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Horseshoe kidney.

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Horseshoe kidney is often asymptomatic but can lead to complications like infections, stones, and hypertension. Early detection through imaging and monitoring is essential.
Updated On: Dec 11, 2025
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Solution and Explanation

A horseshoe kidney is a congenital condition where both kidneys are fused together at the lower poles, forming a U-shape resembling a horseshoe. This abnormality occurs during fetal development and can lead to various clinical complications.
Step 1: Embryology and Pathophysiology:
- During fetal development, the kidneys begin as two separate entities that ascend from the pelvis to their normal position in the abdomen. In horseshoe kidney, the kidneys fail to separate properly and remain fused at the lower poles. This fusion occurs due to a defect in the development of the mesoderm, which gives rise to the renal system. The fused kidneys usually lie lower in the abdomen than normal, and the renal arteries may originate from different parts of the aorta.
- The fused kidney is often shaped like a horseshoe, with the isthmus (connecting tissue) typically located at the lower part of the kidney, near the renal pelvis.
Step 2: Associated Anatomical Features:
- Renal Arteries and Veins: The renal arteries of a horseshoe kidney may arise from various locations on the aorta, often at a lower position than in normal kidneys. This can lead to variations in the vascular supply of the kidney. Similarly, the veins may drain into the inferior vena cava or iliac veins.
- Ureters: The ureters may be displaced laterally, and their insertion into the bladder may be slightly altered. This can cause complications such as urinary stasis and increased risk of infection.
Step 3: Clinical Manifestations:
- Asymptomatic Cases: In many individuals, a horseshoe kidney may remain asymptomatic and be discovered incidentally on imaging studies such as ultrasound or CT scans.
- Complications: Individuals with a horseshoe kidney are at higher risk for developing urinary tract infections (UTIs), kidney stones, and hydronephrosis. Additionally, the condition is associated with a higher incidence of certain cancers, including renal cell carcinoma and Wilms' tumor.
- Hypertension: There is also an increased risk of hypertension due to abnormal blood flow or compression of the renal arteries.
Step 4: Diagnosis and Imaging:
- The diagnosis is usually made via imaging, such as ultrasound, CT scan, or MRI, which can clearly show the fusion of the kidneys and associated anatomical features. Contrast-enhanced imaging may be used to evaluate renal function and any associated structural abnormalities such as hydronephrosis or stones.
Step 5: Treatment and Management:
- Conservative Management: In asymptomatic patients, no treatment may be required other than regular monitoring.
- Surgical Treatment: In cases of recurrent infections, hydronephrosis, or other complications, surgical intervention may be necessary. This may involve correction of the renal pelvis, drainage of any obstruction, or removal of kidney stones.
- Transplantation: In severe cases, where kidney function is compromised, a kidney transplant may be considered, though this is rare.
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