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Macroglossia in rapidly progressive inclusion body myositis
Inclusion body myositis (IBM) is a refractory muscle disease characterized by inflammatory and degenerative features in myofibers. Macroglossia is common in systemic amyloid light chain amyloidosis; however, no reports have been published on patients with IBM. We encountered a female patient with cl...
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Published in: | Neuropathology 2023-06, Vol.43 (3), p.252-256 |
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creator | Yamasaki, Yoshimune Mukaino, Akihiro Yamashita, Satoshi Takeuchi, Yousuke Tawara, Nozomu Yoshida, Ryoji Honda, Yumi Yamashita, Taro Kakimoto, Asako Ueyama, Hidetsugu Ando, Yukio |
description | Inclusion body myositis (IBM) is a refractory muscle disease characterized by inflammatory and degenerative features in myofibers. Macroglossia is common in systemic amyloid light chain amyloidosis; however, no reports have been published on patients with IBM. We encountered a female patient with clinicopathologically defined IBM who exhibited relatively rapid progression of dysphagia, gait disturbance, and macroglossia. Muscle biopsy demonstrated endomysial mononuclear inflammatory infiltrates, fiber necrosis and regeneration with rimmed vacuoles, and sarcoplasmic inclusions of p62. Tongue biopsy demonstrated fiber degeneration with fatty replacement and fibrosis, nonnecrotic fibers surrounded and invaded by mononuclear cells, and sarcoplasmic dotlike inclusions of p62. Based on the parotid gland, lip, and muscle biopsy, she was diagnosed as having IBM with Sjögren's syndrome. She was treated with steroid pulse and intravenous immunoglobulin therapy followed by oral administration of prednisolone, which resulted in temporary clinical improvement. Macroglossia might be an indicator of immunotherapy effectiveness. |
doi_str_mv | 10.1111/neup.12879 |
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Macroglossia is common in systemic amyloid light chain amyloidosis; however, no reports have been published on patients with IBM. We encountered a female patient with clinicopathologically defined IBM who exhibited relatively rapid progression of dysphagia, gait disturbance, and macroglossia. Muscle biopsy demonstrated endomysial mononuclear inflammatory infiltrates, fiber necrosis and regeneration with rimmed vacuoles, and sarcoplasmic inclusions of p62. Tongue biopsy demonstrated fiber degeneration with fatty replacement and fibrosis, nonnecrotic fibers surrounded and invaded by mononuclear cells, and sarcoplasmic dotlike inclusions of p62. Based on the parotid gland, lip, and muscle biopsy, she was diagnosed as having IBM with Sjögren's syndrome. She was treated with steroid pulse and intravenous immunoglobulin therapy followed by oral administration of prednisolone, which resulted in temporary clinical improvement. Macroglossia might be an indicator of immunotherapy effectiveness.</description><identifier>ISSN: 0919-6544</identifier><identifier>EISSN: 1440-1789</identifier><identifier>DOI: 10.1111/neup.12879</identifier><identifier>PMID: 36349419</identifier><language>eng</language><publisher>Melbourne: John Wiley & Sons Australia, Ltd</publisher><subject>Amyloid ; Amyloidosis ; Biopsy ; Dysphagia ; Female ; Fibrosis ; Gait ; Humans ; Immunotherapy ; Inclusion bodies ; inclusion body myositis ; Inflammatory diseases ; Leukocytes (mononuclear) ; Macroglossia ; Movement disorders ; Musculoskeletal diseases ; Myocardium - pathology ; Myositis ; Myositis, Inclusion Body - complications ; Myositis, Inclusion Body - diagnosis ; Myositis, Inclusion Body - pathology ; Oral administration ; Parotid gland ; Prednisolone ; rapid progression ; Sjogren's syndrome ; Sjögren's syndrome ; Vacuoles</subject><ispartof>Neuropathology, 2023-06, Vol.43 (3), p.252-256</ispartof><rights>2022 Japanese Society of Neuropathology.