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Drop Head Syndrome as a Rare Complication in Mixed Connective Tissue Disease
A 54-year-old woman developed drop head syndrome (DHS), Raynaud's phenomenon and creatine kinase (CK) elevation. She did not meet the international classification criteria of dermatomyositis/polymyositis, as we observed no muscle weakness, grasping pain or electromyography abnormality in her li...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Internal Medicine
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086316/ https://www.ncbi.nlm.nih.gov/pubmed/31735790 http://dx.doi.org/10.2169/internalmedicine.3626-19 |
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author | Akagi, Midori Umeda, Masataka Hashisako, Mikiko Hara, Kazusato Tsuji, Sousuke Endo, Yushiro Takatani, Ayuko Shimizu, Toshimasa Fukui, Shoichi Koga, Tomohiro Kawashiri, Shin-ya Iwamoto, Naoki Igawa, Takashi Ichinose, Kunihiro Tamai, Mami Nakamura, Hideki Origuchi, Tomoki Niino, Daisuke Kawakami, Atsushi |
author_facet | Akagi, Midori Umeda, Masataka Hashisako, Mikiko Hara, Kazusato Tsuji, Sousuke Endo, Yushiro Takatani, Ayuko Shimizu, Toshimasa Fukui, Shoichi Koga, Tomohiro Kawashiri, Shin-ya Iwamoto, Naoki Igawa, Takashi Ichinose, Kunihiro Tamai, Mami Nakamura, Hideki Origuchi, Tomoki Niino, Daisuke Kawakami, Atsushi |
author_sort | Akagi, Midori |
collection | PubMed |
description | A 54-year-old woman developed drop head syndrome (DHS), Raynaud's phenomenon and creatine kinase (CK) elevation. She did not meet the international classification criteria of dermatomyositis/polymyositis, as we observed no muscle weakness, grasping pain or electromyography abnormality in her limbs, and anti-aminoacyl tRNA synthetase (ARS) antibody was negative. Cervical magnetic resonance imaging and a muscle biopsy of the trapezius muscle revealed myositis findings as the only clinical observations in muscle. These findings, along with her anti-U1-ribonucleoprotein (RNP) antibody positivity and leukopenia, resulted in a diagnosis of mixed connective tissue disease (MCTD). Prednisolone treatment significantly improved her myositis. To our knowledge, this is the first report of DHS as the only muscle complication of MCTD. |
format | Online Article Text |
id | pubmed-7086316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Japanese Society of Internal Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-70863162020-03-26 Drop Head Syndrome as a Rare Complication in Mixed Connective Tissue Disease Akagi, Midori Umeda, Masataka Hashisako, Mikiko Hara, Kazusato Tsuji, Sousuke Endo, Yushiro Takatani, Ayuko Shimizu, Toshimasa Fukui, Shoichi Koga, Tomohiro Kawashiri, Shin-ya Iwamoto, Naoki Igawa, Takashi Ichinose, Kunihiro Tamai, Mami Nakamura, Hideki Origuchi, Tomoki Niino, Daisuke Kawakami, Atsushi Intern Med Case Report A 54-year-old woman developed drop head syndrome (DHS), Raynaud's phenomenon and creatine kinase (CK) elevation. She did not meet the international classification criteria of dermatomyositis/polymyositis, as we observed no muscle weakness, grasping pain or electromyography abnormality in her limbs, and anti-aminoacyl tRNA synthetase (ARS) antibody was negative. Cervical magnetic resonance imaging and a muscle biopsy of the trapezius muscle revealed myositis findings as the only clinical observations in muscle. These findings, along with her anti-U1-ribonucleoprotein (RNP) antibody positivity and leukopenia, resulted in a diagnosis of mixed connective tissue disease (MCTD). Prednisolone treatment significantly improved her myositis. To our knowledge, this is the first report of DHS as the only muscle complication of MCTD. The Japanese Society of Internal Medicine 2019-11-18 2020-03-01 /pmc/articles/PMC7086316/ /pubmed/31735790 http://dx.doi.org/10.2169/internalmedicine.3626-19 Text en Copyright © 2020 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/ The Internal Medicine is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Akagi, Midori Umeda, Masataka Hashisako, Mikiko Hara, Kazusato Tsuji, Sousuke Endo, Yushiro Takatani, Ayuko Shimizu, Toshimasa Fukui, Shoichi Koga, Tomohiro Kawashiri, Shin-ya Iwamoto, Naoki Igawa, Takashi Ichinose, Kunihiro Tamai, Mami Nakamura, Hideki Origuchi, Tomoki Niino, Daisuke Kawakami, Atsushi Drop Head Syndrome as a Rare Complication in Mixed Connective Tissue Disease |
title | Drop Head Syndrome as a Rare Complication in Mixed Connective Tissue Disease |
title_full | Drop Head Syndrome as a Rare Complication in Mixed Connective Tissue Disease |
title_fullStr | Drop Head Syndrome as a Rare Complication in Mixed Connective Tissue Disease |
title_full_unstemmed | Drop Head Syndrome as a Rare Complication in Mixed Connective Tissue Disease |
title_short | Drop Head Syndrome as a Rare Complication in Mixed Connective Tissue Disease |
title_sort | drop head syndrome as a rare complication in mixed connective tissue disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086316/ https://www.ncbi.nlm.nih.gov/pubmed/31735790 http://dx.doi.org/10.2169/internalmedicine.3626-19 |
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