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A primary case presentation of nephrolithiasis from enteric hyperoxaluria due to Crohn's disease.


Learning objective was to recognize colonic oxalate absorption resulting in hyperoxaluria and nephrolithiasis as a long-term metabolic complication of small bowel resection. A 53-year-old man with a history of Crohn's disease presented with progressive fatigue, oliguria oliguria /ol·i·gu·ria/ (ol?i-gu´re-ah) diminished urine production and excretion in relation to fluid intake.oligu´ric

ol·i·gu·ri·a
n.
Abnormally slight or infrequent urination.
, and watery diarrhea over a 2-week period. He had undergone extensive ileal resection 25 years ago for Crohn's disease. Laboratory testing revealed acute renal failure acute renal failure Acute kidney failure Nephrology An abrupt decline in renal function, triggered by various processes–eg, sepsis, shock, trauma, kidney stones, drug toxicity-aspirin, lithium, substances of abuse, toxins, iodinated radiocontrast. , hyperkalemia Hyperkalemia Definition

The normal concentration of potassium in the serum is in the range of 3.5 to 5.0 mM. Hyperkalemia refers to serum or plasma levels of potassium ions above 5.0 mM.
, metabolic acidosis and severe pancytopenia pancytopenia /pan·cy·to·pe·nia/ (-sit-ah-pe´ne-ah) abnormal depression of all the cellular elements of the blood.

pan·cy·to·pe·ni·a
n.
. Urinalysis did not reveal crystalline deposits; 24-hour urine studies demonstrated hyperoxaluria, hypocalciuria, hypocitraturia and hypomagnesuria. X-rays revealed multiple bilateral ureteral calculi and a renal ultrasound showed hydronephrosis. He underwent bilateral ureteral stent placement after which his renal failure dramatically improved. We concluded that the patient had enteric hyperoxaluria due to excess oxalate absorption in his colon leading to subsequent excretion in his urine. The hyperoxaluria served as a nidus nidus /ni·dus/ (ni´dus) pl. ni´di   [L.]
1. the point of origin or focus of a morbid process.

2. nucleus (2).
 for calcium oxalate nephrolithiasis then obstructive uropathy. Dietary restrictions for oxalate, calcium, and fats were advised, and cholestyramine cholestyramine /cho·le·sty·ra·mine/ (ko?le-sti´rah-men) see cholestyramine resin, under resin.

cho·le·styr·a·mine
n.
 with appropriate mineral supplements was prescribed. Enteric hyperoxaluria can complicate small bowel resection in the presence of an intact colon, and is associated with calcium oxalate nephrolithiasis. In the intact intestine, dietary oxalate binds to calcium, forming insoluble calcium oxalate and is not absorbed. In Crohn's disease fat malabsorption occurs, allowing calcium to bind to fatty acids, leaving oxalate unbound for passage to the colon where it gets both absorbed and excreted. This results in hyperoxaluria and oxalate nephropathy. Diagnostic features include a low urinary pH, low urinary volumes, hyperoxaluria, hypocalciuria and hypocitraturia. Medical treatment includes dietary oxalate and fat restriction along with cholestyramine, calcium and citrate supplementation. In severe recurrent cases, an ileostomy ileostomy /il·e·os·to·my/ (il?e-os´tah-me) surgical creation of an opening into the ileum, with a stoma on the abdominal wall.

il·e·os·to·my
n.
1.
 may be indicated.

Farida Millwala, MD, and Samuel Cykert, MD. Moses H. Cone Memorial Hospital, Department of Internal Medicine, Greensboro, NC.
COPYRIGHT 2004 Southern Medical Association
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Copyright 2004, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

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Title Annotation:Section on Gastroenterology
Author:Cykert, Samuel
Publication:Southern Medical Journal
Date:Oct 1, 2004
Words:289
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