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Atopic dermatitis | AD |
Atopic eruption of pregnancy | AEP |
Estrogen receptor | ER |
Intrahepatic cholestasis of pregnancy | ICP |
Malignant melanoma | MM |
Pemphigoid gestationis | PG |
Polymorphic eruption of pregnancy | PEP |
Prurigo of pregnancy | PP |
Pruritic folliculitis of pregnancy | PFP |
Psoralen with ultraviolet light A | PUVA |
Ultraviolet light B | UVB |
This chapter reviews the physiologic skin changes induced by pregnancy, along with preexisting skin diseases and tumors, and outlines the diagnosis and treatment of melanoma, pruritus, and specific dermatoses of pregnancy. Common skin conditions discussed in the text are defined in Table 56.1 .
Condition | Description |
---|---|
Pseudoacanthosis nigricans | Hyperpigmentation of the skin folds and neck that mimic acanthosis nigricans |
Dermal melanocytosis | Clusters of melanocytes abnormally located in the dermis that result in ill-defined bluish-gray patches |
Vulvar melanosis | Irregularly distributed patches of pigmentation on the vulva |
Pregnancy-associated hyperkeratosis of the nipple | Focal hyperkeratosis, at times with wartlike papules, of the apex of the nipple |
Miliaria | Sweat retention that reflects obstruction of eccrine sweat ducts |
Hyperhidrosis | Skin disorder characterized by increased sweat secretion |
Dyshidrosis | Recurrent vesicular eruption of palms and soles |
Fox-Fordyce disease | Chronic pruritic disorder of the apocrine glands characterized by blockage of the apocrine duct and sweat retention |
Onycholysis | Detachment of the nail plate from the nail bed |
Subungual hyperkeratosis | Deposition of keratinous material on the distal nail beds |
Palmoplantar pompholyx eczema | See dyshidrosis above (former name for pompholyx) |
Acne conglobata | Variant of acne vulgaris characterized by severe eruptive nodulocystic lesions without systemic manifestations |
Pemphigus vulgaris | Autoimmune bullous disorder of the skin and oral mucosa produced by antidesmoglein-3 antibodies that cause intraepidermal acantholysis |
Pemphigus vegetans | Variant of pemphigus vulgaris characterized by pustules that form fungoid vegetations or papillomatous proliferations |
Pemphigus foliaceus | Autoimmune bullous skin disorder produced by antidesmoglein-3 antibodies that cause subcorneal acantholysis |
Spitz nevi | Seen predominantly in children or young adults and characterized by prominent epithelioid and/or spindled melanocytes that can have atypical features |
The human skin undergoes substantial changes during pregnancy, which are induced by the combined effect of endocrine, metabolic, mechanical, and blood flow alterations. Although they may prompt cosmetic complaints, such physiologic changes are not associated with risks to the mother or fetus and can be expected to resolve or improve postpartum ( Box 56.1 ). However, some changes, such as melasma, varicosities, and pregnancy-associated hyperkeratosis of the nipple, may persist postpartum.
Hyperpigmentation
Melasma
Jaundice
Pseudoacanthotic changes
Dermal melanocytosis
Hyperkeratosis of the nipple
Vulvar melanosis
Hirsutism
Postpartum telogen effluvium
Postpartum male-pattern alopecia
Diffuse hair thinning (late pregnancy)
Subungual hyperkeratosis
Distal onycholysis
Transverse grooving
Brittleness and softening
Increased eccrine function
Increased sebaceous function
Decreased apocrine function
Striae
Skin tags (molluscum fibrosum gravidarum)
Spider telangiectasias
Pyogenic granuloma (granuloma gravidarum)
Palmar erythema
Nonpitting edema
Severe labial edema
Varicosities
Vasomotor instability
Gingival hyperemia
Hemorrhoids
Gingivitis
Chadwick sign
Goodell sign
Mild forms of localized or generalized hyperpigmentation occur to some extent in up to 90% of pregnant women and are most noticeable in the areolae, nipples, genital skin, axillae, and inner thighs. Familiar examples include the darkening of the linea alba (linea nigra) and periareolar skin. Melasma, also termed chloasma or mask of pregnancy, refers to the facial hyperpigmentation reported in up to 70% of pregnant women. Hyperpigmented, symmetric, poorly demarcated patches are commonly seen on the malar areas (malar pattern) and are often distributed over the entire central face ( centrofacial pattern ; Fig. 56.1 ). In 16% of cases, hyperpigmentation occurs on the ramus of the mandible (mandibular pattern). Melasma results from melanin deposition in the epidermis (70%), dermal macrophages (10% to 15%), or both (20%). It is likely secondary to the hormonal changes of gestation with increased expression of α-melanocyte–stimulating hormone. Melasma is typically exacerbated by exposure to ultraviolet and visible light. Hyperpigmentation is often more pronounced in brunettes and women with more melanocytes than in women with lighter baseline skin tone; the use of a broad-spectrum sunscreen with a high sun protection factor during pregnancy may decrease the severity of hyperpigmentation.
Melasma usually resolves postpartum but may recur in subsequent pregnancies or with the use of oral contraceptives. Troublesome, persistent melasma can be treated postpartum with topical hydroquinone, with or without a topical retinoid, and a mild topical steroid. Strict sun protection with mineral sunblock containing zinc or titanium dioxide must be used during and after treatment. Despite treatment postpartum, melasma persists in approximately 30% of patients, especially in women with the dermal or mixed subtypes in which the deeper level of pigmentation results in decreased efficacy of topical agents. Combination therapies including laser treatment and chemical peels may be effective in resistant cases. There have been no reports of adverse fetal effects from laser skin treatment during pregnancy. Most laser experts agree that laser radiation does not penetrate through the skin into deeper soft tissues, therefore it should not affect the fetus or the placenta. Still, because of potential liability issues, most dermatologists and plastic surgeons prefer not to perform laser procedures during gestation.
Uncommon pigmentary patterns such as pseudoacanthosis nigricans, dermal melanocytosis, vulvar melanosis, and verrucous areolar hyperpigmentation can also be seen in pregnancy (see Box 56.1 ). Postinflammatory hyperpigmentation secondary to specific dermatoses of pregnancy (see the section “ Specific Dermatoses of Pregnancy ”) is also common in women with more highly pigmented skin types.
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