SciELO - Scientific Electronic Library Online

 
vol.26 issue2Eosinophilic esophagitis at pediatric ageKérion celsi: a rare complication of Tinea capitis author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

  • Have no similar articlesSimilars in SciELO

Share


Nascer e Crescer

Print version ISSN 0872-0754On-line version ISSN 2183-9417

Abstract

SOARES, Ana Teresa et al. Pediatric primary hyperparathyroidism: a rare cause of nephrolithiasis. Nascer e Crescer [online]. 2017, vol.26, n.2, pp.122-125. ISSN 0872-0754.

Introduction: Primary hyperparathyroidism is a rare disease in the pediatric age group and a rare cause of nephrolithiasis. It results from an excessive production of the parathyroid hormone due to abnormalities within the parathyroid glands. Case report: The patient was a twelve-year-old male admitted in the paediatrics emergency department with intermitent flank pain and dysuria. An abdominal ultrassound identified nephrolithiasis. Laboratorial tests showed hypercalcemia, an increased serum level of parathyroid hormone and hypercalciuria. A primary hyperparathyroidism was diagnosed and the ultrassound plus scintigraphy of both thyroid and parathyroid glands revealed a right lower parathyroid adenoma. A right lower parathyroidectomy was performed with regularization of the calcium and parathyroid hormone levels. The histopathology revealed main cells hyperplasia and genetic tests were negative. Conclusion: Primary hyperparathyroidism should be considered in the differential diagnosis of nephrolithiasis to allow an early intervention and prevent organ damage.

Keywords : Children; hypercalcemia; Primary hyperparathyroidism; nephrolithiasis.

        · abstract in Portuguese     · text in Portuguese     · Portuguese ( pdf )

 

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License