# An Unusual Case of Flank Pain Late in Life: A Case Report

**Authors:** Kristel Sibaja, Harper Henderson, Alejandro Biglione, RaeAnn Tourangeau-Young

PMC · DOI: 10.7759/cureus.52790 · Cureus · 2024-01-23

## TL;DR

An 88-year-old woman with a rare kidney condition experienced flank pain and other symptoms, highlighting the unusual presentation of horseshoe kidneys in old age.

## Contribution

This case report documents a rare instance of symptomatic horseshoe kidney presenting late in life.

## Key findings

- An 88-year-old female with a history of horseshoe kidney presented with flank pain and hydronephrosis.
- Symptomatic horseshoe kidneys are rarely diagnosed in elderly patients.
- The case highlights the importance of considering CAKUT in elderly patients with unexplained urinary symptoms.

## Abstract

Abnormalities in renal fusion represent a subset of congenital anomalies of the kidneys and urinary tract (CAKUT). Horseshoe kidneys (HSKs) are the fusion of kidneys at their lower poles. It is the most common form of CAKUT. Symptoms are usually subtle. The diagnosis is usually made incidentally during childhood. Rarely does an HSK become symptomatic later in life. We present the case of an 88-year-old female with a history of HSK who presented to the emergency department (ED) with a three-week history of left-sided flank pain, intermittent nausea, and reduced urine output. Her inpatient workup included imaging that revealed an HSK and bilateral hydronephrosis, which was more prominent on the left. The onset of symptoms for an HSK late in life is extremely rare.

## Linked entities

- **Diseases:** hydronephrosis (MONDO:0005510)

## Full-text entities

- **Diseases:** hydronephrosis (MESH:D006869), renal fusion (MESH:D000069337), reduced urine output (MESH:D014555), Flank Pain (MESH:D021501), nausea (MESH:D009325), CAKUT (MESH:C566906)

## Full text

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## Figures

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## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC10882249/full.md

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Source: https://tomesphere.com/paper/PMC10882249