Zenker's diverticulum: a contraindication for wireless capsule endoscopy?
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Biomedical subjects
Publications and source records attributed to Deborah A Baumgarten.
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BACKGROUND: Sporadic renal cysts not associated with genetic polycystic disorders are common and generally thought to be of no clinical significance. Since multiple cysts frequently develop in end-stage renal disease (ESRD), we tested the hypothesis that cysts that are solitary or few in number are an early manifestation of reduced renal function. METHODS: We evaluated 561 hospitalized patients who underwent contrast-enhanced, abdominal computed tomography (CT) and correlated clinical characteristics and parameters of renal function with the presence or absence of renal cysts. RESULTS: Age ranged from 16 to 100 years, mean serum creatinine concentration was 0.88 mg/dL (range 0.4 to 2.1 mg/dL), and mean estimated creatinine clearance was 94 mL/min/1.73 m(2) (range 22 to 218 mL/min/1.73 m(2)). The presence of cysts was significantly correlated with older age (P < 0.001), higher serum creatinine concentration (P < 0.002), and lower estimated creatinine clearance (P < 0.001). In a multivariate analysis, including age and gender, estimated creatinine clearance still correlated with the presence of cysts (P= 0.009). When patients were grouped by age, estimated creatinine clearance correlated with cysts in patients <40 years and 40 to 59 years, but not in patients 60 to 79 years or > or =80 years. There was no association of cysts with hypertension or proteinuria. In patients with cysts, serum creatinine increased progressively but not significantly with cyst number, and did not correlate with size or distribution of cysts. Renal parenchymal volume was slightly but not significantly reduced in patients with cysts. CONCLUSION: The presence of kidney cysts, even single cysts, is associated with reduced renal function in hospitalized patients younger than 60 years. This relationship may be obscured by the reduced renal function and the high incidence of cysts in older patients. These results suggest that acquired cystic kidney disease may begin early in the course of renal disease and that underlying renal disease should be considered in individuals with renal cysts prior to age 60 years.
BACKGROUND: Autosomal-dominant polycystic kidney disease (ADPKD) is characterized by gradual renal enlargement and cyst growth prior to loss of renal function. Standard radiographic imaging has not provided the resolution and accuracy necessary to detect small changes in renal volume or to reliably measure renal cyst volumes. The Consortium for Radiologic Imaging Studies in Polycystic Kidney Disease (CRISP) is longitudinally observing ADPKD individuals using high-resolution magnetic resonance (MR) imaging to determine if change in renal and cyst volumes can be detected over a short period of time, and if they correlate with decline in renal function early in disease. METHODS: Standardization studies were conducted in phantoms and four subjects at each participating clinical center. After, in the full-scale protocol, healthy ADPKD individuals 15 to 45 years old with creatinine clearance>70 mL/min underwent standardized MR renal imaging, renal iothalamate clearance, comprehensive clinical evaluation, and determination of 24-hour urinary albumin and electrolyte excretion. Stereology was used from T1-weighted images to quantify renal volume, and region-growing thresholding was used from T2-weighted images to determine cyst volume. Renal structures were evaluated in relation to demographic, clinical, and biochemical variables using means/medians, standard deviations, and Pearson correlations. RESULTS: Reliability coefficients for MR renal and cyst volume measurements in phantoms were 99.9% and 89.2%, respectively. In the full-scale protocol, 241 ADPKD individuals (145 women and 96 men) were enrolled. Total renal, cyst, and % cyst volume were significantly greater in each decade group. Hypertensive individuals demonstrated greater renal, cyst, and % cyst volume than normotensive subjects. Age-adjusted renal (r = -0.31, P < 0.0001), cyst (r = -0.36, P < 0.0001), and % cyst volume (r = -0.35, P < 0.0001) were inversely related to glomerular filtration rate (GFR). Age-adjusted renal volume (r = 0.42, P < 0.0001), cystic (r = 0.39, P < 0.0001, and % cyst volume (r = 0.41, P < 0.0001) were related with urinary albumin excretion. CONCLUSION: MR measures of renal and cyst volume are reliable and accurate in patients with ADPKD. ADPKD is characterized by significant cystic involvement that increases with age. Structure (renal and cyst volume) and function (GFR) are inversely related and directly related with the presence of hypertension and urinary albumin excretion in individuals with normal renal function.
OBJECTIVES: Incidental findings of thickened luminal GI organs (LGIO) on CT are not uncommon. However, the significance of these findings is unclear. Because of the lack of scientific data, there are no clinical guidelines for the evaluation of these radiologic abnormalities. Our objective was to determine whether endoscopic evaluation of these findings revealed significant abnormalities. METHODS: This study evaluated all incidental findings of thickened LGIO in a large medical center from October, 1997 to March, 1999 that were followed by endoscopic examinations. RESULTS: Ninety-six percent of patients with incidental findings of thickening of the sigmoid colon or rectum, 81% of patients with thickening of the distal esophagus, and 13% of patients with thickening of the cecum had significant abnormalities on further endoscopic work up. CONCLUSIONS: Although positive pathologic findings are less common in thickening of the cecum than in other LGIO, all of these incidental findings on CT warrant further endoscopic examination.
Sonography is a simple, inexpensive, and readily available imaging modality that has become an essential component of the management of renal transplantation. It is indicated in almost all patients with acute renal failure and also is useful in the evaluation of pain, infection, and hematuria and the performance of percutaneous biopsy. Although many aspects of sonography are similar in native and transplanted kidneys, there are important differences and problems unique to the renal allograft, which form the basis for this review. The anatomy of renal transplantation and changes that accompany parenchymal disorders are discussed, but particular attention focuses on problems related to the urinary tract, fluid collections, and vascular disorders. By becoming more familiar with transplant sonography, nephrologists will be better able to incorporate this indispensable tool into the care of their patients.