AssessmentsMedullary sponge kidney
Medullary sponge kidney
Medullary sponge kidney is a congenital renal disorder characterized by cystic dilatation of the in one or both kidneys.
USMLE® Step 1 style questions USMLE
A 28-year-old woman comes to the office because of blood in her urine. She has a history of urinary tract infections. She says she feels abdominal pain, and on occasion, nausea with the pain. An intravenous pyelogram is done, and shows hyperdense papillae and small clusters limited to the calyces, as shown similarly to the diagram below.
The clusters are confirmed to be calcium stones. Which of the following is the most likely cause?
Content Reviewers:Rishi Desai, MD, MPH
Medullary sponge kidney, also known as cacchi-ricci disease is a congenital disease where the medullary part of the kidney, which is deeper inside the kidney, gets loaded with fluid-filled cysts which gives the kidney the appearance of a sponge.
Now, the kidney can be divided into the cortex which is the outer layer and the medulla which is the layer below that.
Kidneys contain millions of tiny nephrons which filter the blood - each of which is like a little tube receiving blood on one end in the cortex.
From there, the nephron dips into the medulla, and then goes back out into the cortex, and finally dips back into the medulla a second time to connect to the collecting ducts which gather up all of the urine. Not every nephron has this exact structure, but a lot of them do.
From there, the urine drains through the papilla which is an inverted cone shaped pyramid, that, like a shower head, pours urine into the calyces, which comes from the latin -calix which means large cup, kinda like a Roman chalice.
From there it enters the renal pelvis which funnels the urine into the ureter, then to the bladder, and then finally leaves the body out the urethra.
Now, medullary sponge kidney has to do with the development of the kidney. So during fetal development, first off you’ve got this structure called the mesonephric duct which is involved in development of urinary and reproductive organs, and during the 5th week of gestation, a little guy called the ureteric bud starts pushing its way into another structure called the metanephric blastema, and together, these two little embryologic structures go on to develop into a kidney.
At about the 7th week, nephrogenesis, or formation of the kidneys, starts under the influence of that ureteric bud.
By about 20 weeks, the ureteric bud has formed the ureters, the renal calyces, collecting ducts, and collecting tubules, while the metanephric blastema develops into the nephron itself, which includes the epithelial cells and the podocytes of Bowman’s capsule.
In the third trimester and throughout infancy, the kidneys continue to grow and mature.
Although not completely known, it’s thought that medullary sponge kidney is a result of some sort of abnormal induction of the metanephric blastema by the ureteric bud.
This failure might be the fault of the mesonephric duct not forming right, or the ureteric bud not forming right, or both.
Whatever the case, in medullary sponge kidney, the hallmark feature are dilated collecting ducts, meaning enlarged, as well as small cysts that form around the collecting ducts.
Even though medullary sponge kidney is present at birth, sometimes complications don’t emerge until adulthood, and even then, they might come and go.
The most common one is nephrolithiasis, or developing kidney stones, which are made of calcium phosphate or calcium oxalate. These form in the collecting ducts and surrounding tissue, and these result mostly from a failure of kidney cells to properly reabsorb or secrete solutes which ultimately results in stone formation.