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Case Reports
. 2006 Sep;44(9):3452-6.
doi: 10.1128/JCM.00721-06.

Diagnosis of gastric syphilis by direct immunofluorescence staining and real-time PCR testing

Affiliations
Case Reports

Diagnosis of gastric syphilis by direct immunofluorescence staining and real-time PCR testing

Cheng-Yen Chen et al. J Clin Microbiol. 2006 Sep.

Abstract

We report on a case of gastric syphilis in a patient with chronic dyspepsia. The diagnosis was established by serology and the demonstration of spirochetes in diffusely inflammed gastric mucosa by staining with a fluorescent monoclonal antibody specific for pathogenic treponemes and by the detection of specific treponemal DNA sequences by a real-time PCR.

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Figures

FIG. 1.
FIG. 1.
Gastric syphilis: histopathology of the stomach antrum. The mucosal glandular architecture is erased by a dense and diffuse lymphoplasmacytic infiltrate. Only residual glands with luminal neutrophilic infiltrates are seen. Inflammatory spillover is present in the submucosa. (Hematoxylin and eosin stain was used. Magnification, ×400.)
FIG. 2.
FIG. 2.
Specific immunofluorescence staining of pathogenic treponemes with monoclonal antibody. The FITC-labeled mouse antitreponemal 37-kDa monoclonal antibody stain demonstrates numerous spirochetes in thin-section specimens by the use of a ×100 oil objective and a ×10 ocular. Filter cubes B-2A and B-2C/E were used in photographs A and B, respectively.
FIG. 3.
FIG. 3.
Detection of pathogenic treponeme-specific DNA from paraffin-embedded thin sections by the real-time PCR. Amplification results of real-time simplex PCR specific for T. pallidum DNA detection are shown. (A) FAM-labeled TaqMan probed targeting polA; (B) ROX-labeled TaqMan probed targeting the 47-kDa lipoprotein gene.

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References

    1. Antal, G. M., S. A. Lukehart, and A. Z. Meheus. 2002. The endemic treponematoses. Microbes Infect. 4:83-94. - PubMed
    1. Guerrero, A. F., T. M. Straight, J. Eastone, and K. Spooner. 2005. Gastric syphilis in an HIV-infected patient. AIDS Patient Care STDs 19:281-285. - PubMed
    1. Ikebe, M., T. Oiwa, M. Mori, H. Kuwan, K. Sugimachi, and T. Yao. 1994. Gastric syphilis: case report and review of the literature. Radiat. Med. 12:171-175. - PubMed
    1. Inagaki, H., T. kawai, M. Miyata, S. Nagaya, H. Tateyama, and T. Eimoto. 1996. Gastric syphilis: polymerase chain reaction detection of treponemal DNA in pseudolymphomatous lesions. Hum. Pathol. 27:761-765. - PubMed
    1. Ito, F., E. F. Hunter, R. W. George, V. Pope, and S. A. Larsen. 1992. Specific immunofluorescent staining of pathogenic treponemes with a monoclonal antibody. J. Clin. Microbiol. 30:831-838. - PMC - PubMed

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