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Christine Ahn MD
Carl Allen DDS, MSD
Brandon Ayres MD
Howard P. Baden MD
Robert Baran MD
Keira Barr MD
Gregory J. Basura MD, Ph.D
Donald Belsito MD
Jeffrey D. Bernhard MD
Jesse Berry MD
Victor Blanco MD
Benjamin R. Bohaty MD
William Bonnez MD
Sarah Brenner MD
Robert A. Briggaman MD
Robert Brodell MD
Roman Bronfenbrener MD
Walter Brooks MD
William Buckley MD
Philip Bulterys MD, PhD (candidate)
Susan Burgin MD
Sonya Burton MD
Sean P. Bush MD, FACEP
Jeffrey Callen MD
Scott Camazine MD
Michael Cardwell
Shelley D. Cathcart MD
Robert Chalmers MD, MRCP, FRCP
Chia-Yu Chu MD, PhD
Flavio Ciferri MD
Maria Rosa Cordisco MD
Noah Craft MD, PhD
John T. Crissey MD
Harold E. Cross MD, PhD
Charles E. Crutchfield III MD
Adriana Cruz MD
Donna Culton MD, PhD
Bart J. Currie MBBS, FRACP, DTM&H
Chicky Dadlani MD
Alexander Dane DO
C. Ralph Daniel III MD
Thomas Darling MD, PhD
William Delaney MD
Damian P. DiCostanzo MD
Ncoza Dlova MD
James Earls MD
Libby Edwards MD
Melissa K. Egge MD
Charles N. Ellis MD
Rachel Ellis MD
David Elpern MD
Nancy Esterly MD
Stephen Estes MD
E. Dale Everett MD
Janet Fairley MD
David Feingold MD
Jennifer J. Findeis-Hosey MD
Benjamin Fisher MD
Henry Foong MBBS, FRCP
David Foster MD, MPH
Brian D. Foy PhD
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Sunir J. Garg MD, FACS
Kevin J. Geary MD
Lowell Goldsmith MD, MPH
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Bernardo Gontijo MD, PhD
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David G. Hicks MD
Sarah Hocker DO
Ryan J. Hoefen MD, PhD
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Robert Kalb MD
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Carl Krucke
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Sue Lewis-Jones FRCP, FRCPCH
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Organizations
Am. Journal of Trop. Med & Hygiene
Armed Forces Pest Management Board
Blackwell Publishing
Bugwood Network
Centers For Disease Control and Prevention
Centro Internacional de Entrenamiento e Investigaciones Mèdicas (CIDEIM)
Dermatology Online Journal
East Carolina University (ECU), Division of Dermatology
Psoriatic arthritis (PsA) is an inflammatory arthritis that occurs in up to 30% of psoriatics. It is typically considered a seronegative inflammatory arthritis, ie, without detectable rheumatoid factor. About 15% of patients develop PsA before skin psoriasis is present.
The etiology of the disease is multifactorial, with both genetic and environmental factors. PsA affects men and women equally and is predominantly seen in white individuals, similar to psoriasis.
Symptoms:
Pain, stiffness in affected joints, with joint stiffness present for >30 minutes in the morning (after waking) or after prolonged inactivity. Improves with activity (versus osteoarthritis / degenerative joint disease, which typically worsens with activity).
With axial involvement – Inflammatory back pain and stiffness that improve with activity; night symptoms can cause waking from sleep; decreased range of motion of the axial spine and neck over time.
Tender / painful; swelling at entheses (sites of tendon insertion into bone).
Tendonitis / tenosynovitis
Ocular inflammation may lead to scleral erythema, dry eye / foreign body sensation, or uveitis with potential visual disturbance and pain.
Signs:
Tender, painful, swollen joints with possible erythema, effusion, and warmth noted in more actively inflamed joints.
Dactylitis – Inflammation and swelling of the entire digit including metacarpophalangeal (MCP) through proximal / distal interphalangeal (PIP/DIP) joints and intervening soft tissue, giving a "sausage digit" appearance.
Enthesitis – Inflammation at tendinous insertion into bone, with tenderness.
Note: Patients do not necessarily fit into any one pattern and may have features of several throughout the course of illness.
Risk factors:
Patients with nail, scalp, and inverse (intertriginous) psoriatic skin disease have a higher risk of developing PsA.
Several genetic risk markers (HLA associations) are associated with development and variable prognosis in PsA.
Timeline:
Progression to PsA among patients with psoriasis has been reported to occur at a rate of around 2% per year.
Episodic flares of the disease in addition to chronic, baseline joint inflammation.
Joint erosion / damage may accrue over time, with the potential for development of functional impairments.
Accepted CASPAR criteria (ClASsification criteria for Psoriatic ARthritis) are routinely used to classify patients with PsA for trials and studies and may also aid in diagnosis of patients. These include the presence of psoriasis skin lesions, a family history of psoriasis, nail lesions, dactylitis, absence of rheumatoid factor, and periarticular bone formation on radiographs, with a point system to grade each feature (refer to CASPAR criteria; see References).
Codes
ICD10CM: L40.59 – Other psoriatic arthropathy
SNOMEDCT: 33339001 – Psoriasis with arthropathy
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Differential Diagnosis & Pitfalls
Rheumatoid arthritis (RA) – Symmetric polyarthritis; presentation, clinical course, and radiologic and serologic features are distinct from PsA (may be rheumatoid factor and anti-cyclic citrullinated peptide [anti-CCP] positive). The absence of DIP involvement, asymmetry, axial involvement, dactylitis, skin psoriasis, psoriatic nail disease, and radiography may help distinguish RA from PsA.
Gout – History of podagra, joint fluid from arthrocentesis demonstrating monosodium urate crystal should help to differentiate; gout and psoriasis / PsA may co-exist, however.
Pseudogout – Chondrocalcinosis on radiographs and calcium pyrophosphate crystals on joint fluid examination.
Reactive arthritis – Would not expect the presence of psoriasis skin disease; associated with other symptoms such as preceding genitourinary symptoms, diarrheal illness, and skin findings such as keratoderma blenorrhagicum.
Ankylosing spondylitis – To be distinguished from axial disease in PsA; PsA tends to have an asymmetric involvement of the sacroiliac joints, formation of "jug-handle" nonmarginal syndesmophytes that are asymmetrically located, skip lesions along the spine (cervical > lumbar involvement).
Fibromyalgia – Diffuse widespread pain involving "tender point" soft tissue areas. Synovitis is not a component of fibromyalgia. It is important to distinguish enthesitis (inflammation at sites of tendon insertion into bone) from the tender points of fibromyalgia, eg, near the lateral epicondyle of the upper extremity. Fatigue may be common to both conditions. Stiffness may be reported but does not improve with activity.