</rights><rights>2023 Japanese Society of Neuropathology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4149-41307ea13c150d633be433915afbf34c857eb055c6de9c9fb35676952a73496e3</citedby><cites>FETCH-LOGICAL-c4149-41307ea13c150d633be433915afbf34c857eb055c6de9c9fb35676952a73496e3</cites><orcidid>0000-0001-7486-0597</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36349419$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yamasaki, Yoshimune</creatorcontrib><creatorcontrib>Mukaino, Akihiro</creatorcontrib><creatorcontrib>Yamashita, Satoshi</creatorcontrib><creatorcontrib>Takeuchi, Yousuke</creatorcontrib><creatorcontrib>Tawara, Nozomu</creatorcontrib><creatorcontrib>Yoshida, Ryoji</creatorcontrib><creatorcontrib>Honda, Yumi</creatorcontrib><creatorcontrib>Yamashita, Taro</creatorcontrib><creatorcontrib>Kakimoto, Asako</creatorcontrib><creatorcontrib>Ueyama, Hidetsugu</creatorcontrib><creatorcontrib>Ando, Yukio</creatorcontrib><title>Macroglossia in rapidly progressive inclusion body myositis</title><title>Neuropathology</title><addtitle>Neuropathology</addtitle><description>Inclusion body myositis (IBM) is a refractory muscle disease characterized by inflammatory and degenerative features in myofibers. Macroglossia is common in systemic amyloid light chain amyloidosis; however, no reports have been published on patients with IBM. We encountered a female patient with clinicopathologically defined IBM who exhibited relatively rapid progression of dysphagia, gait disturbance, and macroglossia. Muscle biopsy demonstrated endomysial mononuclear inflammatory infiltrates, fiber necrosis and regeneration with rimmed vacuoles, and sarcoplasmic inclusions of p62. Tongue biopsy demonstrated fiber degeneration with fatty replacement and fibrosis, nonnecrotic fibers surrounded and invaded by mononuclear cells, and sarcoplasmic dotlike inclusions of p62. Based on the parotid gland, lip, and muscle biopsy, she was diagnosed as having IBM with Sjögren's syndrome. She was treated with steroid pulse and intravenous immunoglobulin therapy followed by oral administration of prednisolone, which resulted in temporary clinical improvement. Macroglossia might be an indicator of immunotherapy effectiveness.</description><subject>Amyloid</subject><subject>Amyloidosis</subject><subject>Biopsy</subject><subject>Dysphagia</subject><subject>Female</subject><subject>Fibrosis</subject><subject>Gait</subject><subject>Humans</subject><subject>Immunotherapy</subject><subject>Inclusion bodies</subject><subject>inclusion body myositis</subject><subject>Inflammatory diseases</subject><subject>Leukocytes (mononuclear)</subject><subject>Macroglossia</subject><subject>Movement disorders</subject><subject>Musculoskeletal diseases</subject><subject>Myocardium - pathology</subject><subject>Myositis</subject><subject>Myositis, Inclusion Body - complications</subject><subject>Myositis, Inclusion Body - diagnosis</subject><subject>Myositis, Inclusion Body - pathology</subject><subject>Oral administration</subject><subject>Parotid gland</subject><subject>Prednisolone</subject><subject>rapid progression</subject><subject>Sjogren's syndrome</subject><subject>Sjögren's syndrome</subject><subject>Vacuoles</subject><issn>0919-6544</issn><issn>1440-1789</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kEtPwzAQhC0EoqFw4QegSNyQUrzxI7E4oao8pPI40LPlOA5ylSbBbkD597ikcGQvK40-zc4OQueAZxDmujF9N4M0z8QBioBSnECWi0MUYQEi4YzSCTrxfo0xZCLNj9GEcEIFBRGhmyelXftet95bFdsmdqqzZT3EXVCdCeqnCbKue2_bJi7acog3Q-vt1vpTdFSp2puz_Z6i1d3ibf6QLF_uH-e3y0RToCKhQHBmFBANDJeckMJQQgQwVRUVoTpnmSkwY5qXRmhRFYTxjAuWqiyk5IZM0eXoGzJ99MZv5brtXRNOyjRPgTKKcx6oq5EK_3jvTCU7ZzfKDRKw3PUkdz3Jn54CfLG37IuNKf_Q32ICACPwZWsz_GMlnxer19H0G0LXcms</recordid><startdate>202306</startdate><enddate>202306</enddate><creator>Yamasaki, Yoshimune</creator><creator>Mukaino, Akihiro</creator><creator>Yamashita, Satoshi</creator><creator>Takeuchi, Yousuke</creator><creator>Tawara, Nozomu</creator><creator>Yoshida, Ryoji</creator><creator>Honda, Yumi</creator><creator>Yamashita, Taro</creator><creator>Kakimoto, Asako</creator><creator>Ueyama, Hidetsugu</creator><creator>Ando, Yukio</creator><general>John Wiley & Sons Australia, Ltd</general><general>Wiley Subscription Services, 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>7TK</scope><scope>K9.