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[先天性尿路畸形病理(后尿道瓣膜)继发的短暂性假性醛固酮减少症:1例具有病理生理性质要素的病例报告]

[Transient pseudohypoaldosteronism secondary to congenital malformation pathology of the urinary tract (valves of the posterior urethra): a report of a case with elements of a physiopathological nature].

作者信息

Parisi G, Rojo S, De Pascale S, Mancinelli C, D'Alonzo L, Galante E, Marinelli L, Damiani F

机构信息

Unità Operativa Pediatrico Neonatologica, Presidio Ospedaliero di Vasto, Azienda USL Lanciano-Vasto, Chieti, Italia.

出版信息

Pediatr Med Chir. 1998 Jul-Aug;20(4):289-93.

PMID:9866855
Abstract

A case of secondary transient pseudohypoaldosteronism (PHA) in a three-month-old infant who had arrived in emergency conditions is reported. Clinically the patient presented dehydration associated with salt loss, metabolic acidosis, severe hyperkalemia, markedly elevated levels both of plasma renin activity and aldosterone concentration. Biochemical and instrumental tests and clinical evolution have given reason to consider it as a case of transient PHA, secondary to an obstructive uropathy (PUV) with urinary infection. Secondary forms of PHA have frequently been documented in young infants with urinary tract infection associated with both obstructive and non obstructive uropathy. After medical or surgical therapy the abnormalities quickly disappear. This reported case suggests that the pediatrician-neonatologist dealing with a young infant with obstructive uropathy should not only consider the surgical treatment but also the medical one, in the light of the associated physiopathological aspects.

摘要

报告了一例三个月大婴儿出现继发性短暂性假性醛固酮减少症(PHA)的病例,该婴儿以紧急情况入院。临床上,患者表现出与失盐相关的脱水、代谢性酸中毒、严重高钾血症,血浆肾素活性和醛固酮浓度均显著升高。生化和仪器检查以及临床进展表明,该病例可被视为继发于梗阻性尿路病(后尿道瓣膜症)合并泌尿系统感染的短暂性PHA。PHA的继发性形式在患有与梗阻性和非梗阻性尿路病相关的泌尿系统感染的幼儿中经常有记录。经过药物或手术治疗后,异常情况迅速消失。该报告病例表明,处理患有梗阻性尿路病的幼儿的儿科医生和新生儿科医生,鉴于相关的生理病理方面,不仅应考虑手术治疗,还应考虑药物治疗。

相似文献

1
[Transient pseudohypoaldosteronism secondary to congenital malformation pathology of the urinary tract (valves of the posterior urethra): a report of a case with elements of a physiopathological nature].[先天性尿路畸形病理(后尿道瓣膜)继发的短暂性假性醛固酮减少症:1例具有病理生理性质要素的病例报告]
Pediatr Med Chir. 1998 Jul-Aug;20(4):289-93.
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A potential serious complication in infants with congenital obstructive uropathy: Secondary pseudohypoaldosteronism.先天性梗阻性尿路病婴儿的一种潜在严重并发症:继发性假性醛固酮减少症。
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[Urinary tract infections in infants, an insidious clinical picture].[婴儿尿路感染,一种隐匿的临床症状]
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Presumptive pseudohypoaldosteronism secondary to chronic urinary tract obstruction from sloughed urinary bladder mucosa and urinary tract infection in a cat.一只猫因膀胱黏膜脱落和尿路感染导致慢性尿路梗阻继发的疑似假性醛固酮减少症。
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Final diagnosis: transient pseudohypoaldosteronism (TPH) caused by UTI without concordant obstructive uropathy.最终诊断:由尿路感染引起的无合并梗阻性尿路病的短暂性假性醛固酮减少症(TPH)。
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Transient pseudohypoaldosteronism in obstructive renal disease.
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[Valves of the anterior urethra without diverticulum. Description of 3 cases].
Pediatr Med Chir. 1987 Mar-Apr;9(2):211-5.
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Salt losing nephropathy simulating congenital adrenal hyperplasia in infants with obstructive uropathy and/or vesicoureteral reflux--value of ultrasonography in diagnosis.梗阻性尿路病和/或膀胱输尿管反流婴儿中模拟先天性肾上腺增生的失盐性肾病——超声检查在诊断中的价值
Pediatr Radiol. 1991;21(6):413-5. doi: 10.1007/BF02026675.

引用本文的文献

1
Transient secondary pseudo-hypoaldosteronism in infants with urinary tract infections: systematic literature review.尿路感染婴儿一过性假性醛固酮减少症:系统文献复习。
Eur J Pediatr. 2024 Oct;183(10):4205-4214. doi: 10.1007/s00431-024-05676-3. Epub 2024 Jul 10.
2
Transient type 1 pseudo-hypoaldosteronism: report on an eight-patient series and literature review.短暂性1型假性醛固酮减少症:8例病例报告及文献综述
Pediatr Nephrol. 2009 Nov;24(11):2167-75. doi: 10.1007/s00467-009-1285-8.