted, and she was admitted to the pediatric intensive care unit (PICU) for electrolyte repletion and emergent hemodialysis. This case demonstrates an atypically benign presentation of end-stage kidney disease secondary to bilateral kidney dysplasia. It emphasizes the challenges of recognizing children with previously undetected congenital kidney disease and underscores the need for early detection in high-risk populations, including those affected by social determinants of health.

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来源期刊
自引率
11.10%
发文量
48
审稿时长
13 weeks
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