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Sonographic findings in type I glycogen storage disease

✍ Scribed by Carlo Pozzato; Anna Botta; Chiara Melgara; Laura Fiori; Maria Lorella Giannì; Enrica Riva


Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
307 KB
Volume
29
Category
Article
ISSN
0091-2751

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✦ Synopsis


Abstract

Purpose

The aim of this study was to document the sonographic appearance and dimensions of the liver and spleen in patients affected by type I glycogen storage disease and to correlate those findings with laboratory data to evaluate the potential role of sonography in diagnosing that disease.

Methods

Fourteen patients (age range, 3–26 years; 10 patients younger than 18 years) with type I glycogen storage disease proved by liver biopsy were studied prospectively with gray‐scale sonography, color Doppler sonography, and spectral analysis. The liver, kidneys, spleen, portal system, hepatic veins, and hepatic arteries were evaluated. Laboratory data were correlated with sonographic findings.

Results

In 13 (93%), of 14 patients, the liver was enlarged, and in 11 patients (79%), hepatic echogenicity was increased. In 9 patients (64%), both kidneys were enlarged, and in 6 cases (43%), the spleen was enlarged. In all patients, flow in the portal, splenic, and superior mesenteric veins was hepatopetal, and flow in the hepatic veins was triphasic. In 5 patients (36%), both triglyceride and total cholesterol levels were higher than normal. No focal hepatic lesions were identified. Analysis found no significant association between sonographic findings and laboratory data.

Conclusions

The most frequent sonographic findings in patients with type I glycogen storage disease were hepatomegaly, increased hepatic echogenicity, and enlarged kidneys. Sonography may help in the diagnosis of type I glycogen storage disease, but a liver biopsy is required for a definitive diagnosis. © 2001 John Wiley & Sons, Inc. J Clin Ultrasound 29:456–461, 2001.


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Hepatocellular carcinoma in type I glyco
✍ Joachim Limmer; Wolfgang E. Fleig; Dorothea Leupold; Reinhard Bittner; Hans Dits 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 English ⚖ 967 KB

Patients suffering from Type I glycogen storage disease frequently develop hepatic tumors. Some of these were classified as carcinoma, with the majority of tumors representing benign adenomata. However, no evidence exists of malignant transformation of adenomata in these patients. Here, we describe