Jump to content

Synovial chondromatosis: Difference between revisions

From Wikipedia, the free encyclopedia
Content deleted Content added
NMR -> MRI
Line 31: Line 31:
In the disease, the thin flexible membrane of the synovium gradually forms blisters which calcify and enlarge. These nodules eventually break free and float around the joint space becoming larger – these add to the discomfort and stiffness of the joint.
In the disease, the thin flexible membrane of the synovium gradually forms blisters which calcify and enlarge. These nodules eventually break free and float around the joint space becoming larger – these add to the discomfort and stiffness of the joint.
The disease is rare and little known and currently no known cure. The affected tissue will show up as a semi-solid mass in an [[NMR]] scan, final diagnosis is usually confirmed by taking a [[biopsy]].
The disease is rare and little known and currently no known cure. The affected tissue will show up as a semi-solid mass in a [[MRI]] scan, final diagnosis is usually confirmed by taking a [[biopsy]].
People suffering from this disease are nearly always (but not exclusively) male, and usually in their forties. The disease generally affects only one of the larger [[weight bearing]] joints ([[hip]], [[ankle]], [[knee]]) – although the [[elbow]], and [[wrist]] can also be affected.
People suffering from this disease are nearly always (but not exclusively) male, and usually in their forties. The disease generally affects only one of the larger [[weight bearing]] joints ([[hip]], [[ankle]], [[knee]]) – although the [[elbow]], and [[wrist]] can also be affected.

Revision as of 00:34, 15 April 2011

Synovial chondromatosis
SpecialtyRheumatology Edit this on Wikidata

Synovial chondromatosis is a disease affecting the synovium, a thin flexible membrane around a joint. It is also known as Reichel's syndrome or Reichel-Jones-Henderson syndrome, named after Friedrich Paul Reichel, Hugh Toland Jones and Melvin Starkey Henderson.[1]

Symptoms

Patients usually complain of pain in one joint, which persists or months, or even years, does not ease with exercise, steroid injection or heat treatment, shows nothing on X-ray, but shows a definite restriction of movement.

There are 3 defined stages to this disease:

  • early: no loose bodies but active synovial disease;
  • transitional: active synovial disease, and loose bodies;
  • late: loose bodies but no synovial disease;

In the early stages of the disease it is often confused with tendinitis and/or arthritis. Once it reaches transitional the loose bodies become apparent with X-ray in greater than 70% of cases, with MRI often showing where xray fails.

In the disease, the thin flexible membrane of the synovium gradually forms blisters which calcify and enlarge. These nodules eventually break free and float around the joint space becoming larger – these add to the discomfort and stiffness of the joint.

The disease is rare and little known and currently no known cure. The affected tissue will show up as a semi-solid mass in a MRI scan, final diagnosis is usually confirmed by taking a biopsy.

People suffering from this disease are nearly always (but not exclusively) male, and usually in their forties. The disease generally affects only one of the larger weight bearing joints (hip, ankle, knee) – although the elbow, and wrist can also be affected.

Treatment

Treatment is frequently by means of removal of the loose bodies and of a partial or full Synovectomy (removal of the synovium)

Full synovectomy is a moderately major operation and involves completely exposing the joint and removing the affected tissue. Partial synovectomy is normally done arthroscopically. Synovectomies are normally carried out by shaving the lining of the knee but there are other ways of achieveing this by either freezing the synovium or by the use of radiation treatment.

The need for further procedures is greater than 25% although normally the frequency of the required removal of loose bodies is reduced by the previous synovectomy. There have been documented cases of malignant transformation however this is rare.

Whilst the condition can be described as a ‘benign growth’ it seldom affects more than one joint, and does not usually affect surrounding tissue.

References