Tietze syndrome

Tietze syndrome refers a benign costochondritis accompanied by hypertrophy of the costal cartilages.

The exact incidence of occurrence is not known. It is seen most commonly in the 2nd to 5th decades of life. Both sexes are affected equally.

It is characterised as a tender, non-suppurative swelling in the upper costosternal region. It can have an acute or gradual onset and may resolve spontaneously. It may mimic a myocardial infarction, but the pain in Tietze syndrome is more localised and is not accompanied by any additional presenting symptoms.

MRI features of Tietze's syndrome were characterised according to one study as follows 1:

  • enlargement and thickening of cartilage at the site of the complaint
  • focal or widespread increased signal intensities of affected cartilage on both TSE T2-weighted and STIR/T2 fat-saturated images
  • bone marrow oedema in the subchondral bone
  • intense gadolinium enhancement in the areas of thickened cartilage, in the subchondral bone marrow, and/or in the capsule and ligaments

Ga-67 imaging often shows increased radiotracer uptake 7.

First described in 1921 by Alexander Tietze (1864-1927), a German surgeon.

It is a benign condition that may subside spontaneously. Some authors suggest local steroid injection as a possible treatment option 6.

The differential diagnosis of Tietze syndrome runs the gamut of musculoskeletal chest wall pain, as well as:

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Article information

rID: 24439
Tag: cases
Synonyms or Alternate Spellings:
  • Tietze's syndrome
  • Tietze's disease
  • Tietze disease
  • Costochondral junction syndrome
  • Chondropathia tuberosa

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