Miosite por Corpos de Inclusão Familiar (MCIF)
Atualização
DOI:
https://doi.org/10.34024/rnc.2009.v17.8579Palavras-chave:
Miosite, Corpos de Inclusão, Doenças NeuromuscularesResumo
Miosite por corpos de inclusão familiar é uma doença extremamente rara, caracterizada por início tardio, seletivo e com precoce envolvimento dos músculos quadríceps, flexores dos dedos e do antebraço, e ligeiro aumento nos níveis séricos de creatina cinase (CK). Histologicamente as fibras musculares apresentam vacúolos marginados e infiltrados inflamatórios. A combinação de achados clínicos, imunopatológicos, histológicos e imunogênicos indicam que esses pacientes apresentam uma doença de características similares a miosite por corpos de inclusão esporádica.
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