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A 30-year-old female with dermatomyositis without high elevation of muscle enzymes: a rare case report from Syria
Dermatomyositis (DM), sometimes referred to as inflammatory and degenerative changes in the skin and muscles, is a rare autoimmune disorder. DM is distinguished by myopathic disease, symmetrical proximal muscle weakness, and increased creatine kinase (CK). A 30-year-old-female presented to the depar...
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Published in: | Annals of medicine and surgery 2024-04, Vol.86 (4), p.2167-2171 |
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creator | Hamsho, Suaad Sleiay, Bilal Sleiay, Mouhammed Batrash, Obeda Alabdullah, Hadi Aboud, Majed |
description | Dermatomyositis (DM), sometimes referred to as inflammatory and degenerative changes in the skin and muscles, is a rare autoimmune disorder. DM is distinguished by myopathic disease, symmetrical proximal muscle weakness, and increased creatine kinase (CK).
A 30-year-old-female presented to the department of dermatology with a history of chronic right hand pain spreading to the shoulder, severe tachycardia, and dyspenia that increased during routine tasks like using the bathroom. What makes this case unique is that the CPK developed without doubling, and the final concentration was 207 ng/ml. Other common clinical symptoms include amyopathic/hypomyopathic muscle involvement and DM-specific rash (Gottron's papules, heliotrope rash), and these manifestations were in our patients. Sun protection, topical treatment with corticosteroids and/or calcineurin inhibitors, and systemic medication should be utilized for all individuals with nonvasculopathic disease. In our case, the patient stopped using azathioprine and began taking methotrexate.
Sun protection, topical therapy with corticosteroids and/or calcineurin inhibitors, and systemic medication should be utilized in layers for all individuals with nonvasculopathic illnesses. Mycophenolat Mofetil is beneficial in treating refractory illnesses as well as individuals with interstitial lung disease or substantial skin disease.
Even if test findings are not conclusive, dermatomyositis should always be considered when muscular weakness manifests. It's important to distinguish the disorder from connective tissue diseases like lupus erythematosus. In fact, to correctly diagnose DM, if there are any doubts, a muscle biopsy is required. |
doi_str_mv | 10.1097/MS9.0000000000001682 |
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A 30-year-old-female presented to the department of dermatology with a history of chronic right hand pain spreading to the shoulder, severe tachycardia, and dyspenia that increased during routine tasks like using the bathroom. What makes this case unique is that the CPK developed without doubling, and the final concentration was 207 ng/ml. Other common clinical symptoms include amyopathic/hypomyopathic muscle involvement and DM-specific rash (Gottron's papules, heliotrope rash), and these manifestations were in our patients. Sun protection, topical treatment with corticosteroids and/or calcineurin inhibitors, and systemic medication should be utilized for all individuals with nonvasculopathic disease. In our case, the patient stopped using azathioprine and began taking methotrexate.
Sun protection, topical therapy with corticosteroids and/or calcineurin inhibitors, and systemic medication should be utilized in layers for all individuals with nonvasculopathic illnesses. Mycophenolat Mofetil is beneficial in treating refractory illnesses as well as individuals with interstitial lung disease or substantial skin disease.
Even if test findings are not conclusive, dermatomyositis should always be considered when muscular weakness manifests. It's important to distinguish the disorder from connective tissue diseases like lupus erythematosus. In fact, to correctly diagnose DM, if there are any doubts, a muscle biopsy is required.</description><identifier>ISSN: 2049-0801</identifier><identifier>EISSN: 2049-0801</identifier><identifier>DOI: 10.1097/MS9.0000000000001682</identifier><identifier>PMID: 38576947</identifier><language>eng</language><publisher>England: Lippincott Williams & Wilkins</publisher><subject>Case Reports</subject><ispartof>Annals of medicine and surgery, 2024-04, Vol.86 (4), p.2167-2171</ispartof><rights>Copyright © 2024 The Author(s). Published by Wolters Kluwer Health, Inc.</rights><rights>Copyright © 2024 The Author(s). Published by Wolters Kluwer Health, Inc. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c255t-2b29bd9ddc45b3b9f7ea60e8173df60185ccdf03b53b50b046d5fa232f2280fb3</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/PMC10990297/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10990297/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38576947$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hamsho, Suaad</creatorcontrib><creatorcontrib>Sleiay, Bilal</creatorcontrib><creatorcontrib>Sleiay, Mouhammed</creatorcontrib><creatorcontrib>Batrash, Obeda</creatorcontrib><creatorcontrib>Alabdullah, Hadi</creatorcontrib><creatorcontrib>Aboud, Majed</creatorcontrib><title>A 30-year-old female with dermatomyositis without high elevation of muscle enzymes: a rare case report from Syria</title><title>Annals of medicine and surgery</title><addtitle>Ann Med Surg (Lond)</addtitle><description>Dermatomyositis (DM), sometimes referred to as inflammatory and degenerative changes in the skin and muscles, is a rare autoimmune disorder. DM is distinguished by myopathic disease, symmetrical proximal muscle weakness, and increased creatine kinase (CK).
A 30-year-old-female presented to the department of dermatology with a history of chronic right hand pain spreading to the shoulder, severe tachycardia, and dyspenia that increased during routine tasks like using the bathroom. What makes this case unique is that the CPK developed without doubling, and the final concentration was 207 ng/ml. Other common clinical symptoms include amyopathic/hypomyopathic muscle involvement and DM-specific rash (Gottron's papules, heliotrope rash), and these manifestations were in our patients. Sun protection, topical treatment with corticosteroids and/or calcineurin inhibitors, and systemic medication should be utilized for all individuals with nonvasculopathic disease. In our case, the patient stopped using azathioprine and began taking methotrexate.
