Literature DB >> 19730931

Dysferlin deficiency treated like refractory polymyositis.

Julien Vinit1, Maxime Samson, Jean-Baptiste Gaultier, Annie Laquerriere, Elisabeth Ollagnon, Philippe Petiot, Isabelle Marie, Hervé Levesque, Hugues Rousset.   

Abstract

When an adult suffers from muscular symptoms, the diagnosis of polymyositis is often accepted if muscular biopsy reveals necrosis, fibrosis and cellular infiltrate with high expression of major histocompatibility complex class I. Late-onset limb-girdle muscular dystrophy (LGMD) can also be considered. We report the case of a young woman who suffers from dysferlin deficiency, and who was mistakenly treated for refractory polymyositis for 5 years. In LGMD, standard pathological analysis can indeed wrongly give a diagnosis of polymyositis. Immunofixation must be performed to avoid this mistake.

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Year:  2010        PMID: 19730931     DOI: 10.1007/s10067-009-1273-1

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN: 0770-3198            Impact factor:   2.980


  8 in total

1.  Muscle inflammation and MHC class I up-regulation in muscular dystrophy with lack of dysferlin: an immunopathological study.

Authors:  Paolo Confalonieri; Laura Oliva; Francesca Andreetta; Rossella Lorenzoni; Patrizia Dassi; Elisabetta Mariani; Lucia Morandi; Marina Mora; Ferdinando Cornelio; Renato Mantegazza
Journal:  J Neuroimmunol       Date:  2003-09       Impact factor: 3.478

2.  A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families.

Authors:  P Dinçer; Z Akçören; E Demir; I Richard; O Sancak; G Kale; S Ozme; A Karaduman; E Tan; J A Urtizberea; J S Beckmann; H Topaloğlu
Journal:  J Med Genet       Date:  2000-05       Impact factor: 6.318

3.  Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients.

Authors:  Michela Guglieri; Francesca Magri; Maria Grazia D'Angelo; Alessandro Prelle; Lucia Morandi; Carmelo Rodolico; Rachele Cagliani; Marina Mora; Francesco Fortunato; Andreina Bordoni; Roberto Del Bo; Serena Ghezzi; Serena Pagliarani; Sabrina Lucchiari; Sabrina Salani; Chiara Zecca; Costanza Lamperti; Dario Ronchi; Mohammed Aguennouz; Patrizia Ciscato; Claudia Di Blasi; Alessandra Ruggieri; Isabella Moroni; Anna Turconi; Antonio Toscano; Maurizio Moggio; Nereo Bresolin; Giacomo P Comi
Journal:  Hum Mutat       Date:  2008-02       Impact factor: 4.878

4.  Clinical heterogeneity in dysferlinopathy.

Authors:  Hidetsugu Ueyama; Toshihide Kumamoto; Hideo Horinouchi; Shin Fujimoto; Hiroshi Aono; Tomiyasu Tsuda
Journal:  Intern Med       Date:  2002-07       Impact factor: 1.271

5.  [Analysis of 12 cases of McArdle's disease diagnosed after 30 years].

Authors:  M Pavic; P Petiot; N Streichenberger; J-L Dupond; A Drouet; F Flocard; F Bouhour; J-Y Colin; P Bielefeld; M Gouttard; I Maire; J Pellat; D Vital Durand; H Rousset
Journal:  Rev Med Interne       Date:  2003-11       Impact factor: 0.728

6.  Diagnostic value of MHC class I staining in idiopathic inflammatory myopathies.

Authors:  J van der Pas; G J D Hengstman; H J ter Laak; G F Borm; B G M van Engelen
Journal:  J Neurol Neurosurg Psychiatry       Date:  2004-01       Impact factor: 10.154

7.  Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypes.

Authors:  Karine Nguyen; Guillaume Bassez; Martin Krahn; Rafaelle Bernard; Pascal Laforêt; Véronique Labelle; Jon Andoni Urtizberea; Dominique Figarella-Branger; Norma Romero; Shahram Attarian; France Leturcq; Jean Pouget; Nicolas Lévy; Bruno Eymard
Journal:  Arch Neurol       Date:  2007-08

8.  Muscle MRI findings in patients with limb girdle muscular dystrophy with calpain 3 deficiency (LGMD2A) and early contractures.

