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Inflammatory and Glandular Skin Disease in Pregnancy
Abstract A switch from cell-mediated to humoral immunity (Th 1 to Th 2 shift) during gestation plays a key role in placental immune tolerance. As a result, skin diseases that are Th 2-mediated often worsen while skin diseases that are Th 1-mediated often improve during gestation. Also, due to fluctu...
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Published in: | Clinics in dermatology 2016-05, Vol.34 (3), p.335-343 |
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creator | Yang, Catherine S., MD Teeple, Mary, MD Muglia, Jennie, MD Robinson-Bostom, Leslie, MD |
description | Abstract A switch from cell-mediated to humoral immunity (Th 1 to Th 2 shift) during gestation plays a key role in placental immune tolerance. As a result, skin diseases that are Th 2-mediated often worsen while skin diseases that are Th 1-mediated often improve during gestation. Also, due to fluctuations in glandular activity, skin diseases involving sebaceous and eccrine glands may flare, while those involving apocrine glands may improve during pregnancy. Despite these trends, inflammatory and glandular skin diseases do not always follow the predicted pattern, and courses are often diverse. We review the gestational course of inflammatory skin diseases, such as atopic dermatitis (atopic eruption of pregnancy), psoriasis, impetigo herpetiformis, urticaria, erythema annulare centrifugum, pityriasis rosea, sarcoidosis, Sweet syndrome, and erythema nodosum, as well as glandular skin diseases, including acne vulgaris, acne rosacea, perioral dermatitis, hidradenitis suppurativa, Fox-Fordyce disease, hyperhidrosis, and miliaria. For each of the above diseases, we discuss the pathogenesis, clinical presentation, and management with special consideration for maternal and fetal safety. |
doi_str_mv | 10.1016/j.clindermatol.2016.02.005 |
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As a result, skin diseases that are Th 2-mediated often worsen while skin diseases that are Th 1-mediated often improve during gestation. Also, due to fluctuations in glandular activity, skin diseases involving sebaceous and eccrine glands may flare, while those involving apocrine glands may improve during pregnancy. Despite these trends, inflammatory and glandular skin diseases do not always follow the predicted pattern, and courses are often diverse. We review the gestational course of inflammatory skin diseases, such as atopic dermatitis (atopic eruption of pregnancy), psoriasis, impetigo herpetiformis, urticaria, erythema annulare centrifugum, pityriasis rosea, sarcoidosis, Sweet syndrome, and erythema nodosum, as well as glandular skin diseases, including acne vulgaris, acne rosacea, perioral dermatitis, hidradenitis suppurativa, Fox-Fordyce disease, hyperhidrosis, and miliaria. For each of the above diseases, we discuss the pathogenesis, clinical presentation, and management with special consideration for maternal and fetal safety.</description><identifier>ISSN: 0738-081X</identifier><identifier>EISSN: 1879-1131</identifier><identifier>DOI: 10.1016/j.clindermatol.2016.02.005</identifier><identifier>PMID: 27265071</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Acne Vulgaris - drug therapy ; Acne Vulgaris - etiology ; Dermatitis, Atopic - diagnosis ; Dermatitis, Atopic - drug therapy ; Dermatitis, Perioral - etiology ; Dermatology ; Erythema Nodosum - diagnosis ; Female ; Fox-Fordyce Disease - therapy ; Hidradenitis Suppurativa - therapy ; Humans ; Pityriasis Rosea - diagnosis ; Pityriasis Rosea - etiology ; Pregnancy ; Pregnancy Complications - diagnosis ; Pregnancy Complications - etiology ; Pregnancy Complications - therapy ; Psoriasis - complications ; Psoriasis - therapy ; Remission, Spontaneous ; Rosacea - therapy ; Sarcoidosis - complications ; Sarcoidosis - drug therapy ; Skin Diseases - diagnosis ; Skin Diseases - etiology ; Skin Diseases - therapy ; Sweet Syndrome - diagnosis ; Symptom Flare Up ; Urticaria - drug therapy</subject><ispartof>Clinics in dermatology, 2016-05, Vol.34 (3), p.335-343</ispartof><rights>2016 Elsevier Inc.