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Poliartrite acuta

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What is acute polyarthritis?

Acute polyarthritis has a very wide differential diagnosis, presenting significant diagnostic difficulties. This article also considers conditions which may cause polyarthralgia which can present in a similar fashion to the inflammatory diseases.

Definizioni

Acute monoarthritis - acute inflammation of a single joint; the most important differential diagnosis is artrite settica.

Oligoarthritis - more than one but fewer than five joints are affected.

Polyarthritis - five or more joints are affected.

Vedi anche il separato Articolazioni doloranti - valutazione, indagini e gestione nell'assistenza primaria e Storia reumatologica, esame e indagini articoli.

Careful clinical assessment should give a differential diagnosis which can be further narrowed down by appropriate investigations. Autoantibody tests can be misleading if not considered in the context of the clinical presentation. They are best used to confirm a clinical suspicion, rather than as suggesters of a diagnosis and should not be requested if you are not clear which condition you are looking to diagnose or exclude by a particular test.

Conditions more commonly considered to be chronic and indolent can present floridly in the acute phase. It can take time for a disease to evolve into its classical pattern and for the decision to be reached as to whether it is a chronic condition or a one-off phenomenon. In some cases a definitive diagnosis may never be reached. 1

  • Details such as age, sex, ethnic origin and occupation can give useful diagnostic clues. For example, juvenile idiopathic arthritis is the most common arthritis in children.

  • Family history may be present in cases of artrite reumatoide (AR), seronegative arthropathies e osteoarthritis (OA).

  • Character of the pain is not always discriminatory in diagnostic terms; acute joint swelling may indicate an inflammatory condition.

  • Speed of onset and severity at the start may help - gotta tends to come on abruptly, whereas RA is usually more gradual. Similarly, gout tends to cause very severe, excruciating pain.

  • Diurnal variation of symptoms is important to establish. An inflammatory arthritis tends to be worse on waking and eases as the day goes on. Mechanical pain tends to have the opposite effect. Most causes of polyarthritis are inflammatory, with osteoarthritis being the exception.

  • Migratory arthritis (flitting from joint to joint over a period of days) might suggest gonococcal infection, rheumatic fever (RF), sarcoidosi, lupus eritematoso sistemico (LES), malattia di Lyme o bacterial endocarditis.

  • The pattern of joint involvement may be useful in suggesting a diagnosis. For example:

    • OA of the hand affects the distal interphalangeal (DIP) and proximal interphalangeal (PIP) joints but spares the metacarpophalangeal (MCP) joints.

    • RA affects the MCP and PIP joints but spares the DIP joints.

    • Psoriatic arthritis, crystal arthropathies and sarcoidosis can affect all these joints.

    • Large weight-bearing joints and facet joints of the spine are often affected by OA.

    • Axial involvement in younger patients suggests a seronegative arthropathy such as ankylosing spondylitis or inflammatory bowel disease-associated arthropathy.

  • Symmetrical joint involvement tends to occur in systemic syndromes such as RA, SLE, viral arthritis and drug/serum sickness reactions.

  • In asymmetrical joint involvement consider gout, septic arthritis, psoriatic arthritis and reactive arthritis.

  • Extra-articular symptoms should be asked about and can aid diagnosis. The eyes, parotid glands, skin, mouth, genitals and muscles can all be affected by rheumatological diagnoses.

  • Take a full drug history - some drugs (eg, hydralazine, procainamide, quinidine and minocycline) can cause a lupus-like syndrome and there have been reports of a variety of drugs associated with polyarthralgia (eg, moxifloxacin). 2 34

  • A direct enquiry should be made as to the presence of systemic symptoms such as fever and weight loss, as well as extra-articular features as given in the table.

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  • Check the temperature if concerned about infection.

  • Nail changes (eg, pitting) may suggest psoriatic arthropathy.

  • Look at the eyes for signs of inflammation.

  • Check major lymph nodes for evidence of lymphadenopathy.

  • Check the skin for rashes (eg, psoriasis, SLE) and evidence of vasculitis. Feel extensor aspects of forearms for nodules. Check shins for evidence of erythema nodosum.

