Atypical Proximal Cervical Spondylotic Amyotrophy: Case Report Demonstrating Clinical/Imaging Discrepancy

The aim of this study was to present a novel case of unilateral proximal cervical spondylotic amyotrophy (CSA) with contralateral spinal cord compression, which is subject to misdiagnosis and missed diagnosis. CSA is the rare form of cervical spondylosis, which is characterized by severe muscle atro...

Full description

Saved in:
Bibliographic Details
Published inInternational journal of general medicine Vol. 13; pp. 1367 - 1372
Main Authors Feng, Shitong, Fan, Zihan, Yang, Yong, Fei, Qi, Li, Xiang
Format Journal Article
LanguageEnglish
Published New Zealand Dove Medical Press Limited 01.01.2020
Taylor & Francis Ltd
Dove
Dove Medical Press
Subjects
Online AccessGet full text
ISSN1178-7074
1178-7074
DOI10.2147/IJGM.S288588

Cover

Abstract The aim of this study was to present a novel case of unilateral proximal cervical spondylotic amyotrophy (CSA) with contralateral spinal cord compression, which is subject to misdiagnosis and missed diagnosis. CSA is the rare form of cervical spondylosis, which is characterized by severe muscle atrophy in the upper extremities. It can be classified in the proximal subtype and the distal subtype. The etiology, pathophysiology and treatment of CSA are still controversial. A rare case of atypical proximal CSA, who presented with left shoulder and arm weakness, but cervical magnetic resonance imaging (MRI) showed large right paracentral disc herniation in the C4-5 level. Twelve weeks after undergoing anterior cervical discectomy and fusion technique in C4-5 level, the patient's symptoms obviously recovered. The opposite sides between disc herniation and clinical symptoms of upper extremity may be attributed to C5 ventral rootlet becoming stretched caused by spinal cord rotation or shift to the opposite side.
AbstractList Purpose: The aim of this study was to present a novel case of unilateral proximal cervical spondylotic amyotrophy (CSA) with contralateral spinal cord compression, which is subject to misdiagnosis and missed diagnosis. Background: CSA is the rare form of cervical spondylosis, which is characterized by severe muscle atrophy in the upper extremities. It can be classified in the proximal subtype and the distal subtype. The etiology, pathophysiology and treatment of CSA are still controversial. Methods: A rare case of atypical proximal CSA, who presented with left shoulder and arm weakness, but cervical magnetic resonance imaging (MRI) showed large right paracentral disc herniation in the C4-5 level. Twelve weeks after undergoing anterior cervical discectomy and fusion technique in C4-5 level, the patient's symptoms obviously recovered. Conclusion: The opposite sides between disc herniation and clinical symptoms of upper extremity may be attributed to C5 ventral rootlet becoming stretched caused by spinal cord rotation or shift to the opposite side. Keywords: cervical spondylotic amyotrophy, muscle atrophy, anterior decompression
Purpose: The aim of this study was to present a novel case of unilateral proximal cervical spondylotic amyotrophy (CSA) with contralateral spinal cord compression, which is subject to misdiagnosis and missed diagnosis. Background: CSA is the rare form of cervical spondylosis, which is characterized by severe muscle atrophy in the upper extremities. It can be classified in the proximal subtype and the distal subtype. The etiology, pathophysiology and treatment of CSA are still controversial. Methods: A rare case of atypical proximal CSA, who presented with left shoulder and arm weakness, but cervical magnetic resonance imaging (MRI) showed large right paracentral disc herniation in the C4-5 level. Twelve weeks after undergoing anterior cervical discectomy and fusion technique in C4-5 level, the patient’s symptoms obviously recovered. Conclusion: The opposite sides between disc herniation and clinical symptoms of upper extremity may be attributed to C5 ventral rootlet becoming stretched caused by spinal cord rotation or shift to the opposite side.
