Medullary sponge kidney: Difference between revisions

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==Natural History,Complications and Prognosis==
Complications such as infection, hematuria, and [[nephrolithiasis]] may be the presenting complaint in approximately 10% of patients.


==References==
==References==

Revision as of 14:53, 28 September 2012

Medullary sponge kidney
Medullary sponge kidney.
Image courtesy of RadsWiki

Medullary sponge kidney Microchapters

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Overview

Historical Perspective

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Differentiating Medullary sponge kidney from other Diseases

Epidemiology and Demographics

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Natural History, Complications and Prognosis

Diagnosis

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] ; Associate Editor(s)-in-Chief: Cafer Zorkun M.D., PhD.

Overview

Medullary sponge kidney is a congenital disorder of the kidneys characterized by a cystic dilatation of the collecting tubules in one or both kidneys.

Diagnosis

Symptoms

In most cases, medullary sponge kidney affects only one kidney, in which case kidney function is usually preserved and individuals may be asymptomatic. However, these individuals are at increased risk for nephrolithiasis (kidney stones) and urinary tract infection.

Ultrasonography

  • Echogenic medullary pyramids in patients with medullary sponge kidney, irrespective of the presence of medullary nephrocalcinosis.
  • US findings can demonstrate complications related to calculus disease.

Computed Tomography

  • Unenhanced CT scan findings may be normal or demonstrate medullary nephrocalcinosis.
  • Enhanced scans may demonstrate contrast accumulation within the papillae.

Patient #1

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Patient #2'

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References

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