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Muscle MRI in neutral lipid storage disease (NLSD).
Garibaldi, Matteo; Tasca, Giorgio; Diaz-Manera, Jordi; Ottaviani, Pierfancesco; Laschena, Francesco; Pantoli, Donatella; Gerevini, Simonetta; Fiorillo, Chiara; Maggi, Lorenzo; Tasca, Elisabetta; D'Amico, Adele; Musumeci, Olimpia; Toscano, Antonio; Bruno, Claudio; Massa, Roberto; Angelini, Corrado; Bertini, Enrico; Antonini, Giovanni; Pennisi, Elena Maria.
Afiliação
  • Garibaldi M; Unit of Neuromuscular Diseases, Department of Neurology Mental Health and Sensory Organs (NESMOS), Faculty of Medicine and Psychology, 'Sapienza' University of Rome, Sant'Andrea Hospital, Rome, Italy. matteo.garibaldi@uniroma1.it.
  • Tasca G; Institute of Neurology, Policlinico "A.Gemelli" Foundation University Hospital, Rome, Italy.
  • Diaz-Manera J; Neuromuscular Diseases Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
  • Ottaviani P; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Barcelona, Spain.
  • Laschena F; Department of Radiology, Istituto Dermopatico dell'Immacolata, IRCCS, Rome, Italy.
  • Pantoli D; Department of Radiology, Istituto Dermopatico dell'Immacolata, IRCCS, Rome, Italy.
  • Gerevini S; Neuroradiology Unit, Department of Radiology, San Filippo Neri Hospital, Rome, Italy.
  • Fiorillo C; Neuroradiology Department, IRCCS San Raffaele Hospital, Milan, Italy.
  • Maggi L; Pediatric Neurology and Muscular Disorders, Istituto Giannina Gaslini, Genoa, Italy.
  • Tasca E; Neuroimmunology and Neuromuscular Diseases Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
  • D'Amico A; IRCCS S.Camillo, Lido di Venezia, Italy.
  • Musumeci O; Unit of Neuromuscular and Neurodegenerative Disorders, Laboratory of Molecular Medicine, 'Bambino Gesù' Children's Hospital, IRCCS, Rome, Italy.
  • Toscano A; Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
  • Bruno C; Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
  • Massa R; Pediatric Neurology and Muscular Disorders, Istituto Giannina Gaslini, Genoa, Italy.
  • Angelini C; Department of Systems Medicine (Neurology), University of Rome Tor Vergata, Rome, Italy.
  • Bertini E; IRCCS S.Camillo, Lido di Venezia, Italy.
  • Antonini G; Unit of Neuromuscular and Neurodegenerative Disorders, Laboratory of Molecular Medicine, 'Bambino Gesù' Children's Hospital, IRCCS, Rome, Italy.
  • Pennisi EM; Unit of Neuromuscular Diseases, Department of Neurology Mental Health and Sensory Organs (NESMOS), Faculty of Medicine and Psychology, 'Sapienza' University of Rome, Sant'Andrea Hospital, Rome, Italy.
J Neurol ; 264(7): 1334-1342, 2017 Jul.
Article em En | MEDLINE | ID: mdl-28503705
ABSTRACT
Neutral lipid storage disease (NLSD) is a rare inherited disorder of lipid metabolism resulting in lipid droplets accumulation in different tissues. Skeletal muscle could be affected in both two different form of disease NLSD with myopathy (NLSD-M) and NLSD with ichthyosis (NLSD-I). We present the muscle imaging data of 12 patients from the Italian Network for NLSD ten patients presenting NLSD-M and two patients with NLSD-I. In NLSD-M gluteus minimus, semimembranosus, soleus and gastrocnemius medialis in the lower limbs and infraspinatus in the upper limbs were the most affected muscles. Gracilis, sartorius, subscapularis, pectoralis, triceps brachii and sternocleidomastoid were spared. Muscle involvement was not homogenous and characteristic "patchy" replacement was observed in at least one muscle in all the patients. Half of the patients showed one or more STIR positive muscles. In both NLSD-I cases muscle involvement was not observed by T1-TSE sequences, but one of them showed positive STIR images in more than one muscle in the leg. Our data provides evidence that muscle imaging can identify characteristic alterations in NLSD-M, characterized by a specific pattern of muscle involvement with "patchy" areas of fatty replacement. Larger cohorts are needed to assess if a distinct pattern of muscle involvement exists also for NLSD-I.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imageamento por Ressonância Magnética / Eritrodermia Ictiosiforme Congênita / Músculo Esquelético / Erros Inatos do Metabolismo Lipídico / Doenças Musculares Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged País como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imageamento por Ressonância Magnética / Eritrodermia Ictiosiforme Congênita / Músculo Esquelético / Erros Inatos do Metabolismo Lipídico / Doenças Musculares Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged País como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article