Continuing Medical Education: Synovitis.
Edited By: Gregory C. Gardner, M.D. Last updated Thursday, February 10, 2005
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Pattern recognition and the differential diagnosis
What are the three classes of synovitis?
Rheumatologists spend a good deal of their training learning to
recognize various forms of arthritis by their pattern of joint
involvement.
I divide the conditions into monoarticular (one joint only),
pauciarticular (2-5 joints), and polyarticular (more than 6 joints).
These are not set in stone as there is some overlap but is a useful
construct and has withstood the test of time and medical students. The
following lists are not all inclusive. They include the most common
entities someone in the primary care setting would encounter. The
purpose of this differentiation is to focus the initial evaluation and
help the "splitters" among us. The "don't forget" (because of potential
serious consequences) conditions are in italics and the most common causes in each category are bold.
What causes monoarticular arthritis?
Table 3. Causes of monoarthritis
| Inflammatory | Noninflammatory |
- Infection
- Disseminated gonorrhea
- Other bacteria
- Tuberculosis
- Fungi
- Lyme athritis
- Endocarditis
- Crystals
- Monosodium urate
- Calcium pyrophosphate
- Hydroxyappatite
- Spondyloarthropathy
- Ankylosing spondylitis
- Reiter's syndrome
- Psoriatic arthritis
- Miscellaneous
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- Trauma/fracture
- Osteoarthritis
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Nongonococcal septic arthritis is the most serious cause of
monoarthritis. The presentation is that of an acute or subacute onset
of mono- or rarely pauciarthritis. Large joints are usually affected
especially knees. Patients most often look systemically ill and will
have fever, chills, and will have an elevated WBC and ESR. Patients
with underlying arthritis especially rheumatoid arthritis are at
increased risk of septic arthritis and may not have the usual symptoms
due to antiinflammatory medications. The most common organisms are
Staphylococcus aureus, Streptococcus sp. and much less common are gram
negatives but think of the latter in the immunosuppressed or in IV drug
users. The initial evaluation should include arthrocentesis for gram
stain and culture and WBC, blood cultures, as well as an ESR. The
patient should be admitted and IV antibiotics started while waiting for
culture results. If there is any concern for a septic joint do an
arthrocentesis!
Gonococcal arthritis is seen in sexually active young adults
and only 25% have local genitourinary symptoms. Patients are usually
systemically ill and have dermatitis, tenosynovitis, and migratory
arthritis. Blood cultures are positive in only 5%, GU cultures in 80%,
and synovial fluid cultures in 30%. One often resorts to treatment of
presumptive gonococcal arthritis. Luckily, most strains that cause
gonococcal arthritis are penicillin sensitive although , resistant
strains are emerging. Initial evaluation should include the above
cultures plus consideration of pharyngeal and rectal cultures. Patients
often need a few days of hospitalization then can be treated as an
outpatient.
Endocarditis causes musculoskeletal symptoms in up to 40% of
affected patients. Inflammatory low back pain is common as is mono- or
pauciarthritis. It is interesting to note that the fluid while
inflammatory is usually sterile. This is thought to be due to immune
complex deposition in the synovium. Look for peripheral signs of immune
complex deposition such as cutaneous vasculitis, painful nodules,
listen for a murmur, check an ESR, blood cultures, CBC, cultures of
synovial fluid, and if endocarditis is likely, admit the patient and
begin antibiotics. Of note, rheumatoid factor is frequently positive in
these patients.
Crystals causing arthritis include urate, calcium
pyrophosphate, and appatite. Urate gout is probably the most common
cause of acute inflammatory monoarthritis. Inflammation is usually
intense and the patient will relate a history of previous self-limited
attacks. First MTP is a common site for urate gout and knee for calcium
pyrophosphate. Young women can have so called hydroxyappatite
pseudopodagra affecting the 1st MTP. Patients can have a pauciarticular
presentation with urate and pyrophosphate. For urate gout, a history of
ETOH use, history of kidney stones, or a family history of urate gout
is helpful. Females rarely get urate gout before menopause. There are
some distinctive X-ray findings for calcium pyrophosphate and appatite
arthritis (chondrocalcinosis and fluffy calcification respectively) On
examination, look for tophi and synovial fluid analysis is very helpful
in the definitive diagnosis of all but hydroxyappatite. A useful hint
to remember is that bugs, blood, and crystals (BBC) cause the most
intense joint pain.
Palindromic rheumatism is an episodic condition usually
affecting one joint at a time. The attacks can be fairly intense and
the fluid can be quite inflammatory. Attacks usually last several days
and resolve. With time, many individuals progress on to frank
rheumatoid arthritis.
TB and fungi are relatively rare but any chronic
monoarthritis without a diagnosis should be considered for synovial
biopsy and granulomatous synovitis considered.
Osteoarthritis is probably the overall most common cause of
monoarthritis and trauma/internal derangement of the knee is not far
behind. Meniscal tears can cause chronic noninflammatory type pain and
may give symptoms of knee locking or giveway.
Avascular necrosis is caused by trauma, alcohol abuse,
steroid use, divers, and in patients with hemaglobinopathies. Pain is
initially out of proportion to X-rays. Hips, knees and shoulders are
usually involved. Early diagnosis is by MRI scan.
Synovial neoplasm to remember and is pigmented villonodular synovitis. It can cause dark bloody effusions and is diagnosed by MRI/arthroscopy.
What causes pauciarticular arthritis?
Table 4. Causes of pauciarthritis
| Inflammatory | Noninflammatory |
- Infection
- Endocarditis
- Disseminated gonorrhea
- Rheumatic fever
- Lyme disease
- Crystals
- Monosodium urate
- Calcium pyrophosphate
- Spondyloarthropathy
- Miscellaneous
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Rheumatic fever - In many of these conditions systemic
features play an important role in the differential diagnosis.