  • Cardiac examination - listen for murmurs if there is reason to suspect rheumatic fever.

  • Abdominal examination may reveal evidence of hepatomegaly and/or splenomegaly.

  • Examine other systems as indicated by the history and clinical hypotheses.

  • Joint examination:

    • Look for signs of inflammation in the joint, such as heat, tenderness and synovial thickening.

    • Establish whether there the affected joints are symmetrical or asymmetrical.

    • Active and passive movements of affected joints and the degree of pain and/or crepitus may also be helpful. However, crepitus and pain will not differentiate between inflammatory and non-inflammatory causes of joint pain. They may, however, give some indication as to the degree of damage.

    • Also examine the structures around the joint and determine if the symptoms are intra-articular or periarticular.

Discriminating features of common causes of polyarthritis

Pattern of joint/axial involvement

Extra-articular manifestations/other features

Artrite reumatoide (AR)

Small and large joints.

Symmetrical.

May involve the neck.

Nodules

Osteoartrite (OA)

Weight-bearing joints, proximal interphalangeal (PIP) joint, distal interphalangeal (DIP) joint, first carpometacarpal (CMC) joint.

May or may not be symmetrical.

May involve the neck and lower back.

None, Heberden's nodes (distal) and Bouchard's nodes (proximal)

Lupus eritematoso sistemico (LES)

Small joints

Symmetrical.

Does not involve the neck or back.

Malar rash, mouth ulcers, pleuritis, pericarditis

Artrite psoriasica

Large and small joints.

May or may not be symmetrical.

Sometimes involves the neck and back.

Psoriatic rash, dactylitis, nail changes, tendinopathy

Human parvovirus B19 infection

Small joints.

Symmetrical.

Does not involve the neck and back.

Lacy rash, malar rash

Spondilite anchilosante

Large joints.

Symmetrical,

Involves the back.

Iritis, aortic regurgitation, tendinopathy

The diagnoses below are not exhaustive but cover the vast majority of causes of polyarthritis.

Viral infections 5

Parvovirus B19

Enteroviruses

Adenoviruses

Epstein-Barr virus

Coxsackievirus

Cytomegalovirus

Hepatitis viruses - especially epatite B

Parotite

Rosolia

test HIV

Tropical viruses such as chikungunya and Zika

Direct bacterial infections

Gonococcal infection

Staphylococcus aureus

Streptococci

Gram-negative organisms

Bacterial endocarditis

Other infections

malattia di Lyme (Borrelia burgdorferi)

Tubercolosi (mycobacterial)

Fungal infection

Weil's disease (leptospirosis)

Whipple's disease (Tropheryma whippelii)

Reactive to bacterial infection

Gonococcal infection

Campylobacter spp.

Clamidia spp.

Salmonella spp.

Shigella spp.

Yersinia spp.

Rheumatic fever (RF) - group A streptococci

Artrite reattiva

Crystal arthropathy/metabolic disease

Gotta (urate)

Pseudogotta (calcium pyrophosphate)

Hydroxyapatite

la malattia di Wilson

Emocromatosi

Amiloidosi

Iperlipidemia

Multicentric reticulohistiocytosis

Alkaptonuria

Systemic rheumatological disease

Artrite reumatoide (AR)

Lupus eritematoso sistemico (LES)

Polymyositis/dermatomyositis

Artrite idiopatica giovanile

Sclerodermia

Sindrome di Sjögren

Malattia di Behçet

Familial Mediterranean fever

Fibromialgia

Systemic vasculitic disease

Vasculite - ad esempio, Porpora di Henoch-Schönlein

Poliarterite nodosa

Granulomatosi con poliangioite

Arterite a cellule giganti

Vasculite da ipersensibilità

Spondyloarthropathies

Spondilite anchilosante

Artrite psoriasica

Enteropathic arthropathy (inflammatory bowel disease-associated)

