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Peripheral neuropathy in pediatric systemic lupus erythematosus
Peripheral neuropathy is an uncommon manifestation of systemic lupus erythematosus and has not yet been characterized in pediatric patients. We report the clinical and electrophysiologic features of peripheral neuropathy in one child and three adolescents with lupus erythematosus. There were three f...
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Published in: | Pediatric neurology 2002-07, Vol.27 (1), p.53-56 |
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creator | Harel, Liora Mukamel, Masha Brik, Riva Blau, Hannah Straussberg, Rachel |
description | Peripheral neuropathy is an uncommon manifestation of systemic lupus erythematosus and has not yet been characterized in pediatric patients. We report the clinical and electrophysiologic features of peripheral neuropathy in one child and three adolescents with lupus erythematosus. There were three females and one male. The peripheral neuropathy followed the onset of lupus erythematosus by a mean of 3 years. The onset of the neuropathy correlated with lupus erythematosus activity and presented with either severe pain or dropfoot. Nerve conduction studies revealed sensory and motor polyneuropathy in all patients and mononeuritis multiplex in two patients. Only one patient had associated central nervous system involvement at that time. All patients were positive for IgM and IgG anticardiolipin antibodies. Patients were treated with steroids, gabapentin, carbamazepine, azathioprine, and cyclophosphamide. Response to treatment was variable: two patients recovered and two had a partial response. Although an unusual manifestation, peripheral neuropathy should be kept in mind as part of the neurologic spectrum in lupus erythematosus. It is not necessarily associated with central nervous system disease. A role for antiphospholipid antibodies in the pathogenesis is suggested. |
doi_str_mv | 10.1016/S0887-8994(02)00377-6 |
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We report the clinical and electrophysiologic features of peripheral neuropathy in one child and three adolescents with lupus erythematosus. There were three females and one male. The peripheral neuropathy followed the onset of lupus erythematosus by a mean of 3 years. The onset of the neuropathy correlated with lupus erythematosus activity and presented with either severe pain or dropfoot. Nerve conduction studies revealed sensory and motor polyneuropathy in all patients and mononeuritis multiplex in two patients. Only one patient had associated central nervous system involvement at that time. All patients were positive for IgM and IgG anticardiolipin antibodies. Patients were treated with steroids, gabapentin, carbamazepine, azathioprine, and cyclophosphamide. Response to treatment was variable: two patients recovered and two had a partial response. Although an unusual manifestation, peripheral neuropathy should be kept in mind as part of the neurologic spectrum in lupus erythematosus. It is not necessarily associated with central nervous system disease. A role for antiphospholipid antibodies in the pathogenesis is suggested.</description><identifier>ISSN: 0887-8994</identifier><identifier>EISSN: 1873-5150</identifier><identifier>DOI: 10.1016/S0887-8994(02)00377-6</identifier><identifier>PMID: 12160975</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adolescent ; Antibodies, Anticardiolipin - blood ; Biological and medical sciences ; Child ; Female ; Humans ; Lupus Erythematosus, Systemic - complications ; Lupus Erythematosus, Systemic - immunology ; Male ; Medical sciences ; Motor Neurons - physiology ; Neural Conduction ; Neurons, Afferent - physiology ; Peripheral Nervous System Diseases - diagnosis ; Peripheral Nervous System Diseases - etiology ; Peripheral Nervous System Diseases - immunology ; Retrospective Studies ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; Tropical medicine</subject><ispartof>Pediatric neurology, 2002-07, Vol.27 (1), p.53-56</ispartof><rights>2002 Elsevier Science Inc.</rights><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-b8618e72d73f9eb72317211d2373ede82221e6019a78b9f1aa8a2aa4e27708753</citedby><cites>FETCH-LOGICAL-c443t-b8618e72d73f9eb72317211d2373ede82221e6019a78b9f1aa8a2aa4e27708753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13842489$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12160975$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Harel, Liora</creatorcontrib><creatorcontrib>Mukamel, Masha</creatorcontrib><creatorcontrib>Brik, Riva</creatorcontrib><creatorcontrib>Blau, Hannah</creatorcontrib><creatorcontrib>Straussberg, Rachel</creatorcontrib><title>Peripheral neuropathy in pediatric systemic lupus erythematosus</title><title>Pediatric neurology</title><addtitle>Pediatr Neurol</addtitle><description>Peripheral neuropathy is an uncommon manifestation of systemic lupus erythematosus and has not yet been characterized in pediatric patients. We report the clinical and electrophysiologic features of peripheral neuropathy in one child and three adolescents with lupus erythematosus. There were three females and one male. The peripheral neuropathy followed the onset of lupus erythematosus by a mean of 3 years. The onset of the neuropathy correlated with lupus erythematosus activity and presented with either severe pain or dropfoot. Nerve conduction studies revealed sensory and motor polyneuropathy in all patients and mononeuritis multiplex in two patients. Only one patient had associated central nervous system involvement at that time. All patients were positive for IgM and IgG anticardiolipin antibodies. Patients were treated with steroids, gabapentin, carbamazepine, azathioprine, and cyclophosphamide. Response to treatment was variable: two patients recovered and two had a partial response. Although an unusual manifestation, peripheral neuropathy should be kept in mind as part of the neurologic spectrum in lupus erythematosus. It is not necessarily associated with central nervous system disease. A role for antiphospholipid antibodies in the pathogenesis is suggested.