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Non-human immunodeficiency virus-related Kaposi’s sarcoma of the oropharynx: a case report and review of the literature

INTRODUCTION: Kaposi’s sarcoma is a malignant, slowly progressing, mesenchymal neoplasm characterized by a proliferation of connective tissue and capillaries. Clinical presentation is usually as nodules and red-purple plaques. This case report not only represents an uncommon presentation of Kaposi’s...

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Autores principales: Crosetti, Erika, Succo, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3892013/
https://www.ncbi.nlm.nih.gov/pubmed/24378063
http://dx.doi.org/10.1186/1752-1947-7-293
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author Crosetti, Erika
Succo, Giovanni
author_facet Crosetti, Erika
Succo, Giovanni
author_sort Crosetti, Erika
collection PubMed
description INTRODUCTION: Kaposi’s sarcoma is a malignant, slowly progressing, mesenchymal neoplasm characterized by a proliferation of connective tissue and capillaries. Clinical presentation is usually as nodules and red-purple plaques. This case report not only represents an uncommon presentation of Kaposi’s sarcoma in a non-immunocompromised patient, but also supports the role of viral infection in the pathogenesis of this disease. It provides some interesting information about this rare disease, particularly in patients who are human immunodeficiency virus negative. CASE PRESENTATION: A 48-year-old Caucasian man presented with a sensation of a foreign body in his throat, accompanied by stomatolalia. Maxillofacial and neck magnetic resonance imaging confirmed the presence of a voluminous solid mass at the base of his tongue with oropharyngeal space reduction. Histological analysis indicated that the lesion was compatible with ulcerated Kaposi’s sarcoma of the oropharynx. Results of serological tests for human immunodeficiency virus infection were negative as was the result of the human herpesvirus-8 test, but the cytomegalovirus test result was positive. CONCLUSIONS: This case is unusual because the patient had only oropharyngeal localization of disease, without evidence of immunosuppression or the typical background or risk factors suggesting the classic or endemic form of Kaposi’s sarcoma. Isolated cases of Kaposi’s sarcoma with oropharyngeal manifestations not associated with human immunodeficiency virus infection are rare, and only 15 cases have been reported to date. At present, its localization, microscopic and histological characteristics, and patterns of progression are the main tools used for differential diagnosis of Kaposi’s sarcoma from other vascular neoplasms.
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spelling pubmed-38920132014-01-15 Non-human immunodeficiency virus-related Kaposi’s sarcoma of the oropharynx: a case report and review of the literature Crosetti, Erika Succo, Giovanni J Med Case Rep Case Report INTRODUCTION: Kaposi’s sarcoma is a malignant, slowly progressing, mesenchymal neoplasm characterized by a proliferation of connective tissue and capillaries. Clinical presentation is usually as nodules and red-purple plaques. This case report not only represents an uncommon presentation of Kaposi’s sarcoma in a non-immunocompromised patient, but also supports the role of viral infection in the pathogenesis of this disease. It provides some interesting information about this rare disease, particularly in patients who are human immunodeficiency virus negative. CASE PRESENTATION: A 48-year-old Caucasian man presented with a sensation of a foreign body in his throat, accompanied by stomatolalia. Maxillofacial and neck magnetic resonance imaging confirmed the presence of a voluminous solid mass at the base of his tongue with oropharyngeal space reduction. Histological analysis indicated that the lesion was compatible with ulcerated Kaposi’s sarcoma of the oropharynx. Results of serological tests for human immunodeficiency virus infection were negative as was the result of the human herpesvirus-8 test, but the cytomegalovirus test result was positive. CONCLUSIONS: This case is unusual because the patient had only oropharyngeal localization of disease, without evidence of immunosuppression or the typical background or risk factors suggesting the classic or endemic form of Kaposi’s sarcoma. Isolated cases of Kaposi’s sarcoma with oropharyngeal manifestations not associated with human immunodeficiency virus infection are rare, and only 15 cases have been reported to date. At present, its localization, microscopic and histological characteristics, and patterns of progression are the main tools used for differential diagnosis of Kaposi’s sarcoma from other vascular neoplasms. BioMed Central 2013-12-31 /pmc/articles/PMC3892013/ /pubmed/24378063 http://dx.doi.org/10.1186/1752-1947-7-293 Text en Copyright © 2013 Crosetti and Succo; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Crosetti, Erika
Succo, Giovanni
Non-human immunodeficiency virus-related Kaposi’s sarcoma of the oropharynx: a case report and review of the literature
title Non-human immunodeficiency virus-related Kaposi’s sarcoma of the oropharynx: a case report and review of the literature
title_full Non-human immunodeficiency virus-related Kaposi’s sarcoma of the oropharynx: a case report and review of the literature
title_fullStr Non-human immunodeficiency virus-related Kaposi’s sarcoma of the oropharynx: a case report and review of the literature
title_full_unstemmed Non-human immunodeficiency virus-related Kaposi’s sarcoma of the oropharynx: a case report and review of the literature
title_short Non-human immunodeficiency virus-related Kaposi’s sarcoma of the oropharynx: a case report and review of the literature
title_sort non-human immunodeficiency virus-related kaposi’s sarcoma of the oropharynx: a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3892013/
https://www.ncbi.nlm.nih.gov/pubmed/24378063
http://dx.doi.org/10.1186/1752-1947-7-293
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