</rights><rights>Copyright © 2016 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c435t-390ff8c05aac0622e250e131737937ae9a96028fabbb85568f464094f1bc7e993</citedby><cites>FETCH-LOGICAL-c435t-390ff8c05aac0622e250e131737937ae9a96028fabbb85568f464094f1bc7e993</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27265071$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Catherine S., MD</creatorcontrib><creatorcontrib>Teeple, Mary, MD</creatorcontrib><creatorcontrib>Muglia, Jennie, MD</creatorcontrib><creatorcontrib>Robinson-Bostom, Leslie, MD</creatorcontrib><title>Inflammatory and Glandular Skin Disease in Pregnancy</title><title>Clinics in dermatology</title><addtitle>Clin Dermatol</addtitle><description>Abstract A switch from cell-mediated to humoral immunity (Th 1 to Th 2 shift) during gestation plays a key role in placental immune tolerance. As a result, skin diseases that are Th 2-mediated often worsen while skin diseases that are Th 1-mediated often improve during gestation. Also, due to fluctuations in glandular activity, skin diseases involving sebaceous and eccrine glands may flare, while those involving apocrine glands may improve during pregnancy. Despite these trends, inflammatory and glandular skin diseases do not always follow the predicted pattern, and courses are often diverse. We review the gestational course of inflammatory skin diseases, such as atopic dermatitis (atopic eruption of pregnancy), psoriasis, impetigo herpetiformis, urticaria, erythema annulare centrifugum, pityriasis rosea, sarcoidosis, Sweet syndrome, and erythema nodosum, as well as glandular skin diseases, including acne vulgaris, acne rosacea, perioral dermatitis, hidradenitis suppurativa, Fox-Fordyce disease, hyperhidrosis, and miliaria. For each of the above diseases, we discuss the pathogenesis, clinical presentation, and management with special consideration for maternal and fetal safety.</description><subject>Acne Vulgaris - drug therapy</subject><subject>Acne Vulgaris - etiology</subject><subject>Dermatitis, Atopic - diagnosis</subject><subject>Dermatitis, Atopic - drug therapy</subject><subject>Dermatitis, Perioral - etiology</subject><subject>Dermatology</subject><subject>Erythema Nodosum - diagnosis</subject><subject>Female</subject><subject>Fox-Fordyce Disease - therapy</subject><subject>Hidradenitis Suppurativa - therapy</subject><subject>Humans</subject><subject>Pityriasis Rosea - diagnosis</subject><subject>Pityriasis Rosea - etiology</subject><subject>Pregnancy</subject><subject>Pregnancy Complications - diagnosis</subject><subject>Pregnancy Complications - etiology</subject><subject>Pregnancy Complications - therapy</subject><subject>Psoriasis - complications</subject><subject>Psoriasis - therapy</subject><subject>Remission, Spontaneous</subject><subject>Rosacea - therapy</subject><subject>Sarcoidosis - complications</subject><subject>Sarcoidosis - drug therapy</subject><subject>Skin Diseases - diagnosis</subject><subject>Skin Diseases - etiology</subject><subject>Skin Diseases - therapy</subject><subject>Sweet Syndrome - diagnosis</subject><subject>Symptom Flare Up</subject><subject>Urticaria - drug therapy</subject><issn>0738-081X</issn><issn>1879-1131</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkUlLxTAUhYMo-hz-ghRXblpvhjaNC0GcQVBQwV1I01vJs4Mmr8L796Y8FXHlJhPnnHvzXUIOKGQUaHE0z2zr-hp9ZxZDm7H4lgHLAPI1MqOlVCmlnK6TGUheplDS5y2yHcIcAAQUsEm2mGRFDpLOiLjpm9Z0U5JfJqavk6s2rmNrfPLw6vrk3AU0AZN4vPf40pveLnfJRmPagHtf-w55urx4PLtOb--ubs5Ob1MreL5IuYKmKS3kxlgoGEOWA8bOJJeKS4PKqAJY2Ziqqso8L8pGFAKUaGhlJSrFd8jhKvfND-8jhoXuXLDYxg5xGIOmUgkheS5YlB6vpNYPIXhs9Jt3nfFLTUFP1PRc_6amJ2oamI7Uonn_q85YdVj_WL8xRcH5SoDxtx8OvQ7WYW-xdh7tQteD-1-dkz8xk9RZ077iEsN8GH0feWqqQzToh2l-0_howQFYvH0CrcaYTw</recordid><startdate>20160501</startdate><enddate>20160501</enddate><creator>Yang, Catherine S., MD</creator><creator>Teeple, Mary, MD</creator><creator>Muglia, Jennie, MD</creator><creator>Robinson-Bostom, Leslie, MD</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20160501</creationdate><title>Inflammatory and Glandular Skin Disease in Pregnancy</title><author>Yang, Catherine S., MD ; Teeple, Mary, MD ; Muglia, Jennie, MD ; Robinson-Bostom, Leslie, MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-390ff8c05aac0622e250e131737937ae9a96028fabbb85568f464094f1bc7e993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acne