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聚合酶链反应扩增技术在疱疹病毒感染诊断中的临床应用。

Clinical application of polymerase chain reaction amplification to diagnosis of herpes virus infection.

作者信息

Thomas C A, Smith S E, Morgan T M, White W L, Feldman S R

机构信息

Department of Dermatology, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, North Carolina.

出版信息

Am J Dermatopathol. 1994 Jun;16(3):268-74. doi: 10.1097/00000372-199406000-00007.

Abstract

Amplification of viral DNA offers a potentially sensitive and specific method for identifying herpes viruses in pathologic specimens. The purpose of this study is to assess the value of polymerase chain reaction amplification of DNA as a diagnostic test for herpes virus in pathologic specimens. The purpose of this study is to assess for herpes virus infections. We examined 79 paraffin-embedded tissue samples from 43 patients and 55 viral culture samples from 45 patients. Herpes virus DNA in the specimens was amplified by polymerase chain reaction. Using paraffin-embedded tissue on which a diagnosis of herpes virus was made by morphologic criteria, 11 of 19 patients had herpes virus DNA identified by PCR; herpes virus DNA was not identified in any of 35 negative control specimens. Herpes virus DNA was also identified by polymerase chain reaction in all of the positive herpes virus culture specimens. Of 29 culture negative specimens, herpes virus DNA was identified in six. We conclude that polymerase chain reaction is useful to establish or confirm the presence of a herpes virus infection in paraffin-embedded tissue samples and that it is more sensitive than viral culture.

摘要

病毒DNA扩增为在病理标本中鉴定疱疹病毒提供了一种潜在的敏感且特异的方法。本研究的目的是评估DNA聚合酶链反应扩增作为病理标本中疱疹病毒诊断检测方法的价值。本研究的目的是评估疱疹病毒感染情况。我们检查了来自43例患者的79份石蜡包埋组织样本和来自45例患者的55份病毒培养样本。通过聚合酶链反应扩增标本中的疱疹病毒DNA。在通过形态学标准诊断为疱疹病毒感染的石蜡包埋组织上,19例患者中有11例通过PCR鉴定出疱疹病毒DNA;在35份阴性对照标本中均未鉴定出疱疹病毒DNA。在所有疱疹病毒培养阳性的标本中也通过聚合酶链反应鉴定出了疱疹病毒DNA。在29份培养阴性的标本中,有6份鉴定出了疱疹病毒DNA。我们得出结论,聚合酶链反应对于确定或证实石蜡包埋组织样本中疱疹病毒感染的存在是有用的,并且它比病毒培养更敏感。

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