The aim of this study was to present a novel case of unilateral proximal cervical spondylotic amyotrophy (CSA) with contralateral spinal cord compression, which is subject to misdiagnosis and missed diagnosis.PURPOSEThe aim of this study was to present a novel case of unilateral proximal cervical spondylotic amyotrophy (CSA) with contralateral spinal cord compression, which is subject to misdiagnosis and missed diagnosis.CSA is the rare form of cervical spondylosis, which is characterized by severe muscle atrophy in the upper extremities. It can be classified in the proximal subtype and the distal subtype. The etiology, pathophysiology and treatment of CSA are still controversial.BACKGROUNDCSA is the rare form of cervical spondylosis, which is characterized by severe muscle atrophy in the upper extremities. It can be classified in the proximal subtype and the distal subtype. The etiology, pathophysiology and treatment of CSA are still controversial.A rare case of atypical proximal CSA, who presented with left shoulder and arm weakness, but cervical magnetic resonance imaging (MRI) showed large right paracentral disc herniation in the C4-5 level. Twelve weeks after undergoing anterior cervical discectomy and fusion technique in C4-5 level, the patient's symptoms obviously recovered.METHODSA rare case of atypical proximal CSA, who presented with left shoulder and arm weakness, but cervical magnetic resonance imaging (MRI) showed large right paracentral disc herniation in the C4-5 level. Twelve weeks after undergoing anterior cervical discectomy and fusion technique in C4-5 level, the patient's symptoms obviously recovered.The opposite sides between disc herniation and clinical symptoms of upper extremity may be attributed to C5 ventral rootlet becoming stretched caused by spinal cord rotation or shift to the opposite side.CONCLUSIONThe opposite sides between disc herniation and clinical symptoms of upper extremity may be attributed to C5 ventral rootlet becoming stretched caused by spinal cord rotation or shift to the opposite side.
Shitong Feng,* Zihan Fan,* Yong Yang, Qi Fei, Xiang Li Department of Orthopaedics, Beijing Friendship Hospital, Capital Medical University, Beijing, 100050, People's Republic of China*These authors contributed equally to this workCorrespondence: Xiang Li; Yong YangDepartment of Orthopaedics, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, People's Republic of ChinaTel +86-10-63138353; +86-13641225060Fax +86-10-83911029Email lixiang@ccmu.edu.cn; spineyang@126.comPurpose: The aim of this study was to present a novel case of unilateral proximal cervical spondylotic amyotrophy (CSA) with contralateral spinal cord compression, which is subject to misdiagnosis and missed diagnosis.Background: CSA is the rare form of cervical spondylosis, which is characterized by severe muscle atrophy in the upper extremities. It can be classified in the proximal subtype and the distal subtype. The etiology, pathophysiology and treatment of CSA are still controversial.Methods: A rare case of atypical proximal CSA, who presented with left shoulder and arm weakness, but cervical magnetic resonance imaging (MRI) showed large right paracentral disc herniation in the C4-5 level. Twelve weeks after undergoing anterior cervical discectomy and fusion technique in C4-5 level, the patient's symptoms obviously recovered.Conclusion: The opposite sides between disc herniation and clinical symptoms of upper extremity may be attributed to C5 ventral rootlet becoming stretched caused by spinal cord rotation or shift to the opposite side.Keywords: cervical spondylotic amyotrophy, muscle atrophy, anterior decompression
The aim of this study was to present a novel case of unilateral proximal cervical spondylotic amyotrophy (CSA) with contralateral spinal cord compression, which is subject to misdiagnosis and missed diagnosis. CSA is the rare form of cervical spondylosis, which is characterized by severe muscle atrophy in the upper extremities. It can be classified in the proximal subtype and the distal subtype. The etiology, pathophysiology and treatment of CSA are still controversial. A rare case of atypical proximal CSA, who presented with left shoulder and arm weakness, but cervical magnetic resonance imaging (MRI) showed large right paracentral disc herniation in the C4-5 level. Twelve weeks after undergoing anterior cervical discectomy and fusion technique in C4-5 level, the patient's symptoms obviously recovered. The opposite sides between disc herniation and clinical symptoms of upper extremity may be attributed to C5 ventral rootlet becoming stretched caused by spinal cord rotation or shift to the opposite side.