Rheumatic fever is certainly one of these although most adults with
rheumatic fever present with only arthritis. The pain is usually out of
proportion to the swelling and the symptoms tend to be migratory. Other
Jones criteria include carditis, erythema marginatum, chorea, and
subcutaneous nodules. Be sure to listen for a murmur and check
ASO/streptozyme. The ASO should be followed serially and remember that
a positive test still does not prove rheumatic fever. Throat cultures
are usually negative by the time rheumatic fever occurs. One often
spends time ruling out other diseases even with a suspicion for
rheumatic fever due to the lack of definitive diagnostic testing. The
presence of carditis though, is very compelling and can be made by
echocardiogram.
Lyme arthritis is a late manifestation of lyme disease and
usually presents with recurrent attacks of mono- or pauciarthritis
especially including the knee. In this condition, the swelling is often
out of proportion to the pain!. A history of exposure and the
characteristic rash of Lyme disease are important. By time the
arthritis is present, the vast majority of patients have a positive
Lyme antibody test. One may have to treat presumptively for at least
one course of antibiotics in some marginal cases.
Spondyloarthropathies are characterized by their association
with the HLA-B27 gene (except the peripheral arthritis of psoriatic
arthritis). Features of these illness that are helpful in the diagnosis
include inflammatory low back pain, history of inflammatory eye disease
(uveitis, iritis, conjunctivitis), urethritis, cervicitis, diarrhea, a
variety of hyperkeratotic rashes, and diffuse swelling of digits called
sausage digits. Joints most often affected are the large joints of the
lower extremities. In my experience, the most common cause of
inflammatory pauciarthritis is a spondyloarthropathy, especially
Reiter's disease or psoriatic arthritis. Up to 7% of patients with
psoriasis will have arthritis.
Sarcoidosis frequently presents with pauciarthritis. One
typical presentation is called Lofgren syndrome and consists of
erythema nodosum, hilar adenopathy, and pauciarthritis usually
affecting the large joints of the lower extremities. A chronic
destructive form also exists and is often seen along with extensive
bone cysts on X-ray. Other important features include uveitis and skin
lesions.
Polymyalgia rheumatica will be discussed below.
What causes polyarticular arthritis?
Table 5. Causes of polyarthritis
| Inflammatory | Noninflammatory |
- Viruses
- Parvovirus
- Hepatitis B
- Rubella
- Hepatitis C
- Autoimmune diseases
- Rheumatoid arthritis
- Systemic lupus erythematosus
- Sjogren's syndrome
- Scleroderma
- Polymyositis/Dermatomyositis
- Serum sickness
- Antibiotics
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- Primary osteoarthritis
- Secondary osteoarthritis
- Hemachromatosis
- CPPD
- Ochronosis
- Acromegaly
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Viruses are a common cause of acute self limited arthritis. The ones to remember include hepatitis B, parvovirus B19, and rubella.
HIV can cause a variety of rheumatologic syndromes but polyarthritis is
unusual. Viral arthridities are usually symetrical and cause more pain
than swelling. They usually are self limited and are associated with
rash. The prodrome of hepatitis B can be polyarthritis even before
liver function tests are abnormal. Be sure to check for hepatitis B
surface antigen. The arthritis usually goes away by the time the
patient has clinical hepatitis. Hepatitis C is being recognized
as a common infection. It can cause a symmetric polyarthritis that is
often accompanied by a positive rheumatoid factor thus being confused
with rheumatoid arthritis. There are no nodules with hepatitis C nor
does it cause erosive joint changes. Parvovirus will be discussed below.
Rheumatoid arthritis is a relatively common disease affecting
1-2% of the US population. Remember that rheumatoid factor is seen in
only 70% of patients and may not appear for 1 year. RA is a symmetric
arthritis and almost always affects the small joints of the hands and
feet.
Diagnosis of systemic lupus erythematosus is aided greatly by
the ANA testing. A negative ANA plus a negative antiSSA antibody rules
out SLE! On the other hand, a positive ANA does not mean SLE! One has
to look for other features to go along with the positive ANA not just
fatigue and arthralgias. I usually am not impressed with an ANA of less
than 1:160 and look for the presence of other autoantibodies as well as
objective evidence of inflammation on laboratory testing and
examination. Urgent cases of SLE include those with new onset or
exacerbation of nephritis or cerebritis.
Secondary causes of osteoarthrits especially metabolic
causes, are conditions I keep in the back of my mind when I see a
patient with clinical osteoarthritis in a symmetric pattern but in
places atypical for primary OA. These include the shoulders, elbows,
wrists, and MCP joints. The most important cause is idiopathic calcium
pyrophosphate disease and less common, but with more significant
implications, is hemachromatosis. I usually check a calcium, FE, TIBC,
and TSH in a patient with what may be a secondary cause of OA without
other explanation (old RA) and or significant chondrocalcinosis on
X-ray.
Serum sicknesses are actually in this day and age serum
sickness-like reactions. Symptoms include rash often uriticarial, and
inflammatory arthritis affecting large joints. Fever is common and
laboratory abnormalities include mild hypocompletemia and normal
eosinophil count. The process is self limited resolving in 1-3 weeks
after exposure. Typical causes of serum sickness-like reactions are
antibiotics especially penicillins and sulfa drugs.
Surgery for arthritis at the University of Washington, Department of Orthopaedics and Sports Medicine, Seattle, Washington
If you are interested in making an appointment to discuss this procedure in Seattle, you can request an appointment using our online referrals website. To request a referral online, please click here. You can also call 206-598-4288 to make an appointment. Our clinical center is located in Seattle Washington, USA
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