Renom G, Maisonneuve N, Kim I, Dehon B, Azar R
Laboratoire de Biochimie et de Biologie Moléculaire, Hôpital Huriez, Lille, France.
Ann Clin Biochem. 2003 Jul;40(Pt 4):424-6. doi: 10.1258/000456303766477110.
A new case of alcoholic ketoacidosis (AKA) is presented because of unusual clinical and biochemical features. Although it shares some similarities with typical cases of AKA, it appears as unique because of predominantly neurological, rather than abdominal symptoms, major ketogenesis with normal ketone body ratio, the presence of large amounts of propanediol and the absence of an osmolar gap.
本文报告了一例酒精性酮症酸中毒(AKA)新病例,因其具有不寻常的临床和生化特征。尽管它与典型的AKA病例有一些相似之处,但由于主要表现为神经症状而非腹部症状、酮体生成主要但酮体比例正常、存在大量丙二醇且无渗透压间隙,故而显得独特。