Medullary sponge kidney

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Medullary sponge kidney
Classification and external resources

Medullary sponge kidney as seen on an intravenous pyelogram
ICD-10 Q61.5
ICD-9 753.17
eMedicine article/379323
MeSH D007691

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. In the general population, the frequency of medullary sponge kidney disease is reported to be 0.02% - 0.005%; that is, 1 in 5000 to 1 in 20,000. The frequency of medullary sponge kidney has been reported by various authors to be 12 – 21% in patients with nephrolithiasis.[1] The disease is bilateral in 70% of cases. Individuals with medullary sponge kidney are at increased risk for kidney stones and urinary tract infection. Patients with MSK typically pass twice as many stones per year as do other stone formers without MSK. While described as a "benign" disorder with a low morbidity rate, as many as 10% of patients with MSK have an increased risk of morbidity associated with frequent stones and UTIs. While some patients report increased chronic kidney pain, the source of the pain, when a UTI or blockage is not present, is unclear at this time. Renal colic (flank and back pain) is present in 55% of patients. Women with MSK experience more stones, UTIs and complications than men.


[edit] Notes

  1. ^ Ginalski, JM; Portmann L, Jaeger P (1990). "Does medullary sponge kidney cause nephrolithiasis?". American Journal of Roentgenology 155 (2): 299–302. PMID 2115256. http://www.ajronline.org/cgi/reprint/155/2/299.pdf. 
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