Principles of Ambulatory Medicine, 7th Edition
Chapter 113
Diagnoses and Treatment of Skin Disorders
- Elizabeth Whitmore
Skin Examination and Definitions
The primary goal of the skin examination is to define the morphology (appearance) of the lesion and the extent of disease. The former allows the correct diagnosis to be made and the latter aids in the determination of prognosis and treatment. The examination of the lesion or eruption of concern is ideally followed by a complete skin examination. This latter may reveal findings helpful in diagnosis or may expose a previously unrecognized skin disease. The examination is most easily done in a systematic fashion, starting at the top with the scalp, face, and oral mucosa and then moving to the anterior then posterior aspect of the body. Good lighting is essential.
Mastering the definitions of commonly used dermatologic terms should aid in both diagnosis and communication with other physicians,
- Atrophy, Thinning of the epidermis or dermis causing fine wrinkling or depression of the skin (e.g., discoid lupus erythematosus, steroid-induced atrophy, normal aging).
- Bulla, A blister, similar to a vesicle but larger than 5 mm in diameter, filled with serous or serosanguinous fluid (e.g., friction blister, bullous pemphigoid).
- Burrow, A linear thread-like elevation of the skin, typically a few millimeters long (pathognomonic for scabies).
- Comedone, A plugged pilosebaceous follicle (e.g., a closed comedone or “whitehead” seen in acne).
- Crust, Yellowish-brown sticky debris consisting of dried serum, scale, and usually bacteria (e.g., impetigo, impetiginized eczema).
- Cyst, A circumscribed, firm, yet often slightly compressible, spherical lesion, fixed in the dermis (e.g., epidermal inclusion cyst).
- Erosion, A focal loss of a portion of the epidermis, nonscarring (e.g., candidiasis in the inframammary crease with a moist surface, impetigo).
- Excoriation, A self-inflicted disruption of the epidermis.
- Fissure, A vertical cut extending into the dermis (e.g., angular cheilitis or “cracks at the angle of the mouth” caused by Candida, salivary enzymes, or a vitamin deficiency).
- Hive, See Wheal.
- Hyperkeratotic, Heaped up or stacked scale (e.g., hypertrophic actinic keratosis, squamous cell carcinoma, wart).
- Maculeor macular, A flat color change (e.g., freckle, café-au-lait spot, junctional nevus, or “flat brown mole”).
- Morphology, Shape of the primary lesion (e.g., stellate, linear, round, or diffuse).
- Nodule, A solid lesion up to 2 cm in diameter with an appreciable deep (dermal or subcutaneous) component (e.g., dermatofibroma, nodular melanoma, erythema nodosum, lipoma).
- Papule, An elevated often dome-shaped bump up to 10 mm in diameter, (e.g., intradermal nevus or “skin-colored mole,” molluscum contagiosum).
- Plaque, A flat-topped elevated area of skin, the surface area of which is much greater than the thickness (e.g., psoriasis, cutaneous T-cell lymphoma, or “mycosis fungoides”).
- Pustule, A circumscribed lesion visibly filled with purulent material (e.g., folliculitis, acne pustule, pustular psoriasis).
P.1882
- Scale, Surface alteration resulting in a flaky surface, caused by abnormal proliferation or desquamation of the outermost epidermal layer, the stratum corneum (e.g., psoriasis, seborrheic dermatitis, tinea).
- Sclerosis, Scar-like induration (e.g., systemic sclerosis, localized scleroderma or “morphea”).
- Secondary changes, Changes that occur as a result of the natural development or external manipulation of the primary lesion.
- Telangiectasia, A dilated superficial capillary or venule; may be linear, spider-like, or mat-like (e.g., starburst leg telangiectasias, telangiectasias in a basal cell carcinoma or in an area of steroid- or lupus-induced atrophy).
- Tumor, A large mass, greater than 2 cm in diameter, with significant thickness (e.g., neglected squamous cell carcinoma, cutaneous lymphoma).
- Ulcer, A loss of skin extending into the dermis that always heals with scarring (any loss that penetrates the dermal–epidermal junction scars; e.g., venous stasis ulcer, pyoderma gangrenosum).
