Copper deficiency myelopathy mimicking cervical spondylitic myelopathy: a systematic review of the literature with case report

•Copper deficiency myelopathy (CDM) is a rare disease of progressive dorsal column dysfunction resulting in sensory ataxia, weakness, and spasticity.•Patients presenting to a spine surgeon with myelopathy that progress in spite of adequate surgical decompression, or myelopathy concomitant with cytop...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The spine journal 2024-11, Vol.24 (11), p.2026-2034
Hauptverfasser: Chen, Jeffrey W., Zeoli, Tyler, Hughes, Natasha C., Lane, Amanda, Berkman, Richard A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2034
container_issue 11
container_start_page 2026
container_title The spine journal
container_volume 24
creator Chen, Jeffrey W.
Zeoli, Tyler
Hughes, Natasha C.
Lane, Amanda
Berkman, Richard A.
description •Copper deficiency myelopathy (CDM) is a rare disease of progressive dorsal column dysfunction resulting in sensory ataxia, weakness, and spasticity.•Patients presenting to a spine surgeon with myelopathy that progress in spite of adequate surgical decompression, or myelopathy concomitant with cytopenia, require further investigation for copper deficiency myelopathy.•Clues to copper deficiency include a distinct MRI T2 hyperintense inverted “V” signal in the dorsal columns in a patient with risk factors for copper deficiency such as gastric bypass, bariatric surgery, or excessive zinc exposure.•Hematological abnormalities resolve rapidly with replenishment of copper, while neurological deficits only stabilize or partially improve Appropriate copper supplementation therapy may lead to a reversal of T2 signal-intensity changes in the dorsal columns. Copper deficiency myelopathy (CDM) is a rare disease that can present with spastic quadriparesis and sensory ataxia. As a result, it can precisely mimic cervical spondylitic myelopathy (CSM). Copper deficiency may be seen following gastric bypass surgery, malabsorption syndromes such as celiac disease, and with excessive exogenous zinc intake. We present a systematic review of the literature for CDM and an illustrative case. Provide a systematic review of CDM to highlight the importance of recognizing the consideration of CDM in patients presenting to a spine surgeon with myelopathy that progress despite adequate surgical decompression, or myelopathy concomitant with cytopenia, thus requiring further workup. Retrospective medical record review and systematic review of the literature. PubMed and Ovid-Embase database search was conducted in July 2022. Self-reported measures include PRISMA flow diagram for retrospective review; Physiological measures include retrospective review of MRI imaging of cervical spine; alternate demographic and laboratory value data extracted via literature review. A PubMed and Ovid-Embase database search was conducted in July 2022 searching for “copper deficiency myelopathy (MeSH)” from 2000 to 2022 via PRISMA guidelines. Following title and abstract review, the following data was extracted from full text: age, sex, etiology, hematological values upon presentation (mean corpuscular volume, white blood count, platelet count, and hemoglobin level), metal serum studies (serum copper, ceruloplasmin, and zinc), 24-hour collection of copper and zinc, and distinct radiographic findings on MRI. A
doi_str_mv 10.1016/j.spinee.2024.06.018
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3071513006</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1529943024002985</els_id><sourcerecordid>3071513006</sourcerecordid><originalsourceid>FETCH-LOGICAL-c241t-a19f25ab84128f9573aa7098096ad2212ba57ef4d877b95de1341ad4161c5e0d3</originalsourceid><addsrcrecordid>eNp9kE1v1DAQhiMEoh_wDxDykUvCjPNlc0BCKyhIlXppz5bXnrBekjjY3la58NvxsgVx6mleaZ6Z0TxF8QahQsDu_b6Ki5uJKg68qaCrAMWz4hxFL0rsav4855bLUjY1nBUXMe4BQPTIXxZntZAgJcJ58Wvjl4UCszQ442g2K5tWGv2i0y5HNznzw83fmaFw74weWVz8bNfRJWf-Iz8wzeIaE0362Ah07-iB-YGlHbEMU9DpEIg9uLRjRkfKyOJDelW8GPQY6fVjvSzuvny-3Xwtr2-uvm0-XZeGN5hKjXLgrd6KBrkYZNvXWvcgBchOW86Rb3Xb09BY0fdb2VrCukFtG-zQtAS2vizenfYuwf88UExqctHQOOqZ_CGqGnpssQboMtqcUBN8jIEGtQQ36bAqBHU0r_bqZF4dzSvoVDafx94-XjhsJ7L_hv6qzsDHE0D5z6wnqPhHOFkXyCRlvXv6wm_z2pl7</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3071513006</pqid></control><display><type>article</type><title>Copper deficiency myelopathy mimicking cervical spondylitic myelopathy: a systematic review of the literature with case report</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Chen, Jeffrey W. ; Zeoli, Tyler ; Hughes, Natasha C. ; Lane, Amanda ; Berkman, Richard A.