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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2019
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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. |
format | Online Article Text |
id | pubmed-6601505 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
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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