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Benign Acute Childhood Myositis: Our Experience on Clinical Evaluation
Silvia D'Amico1, Gloria Gangi1, Massimo Barbagallo2
1Department of Clinical and Experimental Medicine, Postgraduate Training Program in Pediatrics, University of Catania, Catania, Italy.
Insights
Benign acute childhood myositis (BACM) is a common, transient condition in school-aged children, typically following viral infections. This study found BACM has a favorable prognosis with supportive care, resolving without recurrence.
Area of Science:
- Pediatrics
- Infectious Diseases
- Neurology
Background:
- Benign acute childhood myositis (BACM) is a temporary condition affecting school-aged children, causing muscle pain and walking difficulties.
- Symptoms often follow viral infections like influenza, parainfluenza, rotavirus, and Mycoplasma.
- BACM is characterized by symmetrical lower extremity pain, primarily in the calf muscles.
Purpose of the Study:
- To analyze the clinical characteristics, etiology, and outcomes of Benign acute childhood myositis (BACM) in a pediatric population.
- To evaluate the effectiveness of supportive therapy and the long-term prognosis of BACM.
- To highlight the importance of early diagnosis and follow-up for BACM.
Main Methods:
- A 12-year observational case series conducted across four pediatric hospitals in Catania, Italy.
- Inclusion of 50 children diagnosed with BACM.
- Data collection included clinical examination, laboratory findings, disease course, treatment, and complications from electronic medical records.
Main Results:
- The mean age of affected children was 5.35 years, with 86% being male and 56% of cases occurring in winter.
- Common preceding symptoms included fever and upper respiratory tract inflammation; influenza virus B was the most frequent etiological agent identified.
- All children experienced symptom resolution with supportive care, showing reduced pain and creatine kinase (CK) levels, with no reported recurrences or sequelae.
Conclusions:
- Benign acute childhood myositis (BACM) generally has a favorable evolution and good prognosis with spontaneous symptom remission.
- Despite the benign course, the acute presentation can cause parental distress, underscoring the need for rapid diagnosis.
- Careful follow-up is recommended to rule out persistent symptoms or elevated creatine kinase (CK) levels.
Background:
Benign acute childhood myositis (BACM) is a transient condition mainly affecting children of school age characterized by muscle pain, typically localized to the calf muscle with symmetrical lower extremity pain and difficulty in walking. Usually, the symptomatology is preceded by a viral infection including influenza, parainfluenza, rotavirus, and mycoplasma.
Methods:
The case series was conducted in four pediatric hospitals in Catania, Italy, over a 12-year observational period. Clinical examination, laboratory data, course, treatment, and complications of the affected children were extracted from electronic medical records of each hospital.
Results:
For the case series, 50 children diagnosed with BACM were enrolled: the mean age of affected children was 5.35 years, 86% of were males, and in 56% the affections occurred during the winter. In the affected children, the clinical picture was characterized by previous fever and/or symptoms of inflammation of the upper airways, and followed by pain in the lower extremities up to uncoordinated gait. In 17 cases the etiological agent was isolated, including the influenza virus type B as the most frequent and influenza virus type A, Mycoplasma pneumoniae, beta-hemolytic streptococcus, and herpes simplex virus. Children were treated with supportive therapy. In all the children the muscular symptomatology had a good evolution with progressive marked reduction of pain and of the high level of CKemia. Neither clinical recurrences nor sequelae were reported.
Conclusion:
BACM shows to have in most of the cases a favorable evolution, a spontaneous remission of symptoms, and a good prognosis. However, the disorder generates parental distress for the acute presentation and the striking muscle dysfunction. It is worthy a rapid and early diagnosis to avoid unnecessary diagnostic investigations and a careful follow-up necessary to exclude persistence of symptoms or creatine kinase elevation.
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