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Back to the 22 October 2026 edition

Practice changer · 06 of 06

Myositis immunostains on paraffin muscle: three that work, two that do not

Laboratories without frozen muscle processing can consider paraffin MHC-II, MxA and p62 staining, validated locally, but not MHC-I or MAC.

Design
Method development and paired comparison with frozen sections
Population
20 muscle biopsies including dermatomyositis, IBM, IMNM and mimics
Primary outcome
Concordance of FFPE versus frozen immunohistochemistry
Effect
MHC-II 90%, MxA 90%, p62 80%; MHC-I and MAC unsuccessful on FFPE

Myositis classification relies on immunohistochemistry usually done on snap-frozen muscle, which many laboratories cannot process. A Histopathology study, published in June 2026, developed a protocol for formalin-fixed, paraffin-embedded muscle using heat-induced antigen retrieval and overnight antibody incubation, and compared it with frozen sections in 20 biopsies covering dermatomyositis, inclusion body myositis, immune-mediated necrotising myopathy and mimics.

MHC-II, MxA and p62 stained well on paraffin, with concordance against frozen sections of 90%, 90% and 80%, and no statistically significant differences. Every discrepancy involved a single marker and may reflect the patchy nature of the disease. MHC-I and the membrane attack complex could not be reliably stained on paraffin.

For laboratories without a frozen-section muscle service, which many smaller laboratories lack,this offers a usable partial panel: MxA for dermatomyositis, p62 for inclusion body myositis, MHC-II for antisynthetase and inclusion body myositis patterns. The study is small, and losing MHC-I and MAC means some diagnoses, particularly necrotising myopathy, will still need frozen tissue or serology.

  • Where frozen muscle is unavailable, consider MHC-II, MxA and p62 immunohistochemistry on paraffin sections.
  • Do not rely on MHC-I or membrane attack complex staining on paraffin; they failed in this protocol.
  • Validate the protocol locally against frozen sections or referral cases before reporting.
  • Correlate with myositis-specific antibodies, especially when necrotising myopathy is suspected.
  • Send a frozen sample to a reference centre where feasible for full classification.

Why it matters

Myositis classification need not wait for a referral centre when frozen tissue is not available.

Don't overread it

Twenty cases with a few per diagnosis cannot establish diagnostic accuracy for each myositis subtype.

The statistics, in plain English

Concordance of 90% means 18 of 20 cases matched between paraffin and frozen sections for that marker. Non-significant p-values in 20 cases show no large difference, not equivalence.

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