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Successful plasmapheresis and immunoglobulin treatment for severe lipid storage myopathy: Doing the right thing for the wrong reason.

Authors :
Kleefeld, Felix
von Renesse, Anja
Dittmayer, Carsten
Harms, Lutz
Radke, Josefine
Radbruch, Helena
Goebel, Hans‐Hilmar
Pache, Florence
Schneider, Udo
Schuelke, Markus
Uruha, Akinori
Stenzel, Werner
Source :
Neuropathology & Applied Neurobiology; Feb2022, Vol. 48 Issue 1, p1-5, 5p
Publication Year :
2022

Abstract

Multiple acyl coenzyme A dehydrogenase deficiency, mitochondrial myopathy, electron microscopy, lipid storage myopathy Of note, sarcoplasmic lipid storage compatible with lipid-storage myopathy was only observed in the muscle biopsy specimen taken at the height of her symptoms (second biopsy) by Oil-Red-O staining and on ultrastructural examination. Keywords: multiple acyl coenzyme A dehydrogenase deficiency; mitochondrial myopathy; lipid storage myopathy; electron microscopy EN multiple acyl coenzyme A dehydrogenase deficiency mitochondrial myopathy lipid storage myopathy electron microscopy 1 5 5 01/19/22 20220201 NES 220201 Three consecutive skeletal muscle biopsies during a several months time-frame, showing different degrees of neutral lipid storage. [Extracted from the article]

Details

Language :
English
ISSN :
03051846
Volume :
48
Issue :
1
Database :
Complementary Index
Journal :
Neuropathology & Applied Neurobiology
Publication Type :
Academic Journal
Accession number :
154716153
Full Text :
https://doi.org/10.1111/nan.12731