Osteochondrosis

Definition

  • Disorders of endochondral ossification in growing children
  • Affect the epiphysis, apophysis or physis
  • Repetitive stress, vascular insult and genetic predisposition
  • Osteonecrosis and fragmentation, then repair

Pathology

  • Disordered ossification, with avascular necrosis in some forms
  • Revascularisation, resorption and new bone formation follow
  • Radiographs show sclerosis, flattening and fragmentation, then reconstitution
  • Outcome depends on age, site and articular remodelling before skeletal maturity

Classification

Siffert classification

TypeDescriptionExamples
ArticularJoint surface and epiphysis, with risk of secondary osteoarthritisPerthes, Freiberg, Kohler, Panner
Non-articularTraction apophysitis at a tendon or ligament insertion, self-limitingOsgood-Schlatter, Sever, Sinding-Larsen-Johansson
PhysealGrowth plate involvement with resulting deformityBlount, Scheuermann

Original publication Siffert RS. Classification of the osteochondroses. Clin Orthop Relat Res. 1981;(158):10-8.

Articular

  • Legg-Calve-Perthes disease, femoral head, boys aged 4 to 8 years
  • Kohler disease, navicular, young children, self-limiting
  • Freiberg disease, metatarsal head (usually second), adolescent girls
  • Panner disease, capitellum, boys under 10, distinct from capitellar OCD in older adolescents
  • Kienbock disease, lunate, young adults, with negative ulnar variance

Non-articular

  • Osgood-Schlatter disease, tibial tubercle apophysis, active adolescents
  • Sinding-Larsen-Johansson syndrome, inferior pole of patella
  • Sever disease, calcaneal apophysis at the Achilles insertion

Physeal

  • Scheuermann disease, vertebral ring apophysis, thoracic kyphosis with wedging of three or more vertebrae
  • Blount disease, posteromedial proximal tibial physis, progressive tibia vara

Clinical Features

  • Activity related pain, limp, local tenderness and swelling
  • Deformity in physeal forms
  • Apophyseal forms often bilateral and linked to growth spurts and sport

Investigations

  • Plain radiographs usually confirm the diagnosis, with comparison views where helpful
  • MRI for early disease, staging of necrosis and articular involvement

Management

  • Non-articular forms resolve at skeletal maturity with activity modification, stretching, ice and analgesia
  • Articular forms aim to preserve congruity and range of motion
  • Surgery for progressive collapse, loose bodies or deformity
  • Physeal forms may need bracing or corrective osteotomy, as in Scheuermann and Blount disease

Reviewed by Professor Phong Tran, Head of Orthopaedic Surgery, Western Health. Last updated 10 October 2026.