Audience Academic
Author Fan, Zihan
Li, Xiang
Feng, Shitong
Yang, Yong
Fei, Qi
Author_xml – sequence: 1
  givenname: Shitong
  surname: Feng
  fullname: Feng, Shitong
– sequence: 2
  givenname: Zihan
  surname: Fan
  fullname: Fan, Zihan
– sequence: 3
  givenname: Yong
  surname: Yang
  fullname: Yang, Yong
– sequence: 4
  givenname: Qi
  orcidid: 0000-0001-9753-2692
  surname: Fei
  fullname: Fei, Qi
– sequence: 5
  givenname: Xiang
  surname: Li
  fullname: Li, Xiang
BackLink https://www.ncbi.nlm.nih.gov/pubmed/33293854$$D View this record in MEDLINE/PubMed
BookMark eNptkk1vEzEQhleoiH7AjTNaCQlxIKm9_kwPSFEKJagIROFsjb3exNWuvXg3Ffvv8TahSqrKB1vjZ17PjN_T7MgHb7PsNUbTAlNxvvx69W16U0jJpHyWnWAs5EQgQY_2zsfZadfdIsQ5x-RFdkxIMSOS0ZPMzfuhdQbq_EcMf12TDgsb7-4jN23w5VCH3pl83gyhj6FdDxf5Ajqb_7RtiH1-aZvguz5C7_wqX9TOj6nnywZWY-DSdSbaFrwZXmbPK6g7-2q3n2W_P3_6tfgyuf5-tVzMryeGCd5PjLSIVhiwNVoSAM0qYKlsW3FggEFXDBNdGFZRbgrQJS0JnjEBvNSMlxU5y5Zb3TLArWpj6ikOKoBT94EQVwpiaqm2ShNNsRZoBhxoqalGDGFBsEG6EoWApPVxq9VudGNLY33qtD4QPbzxbq1W4U4JgWek4Eng_U4ghj8b2_WqSROxdQ3ehk2nCsolZ1IIltC3j9DbsIk-jSpRAjGKCNmjVpAacL5KvwJmFFVzTmdckgKTRE2foNIqbeNM8k_lUvwg4d1ewtpC3a-7UG96l373EHyzP5GHUfx3VAI-bAETQ9dFWz0gGKnRsGo0rNoZNuHFI9y4HsZnU8WufjrpH5Qh7fg
CitedBy_id crossref_primary_10_3389_fsurg_2024_1409283
Cites_doi 10.1016/j.jns.2009.12.009
10.14245/ns.1938210.105
10.1097/BRS.0b013e3181e08d93
10.1007/s00586-019-05990-7
10.1038/srep39512
10.1097/00007632-199411001-00002
10.1097/00007632-199401000-00005
10.3171/2014.4.SPINE13681
10.1007/s00586-010-1544-1
10.1007/s00586-012-2506-6
ContentType Journal Article
Copyright 2020 Feng et al.
COPYRIGHT 2020 Dove Medical Press Limited
2020. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
2020 Feng et al. 2020 Feng et al.
Copyright_xml – notice: 2020 Feng et al.
– notice: COPYRIGHT 2020 Dove Medical Press Limited
– notice: 2020. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: 2020 Feng et al. 2020 Feng et al.
DBID AAYXX
CITATION
NPM
3V.
7X7
7XB
8FI
8FJ
8FK
8G5
ABUWG
AFKRA
AZQEC
BENPR
CCPQU
DWQXO
FYUFA
GHDGH
GNUQQ
GUQSH
K9.
