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Atypical Trigeminal Neuralgia: A Rare Neurological Manifestation of Systemic Lupus Erythematosus
BACKGROUND Systemic lupus erythematosus (SLE) is a multisystem autoimmune disorder of unknown etiology which can present at any age with symptoms of mucocutaneous, musculoskeletal, renal, central nervous system, and nonspecific clinical pictures making the disease a "master of mimicry". CA...
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Published in: | The American journal of case reports 2017-01, Vol.18, p.42-45 |
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description | BACKGROUND Systemic lupus erythematosus (SLE) is a multisystem autoimmune disorder of unknown etiology which can present at any age with symptoms of mucocutaneous, musculoskeletal, renal, central nervous system, and nonspecific clinical pictures making the disease a "master of mimicry". CASE REPORT A 53-year-old female, who was recently diagnosed with SLE, presented with right-sided sharp and electric shock-like facial pain starting at the side of her right nostril and traveling down the naso-labial fold and then back to the angle of the jaw, mostly in the region of V2-V3 distribution with no radiation beyond trigeminal distribution. Her pain had been going for the last 2 years and was regarded as "pretrigeminal neuralgia"; however, it progressed in frequency over the last 2 weeks, with no clear identifying triggering factors. Her laboratory test results showed positive anti-nuclear antibodies (ANA) with raised titer, anti-double-stranded DNA, anti-ribonucleoprotein, anti-Sjögren's syndrome-related antigen A, anti-Sjögren's syndrome-related antigen B, and anti-smooth muscle antibodies. Other possibilities of migraine, postherpetic neuralgia, Bell's palsy, and brain tumor were ruled out. A diagnosis of SLE with trigeminal neuralgia (TN) was made and carbamazepine 100 mg 2 times a day was prescribed. CONCLUSIONS TN is seldom mentioned as a neurological manifestation of SLE; hence, we recommend further studies to investigate the SLE-mediated injury to trigeminal fibers to make a timely diagnosis of TN and to prevent progressive autoimmune process-related vasculitic and demyelinating changes. |
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CASE REPORT A 53-year-old female, who was recently diagnosed with SLE, presented with right-sided sharp and electric shock-like facial pain starting at the side of her right nostril and traveling down the naso-labial fold and then back to the angle of the jaw, mostly in the region of V2-V3 distribution with no radiation beyond trigeminal distribution. Her pain had been going for the last 2 years and was regarded as "pretrigeminal neuralgia"; however, it progressed in frequency over the last 2 weeks, with no clear identifying triggering factors. Her laboratory test results showed positive anti-nuclear antibodies (ANA) with raised titer, anti-double-stranded DNA, anti-ribonucleoprotein, anti-Sjögren's syndrome-related antigen A, anti-Sjögren's syndrome-related antigen B, and anti-smooth muscle antibodies. Other possibilities of migraine, postherpetic neuralgia, Bell's palsy, and brain tumor were ruled out. A diagnosis of SLE with trigeminal neuralgia (TN) was made and carbamazepine 100 mg 2 times a day was prescribed. CONCLUSIONS TN is seldom mentioned as a neurological manifestation of SLE; hence, we recommend further studies to investigate the SLE-mediated injury to trigeminal fibers to make a timely diagnosis of TN and to prevent progressive autoimmune process-related vasculitic and demyelinating changes.