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Unilateral lateral mass hypertrophy: An extremely rare congenital anomaly of atlas

A wide variety of congenital anomalies are observed around the craniovertebral junctional area. However, hypertrophied unilateral lateral mass of atlas in association with chiari-1 malformation leading to myelopathy is extremely uncommon. Herein we report a case of 28-year-old female who presented t...

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Autores principales: Das, Kuntal Kanti, Mehrotra, Anant, Sahu, Rabi Narayan, Srivastava, Arun Kumar, Jaiswal, Awadhesh Kumar, Behari, Sanjay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3980560/
https://www.ncbi.nlm.nih.gov/pubmed/24744566
http://dx.doi.org/10.4103/0974-8237.128534
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author Das, Kuntal Kanti
Mehrotra, Anant
Sahu, Rabi Narayan
Srivastava, Arun Kumar
Jaiswal, Awadhesh Kumar
Behari, Sanjay
author_facet Das, Kuntal Kanti
Mehrotra, Anant
Sahu, Rabi Narayan
Srivastava, Arun Kumar
Jaiswal, Awadhesh Kumar
Behari, Sanjay
author_sort Das, Kuntal Kanti
collection PubMed
description A wide variety of congenital anomalies are observed around the craniovertebral junctional area. However, hypertrophied unilateral lateral mass of atlas in association with chiari-1 malformation leading to myelopathy is extremely uncommon. Herein we report a case of 28-year-old female who presented to us with a high cervical compressive myelopathy. Imaging revealed bony hypertrophy involving right sided C1 lateral mass along with chiari malformation-type 1. She underwent transoral as well as posterior decompression followed by occipito-cervical fusion. The authors discuss their case in light of other such reported cases and present a review of the literature.
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spelling pubmed-39805602014-04-17 Unilateral lateral mass hypertrophy: An extremely rare congenital anomaly of atlas Das, Kuntal Kanti Mehrotra, Anant Sahu, Rabi Narayan Srivastava, Arun Kumar Jaiswal, Awadhesh Kumar Behari, Sanjay J Craniovertebr Junction Spine Case Report A wide variety of congenital anomalies are observed around the craniovertebral junctional area. However, hypertrophied unilateral lateral mass of atlas in association with chiari-1 malformation leading to myelopathy is extremely uncommon. Herein we report a case of 28-year-old female who presented to us with a high cervical compressive myelopathy. Imaging revealed bony hypertrophy involving right sided C1 lateral mass along with chiari malformation-type 1. She underwent transoral as well as posterior decompression followed by occipito-cervical fusion. The authors discuss their case in light of other such reported cases and present a review of the literature. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3980560/ /pubmed/24744566 http://dx.doi.org/10.4103/0974-8237.128534 Text en Copyright: © Journal of Craniovertebral Junction and Spine 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
Das, Kuntal Kanti
Mehrotra, Anant
Sahu, Rabi Narayan
Srivastava, Arun Kumar
Jaiswal, Awadhesh Kumar
Behari, Sanjay
Unilateral lateral mass hypertrophy: An extremely rare congenital anomaly of atlas
title Unilateral lateral mass hypertrophy: An extremely rare congenital anomaly of atlas
title_full Unilateral lateral mass hypertrophy: An extremely rare congenital anomaly of atlas
title_fullStr Unilateral lateral mass hypertrophy: An extremely rare congenital anomaly of atlas
title_full_unstemmed Unilateral lateral mass hypertrophy: An extremely rare congenital anomaly of atlas
title_short Unilateral lateral mass hypertrophy: An extremely rare congenital anomaly of atlas
title_sort unilateral lateral mass hypertrophy: an extremely rare congenital anomaly of atlas
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3980560/
https://www.ncbi.nlm.nih.gov/pubmed/24744566
http://dx.doi.org/10.4103/0974-8237.128534
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