Endocrine disease

Iperparatiroidismo

Ipertiroidismo

Ipotiroidismo

Acromegalia

Malignità

Metastatic cancer

Mieloma multiplo

Degenerative/structural

Primary generalised (erosive) osteoarthritis (OA)

Secondary osteoarthritis

Neuropathic joints

Varie

Sarcoidosi

Fibromialgia

Hypertrophic pulmonary osteoarthropathy

Hypermobility syndromes (eg, Sindrome di Ehlers-Danlos o Marfan's syndrome)

Osteomalacia

Drug/serum reactions

Polimialgia reumatica

Sweet's syndrome

Palindromic rheumatism

Long COVID

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  • Where there is any suspicion of septic arthritis, immediate aspiration of synovial fluid should be carried out; referral for this should not be delayed to wait for blood tests.

  • Blood tests - FBC, ESR, CRP and U&E are useful screening investigations which give diagnostic clues.

  • Autoantibodies can help to confirm a diagnosis but are often relatively nonspecific or insensitive.6 They should be interpreted in the context of the clinical presentation, preferably with specialised rheumatological input for the less common markers.

  • Rheumatoid factor if there is synovitis on clinical examination. Consider measuring anti-cyclic citrullinated peptide (anti-CCP ) antibodies in adults with suspected RA if they are negative for rheumatoid factor.7

  • Radiology - X-rays play a variable role in their contribution to diagnosis but are a useful first-line investigation. X-ray the hands and feet in adults with suspected RA and persistent synovitis.7 Other imaging modalities may need to be conducted with rheumatological/radiological advice.

  • Urinalysis indicates any renal involvement.

This is directed at the underlying diagnosis. See the links to the individual diagnoses for detail.

Symptomatic treatment of inflammatory conditions with non-steroidal anti-inflammatory drugs should be considered whilst awaiting the evolution of an arthritis, where there are no contra-indications or significant drug interactions. It is generally not ideal to give prednisolone in this situation, as that can make it harder to make a definitive diagnosis in secondary care. Discussion with a specialist would be wise if considering this.

Where there is a significant inflammatory illness as revealed by clinical severity and CRP/ESR, etc, early referral for disease-modifying interventions can significantly reduce joint pathology in some conditions.

For patient with possible RA, the National Institute for Health and Care Excellence (NICE) recommends:7

  • Refer for specialist opinion any adult with suspected persistent synovitis of undetermined cause.

  • Refer urgently (even with a normal acute-phase response, negative anti-CCP antibodies or rheumatoid factor) if any of the following apply:

    • Le piccole articolazioni delle mani o dei piedi sono colpite.

    • Più di un'articolazione è interessata.

    • C'è stato un ritardo di tre mesi o più tra l'inizio dei sintomi e la ricerca di un consulto medico.

Ulteriori letture e riferimenti

  1. Mies Richie A, Francis ML; Diagnostic approach to polyarticular joint pain. Am Fam Physician. 2003 Sep 15;68(6):1151-60.
  2. Adwan MH; An update on drug-induced arthritis. Rheumatol Int. 2016 Aug;36(8):1089-97. doi: 10.1007/s00296-016-3462-y. Epub 2016 Mar 21.
  3. Dalle Vedove C, Simon JC, Girolomoni G; Drug-induced lupus erythematosus with emphasis on skin manifestations and the role of anti-TNFalpha agents. J Dtsch Dermatol Ges. 2012 Dec;10(12):889-97. doi: 10.1111/j.1610-0387.2012.08000.x. Epub 2012 Sep 3.
  4. Torres JR, Bajares A; Severe acute polyarthritis in a child after high doses of moxifloxacin. Scand J Infect Dis. 2008;40(6-7):582-4.
  5. Tiwari V, Bergman MJ; Viral Arthritis.
  6. Pujalte GG, Albano-Aluquin SA; Differential Diagnosis of Polyarticular Arthritis. Am Fam Physician. 2015 Jul 1;92(1):35-41.
  7. Artrite reumatoide negli adulti: gestione; Linee guida NICE (luglio 2018 - ultimo aggiornamento ottobre 2020)

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