64例抗Mi2皮肌炎患者的系统回顾性研究：一种伴有坏死性肌炎和高恶性肿瘤风险的典型皮疹。 - Suppr

Systematic retrospective study of 64 patients with anti-Mi2 dermatomyositis: A classic skin rash with a necrotizing myositis and high risk of malignancy.

作者信息

Monseau Grégoire, Landon-Cardinal Océane, Stenzel Werner, Schoindre Yoland, Mariampillai Kubéraka, Barete Stéphane, Martel Clothilde, Masseau Agathe, Meyer Alain, Terrier Benjamin, Guégan Sarah, Verneuil Laurence, Audia Sylvain, Livideanu Cristian Bulai, Hachulla Eric, Kahn Jean-Emmanuel, Lefevre Guillaume, Maurier François, Moulis Guillaume, Papo Thomas, Dossier Antoine, Descamps Vincent, Salort-Campana Emmanuelle, Richard Marie-Aleth, Bergot Emmanuel, Mortier Laurent, Costedoat-Chalumeau Nathalie, Genot Séverine, Perez Florian, Piette Anne-Marie, Samson Maxime, Schleinitz Nicolas, Zénone Thierry, Lacoste Marie, de Boysson Hubert, Madaule Serge, Rigolet Aude, Champtiaux Nicolas, Hervier Baptiste, Bouvier Anne-Marie, Jooste Valérie, Léonard-Louis Sarah, Maisonobe Thierry, Aouba Achille, Benveniste Olivier, Bienvenu Boris, Allenbach Yves

机构信息

Département de Médecine Interne, Centre Hospitalier Universitaire de Caen, France.

Sorbonne Universités Pierre et Marie Curie, Assistance Publique-Hôpitaux de Paris, Groupe Hospitalier Pitié-Salpêtrière, Département de médecine Interne et d'immunologie clinique, France; Institut National de la Santé Et de la Recherche Médicale, Unité Mixte de Recherche 974, Paris, France; Department of Medicine, University of Montreal; Division of Rheumatology and Research Center, Centre Hospitalier de l'Université de Montréal, Quebec, Canada.

出版信息

J Am Acad Dermatol. 2020 Dec;83(6):1759-1763. doi: 10.1016/j.jaad.2020.03.058. Epub 2020 Mar 31.

DOI:10.1016/j.jaad.2020.03.058

PMID:32244015

Abstract

摘要

相似文献

Systematic retrospective study of 64 patients with anti-Mi2 dermatomyositis: A classic skin rash with a necrotizing myositis and high risk of malignancy.

J Am Acad Dermatol. 2020 Dec;83(6):1759-1763. doi: 10.1016/j.jaad.2020.03.058. Epub 2020 Mar 31.

More prominent muscle involvement in patients with dermatomyositis with anti-Mi2 autoantibodies.

Neurology. 2019 Nov 5;93(19):e1768-e1777. doi: 10.1212/WNL.0000000000008443. Epub 2019 Oct 8.

Severe muscle damage with myofiber necrosis and macrophage infiltrates characterize anti-Mi2 positive dermatomyositis.

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Acquired Partial Lipodystrophy Associated with Anti-Mi-2 Antibody-positive Adult-onset Dermatomyositis.

Acta Derm Venereol. 2019 Jan 1;99(1):95-96. doi: 10.2340/00015555-3026.

Autoantibodies in polymyositis and dermatomyositis.

Curr Rheumatol Rep. 2013 Jun;15(6):335. doi: 10.1007/s11926-013-0335-1.

Dermatomyositis: Clinical features and pathogenesis.

J Am Acad Dermatol. 2020 Feb;82(2):267-281. doi: 10.1016/j.jaad.2019.06.1309. Epub 2019 Jul 4.

Specific autoantibodies in dermatomyositis: a helpful tool to classify different clinical subsets.

Arch Dermatol Res. 2017 Mar;309(2):87-95. doi: 10.1007/s00403-016-1704-1. Epub 2016 Dec 7.

Clinical characteristics of four myositis-specific autoantibodies with regulatory-approved testing in Japan: A Japanese multi-centre adult myositis patients' cohort.

J Dermatol Sci. 2021 Jul;103(1):53-56. doi: 10.1016/j.jdermsci.2021.05.005. Epub 2021 May 25.