</creator><creatorcontrib>Chen, Jeffrey W. ; Zeoli, Tyler ; Hughes, Natasha C. ; Lane, Amanda ; Berkman, Richard A.</creatorcontrib><description>•Copper deficiency myelopathy (CDM) is a rare disease of progressive dorsal column dysfunction resulting in sensory ataxia, weakness, and spasticity.•Patients presenting to a spine surgeon with myelopathy that progress in spite of adequate surgical decompression, or myelopathy concomitant with cytopenia, require further investigation for copper deficiency myelopathy.•Clues to copper deficiency include a distinct MRI T2 hyperintense inverted “V” signal in the dorsal columns in a patient with risk factors for copper deficiency such as gastric bypass, bariatric surgery, or excessive zinc exposure.•Hematological abnormalities resolve rapidly with replenishment of copper, while neurological deficits only stabilize or partially improve Appropriate copper supplementation therapy may lead to a reversal of T2 signal-intensity changes in the dorsal columns. Copper deficiency myelopathy (CDM) is a rare disease that can present with spastic quadriparesis and sensory ataxia. As a result, it can precisely mimic cervical spondylitic myelopathy (CSM). Copper deficiency may be seen following gastric bypass surgery, malabsorption syndromes such as celiac disease, and with excessive exogenous zinc intake. We present a systematic review of the literature for CDM and an illustrative case. Provide a systematic review of CDM to highlight the importance of recognizing the consideration of CDM in patients presenting to a spine surgeon with myelopathy that progress despite adequate surgical decompression, or myelopathy concomitant with cytopenia, thus requiring further workup. Retrospective medical record review and systematic review of the literature. PubMed and Ovid-Embase database search was conducted in July 2022. Self-reported measures include PRISMA flow diagram for retrospective review; Physiological measures include retrospective review of MRI imaging of cervical spine; alternate demographic and laboratory value data extracted via literature review. A PubMed and Ovid-Embase database search was conducted in July 2022 searching for “copper deficiency myelopathy (MeSH)” from 2000 to 2022 via PRISMA guidelines. Following title and abstract review, the following data was extracted from full text: age, sex, etiology, hematological values upon presentation (mean corpuscular volume, white blood count, platelet count, and hemoglobin level), metal serum studies (serum copper, ceruloplasmin, and zinc), 24-hour collection of copper and zinc, and distinct radiographic findings on MRI. A total of 116 studies were included in this review which contained 198 cases of copper deficiency myelopathy. The mean age was 53.57±14.14 years, with the majority being females (63.8%). The most common etiology was prior gastric surgery (n=55, 36.2 %) followed by excessive zinc consumption from the use of zinc denture cream (n=39, 19.9%). The mean serum copper was 15.67±17.84 (normal=80.0–155.0) mcg/dL and mean ceruloplasmin was 6.43±5.25 (normal=16–45) mg/dL. In spite of appropriate treatment with copper supplementation, only 47 cases (24%) reported improvement in neurological status, and only 10 (5.1%) recovered to baseline. A hyperintense T2 signal abnormality resembling an inverted “v” in the dorsal columns was the most common radiographic abnormality. Pertinent risk factors for copper deficiency