Chapter 49 Rashes and Skin Lesions
Diagnostic Approach
ETIOLOGY
Surveys indicate that 10% to 20% of visits by pediatric patients to outpatient facilities are associated with a dermatologic problem as the primary reason, a secondary concern, or an incidental finding. Dermatology is a visual discipline and with experience, most common problems and many subtle variations can be recognized. An atlas, text, consultant, or other resource can be used to aid in identification of uncommon problems. This chapter’s approach to the diagnosis of skin problems in children is based on the morphology of the patient’s lesions. The appropriate history and a careful description of what you see will overcome a major obstacle to diagnosis.
EVALUATION
Although dermatology relies heavily on recognition of skin lesions, an appropriate, problem-oriented history is the first step in diagnosis. Some questions that may be useful and their rationale are presented in the following sections.
What Should I Ask about the Present Illness?
When did the rash begin? Has it gotten better or worse? Has it occurred in the past?
Conditions such as atopic dermatitis are chronic and recurrent, whereas others such as viral exanthems are acute and self-limited.
Are there associated symptoms?
A generalized erythematous macular eruption associated with fever, nasal congestion, and cough suggests the presence of a viral exanthem. Fever, petechiae, and purpura in an ill-appearing child may indicate a serious bacterial infection such as meningococcemia. Atopic or contact dermatitis and scabies characteristically produce pruritus.
Is the patient using any medications?
The onset of wheals in a child receiving an oral antibiotic might represent urticaria as a manifestation of drug allergy. Lithium can worsen acne, and minocycline may cause hyperpigmentation. Topical therapies also may be relevant to the patient’s problem; neomycin, diphenhydramine, and certain anesthetics may induce a contact dermatitis when applied topically.
Are there factors that worsen or precipitate the rash?
The malar rash of systemic lupus erythematosus is worsened by sun exposure. For many children with atopic dermatitis, reduced humidity during colder months is associated with an exacerbation of disease.
What Does the Family History Add?
Is there a family history of skin disease or other health problems?
In children with atopic dermatitis, often there is a history of atopic disease, including atopic dermatitis, allergic rhinitis, or asthma. If a child is found to have multiple café au lait macules and a diagnosis of neurofibromatosis type 1 is being considered, determining if there are affected first-degree relatives is vital. Whether other family members are similarly affected is relevant when cutaneous infections or infestations are suspected. Impetigo, tinea capitis, scabies, and head lice often are transmitted within families.
Why Is the Social History Important?
Does the patient work after school?
Occupational exposure to greases or oils (e.g., in a fast-food restaurant or car repair shop) may worsen acne.
Has the patient ever been involved in a sexual relationship?
A confidential sexual history may be important. Secondary syphilis and disseminated gonococcal infection, for example, have cutaneous manifestations. Molluscum contagiosum, infestation with pubic lice, and scabies may be transmitted through sexual contact.
How Do I Describe What I See?
Recognizing and describing skin lesions accurately are essential to diagnosis. The first step is to identify the primary lesion, defined as the earliest lesion and the one most characteristic of the disease. Next, it is important to note the distribution, arrangement, and color of primary lesions, along with any secondary change, such as crusting or scaling.
What Are the Types of Primary Lesions?
Flat lesions include macules and patches. A macule is a small, circumscribed area of color change without elevation or depression, such as a café au lait macule. A patch is a large macule, although specific size criteria are lacking.
Elevated lesions may be solid or fluid filled. Solid lesions include papules (< 0.5 cm in diameter), nodules (≥ 0.5 cm in diameter), wheals (a pink, rounded or flat-topped elevation because of edema in the skin), and plaques (plateau-shaped structures often formed by the coalescence of papules). Elevated fluid-filled lesions may be vesicles (< 0.5 cm in diameter and filled with serous fluid), bullae (≥ 0.5 cm in diameter and filled with serous fluid), pustules (< 0.5 cm in diameter and filled with purulent material), and cysts (≥ 0.5 cm in diameter that represent sacs containing fluid or semisolid material).
Depressed lesions include erosions, which reflect superficial loss of epidermis with a moist base, or ulcers, deeper lesions extending into the dermis or below.
Why Is the Distribution of Lesions Important?
Certain disorders have unique patterns of distribution that can be useful for diagnosis. For example, seborrheic dermatitis commonly involves the scalp, eyebrows, and nasolabial folds. Psoriasis also affects the scalp, but lesions are often seen in areas that are traumatized, such as the elbows and knees. Acne is limited to the face, back, and chest, sites of the highest concentrations of pilosebaceous follicles.