</description><identifier>ISSN: 1941-5923</identifier><identifier>EISSN: 1941-5923</identifier><identifier>DOI: 10.12659/AJCR.901478</identifier><identifier>PMID: 28077839</identifier><language>eng</language><publisher>United States: International Scientific Literature, Inc</publisher><subject>Administration, Oral ; Analgesics, Non-Narcotic - administration & dosage ; Carbamazepine - administration & dosage ; Dose-Response Relationship, Drug ; Female ; Humans ; Lupus Erythematosus, Systemic - complications ; Lupus Erythematosus, Systemic - diagnosis ; Lupus Erythematosus, Systemic - drug therapy ; Middle Aged ; Trigeminal Neuralgia - diagnosis ; Trigeminal Neuralgia - drug therapy ; Trigeminal Neuralgia - etiology</subject><ispartof>The American journal of case reports, 2017-01, Vol.18, p.42-45</ispartof><rights>Am J Case Rep, 2017 2017</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c427t-42498daceeb6e56d41d85299433f0e054040dfb54164700db7edb5b1e94392003</citedby><cites>FETCH-LOGICAL-c427t-42498daceeb6e56d41d85299433f0e054040dfb54164700db7edb5b1e94392003</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240879/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240879/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,883,27907,27908,53774,53776</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28077839$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kumar, Viki</creatorcontrib><creatorcontrib>Kaur, Jaspinder</creatorcontrib><creatorcontrib>Pothuri, Pallavi</creatorcontrib><creatorcontrib>Bandagi, Sahiba</creatorcontrib><title>Atypical Trigeminal Neuralgia: A Rare Neurological Manifestation of Systemic Lupus Erythematosus</title><title>The American journal of case reports</title><addtitle>Am J Case Rep</addtitle><description>BACKGROUND Systemic lupus erythematosus (SLE) is a multisystem autoimmune disorder of unknown etiology which can present at any age with symptoms of mucocutaneous, musculoskeletal, renal, central nervous system, and nonspecific clinical pictures making the disease a "master of mimicry". CASE REPORT A 53-year-old female, who was recently diagnosed with SLE, presented with right-sided sharp and electric shock-like facial pain starting at the side of her right nostril and traveling down the naso-labial fold and then back to the angle of the jaw, mostly in the region of V2-V3 distribution with no radiation beyond trigeminal distribution. Her pain had been going for the last 2 years and was regarded as "pretrigeminal neuralgia"; however, it progressed in frequency over the last 2 weeks, with no clear identifying triggering factors. Her laboratory test results showed positive anti-nuclear antibodies (ANA) with raised titer, anti-double-stranded DNA, anti-ribonucleoprotein, anti-Sjögren's syndrome-related antigen A, anti-Sjögren's syndrome-related antigen B, and anti-smooth muscle antibodies. Other possibilities of migraine, postherpetic neuralgia, Bell's palsy, and brain tumor were ruled out. A diagnosis of SLE with trigeminal neuralgia (TN) was made and carbamazepine 100 mg 2 times a day was prescribed. CONCLUSIONS TN is seldom mentioned as a neurological manifestation of SLE; hence, we recommend further studies to investigate the SLE-mediated injury to trigeminal fibers to make a timely diagnosis of TN and to prevent progressive autoimmune process-related vasculitic and demyelinating changes.</description><subject>Administration, Oral</subject><subject>Analgesics, Non-Narcotic - administration & dosage</subject><subject>Carbamazepine - administration & dosage</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Humans</subject><subject>Lupus Erythematosus, Systemic - complications</subject><subject>Lupus Erythematosus, Systemic - diagnosis</subject><subject>Lupus Erythematosus, Systemic - drug therapy</subject><subject>Middle Aged</subject><subject>Trigeminal Neuralgia - diagnosis</subject><subject>Trigeminal Neuralgia - drug therapy</subject><subject>Trigeminal Neuralgia - etiology</subject><issn>1941-5923</issn><issn>1941-5923</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNpVkc1PxCAQxYnRqNG9eTY9enBXoFCKB5PNxs-smqx6RtpOK6YtK7Qm_e_FXTUrl5kwP97w8hA6InhCaMLl2fRutphITJhIt9A-kYyMuaTx9ka_h0bev-NwEpoIGu-iPZpiIdJY7qPXaTcsTa7r6NmZChrThvYBeqfryujzaBottIPVja1ttSLvdWtK8J3ujG0jW0ZPg-_C0zya98veR5du6N6g0Z31vT9EO6WuPYx-6gF6ubp8nt2M54_Xt7PpfJwzKroxo0ymhc4BsgR4UjBSpJxKyeK4xIA5wwwXZcYZSZjAuMgEFBnPCARCUozjA3Sx1l32WQNFDm0XPKilM412g7LaqP-T1rypyn4qThlOhQwCJz8Czn70wZ5qjM-hrnULtveKpDwlmAscB_R0jebOeu-g_FtDsFrlor5zUetcAn68-bU_-DeF-AuBCYm-</recordid><startdate>20170112</startdate><enddate>20170112</enddate><creator>Kumar, Viki</creator><creator>Kaur, Jaspinder</creator><creator>Pothuri, Pallavi</creator><creator>Bandagi, Sahiba</creator><general>International Scientific Literature, 