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  • 1
    ISSN: 1432-0428
    Keywords: Keywords Non-insulin-dependent diabetes mellitus ; microalbuminuria ; von Willebrand factor ; endothelial function ; renal structure.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Microalbuminuria (MA) is associated with microangiopathy (renal and retinal lesions) in insulin-dependent diabetic (IDDM) patients. In contrast MA does not reflect microvascular damage in a substantial number of non-insulin-dependent diabetic (NIDDM) patients. MA predicts cardiovascular disease in NIDDM patients with increased von Willebrand factor (vWF) plasma levels which are hypothesized to reflect endothelial dysfunction. However, it is not known whether MA is consequent to generalised endothelial dysfunction or to renal injury. Thus, this study evaluated vWF plasma levels in relation to renal and retinal structural abnormalities in NIDDM patients with MA. Kidney biopsies, fundoscopy and measures of vWF plasma levels were performed in 32 NIDDM patients with MA. These patients were allocated to two renal structural categories: A) Without renal structural abnormalities (C I, n = 10): normal or near-normal renal structure, and B) With renal structural abnormalities (n = 22), further divided into: C II (n = 12) with typical diabetic nephropathology, predominantly glomerulopathy, and C III (n = 10) with atypical patterns of renal injury (more advanced tubulo-interstitial and arteriolar than glomerular changes). vWF plasma levels were significantly higher in category B (C II: 195 ± 49 % and C III: 161 ± 46 %) than in category A (C I: 119 ± 42 %), (chi-square, p 〈 0.05). Diabetic retinopathy was also related to vWF plasma levels (ANOVA, p 〈 0.05). These data suggest that there are two types of MA in NIDDM: one associated with increased vWF levels, established renal injury and frequently retinopathy, and the other characterized by normal vWF levels, normal renal structure and absent or mild diabetic retinopathy. We propose that vWF plasma levels in NIDDM patients with MA may help to identify patients with important renal structural changes, increased retinopathy risk and, perhaps, generalised endothelial dysfunction. Whether vWF plasma levels predict end-stage renal disease and cardiovascular events deserves longitudinal studies. [Diabetologia (1998) 41: 233–236]
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1084
    Keywords: Chemoembolisation ; Embolisation, hepatic artery ; Hepatocellular carcinoma ; Iodised oil
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract To evaluate the effectiveness of transcatheter arterial embolisation (TAE) as a treatment of hepatocellular carcinoma (HCC) complicating cirrhosis, the survival of 27 untreated patients and 57 TAE-treated patients was compared. Clinical features, laboratory findings and tumour stage were comparable in the two groups of patients. TAE was undertaken with epirubicin, iodised oil and gelatine esponge. Cumulative survival rates at 6, 12, 24 and 36 months were 0.59, 0.47, 0.17 and 0.08 in the untreated group, and 0.87, 0.75, 0.40 and 0.19 in the TAE-treated group (P = 0.01). Patients with Child's grade B cirrhosis and patients with tumour smaller than 25% of the liver volume responded better to TAE. Twenty-four untreated patients and 25 TAE-treated patients died during the follow-up. The complication rate and mortality rate of TAE were 28% and 1.7% respectively. TAE prolongs the survival of patients with HCC complicating cirrhosis; prognosis depends on tumour stage and the degree of hepatic function impairment.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1076
    Keywords: Key words Congenital absence of portal vein ; Focal nodular hyperplasia of the liver
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Congenital absence of portal vein is a rare malformation. To date, 16 cases have been reported – all in association with other anomalies, i.e. benign or malignant hepatic neoplasms in 6 cases and cardiac malformations in 12. This case report described a girl with congenital absence of portal vein, focal nodular hyperplasia of the liver and cystic kidney dysplasia. Angiography showed the splenic vein and superior mesenteric vein joining to form a common trunk that entered the inferior vena cava directly above the liver. A review of the other cases in the literature is provided and the clinical aspects of our patient are discussed.
    Type of Medium: Electronic Resource
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