M0S
M2O
MBDVC
PHGZM
PHGZT
PIMPY
PKEHL
PQEST
PQQKQ
PQUKI
PRINS
Q9U
7X8
5PM
DOA
DOI 10.2147/IJGM.S288588
DatabaseName CrossRef
PubMed
ProQuest Central (Corporate)
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
ProQuest Hospital Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Research Library
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials
ProQuest Central
ProQuest One
ProQuest Central
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
ProQuest Research Library
ProQuest Health & Medical Complete (Alumni)
Health & Medical Collection (Alumni)
Research Library
Research Library (Corporate)
ProQuest Central Premium
ProQuest One Academic (New)
Publicly Available Content Database
ProQuest One Academic Middle East (New)
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
ProQuest Central Basic
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
PubMed
Publicly Available Content Database
Research Library Prep
ProQuest Central Student
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
Research Library (Alumni Edition)
ProQuest Central China
ProQuest Central
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
ProQuest Research Library
ProQuest Central (New)
ProQuest Central Basic
ProQuest One Academic Eastern Edition
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Hospital Collection (Alumni)
ProQuest Health & Medical Complete
ProQuest One Academic UKI Edition
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList
Publicly Available Content Database
MEDLINE - Academic


PubMed
Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 3
  dbid: BENPR
  name: ProQuest Central
  url: http://www.proquest.com/pqcentral?accountid=15518
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
DocumentTitleAlternate Feng et al
EISSN 1178-7074
EndPage 1372
ExternalDocumentID oai_doaj_org_article_b3b41b709a6a4db4b0501731c0bf727a
PMC7719326
A649683213
33293854
10_2147_IJGM_S288588
Genre Case Reports
GeographicLocations China
Beijing China
GeographicLocations_xml – name: China
– name: Beijing China
GrantInformation_xml – fundername: ;
GroupedDBID ---
0YH
29J
2WC
53G
5GY
5VS
7X7
8FI
8FJ
8G5
AAYXX
ABUWG
ACGFO
ADBBV
ADRAZ
AFKRA
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AOIJS
AZQEC
BAWUL
BCNDV
BENPR
BPHCQ
BVXVI
C1A
CCPQU
CITATION
DIK
DWQXO
E3Z
EBD
F5P
FYUFA
GNUQQ
GROUPED_DOAJ
GUQSH
GX1
HMCUK
HYE
IAO
IHR
IHW
IPNFZ
ITC
KQ8
M2O
M48
MK0
M~E
O5R
O5S
OK1
OVT
P2P
PGMZT
PHGZM
PHGZT
PIMPY
PQQKQ
PROAC
RIG
RNS
RPM
TDBHL
TR2
UKHRP
VDV
NPM
PMFND
3V.
7XB
8FK
K9.
MBDVC
PKEHL
PQEST
PQUKI
PRINS
Q9U
7X8
PUEGO
5PM
ID FETCH-LOGICAL-c576t-c8e04f1a1ecb83aab5fa5661ef6a5a1abf513b2c5f46c2abd4d31957a6db56df3
IEDL.DBID 7X7
ISSN 1178-7074
IngestDate Wed Aug 27 01:23:06 EDT 2025
Thu Aug 21 18:16:06 EDT 2025
Fri Sep 05 10:40:14 EDT 2025
Mon Jun 30 12:23:57 EDT 2025
Tue Jun 17 21:06:59 EDT 2025
Tue Jun 10 20:41:56 EDT 2025
Thu May 22 21:21:59 EDT 2025
Thu Jan 02 22:54:18 EST 2025
Thu Apr 24 22:55:12 EDT 2025
Tue Jul 01 01:04:31 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Keywords cervical spondylotic amyotrophy