Sun protection, topical therapy with corticosteroids and/or calcineurin inhibitors, and systemic medication should be utilized in layers for all individuals with nonvasculopathic illnesses. Mycophenolat Mofetil is beneficial in treating refractory illnesses as well as individuals with interstitial lung disease or substantial skin disease.
Even if test findings are not conclusive, dermatomyositis should always be considered when muscular weakness manifests. It's important to distinguish the disorder from connective tissue diseases like lupus erythematosus. In fact, to correctly diagnose DM, if there are any doubts, a muscle biopsy is required.</description><subject>Case Reports</subject><issn>2049-0801</issn><issn>2049-0801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpdUdtKAzEQDaJYqf0DkfzA1myyt_gipXiDig_V5yWbTLqRTVOTbWX9erdWS3UYmGFmzhk4B6GLmIxjwvOrpzkfk4OIs4IeoTNKEh6RgsTHB_0AjUJ42x6RlGVZcYoGrEjzjCf5GXqfYEaiDoSPXKOwBisawB-mrbECb0XrbOeCaU34Hrp1i2uzqDE0sBGtcUvsNLbrIHsULD87C-EaC-yFByxFAOxh5XyLtXcWzztvxDk60aIJMPqpQ_R6d_syfYhmz_eP08kskjRN24hWlFeKKyWTtGIV1zmIjEAR50zpjMRFKqXShFVpn6QiSaZSLSijmtKC6IoN0c2Od7WuLCgJy9aLplx5Y4XvSidM-XezNHW5cJuyF5gTyvOeIdkxSO9C8KD34Jhsr_Kyt6H8b0MPuzx8vAf9is6-AJwghaI</recordid><startdate>20240401</startdate><enddate>20240401</enddate><creator>Hamsho, Suaad</creator><creator>Sleiay, Bilal</creator><creator>Sleiay, Mouhammed</creator><creator>Batrash, Obeda</creator><creator>Alabdullah, Hadi</creator><creator>Aboud, Majed</creator><general>Lippincott Williams & Wilkins</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20240401</creationdate><title>A 30-year-old female with dermatomyositis without high elevation of muscle enzymes: a rare case report from Syria</title><author>Hamsho, Suaad ; Sleiay, Bilal ; Sleiay, Mouhammed ; Batrash, Obeda ; Alabdullah, Hadi ; Aboud, Majed</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c255t-2b29bd9ddc45b3b9f7ea60e8173df60185ccdf03b53b50b046d5fa232f2280fb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Case Reports</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hamsho, Suaad</creatorcontrib><creatorcontrib>Sleiay, Bilal</creatorcontrib><creatorcontrib>Sleiay, Mouhammed</creatorcontrib><creatorcontrib>Batrash, Obeda</creatorcontrib><creatorcontrib>Alabdullah, Hadi</creatorcontrib><creatorcontrib>Aboud, Majed</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Annals of medicine and surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hamsho, Suaad</au><au>Sleiay, Bilal</au><au>Sleiay, Mouhammed</au><au>Batrash, Obeda</au><au>Alabdullah, Hadi</au><au>Aboud, Majed</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A 30-year-old female with dermatomyositis without high elevation of muscle enzymes: a rare case report from Syria</atitle><jtitle>Annals of medicine and surgery</jtitle><addtitle>Ann Med Surg (Lond)</addtitle><date>2024-04-01</date><risdate>2024</risdate><volume>86</volume><issue>4</issue><spage>2167</spage><epage>2171</epage><pages>2167-2171</pages><issn>2049-0801</issn><eissn>2049-0801</eissn><abstract>Dermatomyositis (DM), sometimes referred to as inflammatory and degenerative changes in the skin and muscles, is a rare autoimmune disorder. DM is distinguished by myopathic disease, symmetrical proximal muscle weakness, and increased creatine kinase (CK).
A 30-year-old-female presented to the department of dermatology with a history of chronic right hand pain spreading to the shoulder, severe tachycardia, and dyspenia that increased during routine tasks like using the bathroom. What makes this case unique is that the CPK developed without doubling, and the final concentration was 207 ng/ml. Other common clinical symptoms include amyopathic/hypomyopathic muscle involvement and DM-specific rash (Gottron's papules, heliotrope rash), and these manifestations were in our patients. Sun protection, topical treatment with corticosteroids and/or calcineurin inhibitors, and systemic medication should be utilized for all individuals with nonvasculopathic disease. In our case, the patient stopped using azathioprine and began taking methotrexate.
Sun protection, topical therapy with corticosteroids and/or calcineurin inhibitors, and systemic medication should be utilized in layers for all individuals with nonvasculopathic illnesses. Mycophenolat Mofetil is beneficial in treating refractory illnesses as well as individuals with interstitial lung disease or substantial skin disease.
Even if test findings are not conclusive, dermatomyositis should always be considered when muscular weakness manifests. It's important to distinguish the disorder from connective tissue diseases like lupus erythematosus. In fact, to correctly diagnose DM, if there are any doubts, a muscle biopsy is required.</abstract><cop>England</cop><pub>Lippincott Williams & Wilkins</pub><pmid>38576947</pmid><doi>10.1097/MS9.0000000000001682</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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title | A 30-year-old female with dermatomyositis without high elevation of muscle enzymes: a rare case report from Syria |
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