家族性多发脂肪瘤病中的胃十二指肠脂肪瘤病
Gastroduodenal Lipomatosis in Familial Multiple Lipomatosis.
作者信息
Djuric-Stefanovic Aleksandra, Ebrahimi Keramatollah, Sisevic Jelena, Saranovic Djordjije
机构信息
Department of Radiology, Faculty of Medicine, University of Belgrade, Belgrade, Serbia.
出版信息
Med Princ Pract. 2017;26(2):189-191. doi: 10.1159/000454714. Epub 2016 Nov 24.
OBJECTIVE
To present a case of gastroduodenal lipomatosis associated with familial multiple lipomatosis (FML).
CLINICAL PRESENTATION AND INTERVENTION
A 58-year-old male presented with FML that manifested as multiple, painless, subcutaneous lipomas on his body; his mother had subcutaneous lipoma without a diagnosis of gastroduodenal lipomatosis. His lipid profile was normal. Abdominal computed tomography showed multiple, submucosal, polypoid lesions (of uniform density) of fat in the stomach and duodenum, and a small, similar lesion in the ileum.
CONCLUSION
This case shows that gastrointestinal lipomatosis can manifest as FML.
目的
报告一例与家族性多发性脂肪瘤病（FML）相关的胃十二指肠脂肪瘤病病例。
临床表现及干预措施
一名58岁男性患有FML，表现为身体上有多个无痛性皮下脂肪瘤；他的母亲有皮下脂肪瘤，但未诊断出胃十二指肠脂肪瘤病。他的血脂水平正常。腹部计算机断层扫描显示胃和十二指肠有多个黏膜下息肉样脂肪病变（密度均匀），回肠有一个小的类似病变。
结论
该病例表明胃肠道脂肪瘤病可表现为FML。
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