muscle atrophy
anterior decompression
Language English
License http://creativecommons.org/licenses/by-nc/3.0
2020 Feng et al.
This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c576t-c8e04f1a1ecb83aab5fa5661ef6a5a1abf513b2c5f46c2abd4d31957a6db56df3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Report-3
ObjectType-Case Study-4
ObjectType-Case Study-2
ObjectType-Feature-4
content type line 23
ObjectType-Report-1
ObjectType-Article-3
These authors contributed equally to this work
ORCID 0000-0001-9753-2692
OpenAccessLink https://www.proquest.com/docview/2470540335?pq-origsite=%requestingapplication%
PMID 33293854
PQID 2470540335
PQPubID 3933151
PageCount 6
ParticipantIDs doaj_primary_oai_doaj_org_article_b3b41b709a6a4db4b0501731c0bf727a
pubmedcentral_primary_oai_pubmedcentral_nih_gov_7719326
proquest_miscellaneous_2468658775
proquest_journals_2470540335
gale_infotracmisc_A649683213
gale_infotracacademiconefile_A649683213
gale_healthsolutions_A649683213
pubmed_primary_33293854
crossref_primary_10_2147_IJGM_S288588
crossref_citationtrail_10_2147_IJGM_S288588
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2020-01-01
PublicationDateYYYYMMDD 2020-01-01
PublicationDate_xml – month: 01
  year: 2020
  text: 2020-01-01
  day: 01
PublicationDecade 2020
PublicationPlace New Zealand
PublicationPlace_xml – name: New Zealand
– name: Macclesfield
PublicationTitle International journal of general medicine
PublicationTitleAlternate Int J Gen Med
PublicationYear 2020
Publisher Dove Medical Press Limited
Taylor & Francis Ltd
Dove
Dove Medical Press
Publisher_xml – name: Dove Medical Press Limited
– name: Taylor & Francis Ltd
– name: Dove
– name: Dove Medical Press
References Tauchi (ref4) 2013; 22
Shinomiya (ref8) 1994; 19
Yanagi (ref1) 1976; 16
Tauchi (ref7) 2014; 21
Jiang (ref2) 2011; 20
Luo (ref11) 2019; 28
Imajo (ref5) 2011; 36
Zhang (ref6) 2016; 6
Takahashi (ref9) 2019; 16
Shinomiya (ref10) 1994; 19
Gebere-Michael (ref3) 2010; 290
References_xml – volume: 290
  start-page: 142
  year: 2010
  ident: ref3
  publication-title: J Neurol Sci
  doi: 10.1016/j.jns.2009.12.009
– volume: 16
  start-page: 579
  year: 2019
  ident: ref9
  publication-title: Neurospine
  doi: 10.14245/ns.1938210.105
– volume: 36
  start-page: E476
  year: 2011
  ident: ref5
  publication-title: Spine
  doi: 10.1097/BRS.0b013e3181e08d93
– volume: 28
  start-page: 2293
  year: 2019
  ident: ref11
  publication-title: Eur Spine J
  doi: 10.1007/s00586-019-05990-7
– volume: 6
  start-page: 39512
  year: 2016
  ident: ref6
  publication-title: Sci Rep
  doi: 10.1038/srep39512
– volume: 19
  start-page: 2501
  year: 1994
  ident: ref10
  publication-title: Spine
  doi: 10.1097/00007632-199411001-00002
– volume: 19
  start-page: 21
  year: 1994
  ident: ref8
  publication-title: Spine
  doi: 10.1097/00007632-199401000-00005
– volume: 16
  start-page: 520
  year: 1976
  ident: ref1
  publication-title: Rinsho Shinkeigaku
– volume: 21
  start-page: 411
  year: 2014
  ident: ref7
  publication-title: J Neurosurg Spine
  doi: 10.3171/2014.4.SPINE13681
– volume: 20
  start-page: 351
  year: 2011
  ident: ref2
  publication-title: Eur Spine J
  doi: 10.1007/s00586-010-1544-1
– volume: 22
  start-page: 156
  year: 2013
  ident: ref4
  publication-title: Eur Spine J
  doi: 10.1007/s00586-012-2506-6
SSID ssj0066613
Score 2.153127
Snippet The aim of this study was to present a novel case of unilateral proximal cervical spondylotic amyotrophy (CSA) with contralateral spinal cord compression,...