Unilateral heliotrope rash: A call for recognizing its warning significance in anti-MDA5 antibody-associated dermatomyositis.

J Dermatol. 2024 Sep;51(9):e319-e320. doi: 10.1111/1346-8138.17228. Epub 2024 Apr 15.

Autoantibodies in children with juvenile dermatomyositis: A single centre experience from North-West India.

Rheumatol Int. 2017 May;37(5):807-812. doi: 10.1007/s00296-017-3707-4. Epub 2017 Mar 22.

引用本文的文献

Calcinosis Universalis: An Atypical Presentation of Mi-2 Positive Juvenile Dermatomyositis - A Case-Based Review.

Mediterr J Rheumatol. 2025 Jun 2;36(2):308-315. doi: 10.31138/mjr.291024.cua. eCollection 2025 Jun.

Risk, risk factors, and screening of malignancies in dermatomyositis: current status and future perspectives.

Front Oncol. 2025 Jun 4;15:1503140. doi: 10.3389/fonc.2025.1503140. eCollection 2025.

Clinico-sero-pathological profiles and risk prediction model of idiopathic inflammatory myopathy (IIM) patients with different perifascicular changes.

CNS Neurosci Ther. 2024 Aug;30(8):e14882. doi: 10.1111/cns.14882.

Malignancy in dermatomyositis: a mono-centric retrospective study of 134 patients in China and a potential predictive model.

Front Med (Lausanne). 2023 Jun 8;10:1200804. doi: 10.3389/fmed.2023.1200804. eCollection 2023.

Anti-Mi-2 antibody-positive lung cancer-associated polymyositis.

Int Cancer Conf J. 2023 Mar 14;12(3):173-176. doi: 10.1007/s13691-023-00601-1. eCollection 2023 Jul.

Subsets of Idiopathic Inflammatory Myositis Enriched for Contemporaneous Cancer Relative to the General Population.

Arthritis Rheumatol. 2023 Apr;75(4):620-629. doi: 10.1002/art.42311. Epub 2023 Feb 16.

Autoantibodies and Cancer Association: the Case of Systemic Sclerosis and Dermatomyositis.

Clin Rev Allergy Immunol. 2022 Dec;63(3):330-341. doi: 10.1007/s12016-022-08944-y. Epub 2022 May 20.

Therapy-resistant dermatomyositis with extensive 'lumbar belt' calcinosis.

BMJ Case Rep. 2022 May 18;15(5):e249110. doi: 10.1136/bcr-2022-249110.

Antinuclear Antibody (ANA) and Anti-Mi-2-Alpha Positive Dermatomyositis Hinting a Cancer Diagnosis.

Cureus. 2022 Feb 2;14(2):e21844. doi: 10.7759/cureus.21844. eCollection 2022 Feb.

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Systematic retrospective study of 64 patients with anti-Mi2 dermatomyositis: A classic skin rash with a necrotizing myositis and high risk of malignancy.

作者信息

机构信息

Département de Médecine Interne, Centre Hospitalier Universitaire de Caen, France.

出版信息

J Am Acad Dermatol. 2020 Dec;83(6):1759-1763. doi: 10.1016/j.jaad.2020.03.058. Epub 2020 Mar 31.

DOI:10.1016/j.jaad.2020.03.058

PMID:32244015

Abstract

摘要

相似文献

Systematic retrospective study of 64 patients with anti-Mi2 dermatomyositis: A classic skin rash with a necrotizing myositis and high risk of malignancy.

J Am Acad Dermatol. 2020 Dec;83(6):1759-1763. doi: 10.1016/j.jaad.2020.03.058. Epub 2020 Mar 31.

More prominent muscle involvement in patients with dermatomyositis with anti-Mi2 autoantibodies.

Neurology. 2019 Nov 5;93(19):e1768-e1777. doi: 10.1212/WNL.0000000000008443. Epub 2019 Oct 8.

Severe muscle damage with myofiber necrosis and macrophage infiltrates characterize anti-Mi2 positive dermatomyositis.

Rheumatology (Oxford). 2021 Jun 18;60(6):2916-2926. doi: 10.1093/rheumatology/keaa739.

Acquired Partial Lipodystrophy Associated with Anti-Mi-2 Antibody-positive Adult-onset Dermatomyositis.

Acta Derm Venereol. 2019 Jan 1;99(1):95-96. doi: 10.2340/00015555-3026.

