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Psoriatic Arthritis Clinical Manifestations

by Don Martin, M.D.

There are five clinical patterns of psoriatic arthritis, which may evolve from one to another, and are not necessarily mutually exclusive:

  1. Asymmetrical mono- and oligoarticular arthritis (30-50% of cases) is the most common presentation of psoriatic arthritis.
  2. Symmetrical polyarticular arthritis (30-50% of cases) is ultimately the most common form of psoriatic arthritis.
  3. Distal interphalangeal (DIP) joint involvement (25% of cases) is nearly always associated with nail manifestationsm (image below).
    dip involvement
  4. Arthritis mutilans (5% of cases) is characterized by resorption of the phalangeal bones. (image below)
    dip involvement
  5. Axial arthritis (30-35% of cases) may be different in character from ankylosing spondylitis, the prototypical HLA-B27-associated spondyloarthropathy. It may present as sacro-iliitis, which may be asymmetrical and asymptomatic, or spondylitis, which may occur without sacro-iliitis and may affect any level of the spine in "skip" fashion.

In addition to psoriatic plaques themselves, there are a number of other characteristic, though not necessarily pathognomonic, features of psoriatic arthritis:

  • Nail involvement may be manifested as pitting, ridging, separation from the nail bed (onycholysis) (image below)
    example of onycholysis
    or yellow-orange discoloration ("oil drop" sign). (image below)
    oil-drop sign
  • Dactylitis presents as the so-called "sausage digit", diffuse swelling of the entire digit likely due to a combination of both arthritis and tenosynovitis. (image below)
    dactylitis
  • Enthesitis, inflammation at the site of ligamentous and tendinous insertion (image below), is characteristic of all the HLA-B27-associated spondyloarthropathies.
    enthesitis
  • Extra-cutaneous and -articular manifestations are uncommon but may include conjunctivitis, uveitis, aortic insufficiency and pulmonary fibrosis.

References

1. Willkens RF, Williams HJ, Ward JR, et al: Randomized, double blind, placebo-controlled trial of low dose pulse methotrexate in psoriatic arthritis. Arthritis Rheum 27:376, 1984.

2. Espinoza LR, Zakraoni L, Espinoza CG, et al: Psoriatic arthritis: Clinical response and side effects of methotrexate therapy. J Rheumatol 19:872, 1992.

3. Gupta AK, Matteson EI, Ellis CN, et al: Cyclosporin in the treatment of psoriatic arthritis. Arch Dematol 125:507, 1989.

4. Salvarani C, Macchioni P, Olivieri I, et al: A comparison of cyclosporine, sulfasalazine, and symptomatic therapy in the treatment of psoriatic arthritis. J Rheumatol 28:2274, 2001.

5. Sarzi-Puttini P, Cazzola M, Panni B, et al: Long-term safety and efficacy of low-dose cyclosporin A in severe psoriatic arthritis. Rheumatol Int 21:234, 2002.

6. Mease PJ: Etanercept in the treatment of psoriatic arthritis and psoriasis: a randomized trial. Lancet 356:385, 2000.

7. Mease PJ: Cytokine blockers in psoriatic arthritis. Ann Rheum Dis 60:iii37, 2001.

8. Iyer S, Yamauchi P, Lowe NJ: Etanercept for severe psoriasis and psoriatic arthritis: observations on combination therapy. Br J Dermatol 146:118, 2002.

9. Cauza R, Spak M, Cauza K, Hanusch-Enserer U, Dunky A, Wagner E. Treatment of psoriatic arthritis and psoriasis vulgaris with the tumor necrosis factor inhibitor infliximab. Rheumatol Int 22(6):227, 2002.

10. Antoni C, Dechant C, Hannis-Martin Lorenz PD, Wendler J, Ogilvie A, Lueftl M, Kalden-Nemeth D, Kalden JR, Manger B. Open-label study of infliximab treatment for psoriatic arthritis: clinical and magnetic resonance imaging measurements of reduction of inflammation. Arthritis Rheum 47(5):506, 2002.

11. Mease PJ, Gladman DD, Ritchlin CT, Ruderman EM, Steinfeld SD, Choy EH, Sharp JT, Ory PA, Perdok RJ, Weinberg MA; Adalimumab Effectiveness in Psoriatic Arthritis Trial Study Group.Arthritis Rheum. Adalimumab for the treatment of patients with moderately to severely active psoriatic arthritis: results of a double-blind, randomized, placebo-controlled trial. Arthritis Rheum 52(10):3279-89, 2005.

*Images within this article are from the American College of Rheumatology Slide Collection.

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