</scope><orcidid>https://orcid.org/0000-0001-7486-0597</orcidid></search><sort><creationdate>202306</creationdate><title>Macroglossia in rapidly progressive inclusion body myositis</title><author>Yamasaki, Yoshimune ; Mukaino, Akihiro ; Yamashita, Satoshi ; Takeuchi, Yousuke ; Tawara, Nozomu ; Yoshida, Ryoji ; Honda, Yumi ; Yamashita, Taro ; Kakimoto, Asako ; Ueyama, Hidetsugu ; Ando, Yukio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4149-41307ea13c150d633be433915afbf34c857eb055c6de9c9fb35676952a73496e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Amyloid</topic><topic>Amyloidosis</topic><topic>Biopsy</topic><topic>Dysphagia</topic><topic>Female</topic><topic>Fibrosis</topic><topic>Gait</topic><topic>Humans</topic><topic>Immunotherapy</topic><topic>Inclusion bodies</topic><topic>inclusion body myositis</topic><topic>Inflammatory diseases</topic><topic>Leukocytes (mononuclear)</topic><topic>Macroglossia</topic><topic>Movement disorders</topic><topic>Musculoskeletal diseases</topic><topic>Myocardium - pathology</topic><topic>Myositis</topic><topic>Myositis, Inclusion Body - complications</topic><topic>Myositis, Inclusion Body - diagnosis</topic><topic>Myositis, Inclusion Body - pathology</topic><topic>Oral administration</topic><topic>Parotid gland</topic><topic>Prednisolone</topic><topic>rapid progression</topic><topic>Sjogren's syndrome</topic><topic>Sjögren's syndrome</topic><topic>Vacuoles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamasaki, Yoshimune</creatorcontrib><creatorcontrib>Mukaino, Akihiro</creatorcontrib><creatorcontrib>Yamashita, Satoshi</creatorcontrib><creatorcontrib>Takeuchi, Yousuke</creatorcontrib><creatorcontrib>Tawara, Nozomu</creatorcontrib><creatorcontrib>Yoshida, Ryoji</creatorcontrib><creatorcontrib>Honda, Yumi</creatorcontrib><creatorcontrib>Yamashita, Taro</creatorcontrib><creatorcontrib>Kakimoto, Asako</creatorcontrib><creatorcontrib>Ueyama, Hidetsugu</creatorcontrib><creatorcontrib>Ando, Yukio</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><jtitle>Neuropathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamasaki, Yoshimune</au><au>Mukaino, Akihiro</au><au>Yamashita, Satoshi</au><au>Takeuchi, Yousuke</au><au>Tawara, Nozomu</au><au>Yoshida, Ryoji</au><au>Honda, Yumi</au><au>Yamashita, Taro</au><au>Kakimoto, Asako</au><au>Ueyama, Hidetsugu</au><au>Ando, Yukio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Macroglossia in rapidly progressive inclusion body myositis</atitle><jtitle>Neuropathology</jtitle><addtitle>Neuropathology</addtitle><date>2023-06</date><risdate>2023</risdate><volume>43</volume><issue>3</issue><spage>252</spage><epage>256</epage><pages>252-256</pages><issn>0919-6544</issn><eissn>1440-1789</eissn><abstract>Inclusion body myositis (IBM) is a refractory muscle disease characterized by inflammatory and degenerative features in myofibers. Macroglossia is common in systemic amyloid light chain amyloidosis; however, no reports have been published on patients with IBM. We encountered a female patient with clinicopathologically defined IBM who exhibited relatively rapid progression of dysphagia, gait disturbance, and macroglossia. Muscle biopsy demonstrated endomysial mononuclear inflammatory infiltrates, fiber necrosis and regeneration with rimmed vacuoles, and sarcoplasmic inclusions of p62. Tongue biopsy demonstrated fiber degeneration with fatty replacement and fibrosis, nonnecrotic fibers surrounded and invaded by mononuclear cells, and sarcoplasmic dotlike inclusions of p62. Based on the parotid gland, lip, and muscle biopsy, she was diagnosed as having IBM with Sjögren's syndrome. She was treated with steroid pulse and intravenous immunoglobulin therapy followed by oral administration of prednisolone, which resulted in temporary clinical improvement. 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subjects | Amyloid Amyloidosis Biopsy Dysphagia Female Fibrosis Gait Humans Immunotherapy Inclusion bodies inclusion body myositis Inflammatory diseases Leukocytes (mononuclear) Macroglossia Movement disorders Musculoskeletal diseases Myocardium - pathology Myositis Myositis, Inclusion Body - complications Myositis, Inclusion Body - diagnosis Myositis, Inclusion Body - pathology Oral administration Parotid gland Prednisolone rapid progression Sjogren's syndrome Sjögren's syndrome Vacuoles |
title | Macroglossia in rapidly progressive inclusion body myositis |
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