Hypertensive emergency due to a delayed dialysis modality transition in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis: a case report.

IF 3.3 4区 医学 Q1 Medicine
D Woszczyk, M Płonka, M Różańska, M Miedziaszczyk, I Idasiak-Piechocka
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引用次数: 0

Abstract

BACKGROUND: This case report presents a history of familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC). The patient was admitted to the hospital with hypertensive encephalopathy. FHHNC is a rare autosomal recessive disease caused by mutations in CLDN16 or CLDN19, resulting in insufficient magnesium and calcium kidney reabsorption. FHHNC manifestation starts in childhood, and over the years, its development leads to nephrocalcinosis and, consequently, chronic kidney disease (CKD), which is not slowed by routine administration of magnesium and thiazide diuretics. Ultimately, all FHHNC patients need kidney replacement therapy (KRT). CASE PRESENTATION: The patient was a 28-year-old male diagnosed with FHHNC and admitted to the emergency room due to hypertensive encephalopathy. The current situation was the patient's second hospitalization related to a hypertensive emergency caused by under-dialysis. Despite the signs of insufficient functioning of peritoneal dialysis (PD) (the primary chosen form of KRT), the patient refused the proposed conversion to hemodialysis (HD). Symptoms observed upon admission included disorientation, anxiety, and severe hypertension, reaching 213/123 mmHg. Due to his clinical condition, the patient was transferred to the intensive care unit (ICU), where the introduction of continuous veno-venous hemodiafiltration and hypotensive therapy stabilized blood pressure. Within the next few days, his state improved, followed by discharge from ICU. Eventually, the patient agreed to transition from PD to in-center HD. At the time, he was qualified for kidney transplantation, waiting for a compatible donation. CKD and dialysis are factors that significantly affect a patient's quality of life, especially in young patients with congenital diseases like FHHNC. CONCLUSIONS: For the aforementioned reasons, appropriate education and psychological support should be ensured to avoid the harmful effects of therapy non-compliance.

Graphical abstract: https://www.europeanreview.org/wp/wp-content/uploads/Graphical-abstract-1.pdf.

家族性低镁血症合并高钙尿症和肾钙化症患者因透析方式转换延迟而导致的高血压急症:病例报告。
背景:本病例报告介绍了家族性低镁血症伴高钙尿症和肾钙化症(FHHNC)的病史。患者因高血压脑病入院。FHHNC 是一种罕见的常染色体隐性遗传病,由 CLDN16 或 CLDN19 基因突变引起,导致肾脏对镁和钙的重吸收不足。FHHNC 从儿童时期开始发病,经过数年的发展,会导致肾钙化,进而引发慢性肾病(CKD),而常规服用镁和噻嗪类利尿剂并不能减缓病情。最终,所有 FHHNC 患者都需要接受肾脏替代治疗(KRT)。病例介绍:患者是一名 28 岁的男性,被诊断患有 FHHNC,因高血压脑病被送入急诊室。目前的情况是患者第二次住院,原因是透析不足导致的高血压急症。尽管有迹象表明腹膜透析(KRT 的主要选择形式)功能不足,但患者拒绝接受转为血液透析(HD)的建议。入院时观察到的症状包括迷失方向、焦虑和严重的高血压,达到 213/123 mmHg。鉴于其临床状况,患者被转入重症监护室(ICU),在那里,持续静脉血液透析和降压治疗使血压趋于稳定。在接下来的几天里,他的病情有所好转,随后从重症监护室出院。最终,患者同意从腹膜透析过渡到中心内血液透析。当时,他符合肾移植条件,正在等待匹配的捐赠。慢性肾脏病和透析是严重影响患者生活质量的因素,尤其是像 FHHNC 这样患有先天性疾病的年轻患者。结论:鉴于上述原因,应确保提供适当的教育和心理支持,以避免不依从治疗带来的有害影响。图文摘要:https://www.europeanreview.org/wp/wp-content/uploads/Graphical-abstract-1.pdf。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.30
自引率
6.10%
发文量
906
审稿时长
2-4 weeks
期刊介绍: European Review for Medical and Pharmacological Sciences, a fortnightly journal, acts as an information exchange tool on several aspects of medical and pharmacological sciences. It publishes reviews, original articles, and results from original research. The purposes of the Journal are to encourage interdisciplinary discussions and to contribute to the advancement of medicine. European Review for Medical and Pharmacological Sciences includes: -Editorials- Reviews- Original articles- Trials- Brief communications- Case reports (only if of particular interest and accompanied by a short review)
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