Köhler's Disease

Paediatric MSK
Lens
Full lens

Overview

Köhler's disease is a self-limiting osteochondrosis of the tarsal navicular in young children, in which the bone passes through a phase of avascular necrosis (AVN) and then reossifies to a normal shape.

It is uncommon, classically affects boys aged around 4 to 7, and usually involves 1 foot. It presents as a painful limp with tenderness over the midfoot. The radiographs can look alarming, but the long-term outcome is excellent.

The priorities are to exclude the serious causes of a painful limp, avoid over-calling a normal ossification variant, and reassure the family while managing symptoms.

Anatomy & Pathophysiology

The navicular sits at the apex of the medial longitudinal arch, between the talus and the 3 cuneiforms, and carries high compressive load. It is the last tarsal bone to ossify, earlier in girls than boys. A late-ossifying bone under high load is central to the disease.

The tarsal navicular sits at the apex of the medial longitudinal arch, between the talus and the cuneiforms, where it carries high compressive load.

Its central third is a relative vascular watershed. Compression of the immature bone between the talus and the cuneiforms is thought to compromise small perforating vessels, causing transient ischaemia of the ossific nucleus. The bone becomes sclerotic, flattened and sometimes fragmented, then reossifies and remodels as the surrounding cartilage keeps growing.

Köhler's disease is distinct from Müller-Weiss disease, a separate navicular osteonecrosis seen mainly in adults.

Clinical Pearl
  • •Last tarsal bone to ossify, at the apex of the medial arch
  • •The central third is the vascular watershed at risk
  • •The bone reossifies and remodels to normal

Keep reading for free

Unlock 10 full topics of your choice with a free account.

Already have an account? Log in

Frequently asked questions