Journal article

Morphological Characteristics of Idiopathic Inflammatory Myopathies in Juvenile Patients


Authors listSchaenzer, Anne; Rager, Leonie; Dahlhaus, Iris; Dittmayer, Carsten; Preusse, Corinna; Della Marina, Adela; Goebel, Hans-Hilmar; Hahn, Andreas; Stenzel, Werner

Publication year2022

JournalCells

Volume number11

Issue number1

eISSN2073-4409

Open access statusGold

DOI Linkhttps://doi.org/10.3390/cells11010109

PublisherMDPI


Abstract
Background: In juvenile idiopathic inflammatory myopathies (IIMs), morphological characteristic features of distinct subgroups are not well defined. New treatment strategies require a precise diagnosis of the subgroups in IIM, and, therefore, knowledge about the pathomorphology of juvenile IIMs is warranted. Methods: Muscle biopsies from 15 patients (median age 8 (range 3-17) years, 73% female) with IIM and seven controls were analyzed by standard methods, immunohistochemistry, and transmission electron microscopy (TEM). Detailed clinical and laboratory data were accessed retrospectively. Results: Proximal muscle weakness and skin symptoms were the main clinical symptoms. Dermatomyositis (DM) was diagnosed in 9/15, antisynthetase syndrome (ASyS) in 4/15, and overlap myositis (OM) in 2/15. Analysis of skeletal muscle tissues showed inflammatory cells and diffuse upregulation of MHC class I in all subtypes. Morphological key findings were COX-deficient fibers as a striking pathology in DM and perimysial alkaline phosphatase positivity in anti-Jo-1-ASyS. Vascular staining of the type 1 IFN-surrogate marker, MxA, correlated with endothelial tubuloreticular inclusions in both groups. None of these specific morphological findings were present in anti-PL7-ASyS or OM patients. Conclusions: Morphological characteristics discriminate IIM subtypes in juvenile patients, emphasizing differences in aetiopathogenesis and supporting the notion of individual and targeted therapeutic strategies.



Citation Styles

Harvard Citation styleSchaenzer, A., Rager, L., Dahlhaus, I., Dittmayer, C., Preusse, C., Della Marina, A., et al. (2022) Morphological Characteristics of Idiopathic Inflammatory Myopathies in Juvenile Patients, Cells, 11(1), Article 109. https://doi.org/10.3390/cells11010109

APA Citation styleSchaenzer, A., Rager, L., Dahlhaus, I., Dittmayer, C., Preusse, C., Della Marina, A., Goebel, H., Hahn, A., & Stenzel, W. (2022). Morphological Characteristics of Idiopathic Inflammatory Myopathies in Juvenile Patients. Cells. 11(1), Article 109. https://doi.org/10.3390/cells11010109



Keywords


ANTI-3-HYDROXY-3-METHYLGLUTARYL-COENZYMEAnti-synthetase syndromeDERMATOMYOSITISjuvenilemuscle pathologyMYOSITISMYOSITIS-SPECIFIC AUTOANTIBODIESoverlap myositisphenotypes

Last updated on 2025-10-06 at 11:36