Abstract
Objectives
Growth failure can result from various underlying causes, necessitating a thorough evaluation. Reninoma, a rare renin-secreting tumor, is an uncommon cause of hypertension, especially in paediatric patients, and has not been associated with growth failure until now.
Case presentation
An 11-year-old girl presented with complaints of poor height gain, headaches, increased thirst, and vomiting. The evaluation revealed severe hypertension and hypokalemic alkalosis. Investigations indicated renin-dependent hypertension, and imaging identified a right renal mass. Renal venous sampling confirmed renin production from the tumor. A right open partial nephrectomy was performed, resulting in the normalization of blood pressure and improved growth. Over the following years, she achieved a significant catch-up growth, regaining her original height percentile and the target adult height.
Conclusions
This case adds to the limited literature on paediatric reninoma. It highlights a rare presentation of reninoma causing hypertension and growth failure in a child. The growth failure was likely due to hypokalemic alkalosis-induced low insulin-like growth factor 1 (IGF-1) levels, a mechanism not previously documented in paediatric reninoma cases. Surgical excision of the tumor led to normalization of blood pressure and metabolic alkalosis with significant growth recovery.
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Research ethics: Not applicable.
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Informed consent: Signed informed consent was obtained from the mother (legal guardian) of the patient for publication of this case report and any accompanying images, as the patient was a minor.
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Author contributions: All authors were involved in case diagnosis, management and follow up. All authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Use of Large Language Models, AI and Machine Learning Tools: None declared.
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Conflict of interest: The authors state no conflict of interest.
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Research funding: None declared.
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Data availability: Not applicable.
References
1. Bell, CS, Samuel, JP, Samuels, JA. Prevalence of hypertension in children. Hypertension 2019;73:148–52. https://doi.org/10.1161/hypertensionaha.118.11673.Search in Google Scholar
2. Thomas, J, Stonebrook, E, Kallash, M. Pediatric hypertension: review of the definition, diagnosis, and initial management. Int J Pediatr Adolesc Med 2022;9:1–6. https://doi.org/10.1016/j.ijpam.2020.09.005.Search in Google Scholar PubMed PubMed Central
3. Hayes, AG, Stowasser, M, Umapathysivam, MM, Falhammar, H, Torpy, DJ. Approach to the patient: reninoma. J Clin Endocrinol Metabolism 2024;109:e809–16. https://doi.org/10.1210/clinem/dgad516.Search in Google Scholar PubMed PubMed Central
4. Wolley, M, Gordon, RD, Stowasser, M. Reninoma: the importance of renal vein renin ratios for lateralisation and diagnosis. Am J Nephrol 2014;39:16–9. https://doi.org/10.1159/000357410.Search in Google Scholar PubMed
5. Nugent, JT, Young, C, Funaro, MC, Jiang, K, Saran, I, Ghazi, L, et al.. Prevalence of secondary hypertension in otherwise healthy youths with a new diagnosis of hypertension: a meta-analysis. J Pediatr 2022;244:30–7.e10. https://doi.org/10.1016/j.jpeds.2022.01.047.Search in Google Scholar PubMed PubMed Central
6. Flynn, JT, Kaelber, DC, Baker-Smith, CM, Blowey, D, Carroll, AE, Daniels, SR, et al.. Clinical practice guideline for screening and management of high blood pressure in children and adolescents. Pediatrics 2017;140:e20171904. https://doi.org/10.1542/peds.2017-1904.Search in Google Scholar PubMed
7. Wong, L, Hsu, TH, Perlroth, MG, Hofmann, LV, Haynes, CM, Katznelson, L. Reninoma: case report and literature review. J Hypertens 2008;26:368–73. https://doi.org/10.1097/hjh.0b013e3282f283f3.Search in Google Scholar
8. Bertulli, C, Hureaux, M, De Mutiis, C, Pasini, A, Bockenhauer, D, Vargas-Poussou, R, et al.. A rare cause of chronic hypokalemia with metabolic alkalosis: case report and differential diagnosis. Children 2020;7:212. https://doi.org/10.3390/children7110212.Search in Google Scholar PubMed PubMed Central
9. Tsuru, N, Chan, JC. Growth failure in children with metabolic alkalosis and with metabolic acidosis. Nephron 1987;45:182–5. https://doi.org/10.1159/000184113.Search in Google Scholar PubMed
10. Flyvbjerg, A, Dørup, I, Everts, ME, Orskov, H. Evidence that potassium deficiency induces growth retardation through reduced circulating levels of growth hormone and insulin-like growth factor I. Metabolism 1991;40:769–75. https://doi.org/10.1016/0026-0495(91)90001-d.Search in Google Scholar PubMed
11. Simopoulos, AP. Growth characteristics in patients with Bartter’s syndrome. Nephron 1979;23:130–5. https://doi.org/10.1159/000181622.Search in Google Scholar PubMed
12. Wong, SC, Dobie, R, Altowati, MA, Werther, GA, Farquharson, C, Ahmed, SF. Growth and the growth hormone-insulin like growth factor 1 Axis in children with chronic inflammation: current evidence, gaps in knowledge, and future directions. Endocr Rev 2016;37:62–110. https://doi.org/10.1210/er.2015-1026.Search in Google Scholar PubMed
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Articles in the same Issue
- Frontmatter
- Review
- Osteogenesis imperfecta: shifting paradigms in pathophysiology and care in children
- Opinion Paper
- CRH receptor antagonist crinecerfont – a promising new treatment option for patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- Original Articles
- Age and sex mark clinical differences in the presentation of pediatric type 1 diabetes mellitus
- Geographic information system mapping and predictors of glycemic control in children and youth with type 1 diabetes: a study from Western India
- Body composition assessment measured via bioelectrical impedance analysis in euthyroid children with newly diagnosed Hashimoto’s thyroiditis
- Outcomes of newborns screened for congenital hypothyroidism in Turkey – a single center experience
- High yield of congenital hypothyroidism among infants attending Children Hospital, Nairobi, Kenya. Facility based study in the absence of newborn screening
- Immune checkpoint inhibitors and endocrinopathies in pediatric brain tumor patients
- Assessment of quality of life in families affected by maple syrup urine disease: a cross sectional study
- Case Reports
- Reninoma: an unusual cause of growth failure
- Persistent hypoglycemia in congenital syphilis: hyperinsulinemic hypoglycemia with a focal pancreatic lesion
- Diagnostic challenges in pediatric Cushing’s disease associated with chronic renal failure: a report of three patients
- A novel de novo missense OTC mutation in an Iranian girl: a case report