Purpose: The aim of this study was to present a novel case of unilateral proximal cervical spondylotic amyotrophy (CSA) with contralateral spinal cord...
Shitong Feng,* Zihan Fan,* Yong Yang, Qi Fei, Xiang Li Department of Orthopaedics, Beijing Friendship Hospital, Capital Medical University, Beijing, 100050,...
SourceID doaj
pubmedcentral
proquest
gale
pubmed
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage 1367
SubjectTerms anterior decompression
Atrophy
Atrophy, Muscular
Care and treatment
Case Report
cervical spondylotic amyotrophy
Consent
Magnetic resonance imaging
muscle atrophy
Patients
Spinal cord
SummonAdditionalLinks – databaseName: DOAJ Directory of Open Access Journals
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3di9QwEA9yD-KL-G31TisoPkjdpkmarG_rnufdwYpwHtxbSNJEF27bZe3B3X_vTNqtW0R88aWUZgrtfP4mnc4Q8pqrwnDqZCY5HLisVGaUd1jTUHoqglGx483iS3l8zk8vxMXOqC-sCevaA3eMm1hmObUyn5rS8MpymwtQIkZdbgPE3giN8mm-TaY6HwyYPA5GphRyJAlRsit5x5k8k5PTz4v3Z4VSIk5b-R2MYs_-Pz3zTmgal03uxKGje-RuDyDTWffg98ktXz8gtxf9J_KHZDlrb9bI-fTrprleruBkHv0BnJytm7qCDB1uTWerm6bdNMDlD-kcQlnaQfH00K8QMqJi1N_Tvm3o5eRkFccZpYdL8DMQwsAnPyLnR5--zY-zfp5C5iCraDOnfM4DNdQ7q5gxFkQBaI76UBphqLFBUGYLJwIvXWFsxSswUCFNWVlRVoE9Jnt1U_unJOXGWiMszQ0N3AOqsJhmU26DoyYonpB3W8Zq1zcbx5kXlxqSDhSDRjHoXgwJeTNQr7smG3-h-4gyGmiwNXa8AAqje4XR_1KYhLxECevuP9PBwPWs5NMS5zaxhLyNFGji8NDO9H8qwKtjs6wR5f6IEkzTjZe3WqR71_BTF1wiTGZMJOTVsIx3Yrlb7ZsrpCkVQEMpgeZJp3TDSzMGCE0JYLEcqeOIK-OVevkjNg6XMsL1Z_-Djc_JnQK3HuJu1D7ZazdX_gDwWWtfRFP8BUHwOEk
  priority: 102
  providerName: Directory of Open Access Journals
– databaseName: Scholars Portal Journals: Open Access
  dbid: M48
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3da9RAEF9qBfFF_G60agTFB7k2m93NbgWR82ptCydCPehb2N3s1oO75Iwp9P57Zza50FD15Qi3s5DM52-ykxlC3nCVak6tHEkOP1wWaqSVs1jTkDkqvFah4830W3Y846fn4nyLbKaNdgz8_dfUDudJzerF3tWv9Scw-I9Yxky53D85_TrdO0uVEkrdIrfDSREW8fH-PAEwOmVt2fuNHYOAFPr23_TO18LTsHTyWiw6uk_udSAyHrdSf0C2XPmQ3Jl2x-SPyHzcrFfI_fh7XV3Nl3AxCT4BLs5WVVlAlg5b4_FyXTV1BZz-EE8gnMUtHI8P3RJhIypHeRF3rUMX-yfLMNIoPpyDr4EwBn75MZkdffkxOR51MxVGFjKLZmSVS7inmjprFNPagDgA0VHnMy001cYLykxqheeZTbUpeAFGKqTOCiOywrMnZLusSrdDYq6N0cLQRFPPHSALg6k25cZbqr3iEXm_YWxuu4bjOPdikUPigWLIUQx5J4aIvO2pV22jjX_QfUYZ9TTYHjv8UdUXeWdtuWGGUyOTA51pXhhuEgGeh1GbGA-ATUfkFUo4b7817Y08H2f8IMPZTSwi7wIFKh7ctNXd1wrw6Ngwa0C5O6AE87TD5Y0W5RvtzlMuESozJiLyul_GnVjyVrrqEmkyBfBQSqB52ipd_9CMAUpTAlgsB-o44MpwpZz_DM3DpQyQ_dn_b-s5uZvii4XwrmmXbDf1pXsB6KsxL4Nh_QFOmDBN
  priority: 102
  providerName: Scholars Portal
Title Atypical Proximal Cervical Spondylotic Amyotrophy: Case Report Demonstrating Clinical/Imaging Discrepancy
URI https://www.ncbi.nlm.nih.gov/pubmed/33293854
https://www.proquest.com/docview/2470540335
https://www.proquest.com/docview/2468658775
https://pubmed.ncbi.nlm.nih.gov/PMC7719326
https://doaj.org/article/b3b41b709a6a4db4b0501731c0bf727a
Volume 13
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3db9MwELfYJiFeEN8rjBIkEA8oNI7t2OMFdd1GN6nTxJhUniLbcUalNSldJ7H_njvHzRYheImi-CIl9_nz5XJHyDuuUs2plbHkcOCyULFWzmJNQ-aoKLXyHW8mJ9n4nB9PxTQk3K5CWeXaJ3pHXdQWc-SDlEtEF4yJL4tfMU6Nwq-rYYTGBtmigERwdIOcthsuQOaUNcXuOI1ncHT8dfLpLFVK-Dkrt2HId-v_2yffCUrdgsk7EejwEXkYoGM0bGT9mNxz1RNyfxI-jj8ls-HqZoE8j06X9e_ZHE5G3hPAydmirgrYm8Ot0XB-U6-WNfD3czSCIBY1IDzad3MEi6gS1UUUGoZeDo7mfpBRtD8DDwPBC7zxM3J-ePB9NI7DJIXYwn5iFVvlEl5STZ01imltQAiA46grMy001aYUlJnUipJnNtWm4AWYppA6K4zIipI9J5tVXbltEnFtjBaGJpqW3AGeMLjBptyUlupS8R75uGZsbkObcZx2cZnDdgPFkKMY8iCGHnnfUi-a9hr_oNtDGbU02BTbX6iXF3mwsdwww6mRya7ONC8MN4kAf8OoTUwJME33yBuUcN78Ydqadj7M-G6GE5tYj3zwFGjc8NBWh38U4NWxTVaHcqdDCUZpu8trLcqDU7jKb1W4R962y3gnFrpVrr5GmkwBKJQSaF40Ste-NGOAzZQAFsuOOna40l2pZj99y3ApPVB_-f_HekUepJhO8BmmHbK5Wl6714C5VqZPNpIf4743rz7Z2js4Of3W9_kLOE64-gOAAzJT
linkProvider ProQuest
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3fb9MwELZGJwEviN8UBgsSEw8otE7sJEOaUNdutNtaTWyT9mZsxxmV2qR0naD_HH8bd47TLULwtpcqqi-R4zvffefY9xHyjiWBZFTHfszgh8Vp4svEaNzTEBnKM5nYijfDUdQ_Ywfn_HyN_K7OwuC2ysonWkedFhrXyFsBixFdhCH_PPvhI2sUfl2tKDSko1ZId2yJMXew49Asf0IKd7kz6IG-t4Jgf--02_cdy4CvAWsvfJ2YNsuopEarJJRSQQcB41CTRZJLKlXGaagCzTMW6UCqlKVgtjyWUap4lGYhPPcOWWe4gNIg67t7o-OvVSyA3ICG5XZ75ANqDQ6-DD-eBEnCLdPLdSC