Clinical Characteristics in Pediatric Patients with Immune-Mediated Necrotizing Myopathy
Discuss this preprint
Start a discussion What are Sciety discussions?Listed in
This article is not in any list yet, why not save it to one of your lists.Abstract
Objective To investigate the clinical characteristics and therapeutic strategies of childhood immune-mediated necrotizing myopathy (IMNM) and to provide evidence for clinical diagnosis and management. Methods We retrospectively analyzedthe clinical data of 10 children diagnosed with IMNM at the Children's Medical Center, Xiangya Hospital, Central South University, from January 2016 to May 2025. The onset features, clinical manifestations, laboratory findings, muscle magnetic resonance imaging (MRI) characteristics, treatment modalities, and prognosis were summarized. Results Among the 10 patients, 4 were male and 6 were female, with a median age at onset of 5.5 years (range: 3–16 years). The mainclinical manifestations included symmetric proximal muscle weakness (100%) and cutaneous manifestations(50%, including Gottron's sign and periorbital rash). Creatine kinase(CK) levels were markedly elevated, with a median of 3988.5 U/L (range: 2080–13524 U/L). Muscle MRI revealed edema or fatty infiltration in the thigh muscles. Anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) antibodies were detected in 4 patients (40%), and anti-signal recognition particle(SRP) antibodies in 6 patients (60%). Electromyography (EMG) showed myopathic changes in all cases. Muscle histopathology demonstrated myofiber necrosis, regeneration, and inflammatory cell infiltration. All patients received glucocorticoid therapy, combined with oral methotrexate. Additionally, 5 patients were treated with rituximab, and 8 received intravenous immunoglobulin (IVIG). During follow-up, 4 patients achieved complete remission, 5 achieved partial remission, and 1 showed noclinical remission. Conclusion Childhood IMNM is characterized by proximal muscle weakness, typical rash, and significantly elevated CK levels, frequently associated with anti-SRP or anti-HMGCR antibodies. Early immunosuppressive therapy, including glucocorticoids combined with immunosuppressants or IVIG, can significantly improve prognosis, emphasizingthe importance of early diagnosis and active intervention.