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Descriptor English: Myositis, Inclusion Body
Descriptor Spanish: Miositis por Cuerpos de Inclusión
Descriptor miositis por cuerpos de inclusión
Entry term(s) miopatía por cuerpos de inclusión esporádica
Scope note: Miopatías progresivas caracterizadas por la presencia de cuerpos de inclusión en la biopsia muscular. Se han descrito formas esporádicas y hereditarias. La forma esporádica es una miopatía vacuolar inflamatoria adquirida, que se inicia en la edad adulta, y afecta a los musculos proximales y distales. Las formas familiares suelen comenzar en la infancia y carecen de cambios inflamatorios. Ambas formas presentan inclusiones intracitoplasmáticas e intranucleares características en el tejido muscular. (Adams et al., Principles of Neurology, 6th ed, pp1409-10)
Descriptor Portuguese: Miosite de Corpos de Inclusão
Descriptor French: Myosite à inclusions
Entry term(s): Inclusion Body Myopathy, Sporadic
Inclusion Body Myositides
Inclusion Body Myositis
Inclusion Body Myositis, Sporadic
Myopathy, Inclusion Body, Sporadic
Myositides, Inclusion Body
Myositis, Inclusion Body, Sporadic
Sporadic Inclusion Body Myositis
Tree number(s): C05.651.594.600
C10.668.491.562.500
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D018979
Scope note: Progressive myopathies characterized by the presence of inclusion bodies on muscle biopsy. Sporadic and hereditary forms have been described. The sporadic form is an acquired, adult-onset inflammatory vacuolar myopathy affecting proximal and distal muscles. Familial forms usually begin in childhood and lack inflammatory changes. Both forms feature intracytoplasmic and intranuclear inclusions in muscle tissue. (Adams et al., Principles of Neurology, 6th ed, pp1409-10)
Annotation: do not coord with INCLUSION BODIES but coord with INCLUSION BODIES, VIRAL if relevant (IM or NIM)
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CN congenital
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Myositis (1968-1995)
Public MeSH Note: 96
History Note: 96
DeCS ID: 32669
Unique ID: D018979
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1996/01/01
Date of Entry: 1995/05/24
Revision Date: 2012/07/03
Myositis, Inclusion Body - Preferred
Concept UI M0028350
Scope note Progressive myopathies characterized by the presence of inclusion bodies on muscle biopsy. Sporadic and hereditary forms have been described. The sporadic form is an acquired, adult-onset inflammatory vacuolar myopathy affecting proximal and distal muscles. Familial forms usually begin in childhood and lack inflammatory changes. Both forms feature intracytoplasmic and intranuclear inclusions in muscle tissue. (Adams et al., Principles of Neurology, 6th ed, pp1409-10)
Preferred term Myositis, Inclusion Body
Entry term(s) Inclusion Body Myositides
Inclusion Body Myositis
Myositides, Inclusion Body
Inclusion Body Myopathy, Sporadic - Narrower
Concept UI M0335634
Preferred term Inclusion Body Myopathy, Sporadic
Entry term(s) Inclusion Body Myositis, Sporadic
Myopathy, Inclusion Body, Sporadic
Myositis, Inclusion Body, Sporadic
Sporadic Inclusion Body Myositis



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