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Tietze's Syndrome
First described by Alexander Tietze in 1921,1,2 Tietze's syndrome has been defined as a benign, painful, non-suppurative localized swelling of the costosternal, sternoclavicular, or costochondral joints, most often involving the area of the second and third ribs. Only one area is usually involved, and young adults are more commonly affected.3 The syndrome is uncommon and self limiting. The cause of Tietze's syndrome is unknown, but preceding upper respiratory infections and excessive coughing have been described in some patients.
- Tietze's syndrome can present at any age but is most common in those aged 20 to 30 years.
- Tietze's syndrome is twice as frequent in men as in women.
- May be acute or gradual onset. The patient complains of pain that is often localized to the costal cartilage.
- The syndrome usually affects the upper ribs, especially the second or third ribs.
- The pain is aggravated by physical activity, movement, coughing or sneezing.
- There is localized tenderness.
- Although the pain usually disappears spontaneously, the swelling may persist long after the tenderness has disappeared.
- Other causes of chest pain: the pain may be confused with that of myocardial infarction and is usually unilateral on the left side.
- Tietze's syndrome and costochondritis are not completely synonymous as Tietze's syndrome is more localised and includes costochondral cartilage swelling whereas costochondritis tend to be more diffuse and does not cause costochondral cartilage swelling.
- Diagnosis can usually be made by careful history and examination.
- Investigations may be required to rule out other possible causes of chest pain.
- ECG to exclude cardiovascular conditions.
- Chest X-ray to exclude other pathologies.
- Ultrasound may have a role in assessment and diagnosis.4
- Reassurance once the diagnosis is confirmed.
- Non-steroidal anti-inflammatory drugs.
- Local injection of long-acting corticosteroids may help.
- Intercostal nerve block may also help but is rarely required.
- The pain usually subsides within a few weeks, with some residual swelling persisting for longer periods of time.
- However the course of the disease varies from spontaneous remission to persistent symptoms over years.
Document References
- Tietze A, Uber eine eigenartige Haufung von Fallen mit Dystrophie der Rippenknorpel. Berliner klinische Wochenschrift, 1921, 58: 829-831.
- Tietze's syndrome - www.whonamedit.com
- Aeschlimann A, Kahn MF; Tietze's syndrome: a critical review. Clin Exp Rheumatol. 1990 Jul-Aug;8(4):407-12. [abstract]
- Kamel M, Kotob H; Ultrasonographic assessment of local steroid injection in Tietze's syndrome. Br J Rheumatol. 1997 May;36(5):547-50. [abstract]
DocID: 2872
Document Version: 20
DocRef: bgp1294
Last Updated: 3 Jul 2007
Review Date: 2 Jul 2009
The authors and editors of this article are employed to create accurate and up to date content reflecting reliable research evidence, guidance and best clinical practice. They are free from any commercial conflicts of interest.
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