How Do I Describe the Color of Skin Lesions?
Although the color of a lesion may be obvious, terms that may be helpful include
Hyperpigmented (tan, brown, or black)
Hypopigmented (pigment is decreased but not entirely absent)
Depigmented (all pigment is absent, as occurs in vitiligo)
When erythematous lesions are observed, it is important to note if they blanch. If red blood cells are within vessels (e.g., as occurs in urticaria), compression of the skin forces the cells into deeper vessels and blanching occurs. However, if the cells are outside vessels, as occurs in forms of vasculitis, blanching will not occur; nonblanching lesions are termed petechiae, purpura, or ecchymoses.
What Are Secondary Changes?
Secondary changes are alterations in the skin that may accompany primary lesions and may be valuable in differential diagnosis.
Crusting represents dried fluid. It is commonly seen following the rupture of vesicles or bullae, as occurs with the “honey-colored” crust of impetigo.
Scaling represents epidermal fragments that are characteristic of several disorders, including fungal infections (e.g., tinea corporis) and psoriasis.
Atrophy is an area of surface depression because of absence of the dermis or subcutaneous fat. Atrophic skin often appears thin and wrinkled.
Lichenification is a thickening of the skin that results from chronic rubbing or scratching (e.g., as occurs in atopic dermatitis); as a result, normal creases appear more prominent.
How Do I Put It All Together?
Once you have identified the primary lesions, along with the distribution, arrangement, color, and secondary changes, your observations can be formulated into one or two sentences. For example, “Erythematous, scaling papules, and plaques are located on the extensor surfaces of the extremities. There is scaling of the scalp and pitting of the nails.” This description assists in differential diagnosis: By identifying scaling papules and plaques, you have placed the patient’s condition into the category of papulosquamous (elevated and scaling) diseases and have eliminated countless other disorders from consideration. In children, the most common papulosquamous disorders are chronic atopic or contact dermatitis, tinea corporis, and pityriasis rosea; less common causes are psoriasis, secondary syphilis, lichen planus, dermatomyositis, and lupus erythematosus. Given the location of the lesions on extensor surfaces and involvement of the scalp and nails, psoriasis becomes a primary consideration.
Tables 49-1 and 49-2 are provided to assist in differential diagnosis based on the morphology of lesions and list the disorders you are most likely to encounter, plus a few less common ones. When the physical findings are unclear, you will need a textbook or atlas of dermatology, a consultant, or another resource.
Table 49-1 Differential Diagnosis of Rashes in Neonates
Elevated Lesions | |
---|---|
Papules | Vesicles or Bullae |
Common | Common |
Erythematous | Erythema toxicum |
Erythema toxicum | Miliaria crystallina |
Miliaria rubra | Sucking blisters |
Acne | Bullous impetigo |
Candidiasis | Herpes simplex virus infection |
Scabies | Uncommon |
White | Incontinentia pigmenti |
Milia | Aplasia cutis congenita |
Yellow | Varicella |
Sebaceous gland hypertrophy | Epidermolysis bullosa |
Skin colored | Bullous ichthyosiform erythroderma |
Epidermal nevus | Pustules |
Skin tags | Common |
Uncommon | Erythema toxicum |
Yellow | Transient neonatal pustular melanosis |
Juvenile xanthogranuloma | Miliaria pustulosa |
Mastocytosis | Herpes simplex virus infection |
Nodules | Folliculitis |
Common | Acne |
Erythematous | Candidiasis |
Hemangioma | Scabies |
Uncommon | Uncommon |
Skin colored | Acropustulosis of infancy |
Condylomata acuminata | |
Dermoid cyst | |
Yellow | |
Mastocytosis | |
Plaques | |
Common | |
Skin colored or yellow | |
Nevus sebaceus | |
Skin colored | |
Epidermal nevus |
