[两例儿童期假性巴特综合征:何时怀疑囊性纤维化的罕见发病模式]。

Q4 Medicine
Gianluca Vergine, Giulia Fressola, Maura Ambroni, Monica Gessaroli, Barbara Bigucci, Martina Mazzocco, Maria Luisa Conte
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引用次数: 0

摘要

囊性纤维化是一种多系统疾病,起病、症状和病程极为多变。假性巴特综合征是该病的发病方式之一,也是一种并发症,其特点是在没有任何肾脏疾病的情况下出现低钠血症、低氯性脱水和代谢性碱中毒。这种综合征多发于婴儿出生后的第一年,在夏季达到高峰。本文描述了两例儿童期伴有假性巴特综合征的囊性纤维化病例。排除代谢性碱中毒伴低钠血症的所有可能病因对我们的诊断路径至关重要,从第一个病例中获得的经验对第二个病例帮助很大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Two Cases of Pseudo-Bartter Syndrome in Childhood: When to Suspect a Rare Onset Pattern of Cystic Fibrosis].

Cystic fibrosis is a multisystem disease with extremely variable onset, symptoms and course. One of the onset modality but also a complication of the disease is the pseudo-Bartter syndrome, characterized by hyponatremia, hypochloremic dehydration and metabolic alkalosis in absence of any renal disease. This syndrome occurs more frequently in the first year of life and has a peak in the summer. In this article, we describe two cases of cystic fibrosis associated with pseudo-Bartter syndrome in childhood. Excluding every possible cause of metabolic alkalosis associated with hyponatremia was crucial for our diagnostic pathway, and the experience gained with the first case helped a lot with the second one.

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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
62
期刊介绍: Il Giornale Italiano di Nefrologia (GIN) è la rivista di educazione continua della Società Italiana di Nefrologia SIN ed è pubblicato bimestralmente. E" il più autorevole organo di informazione nefrologia disponibile a livello nazionale. Il giornale Italiano di Nefrologia offre la più aggiornata informazione medico-scientifica rivolta al nefrologo sotto forma di rassegne, casi clinici e articoli finalizzati all’Educazione Continua in Medicina, oltre ai notiziari ed agli atti dei congressi di questa prestigiosa Società Scientifica
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