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Rare glomus tumor formation following trauma to the first digit

INTRODUCTION: Glomus tumors are rare and few cases are reported in the literature. They typically occur in females on the digits of the hands. CASE PRESENTATION: We report a case of a 30 year-old woman who presented with a mass that developed on the distal tip of her right thumb after traumatic inju...

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Autores principales: Saba, Mohammad, Moser, Austin, Rosenberg, Joshua, Qiao, Jian-Hua, Chen, Gary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8387767/
https://www.ncbi.nlm.nih.gov/pubmed/34425425
http://dx.doi.org/10.1016/j.ijscr.2021.106324
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author Saba, Mohammad
Moser, Austin
Rosenberg, Joshua
Qiao, Jian-Hua
Chen, Gary
author_facet Saba, Mohammad
Moser, Austin
Rosenberg, Joshua
Qiao, Jian-Hua
Chen, Gary
author_sort Saba, Mohammad
collection PubMed
description INTRODUCTION: Glomus tumors are rare and few cases are reported in the literature. They typically occur in females on the digits of the hands. CASE PRESENTATION: We report a case of a 30 year-old woman who presented with a mass that developed on the distal tip of her right thumb after traumatic injury. Magnetic resonance imaging (MRI) was conducted and mass resection was performed. Histopathology confirmed that the mass was a glomus tumor. CLINICAL DISCUSSION: Clinical presentations of glomus tumors are typically non-specific, mainly consisting of a small mass with chronic pain, with a lengthy time to diagnosis and potentially improper management. MRI is the preferred diagnostic step, followed by curative surgical excision and pathological confirmation. CONCLUSION: Glomus tumors can cause significant discomfort for patients, and clinicians should be aware of the rare diagnosis when treating painful masses on the extremities, as surgical excision is often curative.
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spelling pubmed-83877672021-08-31 Rare glomus tumor formation following trauma to the first digit Saba, Mohammad Moser, Austin Rosenberg, Joshua Qiao, Jian-Hua Chen, Gary Int J Surg Case Rep Case Report INTRODUCTION: Glomus tumors are rare and few cases are reported in the literature. They typically occur in females on the digits of the hands. CASE PRESENTATION: We report a case of a 30 year-old woman who presented with a mass that developed on the distal tip of her right thumb after traumatic injury. Magnetic resonance imaging (MRI) was conducted and mass resection was performed. Histopathology confirmed that the mass was a glomus tumor. CLINICAL DISCUSSION: Clinical presentations of glomus tumors are typically non-specific, mainly consisting of a small mass with chronic pain, with a lengthy time to diagnosis and potentially improper management. MRI is the preferred diagnostic step, followed by curative surgical excision and pathological confirmation. CONCLUSION: Glomus tumors can cause significant discomfort for patients, and clinicians should be aware of the rare diagnosis when treating painful masses on the extremities, as surgical excision is often curative. Elsevier 2021-08-19 /pmc/articles/PMC8387767/ /pubmed/34425425 http://dx.doi.org/10.1016/j.ijscr.2021.106324 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Saba, Mohammad
Moser, Austin
Rosenberg, Joshua
Qiao, Jian-Hua
Chen, Gary
Rare glomus tumor formation following trauma to the first digit
title Rare glomus tumor formation following trauma to the first digit
title_full Rare glomus tumor formation following trauma to the first digit
title_fullStr Rare glomus tumor formation following trauma to the first digit
title_full_unstemmed Rare glomus tumor formation following trauma to the first digit
title_short Rare glomus tumor formation following trauma to the first digit
title_sort rare glomus tumor formation following trauma to the first digit
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8387767/
https://www.ncbi.nlm.nih.gov/pubmed/34425425
http://dx.doi.org/10.1016/j.ijscr.2021.106324
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