This document discusses myositis ossificans, a condition where bone forms in muscle tissue or other soft tissues. It presents two main types - non-hereditary myositis ossificans, which usually occurs after trauma in adolescents and young adults, and myositis ossificans progressiva (also called fibrodysplasia ossificans progressiva or stone man syndrome), a rare genetic disorder where muscle and connective tissues are gradually replaced by bone. The document outlines the etiology, clinical features, diagnosis, histopathology, and treatment of both conditions. Surgical excision may be indicated if the condition causes intolerable pain, neurological compression, or limited range of motion.