Chitambar Shobha D, Fadnis Rahul S, Joshi Madhuri S, Habbu A, Bhatia S G
National Institute of Virology, Pune, Maharashtra, India.
J Med Virol. 2006 Aug;78(8):1011-4. doi: 10.1002/jmv.20656.
A case of acute hepatitis A with Guillain-Barré Syndrome subtype AMAN (acute motor axonal neuropathy) in a 17-year-old male is reported. Serum and cerebrospinal fluid were positive for anti-hepatitis A virus (HAV) IgM, IgG, and IgA. The onset of the syndrome was evident in week 3 of illness. The remarkably high titers of serum anti-HAV IgG appeared unique to a hepatitis A patient with the syndrome. Phylogenetic analysis of the HAV genome detected in the serum and feces revealed genotype IIIA, circulating commonly in Pune, western India.
报告了一例17岁男性患急性甲型肝炎合并格林-巴利综合征亚型AMAN(急性运动轴索性神经病)的病例。血清和脑脊液中的抗甲型肝炎病毒(HAV)IgM、IgG和IgA呈阳性。该综合征在发病第3周明显出现。血清抗HAV IgG的高滴度在患有该综合征的甲型肝炎患者中显得独特。对血清和粪便中检测到的HAV基因组进行系统发育分析,发现为IIIA基因型,在印度西部浦那普遍流行。