myelopathy include prior upper gastrointestinal surgery, zinc excess, and malabsorption. Characteristic laboratory and imaging findings include cytopenia, low serum copper and ceruloplasmin, and distinct inverted “v” T2 signal hyperintensity in the dorsal columns. The neurologic deterioration with copper deficiency will progress in spite of decompressive surgery, and can be devastating and irreversible even with copper supplementation, reinforcing the importance of early detection. We thus recommend patients with myelopathy presenting with a history of gastric bypass, malabsorption syndromes, excessive zinc exposure, cytopenia, or imaging resembling an inverted “v” shaped hyperintense T2 MRI signal in the dorsal columns, should first undergo blood tests for copper, ceruloplasmin, and B12 levels prior to surgical consideration.</description><identifier>ISSN: 1529-9430</identifier><identifier>ISSN: 1878-1632</identifier><identifier>EISSN: 1878-1632</identifier><identifier>DOI: 10.1016/j.spinee.2024.06.018</identifier><identifier>PMID: 38909910</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Aged ; Cervical spondylitic myelopathy ; Cervical Vertebrae - surgery ; Copper - blood ; Copper - deficiency ; Copper deficiency myelopathy ; CSM ; Diagnosis, Differential ; Female ; Humans ; Magnetic Resonance Imaging ; Male ; Middle Aged ; Myelopathy ; Spinal Cord Diseases - blood ; Spinal Cord Diseases - diagnosis ; Spinal Cord Diseases - etiology ; Spinal Cord Diseases - surgery ; Spondylosis - complications ; Spondylosis - diagnosis</subject><ispartof>The spine journal, 2024-11, Vol.24 (11), p.2026-2034</ispartof><rights>2024 Elsevier Inc.</rights><rights>Copyright © 2024 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c241t-a19f25ab84128f9573aa7098096ad2212ba57ef4d877b95de1341ad4161c5e0d3</cites><orcidid>0000-0003-2031-3306 ; 0000-0002-3929-5964</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1529943024002985$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38909910$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Jeffrey W.</creatorcontrib><creatorcontrib>Zeoli, Tyler</creatorcontrib><creatorcontrib>Hughes, Natasha C.</creatorcontrib><creatorcontrib>Lane, Amanda</creatorcontrib><creatorcontrib>Berkman, Richard A.</creatorcontrib><title>Copper deficiency myelopathy mimicking cervical spondylitic myelopathy: a systematic review of the literature with case report</title><title>The spine journal</title><addtitle>Spine J</addtitle><description>•Copper deficiency myelopathy (CDM) is a rare disease of progressive dorsal column dysfunction resulting in sensory ataxia, weakness, and spasticity.•Patients presenting to a spine surgeon with myelopathy that progress in spite of adequate surgical decompression, or myelopathy concomitant with cytopenia, require further investigation for copper deficiency myelopathy.•Clues to copper deficiency include a distinct MRI T2 hyperintense inverted “V” signal in the dorsal columns in a patient with risk factors for copper deficiency such as gastric bypass, bariatric surgery, or excessive zinc exposure.•Hematological abnormalities resolve rapidly with replenishment of copper, while neurological deficits only stabilize or partially improve Appropriate copper supplementation therapy may lead to a reversal of T2 signal-intensity changes in the dorsal columns. Copper deficiency myelopathy (CDM) is a rare disease that can present with spastic quadriparesis and sensory ataxia. As a result, it can precisely mimic cervical spondylitic myelopathy (CSM). Copper deficiency may be seen following gastric bypass surgery, malabsorption syndromes such as celiac disease, and with excessive exogenous zinc intake. We present a systematic review of the literature for CDM and an illustrative case. Provide a systematic review of CDM to highlight the importance of recognizing the consideration of CDM in patients presenting to a spine surgeon with myelopathy that progress despite adequate surgical decompression, or myelopathy concomitant with cytopenia, thus