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Fibrolipomatous Hamartoma of Median Nerve – A Diagnostic Challenge

INTRODUCTION: Fibrolipomatous hamartoma (FLH) is an uncommon slow-growing tumor of benign etiology, which predominantly affects the median nerve. CASE REPORT: We report the case study of a 17-year-old male patient, who presented with complaints of a gradually increasing localized swelling over the v...

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Autores principales: Rai, Vikrant, Sabhikhi, G S, Sircar, Pankaj, Kumar, Dev, Kundra, Rohit, Jeyaraman, Madhan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8930339/
https://www.ncbi.nlm.nih.gov/pubmed/35415127
http://dx.doi.org/10.13107/jocr.2021.v11.i11.2520
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author Rai, Vikrant
Sabhikhi, G S
Sircar, Pankaj
Kumar, Dev
Kundra, Rohit
Jeyaraman, Madhan
author_facet Rai, Vikrant
Sabhikhi, G S
Sircar, Pankaj
Kumar, Dev
Kundra, Rohit
Jeyaraman, Madhan
author_sort Rai, Vikrant
collection PubMed
description INTRODUCTION: Fibrolipomatous hamartoma (FLH) is an uncommon slow-growing tumor of benign etiology, which predominantly affects the median nerve. CASE REPORT: We report the case study of a 17-year-old male patient, who presented with complaints of a gradually increasing localized swelling over the volar aspect of left hand for 1 year. A contrast-enhanced Magnetic resonance (MR) scan of the left hand was performed which demonstrated characteristic findings. The patient was treated surgically and post-excision histopathological examination confirmed the diagnosis. CONCLUSION: The characteristic MR imaging features of coaxial cable-like appearance on axial section or spaghetti shaped enlarged nerve fascicles and fibrous tissue is confirmatory for a definitive diagnosis of FLH, which alleviates the need for any unnecessary biopsy.
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spelling pubmed-89303392022-04-11 Fibrolipomatous Hamartoma of Median Nerve – A Diagnostic Challenge Rai, Vikrant Sabhikhi, G S Sircar, Pankaj Kumar, Dev Kundra, Rohit Jeyaraman, Madhan J Orthop Case Rep Case Report INTRODUCTION: Fibrolipomatous hamartoma (FLH) is an uncommon slow-growing tumor of benign etiology, which predominantly affects the median nerve. CASE REPORT: We report the case study of a 17-year-old male patient, who presented with complaints of a gradually increasing localized swelling over the volar aspect of left hand for 1 year. A contrast-enhanced Magnetic resonance (MR) scan of the left hand was performed which demonstrated characteristic findings. The patient was treated surgically and post-excision histopathological examination confirmed the diagnosis. CONCLUSION: The characteristic MR imaging features of coaxial cable-like appearance on axial section or spaghetti shaped enlarged nerve fascicles and fibrous tissue is confirmatory for a definitive diagnosis of FLH, which alleviates the need for any unnecessary biopsy. Indian Orthopaedic Research Group 2021-11 2021-11 /pmc/articles/PMC8930339/ /pubmed/35415127 http://dx.doi.org/10.13107/jocr.2021.v11.i11.2520 Text en Copyright: © Indian Orthopaedic Research Group https://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
Rai, Vikrant
Sabhikhi, G S
Sircar, Pankaj
Kumar, Dev
Kundra, Rohit
Jeyaraman, Madhan
Fibrolipomatous Hamartoma of Median Nerve – A Diagnostic Challenge
title Fibrolipomatous Hamartoma of Median Nerve – A Diagnostic Challenge
title_full Fibrolipomatous Hamartoma of Median Nerve – A Diagnostic Challenge
title_fullStr Fibrolipomatous Hamartoma of Median Nerve – A Diagnostic Challenge
title_full_unstemmed Fibrolipomatous Hamartoma of Median Nerve – A Diagnostic Challenge
title_short Fibrolipomatous Hamartoma of Median Nerve – A Diagnostic Challenge
title_sort fibrolipomatous hamartoma of median nerve – a diagnostic challenge
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8930339/
https://www.ncbi.nlm.nih.gov/pubmed/35415127
http://dx.doi.org/10.13107/jocr.2021.v11.i11.2520
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