- Urticarial, Adjective describing plaques that are edematous, erythematous, or blanched (e.g., urticaria or “wheals” or “hives,” urticarial vasculitis, Sweet syndrome, or “acute febrile neutrophilic dermatosis”).
- Vesicle, A blister up to 5 mm in diameter filled with serous or serosanguinous fluid (e.g., herpes simplex infection, vesicular hand dermatitis).
- Wheal or hive, An erythematous or blanched edematous plaque with no surface change, present for no more than 24 hours(urticaria, by definition).
Based on the morphology of the observed skin changes, a differential diagnosis or diagnosis of the skin lesion or eruption may be made, which may or may not require biopsy for confirmation. Table 113.1 provides a summary of selected disorders categorized by morphology and pathophysiology of disease. Those conditions that are common, diagnostically difficult, and therapeutically complicated are discussed in detail in the chapters that follow.
|
FIGURE 113.1. Multiple seborrheic keratoses (upper back). “Stuck-on,” sharply circumscribed, tan to deep brown, finely papillated to verrucous flat-topped papules and plaques. (See color image.)
|
Topical Therapeutics
Topical Corticosteroids
Topical corticosteroids are categorized based on the degree of vasoconstriction produced upon application to the skin, with superpotent products producing the most vasoconstriction. Vasoconstriction correlates well with biologic activity, therapeutic efficacy, and undesirable side effects. The latter include local effects such as acne, rosacea, striae, atrophy (cigarette paper-like wrinkling of the skin), and increased risk of fungal infection. In addition, systemic effects, as evidenced by hypothalamic–pituitary–adrenal axis suppression, may occur with the use of potent corticosteroids over large areas.
Although there are over 20 different preparations, it is easiest to become familiar with and prescribe just four different corticosteroids based on the strength needed. All topical corticosteroids except 0.5% and 1% hydrocortisone are by prescription only. Examples include,
- Low potency, hydrocortisone 1% or 2.5%;
- Mid-potency, triamcinolone (acetonide) 0.1%;
- High potency, fluocinonide;
- Super potency, clobetasol (propionate).
Generally, only low-potency preparations should be used on the face and in areas of thin skin (e.g., folds and genitalia). Unless a drying effect is desired, ointments are preferred as they aid most in restoring the skin barrier.
An accurate estimation of the amount of corticosteroid needed is important because of the cost of these preparations. Dermatoses are generally treated until clear, and the application is repeated for recurrences. Acute and subacute dermatitis generally clear in 1 to 2 weeks; chronic dermatitis may require chronic intermittent therapy. One gram covers a 10 × 10-cm area, 2 g covers the hands, head, face, or anogenital area; 3 g covers the anterior or posterior trunk or an arm; 4 g covers a single lower extremity; and 30 g covers the entire skin surface. Therefore, for a 1-week two times daily application for each of these areas, 30 g, 45 g, 60 g, and 420 g, respectively, should be prescribed. Most corticosteroids come in 15-, 30-, 60-, and 120-g tubes. Additionally, 1-pound jars of hydrocortisone or 0.1% triamcinolone cream or ointment may be requested.
Emollients (Skin Moisturizers)
Very simply, emollients may be classified as oil in water (mostly water), water in oil (mostly oil), and oil preparations. Because the purpose of emollients is to trap moisture after hydrating the skin with a warm bath or shower, occlusive substances are most efficient. Unfortunately, not all patients are amenable to putting petroleum jelly on their skin one or two times a day. A good compromise is Eucerin Original lotion or Nivea moisturizing cream (water in oil). Still lighter oil-in-water moisturizers include Lubriderm, Moisturel, Curel, Vaseline Intensive Care, and Keri lotions. Formulations that contain α-hydroxy acids aid in normal desquamation of the skin, making it softer and smoother (e.g., Am-Lacten, Eucerin Plus, and AquaGlycolic lotion). Although they are useful, patients who have “sensitive” or irritated skin may experience stinging and develop an irritant contact dermatitis from the added α-hydroxy acid. A good rule to follow is that if it burns or stings, it should not be used.
