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Melanotic Schwannoma of the Vagina: A Report of a Very Rare Tumor and Review of the Literature

Melanotic schwannoma (MS) is a rare nerve sheath tumor with fewer than 200 cases reported. MS has uncertain malignant potential and comprises 1% of all nerve sheath tumors with a predilection for the spinal nerve roots. An even rarer location for this tumor is the vagina. Up to 55% of MSs that conta...

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Autores principales: Effah, Kofi, Seidl, Stefan, Gorges, Edith, Akakpo, Patrick Kafui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6601505/
https://www.ncbi.nlm.nih.gov/pubmed/31316847
http://dx.doi.org/10.1155/2019/8521834
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author Effah, Kofi
Seidl, Stefan
Gorges, Edith
Akakpo, Patrick Kafui
author_facet Effah, Kofi
Seidl, Stefan
Gorges, Edith
Akakpo, Patrick Kafui
author_sort Effah, Kofi
collection PubMed
description Melanotic schwannoma (MS) is a rare nerve sheath tumor with fewer than 200 cases reported. MS has uncertain malignant potential and comprises 1% of all nerve sheath tumors with a predilection for the spinal nerve roots. An even rarer location for this tumor is the vagina. Up to 55% of MSs that contain psammoma bodies are associated with the Carney complex, an autosomal dominant syndrome. Criteria for malignancy in MS are still not well established and long term follow-up of patients is recommended. A 26-year-old woman presented with a bleeding vaginal tumor which was diagnosed as MS following excision. The clinical, histopathological, and immunohistochemical features of this tumor are discussed.
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spelling pubmed-66015052019-07-17 Melanotic Schwannoma of the Vagina: A Report of a Very Rare Tumor and Review of the Literature Effah, Kofi Seidl, Stefan Gorges, Edith Akakpo, Patrick Kafui Case Rep Obstet Gynecol Case Report Melanotic schwannoma (MS) is a rare nerve sheath tumor with fewer than 200 cases reported. MS has uncertain malignant potential and comprises 1% of all nerve sheath tumors with a predilection for the spinal nerve roots. An even rarer location for this tumor is the vagina. Up to 55% of MSs that contain psammoma bodies are associated with the Carney complex, an autosomal dominant syndrome. Criteria for malignancy in MS are still not well established and long term follow-up of patients is recommended. A 26-year-old woman presented with a bleeding vaginal tumor which was diagnosed as MS following excision. The clinical, histopathological, and immunohistochemical features of this tumor are discussed. Hindawi 2019-06-17 /pmc/articles/PMC6601505/ /pubmed/31316847 http://dx.doi.org/10.1155/2019/8521834 Text en Copyright © 2019 Kofi Effah et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Effah, Kofi
Seidl, Stefan
Gorges, Edith
Akakpo, Patrick Kafui
Melanotic Schwannoma of the Vagina: A Report of a Very Rare Tumor and Review of the Literature
title Melanotic Schwannoma of the Vagina: A Report of a Very Rare Tumor and Review of the Literature
title_full Melanotic Schwannoma of the Vagina: A Report of a Very Rare Tumor and Review of the Literature
title_fullStr Melanotic Schwannoma of the Vagina: A Report of a Very Rare Tumor and Review of the Literature
title_full_unstemmed Melanotic Schwannoma of the Vagina: A Report of a Very Rare Tumor and Review of the Literature
title_short Melanotic Schwannoma of the Vagina: A Report of a Very Rare Tumor and Review of the Literature
title_sort melanotic schwannoma of the vagina: a report of a very rare tumor and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6601505/
https://www.ncbi.nlm.nih.gov/pubmed/31316847
http://dx.doi.org/10.1155/2019/8521834
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