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Clinical, histopathological and immunohistochemical features of glomus tumor of the nail bed
Purpose: Glomus tumors account for 1–4% of benign hand tumors. In 65% of cases, it is located in the nail bed. Its rarity makes misdiagnosis problems relatively common. Symptomatology is characterized by the hallmark symptomatic triad. Imaging investigations may guide the diagnosis, but the diagnosi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8597357/ https://www.ncbi.nlm.nih.gov/pubmed/34609426 http://dx.doi.org/10.47162/RJME.62.1.23 |
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author | Perţea, Mihaela Poroch, Vladimir Velenciuc, Natalia Mitrea, Mihaela Luncă, Sorinel Terinte, Cristina Filip, Alexandru Alexa, Ovidiu Veliceasa, Bogdan |
author_facet | Perţea, Mihaela Poroch, Vladimir Velenciuc, Natalia Mitrea, Mihaela Luncă, Sorinel Terinte, Cristina Filip, Alexandru Alexa, Ovidiu Veliceasa, Bogdan |
author_sort | Perţea, Mihaela |
collection | PubMed |
description | Purpose: Glomus tumors account for 1–4% of benign hand tumors. In 65% of cases, it is located in the nail bed. Its rarity makes misdiagnosis problems relatively common. Symptomatology is characterized by the hallmark symptomatic triad. Imaging investigations may guide the diagnosis, but the diagnosis is made by pathological examination doubled by immunohistochemical (IHC) markers. Patients, Materials and Methods: We studied a group of seven female patients, aged 28 to 56 years. Clinical examination revealed the presence of the characteristic symptomatic triad. Ultrasound imaging tests were performed. Results: Anatomopathological examination made a diagnosis of glomus tumor in all seven cases. IHC staining showed that tumor cells were positive for alpha-smooth muscle actin (α-SMA) and h-caldesmon in all seven cases and negative for cluster of differentiation 34 (CD34) in 72.14%. IHC stainings for p63, S100, cytokeratin (CK) AE1/AE3 were negative in all cases. The clinical diagnosis completed by ultrasonography was histopathologically confirmed in all cases. Conclusions: Although the glomus tumor is a rare lesion, we need to be familiar with it because a diagnostic delay also implies a treatment delay which will lead to amplified suffering and even real disability due to the high-intensity pain in these cases. |
format | Online Article Text |
id | pubmed-8597357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest |
record_format | MEDLINE/PubMed |
spelling | pubmed-85973572021-12-01 Clinical, histopathological and immunohistochemical features of glomus tumor of the nail bed Perţea, Mihaela Poroch, Vladimir Velenciuc, Natalia Mitrea, Mihaela Luncă, Sorinel Terinte, Cristina Filip, Alexandru Alexa, Ovidiu Veliceasa, Bogdan Rom J Morphol Embryol Original Paper Purpose: Glomus tumors account for 1–4% of benign hand tumors. In 65% of cases, it is located in the nail bed. Its rarity makes misdiagnosis problems relatively common. Symptomatology is characterized by the hallmark symptomatic triad. Imaging investigations may guide the diagnosis, but the diagnosis is made by pathological examination doubled by immunohistochemical (IHC) markers. Patients, Materials and Methods: We studied a group of seven female patients, aged 28 to 56 years. Clinical examination revealed the presence of the characteristic symptomatic triad. Ultrasound imaging tests were performed. Results: Anatomopathological examination made a diagnosis of glomus tumor in all seven cases. IHC staining showed that tumor cells were positive for alpha-smooth muscle actin (α-SMA) and h-caldesmon in all seven cases and negative for cluster of differentiation 34 (CD34) in 72.14%. IHC stainings for p63, S100, cytokeratin (CK) AE1/AE3 were negative in all cases. The clinical diagnosis completed by ultrasonography was histopathologically confirmed in all cases. Conclusions: Although the glomus tumor is a rare lesion, we need to be familiar with it because a diagnostic delay also implies a treatment delay which will lead to amplified suffering and even real disability due to the high-intensity pain in these cases. Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest 2021 2021-09-24 /pmc/articles/PMC8597357/ /pubmed/34609426 http://dx.doi.org/10.47162/RJME.62.1.23 Text en Copyright © 2020, Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Public License, which permits unrestricted use, adaptation, distribution and reproduction in any medium, non-commercially, provided the new creations are licensed under identical terms as the original work and the original work is properly cited. |
spellingShingle | Original Paper Perţea, Mihaela Poroch, Vladimir Velenciuc, Natalia Mitrea, Mihaela Luncă, Sorinel Terinte, Cristina Filip, Alexandru Alexa, Ovidiu Veliceasa, Bogdan Clinical, histopathological and immunohistochemical features of glomus tumor of the nail bed |
title | Clinical, histopathological and immunohistochemical features of glomus tumor of the nail bed |
title_full | Clinical, histopathological and immunohistochemical features of glomus tumor of the nail bed |
title_fullStr | Clinical, histopathological and immunohistochemical features of glomus tumor of the nail bed |
title_full_unstemmed | Clinical, histopathological and immunohistochemical features of glomus tumor of the nail bed |
title_short | Clinical, histopathological and immunohistochemical features of glomus tumor of the nail bed |
title_sort | clinical, histopathological and immunohistochemical features of glomus tumor of the nail bed |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8597357/ https://www.ncbi.nlm.nih.gov/pubmed/34609426 http://dx.doi.org/10.47162/RJME.62.1.23 |
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