Redefining Dermatomyositis

نویسندگان

  • Yves Troyanov
  • Ira N Targoff
  • Marie-Pier Payette
  • Jean-Pierre Raynauld
  • Suzanne Chartier
  • Jean-Richard Goulet
  • Josiane Bourré-Tessier
  • Eric Rich
  • Tamara Grodzicky
  • Marvin J. Fritzler
  • France Joyal
  • Martial Koenig
  • Jean-Luc Senécal
چکیده

Dermatomyositis (DM) is a major clinical subset of autoimmune myositis (AIM). The characteristic DM rash (Gottron papules, heliotrope rash) and perifascicular atrophy at skeletal muscle biopsy are regarded as specific features for this diagnosis. However, new concepts are challenging the current definition of DM. A modified Bohan and Peter classification of AIM was proposed in which the core concept was the inclusion of the diagnostic significance of overlap connective this clinical classification, a DM rash in the absence of overlap features indicates a ever, overlap features in association with sed: June 24, 2014; accepted: July 14, 2014. icine, Division of Rheumatology, Hôpital du of Montreal School of Medicine, Montreal, t of Medicine, Divisions of Rheumatology R, TG, JLS), Internal Medicine (FJ, MK), re Hospitalier de l’Universit e de Montr eal, ol of Medicine, Montreal; Laboratory for Research Center, Centre Hospitalier de S, MK), Quebec, Canada; Veterans Affairs rsity of Oklahoma Health Sciences Center, arch Foundation, Oklahoma City, Oklahoma, Advanced Diagnostics Laboratory (MJF), ity of Calgary, Calgary, Alberta, Canada. Sen ecal, MD, Division of Rheumatology, Universit e de Montr eal, 1560 Sherbrooke ntreal, Quebec, Canada, H2L 4M1 (e-mail: ts of interest: This work was supported in 6, MOP-68966, and MOP-81252 from the ealth Research (to JLS), by Department of Research Funds (to INT), and by donations c (JLS, MK) and Mrs Gisèle Sarrazin-Locas atory for Research in Autoimmunity. MJF iety Research Chair at the University of niversity of Montreal Scleroderma Research JRG, JBT, TG, FJ, MK, and JLS have no disclose. The authors listed below have t (personal or institutional) from the listed utical companies, unrelated to the present EN, BMS, Janssen, Roche, UCB, Warnera Medical Research Foundation Clinical UpToDate; JPR: Arthrolab, Amgen, BMS, Roche, Pfizer; ER: Abbvie, Amgen, BMS, UCB; MJF: EUROIMMUN, ImmunoCons. Kluwer Health | Lippincott Williams & ccess article distributed under the Creative 4.0, which permits unrestricted use, distribuedium, provided the original work is properly

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Non-Hodgkin lymphoma in a 13-year-old boy with provisional hypomyopathic juvenile Dermatomyositis

Provisional hypomyopathic juvenile dermatomyositis is a subgroup of clinically amyopathic juvenile dermatomyositis provisional. The diagnostic criteria include: Classic dermatomyositis skin lesions – which have to be confirmed by biopsy –, no involvement of proximal muscles, subclinical involvement of these muscles and normal level of muscle enzymes. These criteria should be present for a minim...

متن کامل

Subcutaneous Emphysema, Pneumomediastinum and Pneumothorax in a Patient with Dermatomyositis

Introduction:Spontaneous pneumomediastinum, pneumothorax, and subcutaneous emphysema are rare, but serious complications of inflammatory myopathies and occur more commonly in DM than PM. complications of dermatomyositis (DM) and polymyositis (PM), both of which can be fatal. Case Report:A 20-year-old woman was admitted with neck pain, dyspnea, cough, and fever. She had been diagnosed with derma...

متن کامل

Dermatomyositis associated with Pityriasis Rubra Pilaris: A case report

A 9-year old boy had severe muscle weakness and typical skin rash and EMG with diagnosis of dermatomyositis associated with erythrodermia with islands of normal skin and palmoplantar hyperkeratosis, which was reported. As PRP in skin biopsy. Association dermatomyositis with PRP is very rare.

متن کامل

Breast Cancer Associated with Dermatomyositis

Dermatomyositis (DM) is a rare idiopathic inflammatory myopathy with characteristic skin lesions. Case series have shown an association between dermatomyositis and malignancy. Malignancy has been found in 15-25% of the adult patients with dermatomyositis. A 50-year-old new case of breast cancer, was admitted with muscle weakness and inability to walk. Physical examination revealed fever, perior...

متن کامل

Evaluation of Dermatomyositis patients admitted in Sina Hospital in Ahwaz in 1990-2000

Background: Dermatomyositis is an autoimmune inflammatory myopathy with distinct cutaneous findings. Its etiology is unknown. Objective: The purpose of this study was to evaluate demographic, clinical and paraclinical findings in patients with dermatomyositis in Ahwaz. Patients and Methods: This is descriptive, retrospective study and the records of all patients with dermatomyositis admitted to...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 93  شماره 

صفحات  -

تاریخ انتشار 2014