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><scope>5PM</scope></search><sort><creationdate>20170112</creationdate><title>Atypical Trigeminal Neuralgia: A Rare Neurological Manifestation of Systemic Lupus Erythematosus</title><author>Kumar, Viki ; Kaur, Jaspinder ; Pothuri, Pallavi ; Bandagi, Sahiba</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-42498daceeb6e56d41d85299433f0e054040dfb54164700db7edb5b1e94392003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Administration, Oral</topic><topic>Analgesics, Non-Narcotic - administration & dosage</topic><topic>Carbamazepine - administration & dosage</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Humans</topic><topic>Lupus Erythematosus, Systemic - complications</topic><topic>Lupus Erythematosus, Systemic - diagnosis</topic><topic>Lupus Erythematosus, Systemic - drug therapy</topic><topic>Middle Aged</topic><topic>Trigeminal Neuralgia - diagnosis</topic><topic>Trigeminal Neuralgia - drug therapy</topic><topic>Trigeminal Neuralgia - etiology</topic><toplevel>online_resources</toplevel><creatorcontrib>Kumar, Viki</creatorcontrib><creatorcontrib>Kaur, Jaspinder</creatorcontrib><creatorcontrib>Pothuri, Pallavi</creatorcontrib><creatorcontrib>Bandagi, Sahiba</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>The American journal of case reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kumar, Viki</au><au>Kaur, Jaspinder</au><au>Pothuri, Pallavi</au><au>Bandagi, Sahiba</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Atypical Trigeminal Neuralgia: A Rare Neurological Manifestation of Systemic Lupus Erythematosus</atitle><jtitle>The American journal of case reports</jtitle><addtitle>Am J Case Rep</addtitle><date>2017-01-12</date><risdate>2017</risdate><volume>18</volume><spage>42</spage><epage>45</epage><pages>42-45</pages><issn>1941-5923</issn><eissn>1941-5923</eissn><abstract>BACKGROUND Systemic lupus erythematosus (SLE) is a multisystem autoimmune disorder of unknown etiology which can present at any age with symptoms of mucocutaneous, musculoskeletal, renal, central nervous system, and nonspecific clinical pictures making the disease a "master of mimicry". CASE REPORT A 53-year-old female, who was recently diagnosed with SLE, presented with right-sided sharp and electric shock-like facial pain starting at the side of her right nostril and traveling down the naso-labial fold and then back to the angle of the jaw, mostly in the region of V2-V3 distribution with no radiation beyond trigeminal distribution. Her pain had been going for the last 2 years and was regarded as "pretrigeminal neuralgia"; however, it progressed in frequency over the last 2 weeks, with no clear identifying triggering factors. Her laboratory test results showed positive anti-nuclear antibodies (ANA) with raised titer, anti-double-stranded DNA, anti-ribonucleoprotein, anti-Sjögren's syndrome-related antigen A, anti-Sjögren's syndrome-related antigen B, and anti-smooth muscle antibodies. Other possibilities of migraine, postherpetic neuralgia, Bell's palsy, and brain tumor were ruled out. A diagnosis of SLE with trigeminal neuralgia (TN) was made and carbamazepine 100 mg 2 times a day was prescribed. CONCLUSIONS TN is seldom mentioned as a neurological manifestation of SLE; hence, we recommend further studies to investigate the SLE-mediated injury to trigeminal fibers to make a timely diagnosis of TN and to prevent progressive autoimmune process-related vasculitic and demyelinating changes.</abstract><cop>United States</cop><pub>International Scientific Literature, Inc</pub><pmid>28077839</pmid><doi>10.12659/AJCR.901478</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Oral Analgesics, Non-Narcotic - administration & dosage Carbamazepine - administration & dosage Dose-Response Relationship, Drug Female Humans Lupus Erythematosus, Systemic - complications Lupus Erythematosus, Systemic - diagnosis Lupus Erythematosus, Systemic - drug therapy Middle Aged Trigeminal Neuralgia - diagnosis Trigeminal Neuralgia - drug therapy Trigeminal Neuralgia - etiology |
title | Atypical Trigeminal Neuralgia: A Rare Neurological Manifestation of Systemic Lupus Erythematosus |
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