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Molecular and Clinical Oncology
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Print ISSN: 2049-9450 Online ISSN: 2049-9469
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Experimental and Therapeutic Medicine is an international journal devoted to laboratory and clinical medicine.

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Case Report Open Access

Schwannoma of the vagina - a common tumor but a rare location: A case report

  • Authors:
    • Xin An
    • Meng Zhu
    • Ning Zhang
    • Sanjun Lu
    • Pin Wei
    • Linna Jiang
    • Xueli Yang
  • View Affiliations / Copyright

    Affiliations: Department of Pathology, Handan First Hospital, Handan, Hebei 056002, P.R. China, Department of Gastroenterology, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi 710061, P.R. China, Department of Pathology, General Hospital of Ningxia Medical University, Yinchuan, Ningxia 750004, P.R. China
    Copyright: © An et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 783-786
    |
    Published online on: September 19, 2017
       https://doi.org/10.3892/mco.2017.1420
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Abstract

Schwannomas are nerve sheath tumors arising from Schwann cells. These tumors usually present as benign, relatively slow-growing, solitary, encapsulated, painless masses. Schwannomas rarely occur in the vagina, and have not been fully recognized as gynecological tumors. We herein describe the case of a patient who presented with a schwannoma occurring in the wall of vagina, with non-specific symptoms lasting for ~1 year. The vaginal mass was incidentally detected during a sonographic examination and the patient was referred for surgical resection. The surgery was uncomplicated and the vaginal tumor was diagnosed as benign schwannoma. The immunohistochemical examination revealed positivity for vimentin, S-100 and glial fibrillary acidic protein, whereas discovered on GIST-1, CD117, CD34, desmin, smooth muscle actin and cytokeratin were negative. Tumors occurring in the vagina are common and are of variable histological types, with a wide range of pathological characteristics and complications. Schwannoma should be considered in the differential diagnosis in patients presenting with atypical symptoms from the gynecological tract. Immunohistochemical staining is required for confirmation of the diagnosis of schwannoma, and for distinguishing this entity from other homologous tumors.
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Copy and paste a formatted citation
Spandidos Publications style
An X, Zhu M, Zhang N, Lu S, Wei P, Jiang L and Yang X: Schwannoma of the vagina - a common tumor but a rare location: A case report. Mol Clin Oncol 7: 783-786, 2017.
APA
An, X., Zhu, M., Zhang, N., Lu, S., Wei, P., Jiang, L., & Yang, X. (2017). Schwannoma of the vagina - a common tumor but a rare location: A case report. Molecular and Clinical Oncology, 7, 783-786. https://doi.org/10.3892/mco.2017.1420
MLA
An, X., Zhu, M., Zhang, N., Lu, S., Wei, P., Jiang, L., Yang, X."Schwannoma of the vagina - a common tumor but a rare location: A case report". Molecular and Clinical Oncology 7.5 (2017): 783-786.
Chicago
An, X., Zhu, M., Zhang, N., Lu, S., Wei, P., Jiang, L., Yang, X."Schwannoma of the vagina - a common tumor but a rare location: A case report". Molecular and Clinical Oncology 7, no. 5 (2017): 783-786. https://doi.org/10.3892/mco.2017.1420
Copy and paste a formatted citation
x
Spandidos Publications style
An X, Zhu M, Zhang N, Lu S, Wei P, Jiang L and Yang X: Schwannoma of the vagina - a common tumor but a rare location: A case report. Mol Clin Oncol 7: 783-786, 2017.
APA
An, X., Zhu, M., Zhang, N., Lu, S., Wei, P., Jiang, L., & Yang, X. (2017). Schwannoma of the vagina - a common tumor but a rare location: A case report. Molecular and Clinical Oncology, 7, 783-786. https://doi.org/10.3892/mco.2017.1420
MLA
An, X., Zhu, M., Zhang, N., Lu, S., Wei, P., Jiang, L., Yang, X."Schwannoma of the vagina - a common tumor but a rare location: A case report". Molecular and Clinical Oncology 7.5 (2017): 783-786.
Chicago
An, X., Zhu, M., Zhang, N., Lu, S., Wei, P., Jiang, L., Yang, X."Schwannoma of the vagina - a common tumor but a rare location: A case report". Molecular and Clinical Oncology 7, no. 5 (2017): 783-786. https://doi.org/10.3892/mco.2017.1420
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