Epidermal and Dermal Lesions
Acanthosis nigricans causes thickened, hyperpigmented skin of the posterior neck,axillae, and groin; it is often associated with obesity and hyperinsulinism.
EPIDERMAL AND DERMAL LESIONS
Acanthosis nigricans causes thickened, hyperpigmented skin of the posterior neck,axillae, and groin; it is often associated with obesity and hyperinsulinism. On rare occasions it is associated with internal malignancy (stomach and other gastrointes-tinal malignancies).
Seborrheic keratoses are benign squamoproliferative neoplasms that are very com-mon in middle-aged and elderly individuals; they may occur on the trunk, head, neck, and the extremities. The lesions are tan to brown coin-shaped plaques that have a granular surface with a “stuck on” appearance, characterized microscopi-cally by basaloid epidermal hyperplasia and “horn cysts” (keratin-filled epidermal pseudocysts). They are usually left untreated, but may be removed if they become irritated or for cosmetic purposes. The sign of Leser-Trélat (paraneoplastic syndrome) is the sudden development of multiple lesions which may accompany an internal malignancy.
Psoriasis is an autoimmune disorder with a clear genetic component that causes increased proliferation and turnover of epidermal keratinocytes; it affects 1% of the U.S. population. The most common form is psoriasis vulgaris. Common sites of involvement include the knees, elbows, and scalp; the classic skin lesion is a well-demarcated erythematous plaque with a silvery scale. Removal of scale results in pinpoint bleeding (Auspitz sign). Nail beds show pitting and discoloration. Psoriasis may be associated with arthritis, enteropathy, and myopathy.
Microscopically, the lesions show epidermal hyperplasia (acanthosis), patchy hyperkeratinization with parakeratosis, uniform elongation and thickening of the rete ridges, thinning of the epidermis over the dermal papillae, and Munro microabscesses.
Treatment is topical steroids and ultraviolet irradiation; severe systemic dis-ease may be treated with methotrexate.
Pemphigus is a rare, potentially fatal autoimmune disorder that is characterized by intraepidermal blister formation. Pemphigus Vulgaris is the most common form. The pathogenesis involves the production of autoantibodies directed against a part of the keratinocyte desmosome called desmoglein 3, resulting in loss of intercellular adhesion (acantholysis) and blister formation. Pemphigus causes mucosal lesions and easily ruptured, flaccid blisters. Oral involvement is common.
- Microscopic examination shows intraepidermal acantholysis; the acantholysis leaves behind a basal layer of keratinocytes, which has a tombstone-like arrangement. Immunofluorescence shows a net-like pattern of IgG staining between the epidermal keratinocytes that create bullae.
- Treatment is with immunosuppression.
Bullous pemphigoid is a relatively common autoimmune disorder of older individu-als characterized by subepidermal blister formation with tense bullae that do not rupture easily. The condition results from production of autoantibodies directed against a part of the keratinocyte hemidesmosome called bullous pemphigoidantigens 1 and 2. Immunofluorescence shows linear deposits of IgG at the dermal-epidermal junction.
Dermatitis herpetiformis is a rare immune disorder that is often associated withceliac sprue; it is characterized by subepidermal blister formation with itchy, grouped vesicles and occasional bullae on the extensor surfaces. Production of IgA antibodies directed against gliadin and other antigens deposit in the tips of the dermal papillae and result in subepidermal blister formation. Routine microscopy shows microabscesses at the tips of the dermal papillae that can lead to eventual subepidermal separation results in blister formation; immunofluorescence shows granular IgA deposits at the tips of the dermal papillae. Dermatitis herpetiformis often responds to a gluten-free diet.
Porphyria cutanea tarda is an acquired and familial disorder of heme synthesis. Patients experience upper extremity blistering secondary to sun exposure and minor trauma. Microscopically, there are subepidermal blisters with minimal inflammation. Dermal vessels are thickened. Direct immunofluorescence shows deposition of immunoglobulins and complement at the epidermal basement membrane and around dermal vessels.
Ichthyosis Vulgaris is a common inherited (autosomal dominant) skin disorder characterized by a thickened stratum corneum with absent stratum granulosum. Onset is in childhood. Patients have hyperkeratotic, dry skin on the trunk and extensor surfaces of limb areas.
Xerosis is a common cause of pruritus and dry skin in the elderly that is due to decreased skin lipids. Cancer patients receiving epidermal growth factor receptor inhibitor are susceptible. Treatment is with emollients.
Eczema is a group of related inflammatory skin diseases characterized by pruritus and epidermal spongiosis (oedema).
- Acute eczema causes a vesicular, erythematous rash.
- Chronic eczema develops following repetitive scratching and is characterized by dry, thickened, hyperkeratotic skin.
- Atopic dermatitis is often inherited. Defects in the keratinocyte barrier are due to mutations in the filaggrin gene (FLG).
- Contact dermatitis can be either allergic-type (poison ivy, nickel in jewellery) or photodermatitis type (such as photosensitivity reaction after tetracycline).
The polymorphous light eruption is the most common idiopathic form of photodermatoses and causes pruritic erythematous macules, papules, plaques, or vesicles on exposure to sunlight. There are dermal oedema and inflammation.
Verrucae (warts) are caused by human papillomavirus. Verruca Vulgaris is the most common type.
Cutaneous lupus erythematosus may be acute (facial butterfly rash), subacute (photosensitive rash on anterior chest, upper back and upper extremities), or chronic (discoid plaques, usually above the neck). Direct immunofluorescence shows deposition of immunoglobulin and complement at the dermal-epidermal junction. Serologies for autoantibodies and clinical correlation help establish the diagnosis.
Erythema multiforme is a hypersensitivity skin reaction to infections (Mycoplasmapneumoniae, herpes simplex) or drugs (sulfonamides, penicillin, barbiturates, phenytoin) characterized by vesicles, bullae, and “targetoid” erythematous lesions. The most severe form is Stevens-Johnson syndrome, which has extensive involvement of skin and mucous membranes.
Pityriasis rosea causes a pruritic rash that starts with an oval-shaped “herald patch” and progresses to a papular eruption of the trunk to produce a “Christmas tree” distribution. It is clinically diagnosed, self-limiting and possibly a viral exanthem.
Granuloma annulare is a chronic inflammatory disorder that causes papules and plaques. Palisaded granulomas are present microscopically. The pathogenesis is immunologic, but most cases occur in healthy patients.
Erythema nodosum causes raised, erythematous, painful nodules of subcutaneous adipose tissue, typically on the anterior shins, which can be associated with granulomatous diseases and streptococcal infection.
An epidermoid cyst is a common benign skin cyst lined with stratified squamous epithelium and filled with keratin debris.