2008 04 lecture 2 psoriasiform dermatitis cassarino

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    PSORIASIFORM DERMATITISDavid Cassarino, MD, PhD

    UCLA Department of Pathology & Laboratory

    Medicine

    LASOP Meeting April 2008

    Histology showed psoriasiform epidermal acanthosis with

    parakeratosis, focal hypogranulosis, minimal spongiosis, andexocytosis of scattered lymphocytes

    What is your histologic diagnosis and what special

    studies should be done?

    DIAGNOSIS:

    MYCOSIS FUNGOIDES/LARGE

    PLAQUE PARAPSORIASIS

    Psoriasiform pattern: often mimics chronicspong derm or psoriasis, both clinically and

    histologically

    Clues: look for epidermotropism, cytologic

    atypia of lymphocytes, lining up oflymphocytes along basal epidermis, andPautriers microabscesses (~30%)

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    CD2, CD3,

    CD4+

    CD5, CD7,

    CD8-

    LARGE PLAQUE

    PARAPSORIASIS Somewhat controversial entity, now accepted as a

    variant of MF

    Clinically, presents as large erythematous patches

    and plaques

    Often progresses to poikilodermatous lesions

    Histology: mild psoriasiform hyperplasia with

    spongiosis and few atypical lymphocytes Small plaque parapsoriasis (digitate dermatosis)

    unrelated, and not considered variant of MF

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    PSORIASIFORM DERMATITIS

    DIFFERENTIAL DIAGNOSIS:

    1. Psoriasis

    2. Subacute/chronic spongiotic dermatitis

    3. Lichen simplex chronicus (LSC) & prurigonodularis

    4. Pityriasis rubra pilaris (PRP)

    5. Syphilis (secondary)

    6. Reiters syndrome

    7. Mycosis fungoides/large plaque parapsoriasis

    1. PSORIASIS: Clinical

    Chronic dermatitis characterized by oftensymmetric, erythemetous plaques with silvery scale,

    variants include guttate and pustular psoriasis

    PSORIASIS: Histology Regular acanthosis, hypogranulosis, parakeratosis with

    neutrophils Increased epidermal turnover (increased basal mits) and

    tortuous papillary dermal capillaries Guttate, early and treated psoriasis exhibit less acanthosis

    and may show significant spongiosis

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    GUTTATE PSORIASIS EARLY OR TREATED PSORIASIS

    2. SUBACUTE AND CHRONICSPONGIOTIC DERMATITIS

    Irregular or uneven hyperplasia w/parakeratosis;spongiosis may be minimal

    Almost any spongiotic dermatitis in subacute tochronic phase

    PITYRIASIS ROSEA (PR) Common dermatosis in young patients, scaly plaque-like

    herald patch shows most psoriasiform features

    Spongiosis and spongiotic vesicles, mounds ofparakeratosis, RBC extravasation

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    3. LICHEN SIMPLEX CHRONICUS(LSC) AND PRURIGO

    NODULARIS

    Hyperkeratosis, irregular acanthosis, hypergranulosis,

    papillary dermal fibrosis and chronic inflammation

    4. PITYRIASIS RUBRA PILARIS Rare dermatosis, classic presentation with

    erythroderma, hykeratotic patches and plaques with

    follicular plugging

    Histology shows psoriasiform acanthosis with

    hypergranulosis and alternating hyperkeratosis and

    parakeratosis; follicular plugging

    Lack of neutrophils and suprapapillary thinning

    5. SYPHILIS (SECONDARY)

    Erythematous and scaly papules and nodules, often

    on palms and soles, but may be anywhere on thebody, including scalp and mucosal sites

    Often marked epidermal acanthosis andneutrophilic infiltrate with plasma cells

    Organisms may be difficult to find; use silverstains and/or anti-spirochetal antibody

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    6. REITERSSYNDROME

    Clinical: classic triad of

    urethritis, uveitis andarthritis, with

    mucocutaneous lesions

    Crusted erythematous to

    pustular papules andplaques on feet, genitalia,

    buttocks, and scalp

    Histology shows psoriasiform hyperplasia with

    parakeratosis and numerous neutrophils, often

    forming pustules

    May be indistinguishable from pustular psoriasis