</description><subject>Adolescent</subject><subject>Antibodies, Anticardiolipin - blood</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Female</subject><subject>Humans</subject><subject>Lupus Erythematosus, Systemic - complications</subject><subject>Lupus Erythematosus, Systemic - immunology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Motor Neurons - physiology</subject><subject>Neural Conduction</subject><subject>Neurons, Afferent - physiology</subject><subject>Peripheral Nervous System Diseases - diagnosis</subject><subject>Peripheral Nervous System Diseases - etiology</subject><subject>Peripheral Nervous System Diseases - immunology</subject><subject>Retrospective Studies</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><subject>Tropical medicine</subject><issn>0887-8994</issn><issn>1873-5150</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNqF0MtKxDAUgOEgijOOPoLSjaKLak7SNslqkMEbDCio65BJT5lIbyatMG9v54KzdJUsvnMSfkLOgd4ChezunUopYqlUck3ZDaVciDg7IGOQgscppPSQjP_IiJyE8EUpTRVLjskIGGRUiXRMpm_oXbtEb8qoxt43remWq8jVUYu5M513Ngqr0GE1XMq-7UOEftUtsTJdE_pwSo4KUwY8250T8vn48DF7juevTy-z-3lsk4R38UJmIFGwXPBC4UIwDoIB5IwLjjlKxhhgRkEZIReqAGOkYcYkyISgUqR8Qq62e1vffPcYOl25YLEsTY1NH7QAJZIUYIDpFlrfhOCx0K13lfErDVSvy-lNOb3OoinTm3I6G-Yudg_0iwrz_dQu1QAud8AEa8rCm9q6sHdcJiyRanDTrcMhx49Dr4N1WNshp0fb6bxx_3zlF1nbiow</recordid><startdate>20020701</startdate><enddate>20020701</enddate><creator>Harel, Liora</creator><creator>Mukamel, Masha</creator><creator>Brik, Riva</creator><creator>Blau, Hannah</creator><creator>Straussberg, Rachel</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><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></search><sort><creationdate>20020701</creationdate><title>Peripheral neuropathy in pediatric systemic lupus erythematosus</title><author>Harel, Liora ; Mukamel, Masha ; Brik, Riva ; Blau, Hannah ; Straussberg, Rachel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-b8618e72d73f9eb72317211d2373ede82221e6019a78b9f1aa8a2aa4e27708753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adolescent</topic><topic>Antibodies, Anticardiolipin - blood</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Female</topic><topic>Humans</topic><topic>Lupus Erythematosus, Systemic - complications</topic><topic>Lupus Erythematosus, Systemic - immunology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Motor Neurons - physiology</topic><topic>Neural Conduction</topic><topic>Neurons, Afferent - physiology</topic><topic>Peripheral Nervous System Diseases - diagnosis</topic><topic>Peripheral Nervous System Diseases - etiology</topic><topic>Peripheral Nervous System Diseases - immunology</topic><topic>Retrospective Studies</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>Tropical medicine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Harel, Liora</creatorcontrib><creatorcontrib>Mukamel, Masha</creatorcontrib><creatorcontrib>Brik, Riva</creatorcontrib><creatorcontrib>Blau, Hannah</creatorcontrib><creatorcontrib>Straussberg, Rachel</creatorcontrib><collection>Pascal-Francis</collection><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>Pediatric neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Harel, Liora</au><au>Mukamel, Masha</au><au>Brik, Riva</au><au>Blau, Hannah</au><au>Straussberg, Rachel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Peripheral neuropathy in pediatric systemic lupus erythematosus</atitle><jtitle>Pediatric neurology</jtitle><addtitle>Pediatr Neurol</addtitle><date>2002-07-01</date><risdate>2002</risdate><volume>27</volume><issue>1</issue><spage>53</spage><epage>56</epage><pages>53-56</pages><issn>0887-8994</issn><eissn>1873-5150</eissn><abstract>Peripheral neuropathy is an uncommon manifestation of systemic lupus erythematosus and has not yet been characterized in pediatric patients. We report the clinical and electrophysiologic features of peripheral neuropathy in one child and three adolescents with lupus erythematosus. There were three females and one male. The peripheral neuropathy followed the onset of lupus erythematosus by a mean of 3 years. The onset of the neuropathy correlated with lupus erythematosus activity and presented with either severe pain or dropfoot. Nerve conduction studies revealed sensory and motor polyneuropathy in all patients and mononeuritis multiplex in two patients. Only one patient had associated central nervous system involvement at that time. All patients were positive for IgM and IgG anticardiolipin antibodies. Patients were treated with steroids, gabapentin, carbamazepine, azathioprine, and cyclophosphamide. Response to treatment was variable: two patients recovered and two had a partial response. Although an unusual manifestation, peripheral neuropathy should be kept in mind as part of the neurologic spectrum in lupus erythematosus. It is not necessarily associated with central nervous system disease. A role for antiphospholipid antibodies in the pathogenesis is suggested.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>12160975</pmid><doi>10.1016/S0887-8994(02)00377-6</doi><tpages>4</tpages></addata></record> |
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subjects | Adolescent Antibodies, Anticardiolipin - blood Biological and medical sciences Child Female Humans Lupus Erythematosus, Systemic - complications Lupus Erythematosus, Systemic - immunology Male Medical sciences Motor Neurons - physiology Neural Conduction Neurons, Afferent - physiology Peripheral Nervous System Diseases - diagnosis Peripheral Nervous System Diseases - etiology Peripheral Nervous System Diseases - immunology Retrospective Studies Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis Tropical medicine |
title | Peripheral neuropathy in pediatric systemic lupus erythematosus |
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