requiring further workup. Retrospective medical record review and systematic review of the literature. PubMed and Ovid-Embase database search was conducted in July 2022. Self-reported measures include PRISMA flow diagram for retrospective review; Physiological measures include retrospective review of MRI imaging of cervical spine; alternate demographic and laboratory value data extracted via literature review. A PubMed and Ovid-Embase database search was conducted in July 2022 searching for “copper deficiency myelopathy (MeSH)” from 2000 to 2022 via PRISMA guidelines. Following title and abstract review, the following data was extracted from full text: age, sex, etiology, hematological values upon presentation (mean corpuscular volume, white blood count, platelet count, and hemoglobin level), metal serum studies (serum copper, ceruloplasmin, and zinc), 24-hour collection of copper and zinc, and distinct radiographic findings on MRI. A total of 116 studies were included in this review which contained 198 cases of copper deficiency myelopathy. The mean age was 53.57±14.14 years, with the majority being females (63.8%). The most common etiology was prior gastric surgery (n=55, 36.2 %) followed by excessive zinc consumption from the use of zinc denture cream (n=39, 19.9%). The mean serum copper was 15.67±17.84 (normal=80.0–155.0) mcg/dL and mean ceruloplasmin was 6.43±5.25 (normal=16–45) mg/dL. In spite of appropriate treatment with copper supplementation, only 47 cases (24%) reported improvement in neurological status, and only 10 (5.1%) recovered to baseline. A hyperintense T2 signal abnormality resembling an inverted “v” in the dorsal columns was the most common radiographic abnormality. Pertinent risk factors for copper deficiency myelopathy include prior upper gastrointestinal surgery, zinc excess, and malabsorption. Characteristic laboratory and imaging findings include cytopenia, low serum copper and ceruloplasmin, and distinct inverted “v” T2 signal hyperintensity in the dorsal columns. The neurologic deterioration with copper deficiency will progress in spite of decompressive surgery, and can be devastating and irreversible even with copper supplementation, reinforcing the importance of early detection. We thus recommend patients with myelopathy presenting with a history of gastric bypass, malabsorption syndromes, excessive zinc exposure, cytopenia, or imaging resembling an inverted “v” shaped hyperintense T2 MRI signal in the dorsal columns, should first undergo blood tests for copper, ceruloplasmin, and B12 levels prior to surgical consideration.</description><subject>Adult</subject><subject>Aged</subject><subject>Cervical spondylitic myelopathy</subject><subject>Cervical Vertebrae - surgery</subject><subject>Copper - blood</subject><subject>Copper - deficiency</subject><subject>Copper deficiency myelopathy</subject><subject>CSM</subject><subject>Diagnosis, Differential</subject><subject>Female</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Myelopathy</subject><subject>Spinal Cord Diseases - blood</subject><subject>Spinal Cord Diseases - diagnosis</subject><subject>Spinal Cord Diseases - etiology</subject><subject>Spinal Cord Diseases - surgery</subject><subject>Spondylosis - complications</subject><subject>Spondylosis - diagnosis</subject><issn>1529-9430</issn><issn>1878-1632</issn><issn>1878-1632</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1v1DAQhiMEoh_wDxDykUvCjPNlc0BCKyhIlXppz5bXnrBekjjY3la58NvxsgVx6mleaZ6Z0TxF8QahQsDu_b6Ki5uJKg68qaCrAMWz4hxFL0rsav4855bLUjY1nBUXMe4BQPTIXxZntZAgJcJ58Wvjl4UCszQ442g2K5tWGv2i0y5HNznzw83fmaFw74weWVz8bNfRJWf-Iz8wzeIaE0362Ah07-iB-YGlHbEMU9DpEIg9uLRjRkfKyOJDelW8GPQY6fVjvSzuvny-3Xwtr2-uvm0-XZeGN5hKjXLgrd6KBrkYZNvXWvcgBchOW86Rb3Xb09BY0fdb2VrCukFtG-zQtAS2vizenfYuwf88UExqctHQOOqZ_CGqGnpssQboMtqcUBN8jIEGtQQ36bAqBHU0r_bqZF4dzSvoVDafx94-XjhsJ7L_hv6qzsDHE0D5z6wnqPhHOFkXyCRlvXv6wm_z2pl7</recordid><startdate>202411</startdate><enddate>202411</enddate><creator>Chen, Jeffrey W.</creator><creator>Zeoli, Tyler</creator><creator>Hughes, Natasha C.