Flat Lesions | Depressed Lesions |
---|---|
Macules | Erosions |
Common | Common |
Hypopigmented | Bullous impetigo |
Prehemangioma | Neonatal herpes simplex virus infection |
Postinflammatory hypopigmentation | Staphylococcal scalded skin syndrome |
Hyperpigmented | Uncommon |
Transient neonatal pustular melanosis | Aplasia cutis congenita |
Café au lait macule | Acrodermatitis enteropathica |
Postinflammatory hyperpigmentation | Epidermolysis bullosa |
Congenital melanocytic nevus | Bullous ichthyosiform erythroderma |
Uncommon | |
Hypopigmented | |
Ash leaf macule | |
Patches | |
Common | |
Erythematous | |
Salmon patch (nevus simplex) | |
Hemangioma (early) | |
Port wine stain | |
Atopic dermatitis | |
Seborrheic dermatitis | |
Diaper dermatitis (irritant or seborrheic) | |
Hyperpigmented | |
Mongolian spot | |
Lentigo | |
Uncommon | |
Erythematous | |
Acrodermatitis enteropathica | |
Hyperpigmented | |
Linear and whorled hypermelanosis | |
Hypopigmented | |
Hypomelanosis of Ito | |
Nevus depigmentosus |
Table 49-2 Differential Diagnosis of Rashes in Older Infants, Children, and Adolescents
Elevated Lesions | |
---|---|
Papules without Scaling | Nodules |
Common | Common |
Erythematous | Erythematous |
Viral exanthems | Pyogenic granuloma |
Scarlet fever | Skin colored |
Insect bites | Wart |
Scabies | Callus |
Urticaria | Corn |
Papular urticaria | Epidermal cyst |
Acne | Granuloma annulare |
Early lesions of guttate psoriasis | Uncommon |
Erythema multiforme | Erythematous |
Skin colored | Angiofibroma |
Keratosis pilaris | Skin colored |
Molluscum contagiosum | Neurofibroma |
Flat warts | Yellow |
Hyperpigmented | Mastocytosis |
Nevus (intradermal) | Vesicles or Bullae |
Uncommon | Common |
Yellow | Contact dermatitis |
Mastocytosis | Bullous impetigo |
Plaques without scaling | Varicella |
Common | Herpes simplex virus infection |
Skin colored | Hand, foot, and mouth disease |
Nevus sebaceous | Erythema multiforme |
Epidermal nevus | Uncommon |
Hyperpigmented | Polymorphous light eruption |
Congenital melanocytic nevus | Linear IgA dermatosis |
Papules or Plaques with Scaling (papulosquamous diseases) | Pustules |
Common | Common |
Tinea corporis | Folliculitis |
Pityriasis rosea | Scabies |
Chronic atopic or contact dermatitis | Acne |
Psoriasis | Perioral dermatitis |
Uncommon | Uncommon |
Dermatomyositis | Associated with systemic bacterial infection (e.g., disseminated gonococcal infection) |
Lupus erythematosus | |
Lichen planus |
Flat Lesions | |
---|---|
Macules | Patches |
Common | Common |
Erythematous | Erythematous |
Viral exanthems | Salmon patch (nevus simplex) |
Drug eruptions | Port wine stain |
Hypopigmented | Atopic dermatitis |
Pityriasis alba (postinflammatory hypopigmentation) | Hyperpigmented |
Tinea versicolor | Mongolian spot |
Vitiligo | Becker’s nevus |
Halo nevus | Lentigo |
Hyperpigmented | Uncommon |
Freckles | Erythematous |
Postinflammatory hyperpigmentation | Toxic shock syndrome (diffuse macular erythema) |
Tinea versicolor | Hyperpigmented |
Café au lait macules | Linear and whorled hyperpigmelanosis |
Melanocytic nevus | Incontinentia pigmenti |
Uncommon | |
Hypopigmented | |
Lichen sclerosus et atrophicus | |
Scleroderma | |
Ash leaf macule | |
Piebaldism |
Depressed Lesions | |
---|---|
Erosions | |
Common | |
Bullous impetigo | |
Herpes simplex virus infection | |
Staphylococcal scalded skin syndrome | |
Uncommon | |
Epidermolysis bullosa |
Hair Loss | |
---|---|
Congenital | Acquired |
Localized | Localized |
Nevus sebaceous | Friction alopecia |
Epidermal nevus | Tinea capitis |
Aplasia cutis congenita | Traction alopecia |
Diffuse | Trichotillomania |
Hair shaft abnormalities | Alopecia areata |
Hypothyroidism | Psoriasis |
Secondary syphilis | |
Scleroderma | |
Diffuse | |
Telogen effluvium | |
Chemotherapy | |
Hypothyroidism | |
Acrodermatitis enteropathica |

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