0fAF_R4UbYbG-ZfNGDNx_SB448Op1Smt7RNZM_pjcHbrP80_IuLNYzlDr3vG8-DWewkXX-iK4OJkVebqcFHCr15kui8W8AA1_8roQRr0yDfB6ZopwFY0yv_BcydJJazC1VEpebww-DsInxIOn5OxWRvkZaeRFbl4Qj0mlJFe0LWnGDCAahSk-ZSrTVGYJa5IP1cAK7QqdI9_GREDCg2oQqAbh1NAkWyvpWVng4x9yu6ijlQyW5bZ_FPML4Wa5UKFiVMXtbRlJliqm2hw8Xkh1W2UAFGWTbKKGRXnGdeVcRCdi2xFyRoVN8t5KoHuBTmvpTknAq2OhrprkRk0S3IKuN1dWJJxbuhTXk6hJ3q6a8U7capeb4gplogRgaRyDzPPS6FYvHYaADhMOQxzXzLE2KvWWfPzdFi2PY5sqvPx_tzbJvf7p8EgcDUaHr8j9ABc37HrXBmks5lfmNSDAhXrjpplHvt32zP4Duax0EA
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3db9MwELfGJk28IL7pNliQmHhAoXVixxnShLp2Zd1oVTEm7S3YjjMqtUnpOkH_Rf4q7hynW4TgbS9VVF8ix_f1O-d8R8gbFgeSUS18weCHiTT2ZWw05jREhvJMxrbizWAYHZ-zkwt-sUZ-V2dhMK2ysonWUKeFxj3yZsAEoosw5M3MpUWMur2Psx8-dpDCL61VOw3p2iykB7bcmDvkcWqWPyGcuzrod4H3e0HQO_raOfZdxwFfA-5e-Do2LZZRSY1WcSilgskC3qEmiySXVKqM01AFmmcs0oFUKUtBhLmQUap4lGYhPPce2RDg9SEQ3Dg8Go6-VH4B4gQalqn32Buo2T_5NHh_FsQxt11fbpyi7R3wt4e45SLr6Zu3_GHvIXnggKzXLiXvEVkz-WOyOXCf6p-QcXuxnKEEeKN58Ws8hYuOtUtwcTYr8nQ5KeBWrz1dFot5Adz-4HXApXplSOB1zRShKwpofum58qWTZn9q2yp53THYO3Cl4BuekvM7WeVnZD0vcvOCeEwqJbmiLUkzZgDdKAz3KVOZpjKLWYO8qxY20a7oOfbemCQQ_CAbEmRD4tjQIHsr6llZ7OMfdIfIoxUNlui2fxTzy8RpfKJCxagSrX0ZSZYqplocrF9IdUtlABplg-wih5PyvOvK0CTtiO1H2D8qbJC3lgJNDUxaS3diAl4di3bVKHdqlGAidH24kqLEmair5EahGuT1ahjvxLS73BTXSBPFAFGFAJrnpdCtXjoMASnGHJZY1MSxtir1kXz83RYwF8KGDVv_n9Yu2QQNTz73h6fb5H6A-xx262uHrC_m1-YlgMGFeuW0zCPf7lqx_wALz3hU
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Atypical+Proximal+Cervical+Spondylotic+Amyotrophy%3A+Case+Report+Demonstrating+Clinical%2FImaging+Discrepancy&rft.jtitle=International+journal+of+general+medicine&rft.au=Feng%2C+Shitong&rft.au=Fan%2C+Zihan&rft.au=Yang%2C+Yong&rft.au=Qi+Fei&rft.date=2020-01-01&rft.pub=Taylor+%26+Francis+Ltd&rft.eissn=1178-7074&rft.volume=13&rft.spage=1367&rft_id=info:doi/10.2147%2FIJGM.S288588&rft.externalDBID=HAS_PDF_LINK
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1178-7074&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1178-7074&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1178-7074&client=summon