</creator><creator>Lane, Amanda</creator><creator>Berkman, Richard A.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-2031-3306</orcidid><orcidid>https://orcid.org/0000-0002-3929-5964</orcidid></search><sort><creationdate>202411</creationdate><title>Copper deficiency myelopathy mimicking cervical spondylitic myelopathy: a systematic review of the literature with case report</title><author>Chen, Jeffrey W. ; Zeoli, Tyler ; Hughes, Natasha C. ; Lane, Amanda ; Berkman, Richard A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c241t-a19f25ab84128f9573aa7098096ad2212ba57ef4d877b95de1341ad4161c5e0d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Cervical spondylitic myelopathy</topic><topic>Cervical Vertebrae - surgery</topic><topic>Copper - blood</topic><topic>Copper - deficiency</topic><topic>Copper deficiency myelopathy</topic><topic>CSM</topic><topic>Diagnosis, Differential</topic><topic>Female</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Myelopathy</topic><topic>Spinal Cord Diseases - blood</topic><topic>Spinal Cord Diseases - diagnosis</topic><topic>Spinal Cord Diseases - etiology</topic><topic>Spinal Cord Diseases - surgery</topic><topic>Spondylosis - complications</topic><topic>Spondylosis - diagnosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Jeffrey W.</creatorcontrib><creatorcontrib>Zeoli, Tyler</creatorcontrib><creatorcontrib>Hughes, Natasha C.</creatorcontrib><creatorcontrib>Lane, Amanda</creatorcontrib><creatorcontrib>Berkman, Richard A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The spine journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Jeffrey W.</au><au>Zeoli, Tyler</au><au>Hughes, Natasha C.</au><au>Lane, Amanda</au><au>Berkman, Richard A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Copper deficiency myelopathy mimicking cervical spondylitic myelopathy: a systematic review of the literature with case report</atitle><jtitle>The spine journal</jtitle><addtitle>Spine J</addtitle><date>2024-11</date><risdate>2024</risdate><volume>24</volume><issue>11</issue><spage>2026</spage><epage>2034</epage><pages>2026-2034</pages><issn>1529-9430</issn><issn>1878-1632</issn><eissn>1878-1632</eissn><abstract>•Copper deficiency myelopathy (CDM) is a rare disease of progressive dorsal column dysfunction resulting in sensory ataxia, weakness, and spasticity.•Patients presenting to a spine surgeon with myelopathy that progress in spite of adequate surgical decompression, or myelopathy concomitant with cytopenia, require further investigation for copper deficiency myelopathy.•Clues to copper deficiency include a distinct MRI T2 hyperintense inverted “V” signal in the dorsal columns in a patient with risk factors for copper deficiency such as gastric bypass, bariatric surgery, or excessive zinc exposure.•Hematological abnormalities resolve rapidly with replenishment of copper, while neurological deficits only stabilize or partially improve Appropriate copper supplementation therapy may lead to a reversal of T2 signal-intensity changes in the dorsal columns. Copper deficiency myelopathy (CDM) is a rare disease that can present with spastic quadriparesis and sensory ataxia. As a result, it can precisely mimic cervical spondylitic myelopathy (CSM). Copper deficiency may be seen following gastric bypass surgery, malabsorption syndromes such as celiac disease, and with excessive exogenous zinc intake. We present a systematic review of the literature for CDM and an illustrative case. Provide a systematic review of CDM to highlight the importance of recognizing the consideration of CDM in patients presenting to a spine surgeon with myelopathy that progress despite adequate surgical decompression, or myelopathy concomitant with cytopenia, thus requiring further workup. Retrospective medical record review and systematic review of the literature. PubMed and Ovid-Embase database search was conducted in July 2022. Self-reported measures include PRISMA flow diagram for retrospective review; Physiological measures include