Vulgaris - drug therapy</topic><topic>Acne Vulgaris - etiology</topic><topic>Dermatitis, Atopic - diagnosis</topic><topic>Dermatitis, Atopic - drug therapy</topic><topic>Dermatitis, Perioral - etiology</topic><topic>Dermatology</topic><topic>Erythema Nodosum - diagnosis</topic><topic>Female</topic><topic>Fox-Fordyce Disease - therapy</topic><topic>Hidradenitis Suppurativa - therapy</topic><topic>Humans</topic><topic>Pityriasis Rosea - diagnosis</topic><topic>Pityriasis Rosea - etiology</topic><topic>Pregnancy</topic><topic>Pregnancy Complications - diagnosis</topic><topic>Pregnancy Complications - etiology</topic><topic>Pregnancy Complications - therapy</topic><topic>Psoriasis - complications</topic><topic>Psoriasis - therapy</topic><topic>Remission, Spontaneous</topic><topic>Rosacea - therapy</topic><topic>Sarcoidosis - complications</topic><topic>Sarcoidosis - drug therapy</topic><topic>Skin Diseases - diagnosis</topic><topic>Skin Diseases - etiology</topic><topic>Skin Diseases - therapy</topic><topic>Sweet Syndrome - diagnosis</topic><topic>Symptom Flare Up</topic><topic>Urticaria - drug therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Catherine S., MD</creatorcontrib><creatorcontrib>Teeple, Mary, MD</creatorcontrib><creatorcontrib>Muglia, Jennie, MD</creatorcontrib><creatorcontrib>Robinson-Bostom, Leslie, MD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinics in dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Catherine S., MD</au><au>Teeple, Mary, MD</au><au>Muglia, Jennie, MD</au><au>Robinson-Bostom, Leslie, MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inflammatory and Glandular Skin Disease in Pregnancy</atitle><jtitle>Clinics in dermatology</jtitle><addtitle>Clin Dermatol</addtitle><date>2016-05-01</date><risdate>2016</risdate><volume>34</volume><issue>3</issue><spage>335</spage><epage>343</epage><pages>335-343</pages><issn>0738-081X</issn><eissn>1879-1131</eissn><abstract>Abstract A switch from cell-mediated to humoral immunity (Th 1 to Th 2 shift) during gestation plays a key role in placental immune tolerance. As a result, skin diseases that are Th 2-mediated often worsen while skin diseases that are Th 1-mediated often improve during gestation. Also, due to fluctuations in glandular activity, skin diseases involving sebaceous and eccrine glands may flare, while those involving apocrine glands may improve during pregnancy. Despite these trends, inflammatory and glandular skin diseases do not always follow the predicted pattern, and courses are often diverse. We review the gestational course of inflammatory skin diseases, such as atopic dermatitis (atopic eruption of pregnancy), psoriasis, impetigo herpetiformis, urticaria, erythema annulare centrifugum, pityriasis rosea, sarcoidosis, Sweet syndrome, and erythema nodosum, as well as glandular skin diseases, including acne vulgaris, acne rosacea, perioral dermatitis, hidradenitis suppurativa, Fox-Fordyce disease, hyperhidrosis, and miliaria. For each of the above diseases, we discuss the pathogenesis, clinical presentation, and management with special consideration for maternal and fetal safety.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>27265071</pmid><doi>10.1016/j.clindermatol.2016.02.005</doi><tpages>9</tpages></addata></record> |
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subjects | Acne Vulgaris - drug therapy Acne Vulgaris - etiology Dermatitis, Atopic - diagnosis Dermatitis, Atopic - drug therapy Dermatitis, Perioral - etiology Dermatology Erythema Nodosum - diagnosis Female Fox-Fordyce Disease - therapy Hidradenitis Suppurativa - therapy Humans Pityriasis Rosea - diagnosis Pityriasis Rosea - etiology Pregnancy Pregnancy Complications - diagnosis Pregnancy Complications - etiology Pregnancy Complications - therapy Psoriasis - complications Psoriasis - therapy Remission, Spontaneous Rosacea - therapy Sarcoidosis - complications Sarcoidosis - drug therapy Skin Diseases - diagnosis Skin Diseases - etiology Skin Diseases - therapy Sweet Syndrome - diagnosis Symptom Flare Up Urticaria - drug therapy |
title | Inflammatory and Glandular Skin Disease in Pregnancy |
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