Autoantibodies in polymyositis and dermatomyositis.

Curr Rheumatol Rep. 2013 Jun;15(6):335. doi: 10.1007/s11926-013-0335-1.

Dermatomyositis: Clinical features and pathogenesis.

J Am Acad Dermatol. 2020 Feb;82(2):267-281. doi: 10.1016/j.jaad.2019.06.1309. Epub 2019 Jul 4.

Specific autoantibodies in dermatomyositis: a helpful tool to classify different clinical subsets.

Arch Dermatol Res. 2017 Mar;309(2):87-95. doi: 10.1007/s00403-016-1704-1. Epub 2016 Dec 7.

Clinical characteristics of four myositis-specific autoantibodies with regulatory-approved testing in Japan: A Japanese multi-centre adult myositis patients' cohort.

J Dermatol Sci. 2021 Jul;103(1):53-56. doi: 10.1016/j.jdermsci.2021.05.005. Epub 2021 May 25.

Unilateral heliotrope rash: A call for recognizing its warning significance in anti-MDA5 antibody-associated dermatomyositis.

J Dermatol. 2024 Sep;51(9):e319-e320. doi: 10.1111/1346-8138.17228. Epub 2024 Apr 15.

Autoantibodies in children with juvenile dermatomyositis: A single centre experience from North-West India.

Rheumatol Int. 2017 May;37(5):807-812. doi: 10.1007/s00296-017-3707-4. Epub 2017 Mar 22.

引用本文的文献

Calcinosis Universalis: An Atypical Presentation of Mi-2 Positive Juvenile Dermatomyositis - A Case-Based Review.

Mediterr J Rheumatol. 2025 Jun 2;36(2):308-315. doi: 10.31138/mjr.291024.cua. eCollection 2025 Jun.

Risk, risk factors, and screening of malignancies in dermatomyositis: current status and future perspectives.

Front Oncol. 2025 Jun 4;15:1503140. doi: 10.3389/fonc.2025.1503140. eCollection 2025.

Clinico-sero-pathological profiles and risk prediction model of idiopathic inflammatory myopathy (IIM) patients with different perifascicular changes.

CNS Neurosci Ther. 2024 Aug;30(8):e14882. doi: 10.1111/cns.14882.

Malignancy in dermatomyositis: a mono-centric retrospective study of 134 patients in China and a potential predictive model.

Front Med (Lausanne). 2023 Jun 8;10:1200804. doi: 10.3389/fmed.2023.1200804. eCollection 2023.

Anti-Mi-2 antibody-positive lung cancer-associated polymyositis.

Int Cancer Conf J. 2023 Mar 14;12(3):173-176. doi: 10.1007/s13691-023-00601-1. eCollection 2023 Jul.

Subsets of Idiopathic Inflammatory Myositis Enriched for Contemporaneous Cancer Relative to the General Population.

Arthritis Rheumatol. 2023 Apr;75(4):620-629. doi: 10.1002/art.42311. Epub 2023 Feb 16.

Autoantibodies and Cancer Association: the Case of Systemic Sclerosis and Dermatomyositis.

Clin Rev Allergy Immunol. 2022 Dec;63(3):330-341. doi: 10.1007/s12016-022-08944-y. Epub 2022 May 20.

Therapy-resistant dermatomyositis with extensive 'lumbar belt' calcinosis.

BMJ Case Rep. 2022 May 18;15(5):e249110. doi: 10.1136/bcr-2022-249110.

Antinuclear Antibody (ANA) and Anti-Mi-2-Alpha Positive Dermatomyositis Hinting a Cancer Diagnosis.

Cureus. 2022 Feb 2;14(2):e21844. doi: 10.7759/cureus.21844. eCollection 2022 Feb.

Clinical and Serological Features and Pregnancy Outcomes in Women with Polymyositis/Dermatomyositis: A Case-based Review.

Intern Med. 2022 Jan 15;61(2):143-149. doi: 10.2169/internalmedicine.7924-21. Epub 2021 Jul 30.

Systematic retrospective study of 64 patients with anti-Mi2 dermatomyositis: A classic skin rash with a necrotizing myositis and high risk of malignancy.

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Systematic retrospective study of 64 patients with anti-Mi2 dermatomyositis: A classic skin rash with a necrotizing myositis and high risk of malignancy.

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