retrospective review of MRI imaging of cervical spine; alternate demographic and laboratory value data extracted via literature review. A PubMed and Ovid-Embase database search was conducted in July 2022 searching for “copper deficiency myelopathy (MeSH)” from 2000 to 2022 via PRISMA guidelines. Following title and abstract review, the following data was extracted from full text: age, sex, etiology, hematological values upon presentation (mean corpuscular volume, white blood count, platelet count, and hemoglobin level), metal serum studies (serum copper, ceruloplasmin, and zinc), 24-hour collection of copper and zinc, and distinct radiographic findings on MRI. A total of 116 studies were included in this review which contained 198 cases of copper deficiency myelopathy. The mean age was 53.57±14.14 years, with the majority being females (63.8%). The most common etiology was prior gastric surgery (n=55, 36.2 %) followed by excessive zinc consumption from the use of zinc denture cream (n=39, 19.9%). The mean serum copper was 15.67±17.84 (normal=80.0–155.0) mcg/dL and mean ceruloplasmin was 6.43±5.25 (normal=16–45) mg/dL. In spite of appropriate treatment with copper supplementation, only 47 cases (24%) reported improvement in neurological status, and only 10 (5.1%) recovered to baseline. A hyperintense T2 signal abnormality resembling an inverted “v” in the dorsal columns was the most common radiographic abnormality. Pertinent risk factors for copper deficiency myelopathy include prior upper gastrointestinal surgery, zinc excess, and malabsorption. Characteristic laboratory and imaging findings include cytopenia, low serum copper and ceruloplasmin, and distinct inverted “v” T2 signal hyperintensity in the dorsal columns. The neurologic deterioration with copper deficiency will progress in spite of decompressive surgery, and can be devastating and irreversible even with copper supplementation, reinforcing the importance of early detection. We thus recommend patients with myelopathy presenting with a history of gastric bypass, malabsorption syndromes, excessive zinc exposure, cytopenia, or imaging resembling an inverted “v” shaped hyperintense T2 MRI signal in the dorsal columns, should first undergo blood tests for copper, ceruloplasmin, and B12 levels prior to surgical consideration.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>38909910</pmid><doi>10.1016/j.spinee.2024.06.018</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-2031-3306</orcidid><orcidid>https://orcid.org/0000-0002-3929-5964</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1529-9430
ispartof The spine journal, 2024-11, Vol.24 (11), p.2026-2034
issn 1529-9430
1878-1632
1878-1632
language eng
recordid cdi_proquest_miscellaneous_3071513006
source MEDLINE; Elsevier ScienceDirect Journals
subjects Adult
Aged
Cervical spondylitic myelopathy
Cervical Vertebrae - surgery
Copper - blood
Copper - deficiency
Copper deficiency myelopathy
CSM
Diagnosis, Differential
Female
Humans
Magnetic Resonance Imaging
Male
Middle Aged
Myelopathy
Spinal Cord Diseases - blood
Spinal Cord Diseases - diagnosis
Spinal Cord Diseases - etiology
Spinal Cord Diseases - surgery
Spondylosis - complications
Spondylosis - diagnosis
title Copper deficiency myelopathy mimicking cervical spondylitic myelopathy: a systematic review of the literature with case report
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T04%3A07%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Copper%20deficiency%20myelopathy%20mimicking%20cervical%20spondylitic%20myelopathy:%20a%20systematic%20review%20of%20the%20literature%20with%20case%20report&rft.jtitle=The%20spine%20journal&rft.au=Chen,%20Jeffrey%20W.&rft.date=2024-11&rft.volume=24&rft.issue=11&rft.spage=2026&rft.epage=2034&rft.pages=2026-2034&rft.issn=1529-9430&rft.eissn=1878-1632&rft_id=info:doi/10.1016/j.spinee.2024.06.018&rft_dat=%3Cproquest_cross%3E3071513006%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3071513006&rft_id=info:pmid/38909910&rft_els_id=S1529943024002985&rfr_iscdi=true