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Clinical features of specific dermatoses of pregnancy

Clinical features of specific dermatoses of pregnancy
  Atopic eruption of pregnancy Polymorphic eruption of pregnancy Pemphigoid gestationis Intrahepatic cholestasis of pregnancy
Time of onset 75% of cases before third trimester. Last weeks of pregnancy or immediately postpartum. Last trimester or postpartum. Late pregnancy.
Pregnancy Not relevant. First. Not relevant. Not relevant.
Clinical features

20% of patients suffer from an exacerbation of pre-existing atopic dermatitis with a typical clinical picture.

80% will experience atopic skin changes for the first time ever or after a long remission (ie, after childhood eczema), with two main features: (1) E-type: Widespread, eczematous changes affecting typical atopic sites, such as face, neck, upper chest, and the flexural surfaces of the extremities; and (2) P-type: Small, erythematous P-type disseminated on trunk and limbs and typical prurigo nodules, mostly located on the shins and arms.
Urticarial papules and plaques arise from striae distensae usually on the abdomen, characteristically sparing the umbilical region. After 1 or 2 days, the lesions also spread to the thighs and the buttocks and may become frankly polymorphous, showing vesicles (but never blisters), a nonurticated erythema, targetoid lesion, and E-type. Urticarial papules and plaques with usually tense blisters with typical periumbilical involvement and spreading to the trunk and the extremities. Pruritus and exclusively secondary skin lesions (excoriations, prurigo). Total serum bile acid levels >11 mmol/L.
Diagnostic tests None required. None required. Biopsy for histology and DIF and/or serum ELISA for BP180 antibodies. Total bile acids; liver function tests; consider hepatitis serology.
Maternal prognosis Unimpaired; common development of nipple and hand eczema after delivery. Unimpaired. Exacerbations and remissions during pregnancy, flare-up in 75% after delivery, with resolution within weeks to months. May recur with menstruation and hormonal contraception. Risk for gallstones and intra/postpartum hemorrhage.
Recurrence in subsequent pregnancies Yes. No. Yes, often with earlier onset and more severe course. Yes.
Fetal prognosis Unaffected, but there is a higher risk of developing atopic skin changes later on. Unaffected. No cutaneous involvement of the newborn. Increase for small-for-date and premature babies. 10% of newborns develop mild skin lesions that resolve spontaneously within days to weeks. Increased risk of prematurity (19 to 60%), intrapartal fetal distress (22 to 33%), and stillbirths (1 to 2%).
DIF: direct immunofluorescence; ELISA: enzyme-linked immunosorbent assay; BP180: bullous pemphigoid antigen 180.
From: Massone C, Cerroni L, Heidrun N, et al. Histopathological Diagnosis of Atopic Eruption of Pregnancy and Polymorphic Eruption of Pregnancy: A Study on 41 Cases. Am J Dermatopathol 2014; 36:812. DOI: 10.1097/DAD.0000000000000067. Copyright © 2014 International Society of Dermatopathology. Adapted with permission from Wolters Kluwer Health. Unauthorized reproduction of this material is prohibited.
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