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Case Reports
. 2009 Sep 22;3(3):293-299.
doi: 10.1159/000237736.

Schwannoma of the Colon

Affiliations
Case Reports

Schwannoma of the Colon

Ronaldo Nonose et al. Case Rep Gastroenterol. .

Abstract

Schwannomas are neoplasms originating from Schwann cells, which are the cells forming nerve sheaths. These neoplasms generally involve peripheral nerves. They rarely affect the gastrointestinal tract and primary colon involvement is extremely rare. The objective of the present paper was to present a case of primary schwannoma of the sigmoid colon, unassociated with von Recklinghausen disease, that was histopathologically confirmed by means of an immunohistochemical panel. The patient was a 71-year-old woman who had had rectal bleeding when evacuating, with pain and tenesmus, for 4 months. She underwent colonoscopy, which identified a raised submucous lesion of 2.8 cm in diameter, located in the sigmoid colon, 30 cm from the anal margin. During examination, loop polypectomy with lesion excision was performed. Histopathological evaluation showed that this was a tumor of stromal origin. Its resection margins were compromised by neoplasia, and colon resection by means of videolaparoscopy was indicated. Conventional histopathological examination using the hematoxylin-eosin technique suggested that the neoplasm was of mesenchymal origin. An immunohistochemical panel was run for etiological confirmation, using anti-CD34 antibodies, desmin, cytokeratins (AE1/AE3), cKit, chromogranin and S-100 protein. The panel showed intense immunoexpression of S-100 protein. Investigation of the proliferative activity rate using Ki-67 antibodies showed that there was a low rate of mitotic activity, thus confirming the diagnosis of primary benign schwannoma of the colon. The patient's postoperative evolution was uneventful and she remains in good health, without signs of tumor recurrence, 15 months after surgical excision.

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Figures

Fig. 1
Fig. 1
Schwannoma of the sigmoid colon with histological pattern of Antoni A type (hematoxylin-eosin, 100×).
Fig. 2
Fig. 2
Strongly positive immunoexpression of S-100 protein (immunohistochemistry, 100×).
Fig. 3
Fig. 3
Positive immunoexpression of the Ki-67 nuclear proliferation factor in fewer than 5% of the fields studied (immunohistochemistry, 100×).

References

    1. Fotiadis CI, Kouerinis IA, Papandreou I, Zografos GC, Agapitos G. Sigmoid schwannoma: a rare case. World J Gastroenterol. 2005;11:5079–5081. - PMC - PubMed
    1. Daimaru Y, Kido H, Hashimoto H, Enjoji M. Benign schwannoma of the gastrointestinal tract: a clinicopathologic immunohistochemical study. Hum Pathol. 1988;19:257–264. - PubMed
    1. Sugimura H, Tamura S, Yamada H, Kusumoto S, Watanabe K, Hayashi T, Sumiyoshi A. Benign nerve sheath tumor of the sigmoid colon. Clin Imaging. 1993;17:64–66. - PubMed
    1. Miettinen M, Shekitka KM, Sobin LH. Schwannomas in the colon and rectum. A clinicopathologic and immunohistochemical study of 20 cases. Am J Surg Pathol. 2001;25:846–855. - PubMed
    1. Maciejewski A, Lange D, Wloch J. Case report of schwannoma of the rectum - clinical and pathological contribution. Med Sci Monit. 2000;6:779–782. - PubMed

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