Topical Antifungal Agents
Several topical antifungal agents are available (see Chapter 117). Polyenes such as nystatin (cream, ointment, and
P.1883
P.1884
P.1885
P.1886
P.1887
P.1888
P.1889
powder, by prescription) are used only for candida. In contrast, topicals that may be used for both candida and dermatophytes includeimidazoles, such as clotrimazole (Mycelex OTC and Lotrimin AF cream, lotion, and solution, all over the counter), sulconazole (Exelderm 1% cream or solution, by prescription), and ketoconazole (Nizoral cream or 2% shampoo, by prescription), which are fungistatic. Finally, for dermatophyte but not Candida infections, allylamines, such as terbinafine, may be used and are fungicidal (Lamisil cream, lotion, or spray, over-the-counter).
TABLE 113.1 Selected Skin Disorders Based on Morphology
|
Disorder
|
Description
|
Common Presentation
|
Possible Systemic Associations
|
Risks
|
Recommendations
|
Differential Diagnosis
|
Key to Diagnosis
|
HYPOPIGMENTED AND DEPIGMENTED MACULES AND PATCHES
|
Vitiligo
|
Depigmented patches caused by loss of melanocytes, immunologically mediated; favors periorificial and “tip” areas
|
New-onset stark white skin around the eyes, lips, fingertips, and penis
|
Autoimmune thyroiditis, pernicious anemia, Addison disease, diabetes mellitus
|
Skin cancer
|
Sunscreens
|
Postinflammatory hypopigmentation, albinism, chemical leukoderma
|
Acquired depigmentation without a history of exposure to phenolic compounds which may cause depigmentation
|
Idiopathic guttate hypomelanosis, “snowflakes”
|
Hypopigmented 3- to 8-mm macules caused by focal loss of melanin production
|
Asymptomatic whitish macules on the pretibial and extensor forearm surfaces
|
None
|
None
|
Sunscreens
|
Vitiligo
|
Small macules of hypopigmentation on sun-damaged skin
|
Tinea versicolor
|
See Chapter 117
|
Halo nevus
|
Symmetric depigmented halo around a nevus
|
Small symmetric halo surrounding an evenly pigmented brown papule in a young individual
|
In adults and those with a history of melanoma, suspect melanloma or associated metastatic melanoma
|
Misdiagnosis
|
If halo is asymmetric or nevus is abnormal by the ABCDs, biopsy to rule out melanoma
|
Melanoma with regression, dysplastic nevus
|
Symmetric mole with symmetric halo of depigmentation
|
HYPERPIGMENTED MACULES AND PATCHES
|
Junctional nevus
|
Light to dark macule of uniform shape and brown color, may develop from early childhood to early thirties; formed by nests of melanocytes at the dermal- epidermal junction
|
2- to 6-mm sharply circumscribed, evenly pigmented, brown macule
|
None
|
People with >40 to 50 nevi have an increased risk of melanoma
|
Monthly self examinations; intermittent physican examination
|
Lentigo simplex, freckle
|
May be difficult to clinically distinguish from lentigo and freckles; however, all three are benign
|
Solar lentigo
|
“Liver spot”; brown, 2-mm to 2-cm macule occurring on a background of chronic sun-damaged skin
|
Multiple hyperpigmented 3- to 8-mm brown macules on the face and dorsal hands
|
None
|
None
|
Prevention: sunscreen use; elective treatment: cryosurgery, laser surgery, hydroquinone creams
|
Lentigo simplex, lentigo maligna (i.e., melanoma in situ)
|
Homogeneous pigmentation on background of sun-damaged skin
|
HYPERPIGMENTED MACULES AND PATCHES
|
Café-au-lait spot
|
Evenly pigmented, light to medium brown, 1- to several cm macule; noted at birth or in early childhood
|
Tan brown macule
|
Neurofibromatosis: Presence of six café-au-lait spots greater than 1.5 cm often with axillary freckling; may have tumors, e.g., CNS neoplasms, pheochromocytoma Albright syndrome: large, unilateral, pigmented macule with an irregular border, polyostotic fibrous dysplasia and precocious puberty Tuberous sclerosis: cafe-au-lait spots, seizures, adenoma sebaceum (perinasal skin colored papules), and ash leaf macules (hypopigmented macules)
|
|
Lightening or removal may be attempted with laser surgery
