Ozmen M N, Aygün N, Kiliç I, Kuran L, Yalçin B, Besim A
Department of Radiology, Hacettepe University Medical School, Ankara, Turkey.
Pediatr Radiol. 1992;22(7):541-2. doi: 10.1007/BF02013008.
Acid lipase deficiency which is an inborn error of lipid metabolism leads to an abnormal accumulation of cholesteryl esters and triglycerides in many tissues. It is manifested in two clinical forms: Wolman's disease (WD) which is fatal in infancy and cholesteryl ester storage disease (CESD) which is a milder form and usually presented in adulthood. An infant with a clinical diagnosis of WD was examined with CT and ultrasound. Where as CT showed an enlarged liver with decreased density and heavily calcified adrenal glands, ultrasound revealed an enlarged liver with normal echogenicity, adrenal calcification and thickening of bowel loops. Bowel wall thickening in WD was not demonstrated in the literature before with any imaging modality.
酸性脂肪酶缺乏症是一种脂质代谢的先天性缺陷,会导致胆固醇酯和甘油三酯在许多组织中异常蓄积。它有两种临床形式:婴儿期致命的沃尔曼病(WD)和症状较轻、通常在成年期出现的胆固醇酯贮积病(CESD)。对一名临床诊断为WD的婴儿进行了CT和超声检查。CT显示肝脏肿大、密度降低以及肾上腺重度钙化,而超声显示肝脏肿大、回声正常、肾上腺钙化和肠袢增厚。此前文献中未通过任何成像方式证实WD存在肠壁增厚的情况。