• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

囊性纤维化脱水患者的酸碱平衡紊乱:四例病例报告并文献复习

Acid-base disturbances in dehydrated patients with cystic fibrosis : four case reports with review of literature.

作者信息

Peremans L, Declercq D, Vande Velde S, De Bruyne R, Van Winckel M, Vande Walle J, Van Biervliet S

机构信息

Department of paediatrics, Ghent University Hospital.

Cystic Fibrosis Centre, Ghent University Hospital.

出版信息

Acta Gastroenterol Belg. 2020 Apr-Jun;83(2):315-318.

PMID:32603052
Abstract

Most episodes of vomiting, reduced intake and diarrhoea in children can be evaluated and treated without additional tests. However, when the degree of clinical dehydration is not in line with the patient's medical history, other diagnoses should be suspected. In the presence of a hyponatraemic hypochloraemic metabolic alkalosis, cystic fibrosis (CF) should be included in the differential diagnosis, especially if there is failure to thrive even in the absence of respiratory symptoms. Furthermore, young patients diagnosed with CF have a higher risk for an acute electrolyte decompensation caused by increased salt and fluid losses. We present 4 paediatric cases to raise the awareness of electrolyte disturbances in CF patients.

摘要

大多数儿童呕吐、摄入量减少和腹泻的情况无需额外检查即可进行评估和治疗。然而,当临床脱水程度与患者病史不符时,应怀疑其他诊断。存在低钠低氯性代谢性碱中毒时,鉴别诊断应包括囊性纤维化(CF),尤其是即使没有呼吸道症状但存在生长发育迟缓的情况。此外,被诊断为CF的年轻患者因盐和液体流失增加而发生急性电解质失衡的风险更高。我们介绍4例儿科病例,以提高对CF患者电解质紊乱的认识。

相似文献

1
Acid-base disturbances in dehydrated patients with cystic fibrosis : four case reports with review of literature.囊性纤维化脱水患者的酸碱平衡紊乱:四例病例报告并文献复习
Acta Gastroenterol Belg. 2020 Apr-Jun;83(2):315-318.
2
Pseudo-Bartter syndrome as the initial presentation of cystic fibrosis in children: an important diagnosis not to be missed.儿童囊性纤维化以假性巴特综合征为首发表现:一个不容忽视的重要诊断。
BMJ Case Rep. 2024 Jan 31;17(1):e257348. doi: 10.1136/bcr-2023-257348.
3
Hyponatremic dehydration as a presentation of cystic fibrosis.低钠血症性脱水作为囊性纤维化的一种表现形式。
Pediatr Emerg Care. 2006 Nov;22(11):725-7. doi: 10.1097/01.pec.0000245170.31343.bb.
4
[Pseudo-Bartter syndrome as manifestation of cystic fibrosis with DF508 mutation].[以DF508突变为表现的囊性纤维化所致假性巴特综合征]
Bol Med Hosp Infant Mex. 2016 Sep-Oct;73(5):331-334. doi: 10.1016/j.bmhimx.2016.04.004. Epub 2016 Sep 17.
5
[Dehydration and metabolic alkalosis: an unusual presentation of cystic fibrosis in an infant].[脱水与代谢性碱中毒:婴儿期囊性纤维化的一种不寻常表现]
Arch Argent Pediatr. 2008 Oct;106(5):443-6. doi: 10.1590/S0325-00752008000500012.
6
Hypoelectrolytemia and metabolic alkalosis in infants with cystic fibrosis.囊性纤维化婴儿的低电解质血症和代谢性碱中毒
Pediatrics. 1979 Apr;63(4):580-3.
7
Clinical features and treatment approaches in cystic fibrosis with pseudo-Bartter syndrome.伴有假性巴特综合征的囊性纤维化的临床特征及治疗方法
Ann Trop Paediatr. 2005 Jun;25(2):119-24. doi: 10.1179/146532805X45719.
8
Episodic seasonal Pseudo-Bartter syndrome in cystic fibrosis.囊性纤维化中的阵发性季节性假性巴特综合征。
Paediatr Respir Rev. 2014 Jun;15 Suppl 1:19-21. doi: 10.1016/j.prrv.2014.04.015. Epub 2014 May 10.
9
Metabolic alkalosis with hypoelectrolytemia in infants with cystic fibrosis.患有囊性纤维化的婴儿出现伴有低电解质血症的代谢性碱中毒。
Pediatr Int. 2002 Jun;44(3):289-92. doi: 10.1046/j.1442-200x.2002.01563.x.
10
[Cystic fibrosis revealed by dehydration with hypochloronatremic alkalosis in 3 infants and a neonate].[3例婴儿及1例新生儿因脱水伴低氯性碱中毒而确诊的囊性纤维化]
Arch Pediatr. 1994 Jan;1(1):42-5.

引用本文的文献

1
A unique presentation of hyponatremia and seizures in a 2-month-old child with cystic fibrosis: a case report.一名患有囊性纤维化的2个月大儿童出现低钠血症和癫痫发作的独特表现:病例报告
Ann Med Surg (Lond). 2023 Jul 8;85(8):4150-4152. doi: 10.1097/MS9.0000000000001048. eCollection 2023 Aug.