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Published on: October 26, 2020
Hypertension and segmental renal infarction in children: apropos of two cases
Júlia Candel-Pau1, Yolanda Castilla-Fernández, Alvaro Madrid-Aris
1Department of Pediatric Nephrology, Hospital Vall d'Hebron, Barcelona, Spain. julicpvs@hotmail.com
Insights
Segmental renal infarction (SRI) is a rare cause of pediatric renovascular hypertension (RVH). This study details two children with idiopathic SRI, highlighting diagnosis and varied treatment approaches for this uncommon condition.
Area of Science:
- Pediatric Nephrology
- Vascular Surgery
- Hypertension Research
Background:
- Renovascular hypertension (RVH) accounts for 8-10% of pediatric hypertension cases.
- Segmental renal infarction (SRI) is a rare etiology of RVH, often idiopathic.
- SRI involves occlusion of small renal arteries, leading to hypertension and potential hyponatremia.
Observation:
- Two pediatric cases of idiopathic SRI presenting with severe arterial hypertension and hyponatremia are described.
- Hypertension was detected during hematuria workup in one child and as a hypertensive emergency in the other.
- Both cases involved occlusion of small renal arteries leading to SRI.
Findings:
- Selective renal arteriography is the gold standard for diagnosing SRI.
- Treatment varied: one patient underwent partial nephrectomy, while the other received antihypertensive medication due to the infarct location.
- Surgical segmentectomy is the definitive treatment when feasible.
Implications:
- This case series underscores the importance of considering rare causes like SRI in pediatric hypertension.
- Management strategies for SRI should be individualized based on infarct localization and surgical feasibility.
- Further research into the idiopathic origins and optimal management of SRI in children is warranted.
Abstract:
Segmental renal infarction (SRI) is a rare condition that causes renovascular hypertension (RVH), which accounts for 8-10% of all causes of pediatric hypertension. We report the clinical course of two children with idiopathic SRI who suffered severe arterial hypertension associated with hyponatremia. Hypertension was diagnosed during the study of hematuria in the first case and due to a hypertensive emergency in the second case. The etiology was found to be renovascular in both patients, involving the occlusion of small renal arteries and causing SRI. Our first patient was treated with partial nephrectomy, and the second patient was treated with antihypertensive medication given the impossibility of removing the infarcted renal area. The occlusion of small renal arteries is a rare disease of unknown origin in which the gold standard for diagnosis is selective renal arteriography. The definitive treatment is surgical segmentectomy. If segmentectomy is not feasible because of the localization of the infarcted area, as in our second patient, medical treatment is required. In view of the importance of RVH in children and the rareness of the particular etiology here reported (SRI), a review of the literature was done.
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