The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2019-04

AUTHORS

G. J. Knuiman, B. Küsters, L. Eshuis, M. Snoeck, M. Lammens, L. Heytens, W. De Ridder, J. Baets, R. S. Scalco, R. Quinlivan, J. Holton, I. Bodi, E. Wraige, A. Radunovic, C. von Landenberg, J. Reimann, E.-J. Kamsteeg, C. Sewry, H. Jungbluth, N. C. Voermans

ABSTRACT

OBJECTIVE: The histopathological features of malignant hyperthermia (MH) and non-anaesthetic (mostly exertional) rhabdomyolysis (RM) due to RYR1 mutations have only been reported in a few cases. METHODS: We performed a retrospective multi-centre cohort study focussing on the histopathological features of patients with MH or RM due to RYR1 mutations (1987-2017). All muscle biopsies were reviewed by a neuromuscular pathologist. Additional morphometric and electron microscopic analysis were performed where possible. RESULTS: Through the six participating centres we identified 50 patients from 46 families, including patients with MH (n = 31) and RM (n = 19). Overall, the biopsy of 90% of patients showed one or more myopathic features including: increased fibre size variability (n = 44), increase in the number of fibres with internal nuclei (n = 30), and type I fibre predominance (n = 13). Abnormalities on oxidative staining, generally considered to be more specifically associated with RYR1-related congenital myopathies, were observed in 52%, and included unevenness (n = 24), central cores (n = 7) and multi-minicores (n = 3). Apart from oxidative staining abnormalities more frequently observed in MH patients, the histopathological spectrum was similar between the two groups. There was no correlation between the presence of cores and the occurrence of clinically detectable weakness or presence of (likely) pathogenic variants. CONCLUSIONS: Patients with RYR1-related MH and RM exhibit a similar histopathological spectrum, ranging from mild myopathic changes to cores and other features typical of RYR1-related congenital myopathies. Suggestive histopathological features may support RYR1 involvement, also in cases where the in vitro contracture test is not informative. More... »

PAGES

876-887

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00415-019-09209-z

DOI

http://dx.doi.org/10.1007/s00415-019-09209-z

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1112260108

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/30788618


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