Medullary sponge kidney

Medullary Sponge Kidney (also known as Cacchi-Ricci disease) is a congenital disorder of the kidneys characterized by cystic dilatation of the collecting tubules in one or both kidneys.

Signs and Symptoms[edit | edit source]

Individuals with Medullary Sponge Kidney often present with hematuria (blood in the urine), nephrolithiasis (kidney stones), and nephrocalcinosis (calcium deposits in the kidneys). Other symptoms may include recurrent urinary tract infections and flank pain.

Causes[edit | edit source]

The exact cause of Medullary Sponge Kidney is unknown. However, it is believed to be congenital (present at birth). Some studies suggest a possible genetic link, but more research is needed to confirm this.

Diagnosis[edit | edit source]

Diagnosis of Medullary Sponge Kidney is often made through imaging studies such as ultrasound, computed tomography (CT) scan, or intravenous pyelogram (IVP). These tests can reveal the characteristic appearance of cystic dilatation in the kidneys.

Treatment[edit | edit source]

Treatment for Medullary Sponge Kidney is primarily aimed at managing symptoms and preventing complications. This may include measures to prevent kidney stones, such as increasing fluid intake, dietary modifications, and medications. In some cases, surgical intervention may be necessary to remove large kidney stones.

Prognosis[edit | edit source]

The prognosis for individuals with Medullary Sponge Kidney is generally good. While the condition can cause discomfort and complications such as kidney stones, it does not typically affect kidney function or lead to kidney failure.

References[edit | edit source]

Medullary sponge kidney Resources
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