Juvenile polymyositis

Description

Juvenile polymyositis is a rare childhood idiopathic inflammatory myopathy. It is frequently misdiagnosed, as it lacks a unique clinical phenotype. Traditionally, it presents with weakness of the proximal muscles that evolves over weeks to months. The primary histologic features are fibre size variability, scattered necrotic and regenerating fibres, and perivascular and endomysial cellular infiltrates.

Excludes

• 4A40 – Lupus erythematosus
• 4A42 – Systemic sclerosis
• 4A43 – Overlap or undifferentiated nonorgan specific systemic autoimmune disease
• 4A44 – Vasculitis
• 4A45 – Antiphospholipid syndrome

Exclusions from above levels

• 02 – Neoplasms
• 18 – Complications of pregnancy, childbirth and the puerperium
• 20 – Developmental anomalies