|
Junctional nevus
|
Macular pigmentation with no surface change (i.e., no epidermal alteration)
|
Melasma
|
Irregular tan to brown pigmentation; favors cheeks, forehead and upper lip
|
Patchy brown discoloration on central forehead and cheeks
|
Pregnancy and exogenous estrogens
|
N/A
|
Sunscreens and avoidance of sun exposure, hydroquinone cream, or elective laser surgery
|
Hydroquinone induced in “pseudo-ochronosis”
|
Female, facial location, intensifies in the summer
|
Xanthelasma
|
See Chapter 82
|
Xanthoma
|
See Chapter 82
|
PAPULES
|
Warts, tumors
|
See Chapter 117
|
Compound nevus
|
Tan to dark brown, 2- to 6-mm dome-shaped papule, formed by nests of melanocytes, both at the dermal epidermal junction and in the dermis
|
Stable brown “mole”
|
None
|
None
|
Patient self- examinations for changes, as with all nevi; biopsy if diagnosis is in question
|
Melanoma, intradermal nevus, dermatofibroma, neurofibroma
|
Soft, circumscribed, symmetric, evenly colored papule
|
Intradermal nevus
|
Skin color to light brown, generally 2- to 6-mm fleshy papule; consists of nests of melanocytes confined to the dermis
|
Dome shaped, skin-colored papule
|
None
|
None
|
Biopsy if diagnosis is in question
|
Amelanotic melanoma, dermatofibroma, neurofibroma
|
Soft, circumscribed, symmetric, skin colored papule
|
Seborrheic keratosis (Fig. 113.1)
|
“Stuck on” appearing tan, yellowish-brown to black-brown plaque with a friable, fine papulated, or smooth surface studded with tiny white flecks of keratin; caused by local proliferation of the epidermis; common after age 30
|
Tan to dark brown finely papulated “stuck on” flat topped papules over the trunk
|
“Sudden” eruption of many inflamed seborrheic keratoses; may herald a malignancy, most often with adenocarcinoma
|
None
|
Liquid nitrogen cryosurgery or curettage may be used on pruritic or troublesome lesions; biopsy, never destroy, if diagnosis is in question
|
Wart, squamous cell carcinoma, basal cell carcinoma, melanoma
|
Characteristic “stuck on” appearance
|
Cherry angioma
|
“Cherry red” 0.5- to 6-mm dome-shaped nonblanching papules which favor the trunk, formed by dilated capillaries; common after age 30
|
Minute to 4-mm red to purple dome-shaped papules
|
Hereditary hemorrhagic telangiectasia: autosomal dominant, punctate telangiectasias on the oral mucosa and fingers +/- AV malformations in the GI tract, lungs, and CNS CREST: sclerodactyly with punctate and matlike telangiectasias on the face and fingers
|
None
|
Cauterize if traumatized or if desired for cosmesis
|
Hemangioma
|
Characteristic size and cherry red appearance
|
Dermatofibroma
|
Smooth, circumscribed, 3- to 10-mm papule in the skin; feels like a “pea in the skin”; composed of fibroblasts
|
Small, brownish ill-defined macule with underlying papule
|
|
None
|
Biopsy if diagnosis is in question
|
Nodular melanoma, nevus
|
Characteristic “pea-like” dermal papule without surface change
|
Condyloma acuminatum
|
See Chapter 117
|
Molluscum contagiosum
|
See Chapter 117
|
Basal cell carcinoma
|
See Chapter 114
|
Squamous cell carcinoma
|
See Chapter 114
|
Kaposi sarcoma
|
See Chapter 39
|
PLAQUES
|
Psoriasis
|
See Chapter 116
|
Seborrheic dermatitis
|
See Chapter 116
|
Atopic dermatitis
|
See Chapter 116
|
Nummular dermatitis
|
See Chapter 116
|
Secondary syphilis
|
See Chapter 37
|
Contact dermatitis
|
See Chapter 116
|
Tinea
|
See Chapter 117
|
Xanthoma
|
See Chapter 82
|
PLAQUES
|
Pityriasis rosea
|
Self-limited eruption, lasting several weeks, initial lesion: herald patch; >1-cm erythematous oval plaque with fine peripheral scale, usually on the chest, followed in 7–14 days by an eruption of smaller plaques over the trunk; pruritus
|
1- to 3-cm oval plaque, followed by a shower of 25–100 similar 3- to 15-mm papules and plaques on the trunk, with the long axes of the lesions oriented along the skin lines in a “Christmas tree” pattern
|
None
|
None
|