Authors:  Eugenio Mercuri; Kate Bushby; Enzo Ricci; Daniel Birchall; Marika Pane; Maria Kinali; Joanna Allsop; Vincenzo Nigro; Amets Sáenz; Annachiara Nascimbeni; Luigi Fulizio; Corrado Angelini; Francesco Muntoni
Journal:  Neuromuscul Disord       Date:  2004-11-26       Impact factor: 4.296

  8 in total
  10 in total

1.  The effects of MyD88 deficiency on disease phenotype in dysferlin-deficient A/J mice: role of endogenous TLR ligands.

Authors:  Kitipong Uaesoontrachoon; Hee-Jae Cha; Beryl Ampong; Arpana Sali; Jack Vandermeulen; Benjamin Wei; Brittany Creeden; Tony Huynh; James Quinn; Kathleen Tatem; Sree Rayavarapu; Eric P Hoffman; Kanneboyina Nagaraju
Journal:  J Pathol       Date:  2013-10       Impact factor: 7.996

2.  Polymyositis, a very uncommon isolated disease: clinical and histological re-evaluation after long-term follow-up.

Authors:  Veronica Silva Vilela; Sergio Prieto-González; José C Milisenda; Albert Selva-O Callaghan; Josep M Grau
Journal:  Rheumatol Int       Date:  2014-12-30       Impact factor: 2.631

Review 3.  Dysferlinopathy misdiagnosed with juvenile polymyositis in the pre-symptomatic stage of hyperCKemia: a case report and literature review.

Authors:  Cecilia Contreras-Cubas; Francisco Barajas-Olmos; Maria Inés Frayre-Martínez; Georgina Siordia-Reyes; Claudia C Guízar-Sánchez; Humberto García-Ortiz; Lorena Orozco; Vicente Baca
Journal:  BMC Med Genomics       Date:  2022-06-20       Impact factor: 3.622

4.  Diagnostic muscle biopsies in the era of genetics: the added value of myopathology in a selection of limb-girdle muscular dystrophy patients.

Authors:  Boel De Paepe; Elise Velghe; Linnea Salminen; Balint Toth; Pieter Olivier; Jan L De Bleecker
Journal:  Acta Neurol Belg       Date:  2021-01-05       Impact factor: 2.396

5.  Clinical, Neurophysiological, Radiological, Pathological, and Genetic Features of Dysferlinopathy in Saudi Arabia.

Authors:  Norah Alharbi; Rawan Matar; Edward Cupler; Hindi Al-Hindi; Hatem Murad; Iftteah Alhomud; Dorota Monies; Ali Alshehri; Mossaed Alyahya; Brian Meyer; Saeed Bohlega
Journal:  Front Neurosci       Date:  2022-02-22       Impact factor: 4.677

6.  Diagnosis by protein analysis of dysferlinopathy in two patients mistaken as polymyositis.

Authors:  Corrado Angelini; Wolfgang Grisold; Vincenzo Nigro
Journal:  Acta Myol       Date:  2011-12

7.  Dysferlinopathy course and sportive activity: clues for possible treatment.

Authors:  C Angelini; E Peterle; A Gaiani; L Bortolussi; C Borsato
Journal:  Acta Myol       Date:  2011-10

8.  The Classification, Natural History and Treatment of the Limb Girdle Muscular Dystrophies.

Authors:  Alexander Peter Murphy; Volker Straub
Journal:  J Neuromuscul Dis       Date:  2015-07-22

Review 9.  Limb-girdle muscular dystrophies: where next after six decades from the first proposal (Review).

Authors:  Omar A Mahmood; Xin Mei Jiang
Journal:  Mol Med Rep       Date:  2014-03-13       Impact factor: 2.952

Review 10.  Muscle Cells Fix Breaches by Orchestrating a Membrane Repair Ballet.

Authors:  Florian Barthélémy; Aurélia Defour; Nicolas Lévy; Martin Krahn; Marc Bartoli
Journal:  J Neuromuscul Dis       Date:  2018
  10 in total

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