Renal Papillary Necrosis as the First Presenting Clinical Feature in a Sickle Beta and Thalassemic Child

Authors

  • Jagadish Kumar Department of Paediatrics, Jagadguru Sri Shivarathreeshwara Medical College, Jagadguru Sri Shivarathreeshwara University, Mysore, India
  • Satyesh Chowdary Department of Paediatrics, Jagadguru Sri Shivarathreeshwara Medical College, Jagadguru Sri Shivarathreeshwara University, Mysore, India
  • Manjunath VG Department of Paediatrics, Jagadguru Sri Shivarathreeshwara Medical College, Jagadguru Sri Shivarathreeshwara University, Mysore, India
  • Sudha Kiran Das Department of Paediatrics, Jagadguru Sri Shivarathreeshwara Medical College, Jagadguru Sri Shivarathreeshwara University, Mysore, India
  • Manovihari Vuyyuru Department of Paediatrics, Jagadguru Sri Shivarathreeshwara Medical College, Jagadguru Sri Shivarathreeshwara University, Mysore, India

DOI:

https://doi.org/10.3126/jnps.v40i3.29617

Keywords:

Renal Papillary Necrosis; Sickle Beta and Thalassemia; Sickle Cell Disease; Sickle Cell Nephropathy

Abstract

In sickle cell disease (SCD), the clinical manifestations are due to episodes of vascular occlusion and haemolysis. Most of the children experience vaso-occlusive pain episodes by the age of six years. Renal injury in sickle cell disease referred to as sickle cell nephropathy is a frequent yet under-recognised complication. Renal papillary necrosis (RPN) as the first presentation in SCD is rare. We are reporting a 12 year old child with no prior vaso-occlusive episodes, presenting with renal papillary necrosis due to Sickle Beta and Thalassemia.

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Published

2020-12-15

How to Cite

Kumar, J., Chowdary, S., VG, M., Das, S. K., & Vuyyuru, M. (2020). Renal Papillary Necrosis as the First Presenting Clinical Feature in a Sickle Beta and Thalassemic Child. Journal of Nepal Paediatric Society, 40(3), 274–277. https://doi.org/10.3126/jnps.v40i3.29617

Issue

Vol. 40 No. 3 (2020)

Section

Case Reports

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