If pruritic, midpotency topical corticosteroids; if extremely pruritic, consider phototherapy
|
Secondary syphilis, primary HIV exanthem, tinea corporis, tinea versicolor, psoriasis
|
Herald patch, negative test for syphilis
|
Pityriasis alba
|
A mild form of dermatitis, in young patients; hypopigmented, slightly scaly, up to several cm macules or minimally elevated plaques; occasionally pruritic
|
Asymptomatic scaly patches over the arms and legs
|
More common in patients with atopy
|
None
|
Emollients, hydrocortisone; phototherapy
|
Tinea versicolor, hypopigmented mycosis fungoides, sarcoidosis
|
May be difficult to exclude other diagnoses without further evaluation (i.e., KOH +/- biopsy)
|
Mycosis fungoides
|
Cutaneous T-cell lymphoma most often affects patients older than age 40; however, any age may be affected; erythematous to brawny patches, plaques, or tumors; may assume bizarre irregular shapes; asymptomatic or pruritic
|
Several-year history of scaly reddish plaques gradually increasing in number over the trunk
|
None
|
Although a lymphoma, evidence of systemic involvement with simple testing is usually absent unless the disease progresses; poor prognosis is associated with greater than 10% body surface area involvement, tumor, and lymphadenopathy (the latter requires biopsy to determine reactive vs. neoplastic)
|
Treatment varies with the stage of the disease and age of patient; PUVA, electron beam, topical nitrogen mustard, interferon-γ, observation
|
Parapsoriasis, psoriasis, sarcoidosis, pityriasis alba
|
Biopsy required
|
Erythema nodosum
|
Hypersensitivity reaction to some antigen, erythematous, tender nodules most often on the pretibial legs; develop in crops and involute over 2–3 weeks, resolve with a local bruise, never suppurate and drain; caused by a localized inflammatory infiltrate in the septum surrounding fat lobules
|
Acute onset of erythematous nodules over the pretibial area associated with mild arthralgias
|
More common associations include streptococcal infection, vaginal candidiasis, tuberculosis, viral hepatitis, coccidioidomycosis, histoplasmosis, lymphogranuloma venereum, Yersinia enterocolitica; inflammatory bowel disease, or reaction to sulfonamides, barbiturates, various antibiotics, salicylates, oral contraceptives, or pregnancy
|
None
|
Evaluation to exclude possible associations; review of Rx and OTC medications, throat culture, ASO titer, chest radiograph, PPD; complete viral hepatitis screen; additional workup based on clinical findings; reassess chronic disease with a search for “occult infection” (dental, sinus, gallbladder, other gastrointestional, etc.)
|
Other forms of panniculitis and polyarteritis nodosa
|
Tender nodules on the pretibial legs that resolve over a few weeks without ever ulcerating
|
Lipoma
|
Benign fatty tumor, often solitary, on the trunk
|
Asymptomatic rubbery nodule, movable under the skin
|
None
|
None
|
Excision if desired or diagnosis is in question
|
Cyst, neurofibroma, soft tissue malignancies
|
Soft nodule, freely movable under the skin
|
CNS, central nervous system; AV, atrioventricular; GI, gastrointestinal; CREST, calcinosis, Raynaud phenomenon, esophageal motility disorders, sclerodactyly, and telangiectasia; HIV, human immunodeficiency virus; OTC, over the counter; ASO, antistreptolysin; PPD, purified protein derivative of tuberculin.
|
|
Creams are applied one or two times per day and should be continued for 2 weeks after clinical resolution of the infection, and as needed for recurrences. Nizoral shampoo is intended for treatment of scalp seborrheic dermatitis, but it may also be used for tinea versicolor. For the former, it is lathered on the scalp and rinsed after 3 minutes, two or three times per week; for the latter, it is applied to the trunk from the neck to the waistline, left 5 minutes, then lathered and rinsed, daily for 10 to 14 days, with a single application repeated every 1 to 2 weeks to prevent recurrences.
