{"title":"视神经脊髓炎频谱障碍伴间质性肺炎和明显的高血血症:1例报告和文献回顾。","authors":"Tomohiro Yoshida, Keisuke Nishimura, Kei Hirose, Hiroyuki Murabe","doi":"10.1620/tjem.2025.J007","DOIUrl":null,"url":null,"abstract":"<p><p>Neuromyelitis optica spectrum disorder is an inflammatory disease of central nervous system. Autoantibodies against aquaporin 4 (anti-AQP4-ab) are often present in neuromyelitis optica spectrum disorder and have pathogenic effects on central nervous system. Aquaporin 4 is also expressed in peripheral organs, and some cases of anti-AQP4-ab-positive neuromyelitis optica spectrum disorder with peripheral organ involvement have recently been reported. Here, we report a unique case of anti-AQP4-ab-positive neuromyelitis optica spectrum disorder. A 58-year-old man was admitted with fever, interstitial pneumonia, and markedly increased serum-creatine kinase levels (up to 300,200 U/L). Skeletal muscle biopsy revealed rhabdomyolysis. Collagen and infectious diseases were excluded; therefore, adverse effects of prescription drugs were initially suspected. Clinical symptoms improved with steroid administration and discontinuation of all previously prescribed medications. However, bilateral vision loss, bilateral lower-limb muscle weakness, and bilateral lower-limb sensory disturbances appeared later, and fever and increased serum-creatine kinase levels recurred. The patient was diagnosed with neuromyelitis optica spectrum disorder with peripheral organ (lung and skeletal muscles) involvement based on magnetic resonance imaging findings and serum anti-AQP4-ab positivity. Our case demonstrates that interstitial pneumonia and rhabdomyolysis can be the initial symptoms and indicators of the relapse of anti-AQP4-ab-positive neuromyelitis optica spectrum disorder, and skeletal muscle involvement can lead to markedly elevated creatine kinase levels.</p>","PeriodicalId":23187,"journal":{"name":"Tohoku Journal of Experimental Medicine","volume":" ","pages":"327-334"},"PeriodicalIF":1.6000,"publicationDate":"2025-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Neuromyelitis Optica Spectrum Disorder with Interstitial Pneumonia and Marked HyperCKemia as an Initial Presentation: A Case Report and Literature Review.\",\"authors\":\"Tomohiro Yoshida, Keisuke Nishimura, Kei Hirose, Hiroyuki Murabe\",\"doi\":\"10.1620/tjem.2025.J007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Neuromyelitis optica spectrum disorder is an inflammatory disease of central nervous system. Autoantibodies against aquaporin 4 (anti-AQP4-ab) are often present in neuromyelitis optica spectrum disorder and have pathogenic effects on central nervous system. Aquaporin 4 is also expressed in peripheral organs, and some cases of anti-AQP4-ab-positive neuromyelitis optica spectrum disorder with peripheral organ involvement have recently been reported. Here, we report a unique case of anti-AQP4-ab-positive neuromyelitis optica spectrum disorder. A 58-year-old man was admitted with fever, interstitial pneumonia, and markedly increased serum-creatine kinase levels (up to 300,200 U/L). Skeletal muscle biopsy revealed rhabdomyolysis. Collagen and infectious diseases were excluded; therefore, adverse effects of prescription drugs were initially suspected. Clinical symptoms improved with steroid administration and discontinuation of all previously prescribed medications. However, bilateral vision loss, bilateral lower-limb muscle weakness, and bilateral lower-limb sensory disturbances appeared later, and fever and increased serum-creatine kinase levels recurred. The patient was diagnosed with neuromyelitis optica spectrum disorder with peripheral organ (lung and skeletal muscles) involvement based on magnetic resonance imaging findings and serum anti-AQP4-ab positivity. Our case demonstrates that interstitial pneumonia and rhabdomyolysis can be the initial symptoms and indicators of the relapse of anti-AQP4-ab-positive neuromyelitis optica spectrum disorder, and skeletal muscle involvement can lead to markedly elevated creatine kinase levels.</p>\",\"PeriodicalId\":23187,\"journal\":{\"name\":\"Tohoku Journal of Experimental Medicine\",\"volume\":\" \",\"pages\":\"327-334\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2025-08-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tohoku Journal of Experimental Medicine\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1620/tjem.2025.J007\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/30 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tohoku Journal of Experimental Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1620/tjem.2025.J007","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/30 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
Neuromyelitis Optica Spectrum Disorder with Interstitial Pneumonia and Marked HyperCKemia as an Initial Presentation: A Case Report and Literature Review.
Neuromyelitis optica spectrum disorder is an inflammatory disease of central nervous system. Autoantibodies against aquaporin 4 (anti-AQP4-ab) are often present in neuromyelitis optica spectrum disorder and have pathogenic effects on central nervous system. Aquaporin 4 is also expressed in peripheral organs, and some cases of anti-AQP4-ab-positive neuromyelitis optica spectrum disorder with peripheral organ involvement have recently been reported. Here, we report a unique case of anti-AQP4-ab-positive neuromyelitis optica spectrum disorder. A 58-year-old man was admitted with fever, interstitial pneumonia, and markedly increased serum-creatine kinase levels (up to 300,200 U/L). Skeletal muscle biopsy revealed rhabdomyolysis. Collagen and infectious diseases were excluded; therefore, adverse effects of prescription drugs were initially suspected. Clinical symptoms improved with steroid administration and discontinuation of all previously prescribed medications. However, bilateral vision loss, bilateral lower-limb muscle weakness, and bilateral lower-limb sensory disturbances appeared later, and fever and increased serum-creatine kinase levels recurred. The patient was diagnosed with neuromyelitis optica spectrum disorder with peripheral organ (lung and skeletal muscles) involvement based on magnetic resonance imaging findings and serum anti-AQP4-ab positivity. Our case demonstrates that interstitial pneumonia and rhabdomyolysis can be the initial symptoms and indicators of the relapse of anti-AQP4-ab-positive neuromyelitis optica spectrum disorder, and skeletal muscle involvement can lead to markedly elevated creatine kinase levels.
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