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Schwannoma of the Lateral Femoral Cutaneous Nerve, an Unusual Cause of Meralgia Paresthetica: A Case Report

INTRODUCTION: Meralgia paresthetica (MP) is a clinical syndrome usually resulting usually from compression of the lateral femoral cutaneous nerve (LFCN). Tumors arising from this nerve could also be the cause of this syndrome. CASE REPORT: We present an unusual cause of MP in a 67-year-old Caucasian...

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Autores principales: Makris, Anastasios P., Makris, Dimitrios
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933639/
https://www.ncbi.nlm.nih.gov/pubmed/33708718
http://dx.doi.org/10.13107/jocr.2020.v10.i08.1870
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author Makris, Anastasios P.
Makris, Dimitrios
author_facet Makris, Anastasios P.
Makris, Dimitrios
author_sort Makris, Anastasios P.
collection PubMed
description INTRODUCTION: Meralgia paresthetica (MP) is a clinical syndrome usually resulting usually from compression of the lateral femoral cutaneous nerve (LFCN). Tumors arising from this nerve could also be the cause of this syndrome. CASE REPORT: We present an unusual cause of MP in a 67-year-old Caucasian male. The cause of the syndrome appeared to be a schwannoma tumor of the LFCN. Such a cause of MP has not been reported previously in the literature. CONCLUSION: Medical practitioners should also consider other causes of MP syndrome, such as peripheral nerve tumors. Although diagnosis is considered to be clinical, ultrasound or magnetic resonance imaging (MRI) could be helpful to establish the diagnosis.
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spelling pubmed-79336392021-03-10 Schwannoma of the Lateral Femoral Cutaneous Nerve, an Unusual Cause of Meralgia Paresthetica: A Case Report Makris, Anastasios P. Makris, Dimitrios J Orthop Case Rep Case Report INTRODUCTION: Meralgia paresthetica (MP) is a clinical syndrome usually resulting usually from compression of the lateral femoral cutaneous nerve (LFCN). Tumors arising from this nerve could also be the cause of this syndrome. CASE REPORT: We present an unusual cause of MP in a 67-year-old Caucasian male. The cause of the syndrome appeared to be a schwannoma tumor of the LFCN. Such a cause of MP has not been reported previously in the literature. CONCLUSION: Medical practitioners should also consider other causes of MP syndrome, such as peripheral nerve tumors. Although diagnosis is considered to be clinical, ultrasound or magnetic resonance imaging (MRI) could be helpful to establish the diagnosis. Indian Orthopaedic Research Group 2020-11 /pmc/articles/PMC7933639/ /pubmed/33708718 http://dx.doi.org/10.13107/jocr.2020.v10.i08.1870 Text en Copyright: © Indian Orthopaedic Research Group http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Makris, Anastasios P.
Makris, Dimitrios
Schwannoma of the Lateral Femoral Cutaneous Nerve, an Unusual Cause of Meralgia Paresthetica: A Case Report
title Schwannoma of the Lateral Femoral Cutaneous Nerve, an Unusual Cause of Meralgia Paresthetica: A Case Report
title_full Schwannoma of the Lateral Femoral Cutaneous Nerve, an Unusual Cause of Meralgia Paresthetica: A Case Report
title_fullStr Schwannoma of the Lateral Femoral Cutaneous Nerve, an Unusual Cause of Meralgia Paresthetica: A Case Report
title_full_unstemmed Schwannoma of the Lateral Femoral Cutaneous Nerve, an Unusual Cause of Meralgia Paresthetica: A Case Report
title_short Schwannoma of the Lateral Femoral Cutaneous Nerve, an Unusual Cause of Meralgia Paresthetica: A Case Report
title_sort schwannoma of the lateral femoral cutaneous nerve, an unusual cause of meralgia paresthetica: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7933639/
https://www.ncbi.nlm.nih.gov/pubmed/33708718
http://dx.doi.org/10.13107/jocr.2020.v10.i08.1870
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