Compresses and Baths
Compresses are used to dry and débride localized areas of acute dermatitis, characterized by moist, erythematous, edematous papules, plaques, and vesicles or bullae with serous discharge. Several solutions dry by precipitating protein (Burow aluminum acetate solution, 1,20 dilution; Domeboro aluminum sulfate and calcium acetate solution, 1,20 dilution; Aveeno Colloidal Oatmeal Packet). Some act as germicidals (silver nitrate 0.1% to 0.5% solution, acetic acid 1% to 5% solution). All, including saline made by adding 2 teaspoons salt per 1 L of water, promote drying through evaporation and remove devitalized tissue through physical softening, allowing mechanical removal upon lifting the damp (“wet to damp”) or dry (“wet to dry”) dressing.
Compresses may be gauze or cotton sheeting. For the latter, a clean sheet should be cut and folded into six to eight layers to approximate the area of affected skin. This is immersed in the soaking solution and squeezed just short of dripping wet. It is placed on the site for 15 to 30 minutes, three or four times per day, and is rewetted every 15 minutes for a “wet to damp” dressing.
When more than one third of the body surface area is affected by acute dermatitis or impetiginization, compresses are not only impractical but may cause hypothermia. Warm baths are used instead. Preferred drying and soothing additives include Aveeno Oatmeal Packet, sodium bicarbonate (baking soda, 3 cups), hydrolyzed starch (Lint, 4 cups mixed with water in a large mixing bowl and then added to the bath water), and a mix of half of each of the bicarbonate and starch mixtures.
Baths are also useful for generalized dry pruritic dermatoses such as atopic dermatitis, generalized psoriasis, morbilliform drug eruptions, and erythroderma. Instead of drying additives, oil (one eighth cup bath oil or Aveeno Oilated Oatmeal Packet) is added to the bath water to help trap moisture in the skin. Patients must be warned about oil making the bathtub slippery and should be advised to purchase secure bath mats for the tub and for the floor outside the tub. Unsteady or frail patients should not use bath oil. Baths should be taken three or four times a day for 20 minutes and a heavy moisturizer (e.g., Vaseline jelly, Aquaphor ointment, Eucerin Original Lotion) must be reapplied immediately after lightly patting dry, leaving some moisture on the skin.
Skin Biopsy
Skin biopsy for histologic examination of the skin is required to confirm the diagnosis of many skin conditions. Types of biopsies that may be used include punch, ellipse, and shave. They may be incisional (sampling a portion of the lesion) or excisional (removing the entire lesion). Skin biopsy is a simple and invaluable procedure that may be easily mastered with the help of a skilled instructor and practice.
Specific References
Ackerman BA, Kerl H, Sanchez J. A clinical atlas of 101 common skin diseases with histopathologic correlation. New York: Ardor Scribendi, 2000.
Fitzpatrick TP, Johnson RA, Wolff K, et al. Color atlas and synopsis of clinical dermatology. 3rd ed. New York: McGraw-Hill, 1997. A concise disease discussion, with excellent photographs.
Habib TP, Quitadamo MJ, Campbell JL, et al. Skin disease: diagnosis and treatment. St. Louis: Mosby, 2001.An excellent text of clinical diagnosis and therapy.
Kazin, RA, Lowitt NR, Lowitt MH. Update in dermatology. Ann Intern Med 2001;135:124. Highlights 10 articles of interest to the generalist.
Lamberg SI. The little black book of dermatology. Malden, MA: Blackwell, 2000. A comprehensive clinical handbook organized by chief complaint, body part affected, or associated condition.
Lookingbill DP, Marks JG Jr. Principals of dermatology. 3rd ed. Philadelphia, PA: WB Saunders, 2000.
Websites
American Cancer Society website; also telephone 800-ACS-2345). Available at: http://www.cancer.org. An excellent resource for educational materials on skin cancer for physicians and patients.
American Academy of Dermatology website. Available at: http://www.aad.org.
National Psoriasis Foundation website. Available at: http://www.psoriasis.org.
P.1890
University of Iowa. Available at: http://www.tray.dermatology.uiowa.edu/home.html. University of Iowa Website with over 300 clinical photographs; also resource for dermatology patient support group.)
Available at: http://www.med.jhu.edu/peds/dermatlas. Last accessed DATE. Also see review: Lamberg L. Internet dermatology atlas aids physicians and parents. JAMA 2001;25:2065.
If you find an error or have any questions, please email us at admin@doctorlib.org. Thank you!